Haplogroup O-M175
Haplogroup O, also known as O-M175, is a human Y-chromosome DNA haplogroup. It is primarily found among populations in Southeast Asia and East Asia. It also is found in various percentages of populations of the Russian Far East, South Asia, Central Asia, Caucasus, Crimea, Ukraine, Iran, Oceania, Madagascar and the Comoros. Haplogroup O is a primary descendant of haplogroup NO-M214.
Haplogroup O-M175 | |
---|---|
Possible time of origin | 41,750 (95% CI 30,597<-> 46,041) years ago[1] 44,700 or 38,300 ybp[2] |
Coalescence age | 33,943 (95% CI 25,124 <-> 37,631) years (Karmin 2022[1]) 35,000 or 30,000 years ago depending on mutation rate[2] |
Possible place of origin | Southeast Asia or East Asia |
Ancestor | NO |
Descendants | Primary: O1 (O-F265); O2 (O-M122) Secondary: O1a (O-M119); O1b (O-M268); O2a (O-M324); O2b (O-F742) |
Defining mutations | M175 (+ numerous other SNPs).[3] |
The O-M175 haplogroup is very common amongst males from East and Southeast Asia. It has two primary branches: O1 (O-F265) and O2 (O-M122). O1 is found at high frequencies amongst males native to Southeast Asia, Taiwan, the Japanese Archipelago, the Korean Peninsula, Madagascar and some populations in southern China and Austroasiatic speakers of India. O2 is found at high levels amongst Han Chinese, Tibeto-Burman populations (including many of those in Yunnan, Tibet, Burma, Northeast India, and Nepal), Manchu, Mongols (especially those who are citizens of the PRC), Koreans, Vietnamese, Filipinos, Thais, Polynesians, Miao people, Hmong, the Naiman tribe of Kazakhs in Kazakhstan,[4] Kazakhs in the southeast of Altai Republic,[5] and Kazakhs in the Ili area of Xinjiang.[6]
Origins
Haplogroup O-M175 is a descendant haplogroup of Haplogroup NO-M214, and first appeared according to different theories either in Southeast Asia (see Rootsi 2006, TMC 1998, Shi 2005, and Bradshaw Foundation) or East Asia (see ISOGG 2012) approximately 40,000 years ago (or between 31,294 and 51,202 years ago according to Karmin et al. 2015).[7][8]
Haplogroup O-M175 is one of NO-M214's two branches. The other is Haplogroup N, which is common throughout North Eurasia.
Distribution
This haplogroup appears in high to moderate frequencies in most populations in both East Asia and Southeast Asia, and it is almost exclusive to that region: It is almost nonexistent in Western Siberia, Western Asia, Europe, most of Africa, India and the Americas, where its presence may be the result of recent migrations. However, certain O subclades do achieve significant frequencies among some populations of Central Asia, South Asia, and Oceania. For example, one study found it at a rate of 65.81% among the Naimans, a tribe in Kazakhstan,[4] even though the rate among Kazakhs in general is believed to be only about 9% (Wells et al. 2001). It has been estimated that 25% of the entire male population of the world carries different subclades of O.[8][9] Karafet et al. (2015) have assigned the Y-DNA of 46.2% (12/26) of a sample of Papuan from Pantar Island to haplogroup NO-M214;[10] considering their location in the Malay Archipelago, all or most of these individuals should belong to haplogroup O-M175.
An association with the spread of Austronesian languages in late antiquity is suggested by significant levels of O-M175 among island populations of the South Pacific and Indian Ocean, including the East African littoral. For example, Haplogroup O-M50 has even been found in Bantu-speaking populations of the Comoros along 6% of O-MSY2.2(xM50),[11] while both O-M50 and O-M95(xM88) occur commonly among the Malagasy people of Madagascar with a combined frequency of 34%.[12][13] O-M175 has been found in 28.1% of Solomon Islanders from Melanesia.[14] 12% of Uyghurs (Wells et al. 2001), 6.8% of Kalmyks[15] (17.1% of Khoshuud, 6.1% of Dörwöd, 3.3% of Torguud, 0% of Buzawa), 6.2% of Altaians (Kharkov et al. 2007), 4.1% of Uzbeks on average but Uzbeks from Bukhara 12.1%, Karakalpaks (Uzbekistan) 11.4%, Sinte (Uzbekistans) 6.7% (Wells et al. 2001) and 4.0% of Buryats.[16] In the Caucasus region it has been found in the Nogais 6%[17] but 5.3% in the Karan Nogais, it is also found in the Dargins of Dargwa speakers at 2.9%.[18] In the Iranic population, it is found in Iranian (Esfahan) at 6.3% (Wells et al. 2001), 8.9% of Tajiks in Afghanistan[19] 4.2% in the Pathans in Pakistan (Firasat 2007) but 1% in Afghanistan, 3.1% in Burusho (Firasat 2007).
Haplogroup O-M175 ranges in various moderate to high frequencies in the ethnic minorities of South Africa. The frequency of this haplogroup is 6.14% in the Cape colored population.[20] 18% in Cape Coloured Muslim, 38% in Cape Indian Muslims and 10% in other Cape Other Muslim.[20] It's found 11.5% in the Réunion Creole.[21] Haplogroup O-M175 had also been found in Latin America and Caribbean as a result of massive Chinese male migration from the 19th century. It was found in the Jamaicans at 3.8,[22] Cubans 1.5%[23]
Haplogroup O-M175 has been found in 88.7% of Asian American. 1.6% in Hispanic American, White Americans 0.5%, and 0.3% in African American.[24] Another study gives 0.5% African American.[25]
Among the sub-branches of haplogroup O-M175 are O-M119(O1a), O-M268(O1b), and O-M122(O2).
O-M175*
A broad survey of Y-chromosome variation among populations of central Eurasia found haplogroup O-M175(xM119,M95,M122) in 31% (14/45) of a sample of Koreans and in smaller percentages of Crimean Tatars (1/22 = 4.5%), Tajiks (1/16 = 6.25% Dushanbe, 1/40 = 2.5% Samarkand), Uyghurs (2/41 = 4.9%), Uzbeks (1/68 = 1.5% Surxondaryo, 1/70 = 1.4% Xorazm), and Kazakhs (1/54 = 1.9%) (Wells et al. 2001). However, nearly all of the purported Korean O-M175(xM119,M95,M122) Y-chromosomes may belong to Haplogroup O-M176,[Note 1] and later studies do not support the finding of O-M175* among similar population samples (Xue 2006, Kim 2011). The reported examples of O-M175(xM119,M95,M122) Y-chromosomes that have been found among these populations might therefore belong to Haplogroup O-M268*(xM95,M176) or Haplogroup O-M176 (O1b2).
A study published in 2013 found O-M175(xM119, M95, M176, M122) Y-DNA in 5.5% (1/18) Iranians from Teheran, 5.4% (2/37) Tajiks from Badakhshan Province of Afghanistan, and 1/97 Mongols from northwest Mongolia, while finding O-M176 only in 1/20 Mongols from northeast Mongolia.[26]
O-F265 (O1)
O1a-M119 and O1b-M268 share a common ancestor, O1-F265 (a.k.a. O-F75) approximately 33,181 (95% CI 24,461 to 36,879) YBP.[1][27] O1-F265, in turn, coalesces to a common ancestor with O2-M122 approximately 33,943 (95% CI 25,124 to 37,631) YBP.[1] Thus, O1-F265 should have existed as a single haplogroup parallel to O2-M122 for a duration of approximately 762 years (or anywhere from 0 to 13,170 years considering the 95% CIs and assuming that the phylogeny is correct) before breaking up into its two extant descendant haplogroups, O1-MSY2.2 and O1b-M268.
O-M119 (O1a)
O-M119 (which was known briefly as O-MSY2.2, until the SNP MSY2.2 was found to be unreliable) is found frequently in Austronesian-speaking people, with a moderate distribution in southern and eastern Chinese and Kra-dai peoples.
O-M268 (O1b)
- O-K18 Naxi[28]
- O-CTS4040
- O-MF56251 Observed sporadically in China (Guangxi,[28][29] Guangdong,[29] Sichuan,[29] Zhejiang,[29] Jiangsu,[29] Beijing[29]), Thailand (Phuan,[30] Yuan,[30] Central Thai[30]), Vietnam (Nùng,[30] Tày[30])
- O-Page59/CTS10887 Found among North Han Chinese (5%), East Han Chinese (4%), South Han Chinese (3%) [31]
- O-F4070
- O-MF106398 Observed sporadically in China (Guangdong, Henan, Hubei, Jiangxi, Sichuan, Zhejiang, Guangxi, Heilongjiang, Jiangsu, Shandong[29])
- O-F779/F993/F3135 China,[29] Vietnam (Lahu[32]), Qatar[33]
- O-MF107014 Observed sporadically in China (Jiangsu, Anhui, Heilongjiang[29])
- O-CTS5160/MF61620 China (Han,[28] mostly Guangdong or Fujian[29])
- O-F2064/F1759 China (Han from Fujian,[28] Shandong[28]), Singapore,[28] Vietnam (Sila,[32] Hanhi,[32] Kinh[32]), Korea[28]
- O-PH2797/CTS1127 China (especially Shandong, Jiangsu, Liaoning, Hebei, Anhui, Beijing, Henan, and Shanghai[29])
- O-Y148532 China (Shandong, Heilongjiang, Liaoning, Jilin, Jiangsu, Shanghai, Sichuan,[28] Beijing, Shaanxi[29]), Afghanistan (Hazara[28])
- O-Y239146/MF31164 Singapore,[28] Taiwan[28]
- O-Y47392/MF17288 China (Zhejiang[28])
- O-BY182144/Y157814 China (Shandong,[28][29] Gansu[29]), Taiwan[34]
- O-PH4822 China (Beijing,[28] Jiangsu[28])
- O-F417/M1654/CTS469 Japan (Tokyo[28])
- O-CTS9996/PF4341 Philippines[34]
- O-F4070
- O-PK4
- O-F838 Found in about 1.4% of Han Chinese[31] (and esp. in Hunan, Chongqing, Jiangxi, Sichuan, Guizhou[29])
- O-M95
- O-CTS350 China (Ningxia, Yunnan, Heilongjiang, Hunan, Shaanxi, Anhui, etc.[29])
- O-M1310
- O-Y172653/Y172877 Found in China (esp. Zhejiang, Fujian, Guangdong, Sichuan, Hunan, Jiangxi, Hubei, Chongqing[29]) and Japan[29]
- O-F1803/M1348 China (Zhejiang, Shandong, Beijing, Guangdong, Hubei, Sichuan, Jiangsu, Shanghai, etc.[29])
- O-ACT721/ACT1038 Found sporadically in China (Zhejiang,[29] Anhui,[29] Hunan,[29] Hainan,[28] Tianjin,[29] Beijing,[29] Liaoning,[28] Heilongjiang[29])
- O-F789/M1283 Found in China (Blang,[36] Palaung,[36] Wa,[36] Dai,[28][37] Yi,[28][37] Naxi), Vietnam, Cambodia, Singapore (Malay), Java, Borneo, Thailand, Laos, Myanmar, Bhutan, Bangladesh, India (Tripura, Ho, Konda Dora, Gond)
- O-M1283* Lao Isan[38]
- O-MF600645 Gansu (Hui,[28] Dongxiang[29]), Sichuan (Chengdu[29]), Hunan (Yiyang[29])
- O-M1368 Singapore[28]
- O-M1361
- O-MF611153 Found sporadically in China (Hunan, Hubei, Chongqing, Guangxi, Jiangxi[29])
- O-A22938 Vietnam (Kinh from Ho Chi Minh City[28]), China (Hong Kong,[28] Qinzhou,[29] Chongqing,[29] Lijiang[29])
- O-Y9322 China (Dai in Xishuangbanna,[28] Yunnan,[29] Chongqing,[29] Guangdong,[29] Sichuan,[29] etc.)
- O-Y9325
- O-Z39485 China (Dai, Yi)[28]
- O-Z39490
- O-Y9033/B426 Laos (Laotian[38]), Thailand (Blang,[38] Khmu,[38] Lawa,[38] Htin,[38] Padaung Karen,[38] Tai Dam,[38] Suay,[38] Khmer,[38] Mon,[38] Lao Isan,[38] Soa,[38] Shan,[38] Phutai,[38] Nyaw,[38] S'gaw Karen,[38] Thai,[38] Khon Mueang[38]), Vietnam (Mang from Mường Tè District,[32] Ede from Krông Buk District and Tuy An District,[32] Kinh from Hoàng Mai District, Gia Lâm District, and Yên Phong District,[32] Thái from Điện Biên Phủ,[32] Giarai from Ayun Pa[32])
- O-Y9325
- O-M1361
- O-F1252
- O-SK1630/F5504 China (esp. Sichuan and Guizhou, accounting for about 0.25% of the entire Chinese population[29])
- O-ACT5802
- O-MF92614
- O-F16061
- O-MF286118 Found in two Han Chinese from Guangdong[29]
- O-F19607
- O-ACT5802
- O-F2924
- O-CTS5854
- O-Z23810
- O-CTS7399
- O-Y85641 China (esp. Shandong, Liaoning, Jilin, Heilongjiang[29])
- O-Y14024/FGC19706 Japan (Tokyo[28])
- O-FGC19713/Y14026 Laos (Laotian in Vientiane and Luang Prabang[38]), Thailand (Tai Dam,[38] Tai Lue,[38] Nyah Kur,[38] Thai,[38] Eastern Lawa[38]), Vietnam (Thái from Bá Thước District and Tủa Chùa District,[32] Hà Nhì from Mường Tè District[32])
- O-FGC19707
- O-MF14427 China (esp. Jiangsu, Gansu, Henan, Shandong, Shanxi, Hebei, Shaanxi[29])
- O-FGC19716 China (Hong Kong,[28] Guangdong,[29] Hunan,[29] Chongqing[29])
- O-FGC19718 China (esp. Fujian, Jiangxi, Hubei, Jiangsu, Guangdong[29]), Philippines (Capiz[28])
- O-Z23849 China (Chongqing Han,[28] Xishuangbanna Dai,[28] Guangxi Zhuang,[28] Guangdong,[28] Shandong,[28] Tianjin[28])
- O-FGC19707
- O-CTS651/CTS10484 Thailand (Tai Khün,[38] Phuan,[38] Tai Lue,[38] Khon Mueang,[38] Eastern Lawa,[38] Lao Isan,[38] Thai[38]), Laos (Laotian in Vientiane[38]), Vietnam (Dao and Nùng from Hoàng Su Phì District,[32] Tày from Krông Pắk District, Hà Quảng District, and Đình Lập District[32])
- O-CTS7399
- O-Z23781 China (Henan[28])
- O-Z23810
- O-M111/M88 Found frequently among Vietnamese,[40][41][32] Tai peoples[42][43][41][32] (Bouyei,[42] Zhuang,[44][45][43] Nùng,[32] Tày,[32] Thái people in Vietnam,[32] Lao,[46] Northeastern Thai,[44] Northern Thai,[47][46] general population of Bangkok[41]), Lachi,[32] Lô Lô,[32] Hani-Akha,[42][41][32] Bunu,[48] She people,[40] Cambodians,[44] Kuy,[36][48] Bru,[48] and Htin,[36] with a moderate distribution among Qiang,[42] Bai,[49] Yi,[43] Bamar,[50] Jingpo,[50] Lahu,[32] Tujia,[44] Han Chinese,[44][42][40][41] Miao,[40][48] Pathen,[32] Yao,[42][40][48][32] Hlai,[44][42] Taiwanese aborigines[12][40][41] (especially Bunun[47][41]), the Philippines,[40][41] Malaysia[40] (Kota Kinabalu[12]), Kalimantan (Banjarmasin[12]), Java,[41] Chamic-speaking peoples (Cham from Bình Thuận,[46] Ede,[32] Jarai[32]), and Kiribati[47]
- O-M111/M88* Northern Thailand (Htin, Lawa), Cambodia (Jarai, Brao, Kachac, Khmer, Lao, Lun), Yunnan (De'ang)[36]
- O-F2524
- O-F2524* Jiangsu[28]
- O-F2346
- O-F2890 Thailand (Khon Mueang,[38] Phuan,[38] Shan,[38] Htin,[38] Tai Dam,[38] Thai,[38] Lawa,[38] Lao Isan,[38] Mon[38]), Vietnam (Kinh from Gia Lâm District,[32] Tày from Lục Yên District[32])
- O-F2890* Ho Chi Minh City[28]
- O-Z24048
- O-F2758 Vietnam (Kinh,[32] Lahu,[32] Dao, Pathen,[32] Tày,[32] Thái,[32] Ede,[32] Giarai[32]), Cambodia (Kuy, Tampuan, Khmer), Thailand (Phutai,[38] Bru,[38] Tai Khün,[38] Phuan,[38] Tai Dam,[38] Shan,[38] Khon Mueang,[38] Mon,[38] Lao Isan,[38] Tai Lue,[38] Htin,[36][38] Lawa,[36] Khmu,[38] Kaleun,[38] Nyaw,[38] Suay,[38] Thai[38]), Laos (Laotian in Luang Prabang[38]), Yunnan (Bulang, De'ang)[36]
- O-F2758* China (Miao,[28] Hunan[28])
- O-Z24083
- O-Z24083* Ho Chi Minh City (Kinh)
- O-Z24089
- O-SK1627/Z24091 Vietnam (Lô Lô from Mèo Vạc District,[32] La Chí and Nùng from Hoàng Su Phì District,[32] Hà Nhì from Mường Tè District,[32] Tày from Chợ Đồn District and Đăk Mil District,[32] Ede from Ea Kar District,[32] Kinh from Nghĩa Hưng District[32]), Thailand (Soa,[38] Saek,[38] Phutai,[38] Suay,[38] Tai Dam,[38] S'gaw Karen,[38] Nyah Kur,[38] Khmer,[38] Lawa,[38] Lao Isan,[38] Mon,[38] Thai[38]), Laos (Laotian in Vientiane[38])
- O-Z24091* China (Hebei,[28] Xishuangbanna Dai[28]), Vietnam (Kinh from Ho Chi Minh City[28])
- O-Y26364
- O-Y26364* Thailand (Phutai from Sakon Nakhon Province[38][28])
- O-Y26370 China (Tujia[28]), Vietnam (Kinh from Ho Chi Minh City[28])
- O-F923
- O-SK1627/Z24091 Vietnam (Lô Lô from Mèo Vạc District,[32] La Chí and Nùng from Hoàng Su Phì District,[32] Hà Nhì from Mường Tè District,[32] Tày from Chợ Đồn District and Đăk Mil District,[32] Ede from Ea Kar District,[32] Kinh from Nghĩa Hưng District[32]), Thailand (Soa,[38] Saek,[38] Phutai,[38] Suay,[38] Tai Dam,[38] S'gaw Karen,[38] Nyah Kur,[38] Khmer,[38] Lawa,[38] Lao Isan,[38] Mon,[38] Thai[38]), Laos (Laotian in Vientiane[38])
- O-F2890 Thailand (Khon Mueang,[38] Phuan,[38] Shan,[38] Htin,[38] Tai Dam,[38] Thai,[38] Lawa,[38] Lao Isan,[38] Mon[38]), Vietnam (Kinh from Gia Lâm District,[32] Tày from Lục Yên District[32])
- O-CTS5854
- O-SK1630/F5504 China (esp. Sichuan and Guizhou, accounting for about 0.25% of the entire Chinese population[29])
- O-CTS4040
- O-M176
- O-K4: Found frequently among Koreans and with a moderate distribution among Japanese, Ryukyuans, Daurs, Evenks, Hezhe, Manchus, and Sibe. Also found sporadically (<1%) among Han Chinese, Hui, Micronesians, Mongols, Thais, Uyghurs, Vietnamese, etc.
- O-47z: Found frequently among Japanese and Ryukyuans and with a moderate distribution among Koreans. Found sporadically (<1%) among Manchus, Mongols, Han Chinese, Hui, Tujia, Vietnamese, etc.
O-M122 (O2)
Found frequently among populations of East Asia, Southeast Asia, and culturally Austronesian regions of Oceania, with a moderate distribution in Central Asia (Shi 2005).
- O-M122
- O-CTS1754 East & Southeast Asia
- O-M324
- O-L465
- O-CTS727
- O-F915
- O-CTS3709
- O-JST002611/CTS2483
- O-CTS2483* China,[34] Japan,[34] Philippines[34]
- O-CTS10573 Beijing,[51] Sichuan,[51] Henan,[51] Jiangsu[51]
- O-F18
- O-CTS498 China,[28] Japan (Tokyo)[28]
- O-F449 Azerbaijan[34]
- O-F117
- O-F117* Fujian[28]
- O-F11
- O-F11* Gansu,[28] Japanese[28]
- O-F930 Beijing,[28] Armenia,[28] Inner Mongolia,[51] Hebei,[51] Shaanxi,[51] Shandong,[51] Zhejiang,[51] Hubei[51]
- O-F2685 Beijing, Shanghai, Fujian, Guangdong[51]
- O-BY169374
- O-F539 Beijing, Shanghai, Jiangsu, Zhejiang, Jiangxi, Guangdong, Yunnan[51]
- O-CTS12877
- O-Y29837
- O-BY36917 Japan[34]
- O-F4062 Beijing, Shanghai, Guangdong, Jiangsu, Shandong, Shaanxi, Chongqing, Heilongjiang, Liaoning, Henan, Hubei, Hunan, Zhejiang[51]
- O-Y15976 China, Japan,[34] Korea, Pakistan, Vietnam
- O-FGC54474
- O-F971 Beijing, Shanghai, Hubei, Guangdong[51]
- O-F632
- O-F632* Beijing[28]
- O-F16340 Zhejiang[28]
- O-F133 China, Bulgaria[34]
- O-CTS727
- O-P201
- O-M188
- O-M188* Korea[34]
- O-CTS800
- O-CTS445
- O-CTS201 Korea[34]
- O-M159 China (about 0.79% of the national male population[52]), Taiwan, Cambodia, Malaysia, Singapore[34]
- O-FTA21663/O-MF22947 China (Heilongjiang,[28][29] Inner Mongolia,[28][29] Zhejiang,[29] Shanghai,[29] Henan,[29] Hebei,[29] etc.; accounts for about 0.06% of the male population in China at present[53]), Saudi Arabia (al-Qaṣīm[28])
- O-CTS3994
- O-MF18110/FGC50590 China (esp. Guangdong, Zhejiang, Hunan, Shandong, and Guangxi[29])
- O-MF109844
- O-FGC50661 China (esp. Jiangsu and Hunan[29])
- O-MF56709
- O-FGC50643/MF15475 China (Shandong,[29] Hebei,[29] Hubei,[29] Shanxi,[28][29] Anhui,[29] Jiangsu,[29] etc.)
- O-MF56474 China (Jiangsu, Anhui, Jilin, Shandong, etc.[29])
- O-FGC50649
- O-Y169670/O-MF14256 China (esp. Jiangsu,[28][29] Shandong,[29] Zhejiang,[29] and Shanghai[29])
- O-MF50824
- O-MF14135/O-Z12303 China (currently accounts for about 0.44% of the total male population[55])
- O-MF238642
- O-MF37094 China (Zhejiang,[29] Jiangsu[29])
- O-Y169696/O-MF15693 China (Jiangsu,[28][29] Fufeng County,[29] Beijing,[29] Tangshan,[29] Feidong County,[29] Chifeng,[29] Xi County,[29] Min County,[29] Laizhou,[29] Rushan,[29] Harbin,[29] Yanji,[29] Dancheng County[29])
- O-MF18577/O-MF18626 China (currently accounts for about 0.23% of all males in China, especially in Jiangsu [1.08%], Shanghai [0.69%], Ningxia [0.39%], Shandong [0.38%], Anhui [0.33%], Heilongjiang [0.32%], Zhejiang [0.31%], and Jilin [0.26%][56]), Kazakhstan,[57] Thailand[57]
- O-MF238642
- O-FGC50558 Japan,[34] Korea[34]
- O-Y169670/O-MF14256 China (esp. Jiangsu,[28][29] Shandong,[29] Zhejiang,[29] and Shanghai[29])
- O-M159 China (about 0.79% of the national male population[52]), Taiwan, Cambodia, Malaysia, Singapore[34]
- O-M7 Found frequently among human remains associated with the Neolithic Daxi culture[58] and modern Hmong–Mien, Katuic, and Bahnaric peoples,[48] with a moderate distribution among Han Chinese (Xue 2006), Buyei (Xue 2006), Bai (Wen 2004), Mosuo (Wen 2004), Tibetans (Wen 2004), Qiang (Xue 2006), Oroqen (Xue 2006), Tujia (Su 2000), Thai (Su 2000), Orang Asli (Su 2000), western Indonesians (Su 2000 and Kayser 2008), Malaysians (Kayser 2008), Vietnamese (Kayser 2008), and Atayal (Su 2000).
- O-MF106687 China (Jinghu District,[29] etc.)
- O-Z25245
- O-MF9858/O-Z6157 China (approximately 0.08% of all males in present-day China[59]), Thailand (Central Thai in Central Thailand[38][30])
- O-Y26422
- O-F1276
- O-F1863
- O-MF107102 China (Tongchuan District[29])
- O-MF56735 China (Haiyan County, Suzhou, Wuxi, Shanghai, etc.[29])
- O-MF36531 China (Han in Yanping District[29])
- O-Y13816
- O-MF109664 China (Kazakh in Minqin County,[30] Kazakh in Tacheng City,[29] Han in Zizhong County,[29] Han in Furong District[29])
- O-MF36502 Guangdong (Kaiping, Yangjiang, Foshan, Lianjiang, etc.[29])
- O-Y13816
- O-F1134
- O-MF35799/O-Y94171 Thailand (Mon in Central Thailand[38][30]), China (observed sporadically in Pingyang County, Yunan County, Siming District, Longyao County, Shanwei, etc.[29])
- O-F1262/O-Y173492 China[28][57] (accounts for about 0.15% of the male population in China at present and is relatively concentrated in Zhejiang, Taiwan, Anhui, Jiangxi, etc.[60]; also observed in individuals from Zhenjiang,[30] Hejian,[30] and Langfang[30])
- O-FT303223/O-MF106843/O-F15314/O-F20756 China[57] (Changsha,[29] Chancheng District,[29] Wanzhou District,[29] Chaoyang District,[29] Dongying,[29] Chifeng,[29] Liaoyuan,[29] Harbin,[29] Han in Zhengzhou,[30] Dai in Xishuangbanna[28]), Thailand[57] (Khon Mueang in Northern Thailand,[38][30] Black Tai in Loei Province[38][30])
- O-Z25288/O-Z25293 Vietnam[57] (Kinh in Ho Chi Minh City,[28][30] Hanoi,[30] Nam Dinh,[30] and Lao Cai,[30] Giarai in Gia Lai,[30] Tày in Thai Nguyen[30])
- O-CTS6489
- O-MF106428/O-Y94472/O-FTB23660 Thailand[57] (Phayao,[28] Phutai, Lao Isan, Tai Lue, Phuan, Shan, Khon Mueang/Tai Yuan, Khmer, Mon[30]), Vietnam[57] (Tày in Lào Cai[30]), China (Dai in Xishuangbanna,[28] Achang in Yunnan;[30] accounts for about 0.05% of all males in China at present, mainly distributed in Guangxi and Guangdong[61])
- O-F1275 Guangxi (Dushan 4-1 ca. 7024 - 6643 BCE[57])
- O-MF15199/O-FTA25885
- O-F20472
- O-FTB23785 Thailand,[57] Vietnam[57]
- O-F17410/O-F18833/O-MF122643/O-BY177553 Thailand (Lao Isan in Northeast Thailand[38][30])
- O-MF106415/O-MF111486/O-BY122399 Thailand[57] (Shan in Mae Hong Son Province[62][30]), China (observed sporadically in individuals from Hubei, Hunan, Chongqing, Sichuan, Guangxi, Jiangxi, Zhejiang, Jiangsu, Anhui, Gansu, Shaanxi, Shanxi, Henan, and Shandong[29])
- O-Y127482/O-F15988 Thailand (Nyahkur and Lao Isan in Northeast Thailand[38][30])
- O-MF6534/O-MF58872/O-BY27925/O-Y23477 Thailand[57] (Central Thai in Central Thailand, Phuan in Central Thailand, Khon Mueang in North Thailand,[38][30] White Hmong in Chiang Rai Province[62][30]), Singapore,[28][30] China (Guangdong, Guangxi, Hunan, Sichuan, Jiangxi, Zhejiang, Shaanxi, Henan, Shandong[30][29])
- O-CTS6579
- O-CTS123/O-F22573/O-MF48275 China (Hunan Han;[28] accounts for about 0.13% of the male population in China at present, mainly distributed in Jiangxi, Hunan and other south-central provinces and cities[63])
- O-F14832/O-F15788/O-Y208219 China[57] (accounts for about 0.22% of the male population in China at present, mainly distributed in the northern region[64]), Thailand[57] (Mon in Western Thailand,[38][30] Tai Lue in Northern Thailand[38][30])
- O-F20472
- O-Z25411
- O-ACT1126/O-Y140772/O-F1289 China (relatively concentrated in northern China at present, accounting for about 0.24% of the national male population;[65] also found in Fujian[28]), Thailand[57] (Lisu[30])
- O-Z25398
- O-F22005/O-Z25400 Thailand[57] (Black Hmong in North Thailand[28][62]), Vietnam[57] (Kinh in Ho Chi Minh City[28]), China (currently distributed mainly in Guangxi, Sichuan, Guangdong and other places, accounting for about 0.10% of the national male population[66])
- O-F1100/O-Y37861 Hunan[28]
- O-MF17697 Laos,[57] Thailand,[57] China (Jiangsu, Hunan, Jiangxi, Guangxi, Guangdong, Guizhou, Yunnan, Fujian, Sichuan, Hong Kong, Chongqing, Henan, Liaoning[29])
- O-F1234/O-Y37855
- O-Y185160/O-MF36985 Hebei,[28] Beijing,[28] Sichuan, Shaanxi, Guangxi, Zhejiang, Shandong, Ningxia, Inner Mongolia, Hubei, Jiangxi (currently accounts for approximately 0.13% of the Chinese male population[67])
- O-FGC71370
- O-MF193618 Sichuan, Zhejiang, Shandong, Anhui, Hunan, Hubei, Fujian (currently accounts for about 0.08% of the male population in China, mainly distributed in Guangdong, Hunan, Anhui and other provinces and cities[68]), Philippines[57]
- O-F14904/N5 Ningxia,[28] Hmong (Northern Thailand[62]), She,[28] Iu Mien (Phayao Province[62]), Quebec[28]. Huang et al. (2022) found that this is the most common Y-chromosome haplogroup among many Hmongic-speaking ethnic groups (including Guangxi Miao, Hunan Miao, Hunan Pa-hng, and Thailand Hmong), with a frequency of 47.1% among the Guangxi Miao.[69]
- O-MF15199/O-FTA25885
- O-F1863
- O-CTS201 Korea[34]
- O-P164
- O-F996/F3237
- O-A16433 Heilongjiang[28]
- O-MF56976 Anhui[28]
- O-Y125645
- O-F871
- O-F706 Philippines, China, Cambodia,[34] Thailand (Bru in Sakon Nakhon Province[38])
- O-F1010 Thailand (Eastern Lawa, Blang, Palaung, Khon Mueang from Chiang Rai Province[38])
- O-AM01750/AM01861/B451 Singapore (Malay),[7] Indonesia (Bajo),[7] Philippines (Batak)[7]
- O-F2472
- O-F706 Philippines, China, Cambodia,[34] Thailand (Bru in Sakon Nakhon Province[38])
- O-A16433 Heilongjiang[28]
- O-M134: Found frequently among speakers of Sino-Tibetan languages, among members of the Kazakh Naiman tribe with a moderate distribution throughout East Asia and Southeast Asia.
- O-Y20/PAGES00125 Poland[34]
- O-F1725
- O-Y12/F314
- O-Y12* Beijing (Han)[28]
- O-CTS2643/CTS11192
- O-CTS53
- O-F876
- O-F275
- O-F634
- O-CTS3776/F2887
- O-M117/PAGE23
- O-MF1380/CTS4960 China, Korea, Japan,[34] Indonesia[34]
- O-M133/M1706 Shandong[28]
- O-M1706* Japan (Tokyo)[28]
- O-YP4864
- O-CTS7634
- O-M1726
- O-A9459
- O-F6800
- O-F14249
- O-F438 Japan (Tokyo)[28]
- O-CTS1642
- O-Y20/PAGES00125 Poland[34]
- O-F996/F3237
- O-M188
- O-L465
Language families and genes
Haplogroup O is associated with populations which speak Austric languages. The following is a phylogenetic tree of language families and their corresponding SNP markers, or haplogroups, sourced mainly from Edmondson 2007 and Shi 2005. This has been called the "Father Tongue Hypothesis" by George van Driem (van Driem 2011). It does not appear to account for O-M176, which is found among Japanese, Korean, and Manchurian males.
(M175) |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Phylogenetics
Phylogenetic history
Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being, above all, timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.
YCC 2002/2008 (Shorthand) | (α) | (β) | (γ) | (δ) | (ε) | (ζ) | (η) | YCC 2002 (Longhand) | YCC 2005 (Longhand) | YCC 2008 (Longhand) | YCC 2010r (Longhand) | ISOGG 2006 | ISOGG 2007 | ISOGG 2008 | ISOGG 2009 | ISOGG 2010 | ISOGG 2011 | ISOGG 2012 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
O-M175 | 26 | VII | 1U | 28 | Eu16 | H9 | I | O* | O | O | O | O | O | O | O | O | O | O |
O-M119 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1* | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a |
O-M101 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1a | O1a1 | O1a1a | O1a1a | O1a1 | O1a1 | O1a1a | O1a1a | O1a1a | O1a1a | O1a1a |
O-M50 | 26 | VII | 1U | 32 | Eu16 | H10 | H | O1b | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 |
O-P31 | 26 | VII | 1U | 33 | Eu16 | H5 | I | O2* | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 |
O-M95 | 26 | VII | 1U | 34 | Eu16 | H11 | G | O2a* | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a1 | O2a1 |
O-M88 | 26 | VII | 1U | 34 | Eu16 | H12 | G | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1a | O2a1a |
O-SRY465 | 20 | VII | 1U | 35 | Eu16 | H5 | I | O2b* | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b |
O-47z | 5 | VII | 1U | 26 | Eu16 | H5 | I | O2b1 | O2b1a | O2b1 | O2b1 | O2b1a | O2b1a | O2b1 | O2b1 | O2b1 | O2b1 | O2b1 |
O-M122 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3* | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 |
O-M121 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3a | O3a | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1a | O3a1a |
O-M164 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3b | O3b | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a1b | O3a1b |
O-M159 | 13 | VII | 1U | 31 | Eu16 | H6 | L | O3c | O3c | O3a3a | O3a3a | O3a3 | O3a3 | O3a3a | O3a3a | O3a3a | O3a3a | O3a3a |
O-M7 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d* | O3c | O3a3b | O3a3b | O3a4 | O3a4 | O3a3b | O3a3b | O3a3b | O3a2b | O3a2b |
O-M113 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d1 | O3c1 | O3a3b1 | O3a3b1 | - | O3a4a | O3a3b1 | O3a3b1 | O3a3b1 | O3a2b1 | O3a2b1 |
O-M134 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e* | O3d | O3a3c | O3a3c | O3a5 | O3a5 | O3a3c | O3a3c | O3a3c | O3a2c1 | O3a2c1 |
O-M117 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1* | O3d1 | O3a3c1 | O3a3c1 | O3a5a | O3a5a | O3a3c1 | O3a3c1 | O3a3c1 | O3a2c1a | O3a2c1a |
O-M162 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1a | O3d1a | O3a3c1a | O3a3c1a | O3a5a1 | O3a5a1 | O3a3c1a | O3a3c1a | O3a3c1a | O3a2c1a1 | O3a2c1a1 |
Original Research Publications
The following research teams per their publications were represented in the creation of the YCC Tree.
Phylogenetic trees
ISOGG 2017 tree (ver. 12.244).[73]
- O (M175)
- O1 (F265/M1354, CTS2866, F75/M1297, F429/M1415, F465/M1422)
- O1a (M119)
- O1a1 (B384/Z23193)
- O1a1a (M307.1/P203.1)
- O1a1a1 (F446)
- O1a1a1a (F140)
- O1a1a1a1 (F78)
- O1a1a1a1a (F81)
- O1a1a1a1a1 (CTS2458)
- O1a1a1a1a1a (F533)
- O1a1a1a1a1a1 (F492)
- O1a1a1a1a1a1a (F656)
- O1a1a1a1a1a1a1 (A12440)
- O1a1a1a1a1a1a1a (A12439)
- O1a1a1a1a1a1a2 (A14788)
- O1a1a1a1a1a1a3 (F65)
- O1a1a1a1a1a1a4 (MF1068)
- O1a1a1a1a1a1a5 (Z23482)
- O1a1a1a1a1a1a1 (A12440)
- O1a1a1a1a1a1b (FGC66168)
- O1a1a1a1a1a1b1 (CTS11553)
- O1a1a1a1a1a1c (Y31266)
- O1a1a1a1a1a1c1 (Y31261)
- O1a1a1a1a1a1d (A12441)
- O1a1a1a1a1a1e (MF1071)
- O1a1a1a1a1a1e1 (MF1074)
- O1a1a1a1a1a1a (F656)
- O1a1a1a1a1a2 (CTS4585)
- O1a1a1a1a1a1 (F492)
- O1a1a1a1a1a (F533)
- O1a1a1a1a2 (MF1075)
- O1a1a1a1a1 (CTS2458)
- O1a1a1a1a (F81)
- O1a1a1a2 (YP4610/Z39229)
- O1a1a1a2a (AM00330/AMM480/B386)
- O1a1a1a2a1 (AM00333/AMM483/B387)
- O1a1a1a2a1a (B388)
- O1a1a1a2a1 (AM00333/AMM483/B387)
- O1a1a1a2b (SK1555)
- O1a1a1a2a (AM00330/AMM480/B386)
- O1a1a1a1 (F78)
- O1a1a1b (SK1568/Z23420)
- O1a1a1b1 (M101)
- O1a1a1b2 (Z23392)
- O1a1a1b2a (Z23442)
- O1a1a1b2a1 (SK1571)
- O1a1a1b2a (Z23442)
- O1a1a1a (F140)
- O1a1a2 (CTS52)
- O1a1a2a (CTS701)
- O1a1a2a1 (K644/Z23266)
- O1a1a2a (CTS701)
- O1a1a1 (F446)
- O1a1b (CTS5726)
- O1a1a (M307.1/P203.1)
- O1a2 (M110)
- O1a2a (F3288)
- O1a2a1 (B392)
- O1a2a1a (B393)
- O1a2a1 (B392)
- O1a2a (F3288)
- O1a3 (Page109)
- O1a1 (B384/Z23193)
- O1b (M268)
- O1b1 (F2320)
- O1b1a (M1470)
- O1b1a1 (PK4)
- O1b1a1a (M95)
- O1b1a1a1 (F1803/M1348)
- O1b1a1a1a (F1252)
- O1b1a1a1a1 (F2924)
- O1b1a1a1a1a (M111)
- O1b1a1a1a1a1 (F2758)
- O1b1a1a1a1a1a (Z24083)
- O1b1a1a1a1a1a1 (Z24089)
- O1b1a1a1a1a1a1a (F923)
- O1b1a1a1a1a1a1a1 (CTS2022)
- O1b1a1a1a1a1a1a1a (F1399)
- O1b1a1a1a1a1a1a1a1 (F2415)
- O1b1a1a1a1a1a1a1a (F1399)
- O1b1a1a1a1a1a1a2 (Z24131)
- O1b1a1a1a1a1a1a3 (Z24100)
- O1b1a1a1a1a1a1a1 (CTS2022)
- O1b1a1a1a1a1a1b (SK1627/Z24091)
- O1b1a1a1a1a1a1b1 (Z39410)
- O1b1a1a1a1a1a1a (F923)
- O1b1a1a1a1a1a2 (Z24088)
- O1b1a1a1a1a1a1 (Z24089)
- O1b1a1a1a1a1a (Z24083)
- O1b1a1a1a1a2 (F2890)
- O1b1a1a1a1a2a (Z24048)
- O1b1a1a1a1a2a1 (Z24050)
- O1b1a1a1a1a2b (Z24014)
- O1b1a1a1a1a2a (Z24048)
- O1b1a1a1a1a1 (F2758)
- O1b1a1a1a1b (CTS5854)
- O1b1a1a1a1b1 (Z23810)
- O1b1a1a1a1b1a (CTS7399)
- O1b1a1a1a1b1a1 (FGC19713/Y14026)
- O1b1a1a1a1b1a1a (Z23849)
- O1b1a1a1a1b1a1a1 (FGC61038)
- O1b1a1a1a1b1a1a (Z23849)
- O1b1a1a1a1b1a1 (FGC19713/Y14026)
- O1b1a1a1a1b1b (CTS651)
- O1b1a1a1a1b1b1 (CTS9884)
- O1b1a1a1a1b1a (CTS7399)
- O1b1a1a1a1b2 (F4229)
- O1b1a1a1a1b2a (F809)
- O1b1a1a1a1b2a1 (F2517)
- O1b1a1a1a1b2a (F809)
- O1b1a1a1a1b1 (Z23810)
- O1b1a1a1a1a (M111)
- O1b1a1a1a2 (SK1630)
- O1b1a1a1a2a (SK1636)
- O1b1a1a1a1 (F2924)
- O1b1a1a1b (F789/M1283)
- O1b1a1a1b1 (FGC29900/Y9322/Z23667)
- O1b1a1a1b1a (B426/FGC29896/Y9033/Z23671)
- O1b1a1a1b1a1 (FGC29907/YP3930)
- O1b1a1a1b1a2 (B427/Z23680)
- O1b1a1a1b1b (Z39485)
- O1b1a1a1b1c (B418)
- O1b1a1a1b1a (B426/FGC29896/Y9033/Z23671)
- O1b1a1a1b2 (SK1646)
- O1b1a1a1b1 (FGC29900/Y9322/Z23667)
- O1b1a1a1a (F1252)
- O1b1a1a2 (CTS350)
- O1b1a1a3 (Page103)
- O1b1a1a1 (F1803/M1348)
- O1b1a1b (F838)
- O1b1a1b1 (F1199)
- O1b1a1a (M95)
- O1b1a2 (Page59)
- O1b1a2a (F993)
- O1b1a2a1 (F1759)
- O1b1a2a1a (CTS1127)
- O1b1a2a1 (F1759)
- O1b1a2b (F417/M1654)
- O1b1a2b1 (F840)
- O1b1a2b1a (F1127)
- O1b1a2b2 (CTS1451)
- O1b1a2b1 (F840)
- O1b1a2c (CTS9996)
- O1b1a2a (F993)
- O1b1a1 (PK4)
- O1b1a (M1470)
- O1b2 (P49, M176)
- O1b2a (F1942/Page92)
- O1b2a1 (CTS9259)
- O1b2a1a (F1204)
- O1b2a1a1 (CTS713)
- O1b2a1a1a (CTS1875)
- O1b2a1a1a1 (CTS10682)
- O1b2a1a1b (Z24598)
- O1b2a1a1c (CTS203)
- O1b2a1a1a (CTS1875)
- O1b2a1a2 (F2868)
- O1b2a1a2a (L682)
- O1b2a1a2a1 (CTS723)
- O1b2a1a2a1a (CTS7620)
- O1b2a1a2a1b (A12446)
- O1b2a1a2a1b1 (PH40)
- O1b2a1a2a1 (CTS723)
- O1b2a1a2b (F940)
- O1b2a1a2a (L682)
- O1b2a1a3 (CTS10687)
- O1b2a1a3a (CTS1215)
- O1b2a1a1 (CTS713)
- O1b2a1b (CTS562)
- O1b2a1a (F1204)
- O1b2a2 (Page90)
- O1b2a1 (CTS9259)
- O1b2a (F1942/Page92)
- O1b1 (F2320)
- O1a (M119)
- O2 (M122)
- O2a (M324)
- O2a1 (L127.1)
- O2a1a (F1876/Page127)
- O2a1a1 (F2159)
- O2a1a1a (F1867/Page124)
- O2a1a1a1 (F852)
- O2a1a1a1a (F2266)
- O2a1a1a1a1 (L599)
- O2a1a1a1a1a (Z43961)
- O2a1a1a1a1a1 (Z43963)
- O2a1a1a1a1a (Z43961)
- O2a1a1a1a1 (L599)
- O2a1a1a1b (F854)
- O2a1a1a1b1 (Z43966)
- O2a1a1a1c (Page130)
- O2a1a1a1a (F2266)
- O2a1a1a1 (F852)
- O2a1a1b (F915)
- O2a1a1b1 (F1478)
- O2a1a1b1a (PF5390)
- O2a1a1b1a1 (CTS1936)
- O2a1a1b1a1a (Z43975)
- O2a1a1b1a2 (FGC33994)
- O2a1a1b1a (PF5390)
- O2a1a1b1 (F1478)
- O2a1a1a (F1867/Page124)
- O2a1a1 (F2159)
- O2a1b (M164)
- O2a1c (IMS-JST002611)
- O2a1c1 (F18)
- O2a1c1a (F117)
- O2a1c1a1 (F13)
- O2a1c1a1a (F11)
- O2a1c1a1a1 (F632)
- O2a1c1a1a1a (F110/M11115)
- O2a1c1a1a1a1 (F17)
- O2a1c1a1a1a1a (F377)
- O2a1c1a1a1a1a1 (F1095)
- O2a1c1a1a1a1a1a (F856)
- O2a1c1a1a1a1a1a1 (F1418)
- O2a1c1a1a1a1a1a2 (Z25097)
- O2a1c1a1a1a1a1a (F856)
- O2a1c1a1a1a1a2 (CTS7501)
- O2a1c1a1a1a1a1 (F1095)
- O2a1c1a1a1a1b (F793)
- O2a1c1a1a1a1a (F377)
- O2a1c1a1a1a2 (Y20951)
- O2a1c1a1a1a2a (Y20932)
- O2a1c1a1a1a1 (F17)
- O2a1c1a1a1a (F110/M11115)
- O2a1c1a1a2 (F38)
- O2a1c1a1a3 (F12)
- O2a1c1a1a4 (F930)
- O2a1c1a1a4a (F2685)
- O2a1c1a1a5 (F1365/M5420/PF1558)
- O2a1c1a1a5a (Y15976)
- O2a1c1a1a5a1 (Y16154)
- O2a1c1a1a5a1a (Y26383)
- O2a1c1a1a5a1a1 (SK1686)
- O2a1c1a1a5a1a (Y26383)
- O2a1c1a1a5a1 (Y16154)
- O2a1c1a1a5b (FGC54486)
- O2a1c1a1a5b1 (FGC54507)
- O2a1c1a1a5a (Y15976)
- O2a1c1a1a6 (CTS12877)
- O2a1c1a1a6a (F2527)
- O2a1c1a1a6a1 (CTS5409)
- O2a1c1a1a6a2 (F2941)
- O2a1c1a1a6a (F2527)
- O2a1c1a1a7 (F723)
- O2a1c1a1a8 (CTS2107)
- O2a1c1a1a9 (SK1691)
- O2a1c1a1a1 (F632)
- O2a1c1a1b (PH203)
- O2a1c1a1a (F11)
- O2a1c1a1 (F13)
- O2a1c1b (F449)
- O2a1c1b1 (F238)
- O2a1c1b1a (F134)
- O2a1c1b1a1 (F1273)
- O2a1c1b1a2 (F724)
- O2a1c1b1a (F134)
- O2a1c1b2 (F1266)
- O2a1c1b1 (F238)
- O2a1c1c (CTS498)
- O2a1c1a (F117)
- O2a1c2 (FGC3750/SK1673)
- O2a1c1 (F18)
- O2a1a (F1876/Page127)
- O2a2 (IMS-JST021354/P201)
- O2a2a (M188)
- O2a2a1 (F2588)
- O2a2a1a (CTS445)
- O2a2a1a1 (CTS201)
- O2a2a1a1a (M159/Page96)
- O2a2a1a2 (M7)
- O2a2a1a2a (F1276)
- O2a2a1a2a1 (CTS6489)
- O2a2a1a2a1a (F1275)
- O2a2a1a2a1a1 (M113)
- O2a2a1a2a1a2 (N5)
- O2a2a1a2a1a3 (Z25400)
- O2a2a1a2a1a (F1275)
- O2a2a1a2a2 (F1863)
- O2a2a1a2a2a (F1134)
- O2a2a1a2a2a1 (F1262)
- O2a2a1a2a2a (F1134)
- O2a2a1a2a1 (CTS6489)
- O2a2a1a2b (Y26403)
- O2a2a1a2a (F1276)
- O2a2a1a1 (CTS201)
- O2a2a1b (F1837)
- O2a2a1a (CTS445)
- O2a2a2 (F879)
- O2a2a2a (F1226)
- O2a2a2a1 (F2859)
- O2a2a2a (F1226)
- O2a2a1 (F2588)
- O2a2b (P164)
- O2a2b1 (M134)
- O2a2b1a (F450/M1667)
- O2a2b1a1 (M117/Page23)
- O2a2b1a1a (M133)
- O2a2b1a1a1 (F438)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a1a1 (F155)
- O2a2b1a1a1a1a (F813/M6539)
- O2a2b1a1a1a1a1 (Y20928)
- O2a2b1a1a1a1a (F813/M6539)
- O2a2b1a1a1a2 (F1754)
- O2a2b1a1a1a2a (F2137)
- O2a2b1a1a1a2a1 (F1442)
- O2a2b1a1a1a2a1a (F1123)
- O2a2b1a1a1a2a1a1 (F1369)
- O2a2b1a1a1a2a1a (F1123)
- O2a2b1a1a1a2a2 (A16636)
- O2a2b1a1a1a2a1 (F1442)
- O2a2b1a1a1a2a (F2137)
- O2a2b1a1a1a3 (Z25907)
- O2a2b1a1a1a1 (F155)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a2 (FGC23469/Z25852)
- O2a2b1a1a2a (F310)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a1a (F1531)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a (F310)
- O2a2b1a1a3 (CTS7634)
- O2a2b1a1a3a (F317)
- O2a2b1a1a3a1 (F3039)
- O2a2b1a1a3a2 (Y29861)
- O2a2b1a1a3b (CTS5488)
- O2a2b1a1a3a (F317)
- O2a2b1a1a4 (Z25853)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a4a1 (CTS6987)
- O2a2b1a1a4a1a (Z42620)
- O2a2b1a1a4a2 ( F20963)
- O2a2b1a1a4a1 (CTS6987)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a5 (CTS10738/M1707)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a5a1 (Z39663)
- O2a2b1a1a5a2 (M1513)
- O2a2b1a1a5b (A9457)
- O2a2b1a1a5b1 (F17158)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a6 (CTS4658)
- O2a2b1a1a6a (CTS5308)
- O2a2b1a1a6b (Z25928)
- O2a2b1a1a6b1 (SK1730/Z25982)
- O2a2b1a1a6b1a (Z26030)
- O2a2b1a1a6b1b (Z26010)
- O2a2b1a1a6b2 (A9462)
- O2a2b1a1a6b3 (B456)
- O2a2b1a1a6b1 (SK1730/Z25982)
- O2a2b1a1a7 (YP4864)
- O2a2b1a1a7a (Z44068)
- O2a2b1a1a7a1 (F5525/SK1748)
- O2a2b1a1a7b (Z44071)
- O2a2b1a1a7a (Z44068)
- O2a2b1a1a8 (Z44091)
- O2a2b1a1a8a (Z44092)
- O2a2b1a1a1 (F438)
- O2a2b1a1b (CTS4960)
- O2a2b1a1a (M133)
- O2a2b1a2 (F114)
- O2a2b1a2a (F79)
- O2a2b1a2a1 (F46/Y15)
- O2a2b1a2a1a (FGC16847/Z26091)
- O2a2b1a2a1a1 (F48)
- O2a2b1a2a1a1a (F152)
- O2a2b1a2a1a1a1 (F2505)
- O2a2b1a2a1a1b (CTS3149)
- O2a2b1a2a1a1a (F152)
- O2a2b1a2a1a2 (F242)
- O2a2b1a2a1a2a (CTS4266)
- O2a2b1a2a1a2a1 (Z26108)
- O2a2b1a2a1a2a1a (F2173)
- O2a2b1a2a1a2a1 (Z26108)
- O2a2b1a2a1a2a (CTS4266)
- O2a2b1a2a1a3 (F2887)
- O2a2b1a2a1a3a (F3607)
- O2a2b1a2a1a3a1 (F3525)
- O2a2b1a2a1a3b (CTS3763)
- O2a2b1a2a1a3b1 (A9472)
- O2a2b1a2a1a3b2 (FGC16863/Y7110)
- O2a2b1a2a1a3b2a (L1360)
- O2a2b1a2a1a3b2a1 (FGC16889)
- O2a2b1a2a1a3b2b (SK1768/Y7112/Z26257)
- O2a2b1a2a1a3b2b1 (F4249)
- O2a2b1a2a1a3b2b1a (FGC23868)
- O2a2b1a2a1a3b2b2 (CTS335)
- O2a2b1a2a1a3b2b1 (F4249)
- O2a2b1a2a1a3b2a (L1360)
- O2a2b1a2a1a3a (F3607)
- O2a2b1a2a1a1 (F48)
- O2a2b1a2a1b (CTS53)
- O2a2b1a2a1b1 (CTS6373)
- O2a2b1a2a1b1a (A9473)
- O2a2b1a2a1b1 (CTS6373)
- O2a2b1a2a1c (F3386)
- O2a2b1a2a1d (Y29828)
- O2a2b1a2a1d1 (F735)
- O2a2b1a2a1d1a (FGC34973)
- O2a2b1a2a1d1b (F1739)
- O2a2b1a2a1d1 (F735)
- O2a2b1a2a1a (FGC16847/Z26091)
- O2a2b1a2a1 (F46/Y15)
- O2a2b1a2b (F743)
- O2a2b1a2b1 (CTS8481)
- O2a2b1a2b1a (CTS4325)
- O2a2b1a2b1a1 (A16629)
- O2a2b1a2b1a2 (CTS682)
- O2a2b1a2b1a (CTS4325)
- O2a2b1a2b2 (F748)
- O2a2b1a2b2a (F728)
- O2a2b1a2b1 (CTS8481)
- O2a2b1a2c (Page101)
- O2a2b1a2a (F79)
- O2a2b1a1 (M117/Page23)
- O2a2b1a (F450/M1667)
- O2a2b2 (AM01822/F3223)
- O2a2b2a (AM01856/F871)
- O2a2b2a1 (N7)
- O2a2b2a1a (F4110)
- O2a2b2a1a1 (F4068)
- O2a2b2a1a2 (SK1780)
- O2a2b2a1b (F4124)
- O2a2b2a1b1 (IMS-JST008425p6)
- O2a2b2a1b2 (BY15188)
- O2a2b2a1b2a (F16411)
- O2a2b2a1a (F4110)
- O2a2b2a2 (AM01845/F706)
- O2a2b2a2a (F717)
- O2a2b2a2a1 (F3612)
- O2a2b2a2a2 (SK1783)
- O2a2b2a2b (AM01847/B451)
- O2a2b2a2b1 (A17418)
- O2a2b2a2b2 (AM01756)
- O2a2b2a2b2a (B450)
- O2a2b2a2b2b (AM00472/B452)
- O2a2b2a2b2b1 (F18942)
- O2a2b2a2b2c (A16427)
- O2a2b2a2a (F717)
- O2a2b2a1 (N7)
- O2a2b2b (A16433)
- O2a2b2b1 (A16438)
- O2a2b2b1a (SK1775)
- O2a2b2b1a1 (SK1774)
- O2a2b2b1b (A16440)
- O2a2b2b1a (SK1775)
- O2a2b2b1 (A16438)
- O2a2b2a (AM01856/F871)
- O2a2b1 (M134)
- O2a2a (M188)
- O2a3 (M300)
- O2a4 (M333)
- O2a1 (L127.1)
- O2b (F742)
- O2b1 (F1150)
- O2b1a (F837)
- O2b1a1 (F1025)
- O2b1a (F837)
- O2b2 (F1055)
- O2b2a (F3021)
- O2b1 (F1150)
- O2a (M324)
- O1 (F265/M1354, CTS2866, F75/M1297, F429/M1415, F465/M1422)
See also
Genetics
Y-DNA O subclades
Y-DNA backbone tree
Notes
- O-M175(xM119,M95,M122) is sometimes incorrectly called "O*".
- The outlier Kadai branch is called "Kra" by Thai linguist Weera Ostapirat and "Geyang" by Chinese linguists.
References
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- YFull Haplogroup YTree v5.04 at 16 May 2017
- Phylogenetic tree of Haplogroup O at 23mofang
- Phylogenetic tree of Haplogroup O-F175 at TheYtree
- Yan S, Wang CC, Li H, Li SL, Jin L, et al. (Genographic Consortium) (September 2011). "An updated tree of Y-chromosome Haplogroup O and revised phylogenetic positions of mutations P164 and PK4". European Journal of Human Genetics. 19 (9): 1013–5. doi:10.1038/ejhg.2011.64. PMC 3179364. PMID 21505448.
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- O Y-Haplogroup Project at Family Tree DNA
- Y-DNA Haplotree at Family Tree DNA
- Damgaard, Peter de Barros; Marchi, Nina; Rasmussen, Simon; Peyrot, Michaël; Renaud, Gabriel; Korneliussen, Thorfinn; Moreno-Mayar, J. Víctor; Pedersen, Mikkel Winther; Goldberg, Amy; Usmanova, Emma; Baimukhanov, Nurbol; Loman, Valeriy; Hedeager, Lotte; Pedersen, Anders Gorm; Nielsen, Kasper; Afanasiev, Gennady; Akmatov, Kunbolot; Aldashev, Almaz; Alpaslan, Ashyk; Baimbetov, Gabit; Bazaliiskii, Vladimir I.; Beisenov, Arman; Boldbaatar, Bazartseren; Boldgiv, Bazartseren; Dorzhu, Choduraa; Ellingvag, Sturla; Erdenebaatar, Diimaajav; Dajani, Rana; Dmitriev, Evgeniy; Evdokimov, Valeriy; Frei, Karin M.; Gromov, Andrey; Goryachev, Alexander; Hakonarson, Hakon; Hegay, Tatyana; Khachatryan, Zaruhi; Khaskhanov, Ruslan; Kitov, Egor; Kolbina, Alina; Kubatbek, Tabaldiev; Kukushkin, Alexey; Kukushkin, Igor; Lau, Nina; Margaryan, Ashot; Merkyte, Inga; Mertz, Ilya V.; Mertz, Viktor K.; Mijiddorj, Enkhbayar; Moiyesev, Vyacheslav; Mukhtarova, Gulmira; Nurmukhanbetov, Bekmukhanbet; Orozbekova, Z.; Panyushkina, Irina; Pieta, Karol; Smrčka, Václav; Shevnina, Irina; Logvin, Andrey; Sjögren, Karl-Göran; Štolcová, Tereza; Taravella, Angela M.; Tashbaeva, Kadicha; Tkachev, Alexander; Tulegenov, Turaly; Voyakin, Dmitriy; Yepiskoposyan, Levon; Undrakhbold, Sainbileg; Varfolomeev, Victor; Weber, Andrzej; Wilson Sayres, Melissa A.; Kradin, Nikolay; Allentoft, Morten E.; Orlando, Ludovic; Nielsen, Rasmus; Sikora, Martin; Heyer, Evelyne; Kristiansen, Kristian; Willerslev, Eske (May 2018). "137 ancient human genomes from across the Eurasian steppes". Nature. 557 (7705): 369–374. Bibcode:2018Natur.557..369D. doi:10.1038/s41586-018-0094-2. hdl:1887/3202709. PMID 29743675. S2CID 13670282.
- Zhang, Xiaoming; Kampuansai, Jatupol; Qi, Xuebin; Yan, Shi; Yang, Zhaohui; Serey, Bun; Sovannary, Tuot; Bunnath, Long; Aun, Hong Seang; Samnom, Ham; Kutanan, Wibhu; Luo, Xin; Liao, Shiyu; Kangwanpong, Daoroong; Jin, Li; Shi, Hong; Su, Bing (27 June 2014). "An Updated Phylogeny of the Human Y-Chromosome Lineage O2a-M95 with Novel SNPs". PLOS ONE. 9 (6): e101020. Bibcode:2014PLoSO...9j1020Z. doi:10.1371/journal.pone.0101020. PMC 4074153. PMID 24972021.
- Lippold, Sebastian; Xu, Hongyang; Ko, Albert; Li, Mingkun; Renaud, Gabriel; Butthof, Anne; Schröder, Roland; Stoneking, Mark (December 2014). "Human paternal and maternal demographic histories: insights from high-resolution Y chromosome and mtDNA sequences". Investigative Genetics. 5 (1): 13. doi:10.1186/2041-2223-5-13. PMC 4174254. PMID 25254093.
- Kutanan, Wibhu; Kampuansai, Jatupol; Srikummool, Metawee; Brunelli, Andrea; Ghirotto, Silvia; Arias, Leonardo; Macholdt, Enrico; Hübner, Alexander; Schröder, Roland; Stoneking, Mark (1 July 2019). "Contrasting Paternal and Maternal Genetic Histories of Thai and Lao Populations". Molecular Biology and Evolution. 36 (7): 1490–1506. doi:10.1093/molbev/msz083. PMC 6573475. PMID 30980085.
- Xia, Zi-Yang; Yan, Shi; Wang, Chuan-Chao; Zheng, Hong-Xiang; Zhang, Fan; Liu, Yu-Chi; Yu, Ge; Yu, Bin-Xia; Shu, Li-Li; Jin, Li (9 August 2019). "Inland-coastal bifurcation of southern East Asians revealed by Hmong-Mien genomic history". bioRxiv 10.1101/730903.S2CID 202028061
- Karafet, T. M.; Hallmark, B.; Cox, M. P.; Sudoyo, H.; Downey, S.; Lansing, J. S.; Hammer, M. F. (1 August 2010). "Major East-West Division Underlies Y Chromosome Stratification across Indonesia". Molecular Biology and Evolution. 27 (8): 1833–1844. doi:10.1093/molbev/msq063. PMID 20207712.
- Trejaut, Jean A; Poloni, Estella S; Yen, Ju-Chen; Lai, Ying-Hui; Loo, Jun-Hun; Lee, Chien-Liang; He, Chun-Lin; Lin, Marie (2014). "Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia". BMC Genetics. 15 (1): 77. doi:10.1186/1471-2156-15-77. PMC 4083334. PMID 24965575.
- Xue, Yali; Zerjal, Tatiana; Bao, Weidong; Zhu, Suling; Shu, Qunfang; Xu, Jiujin; Du, Ruofu; Fu, Songbin; Li, Pu; Hurles, Matthew E; Yang, Huanming; Tyler-Smith, Chris (1 April 2006). "Male Demography in East Asia: A North–South Contrast in Human Population Expansion Times". Genetics. 172 (4): 2431–2439. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
- Hammer, Michael F.; Karafet, Tatiana M.; Park, Hwayong; Omoto, Keiichi; Harihara, Shinji; Stoneking, Mark; Horai, Satoshi (January 2006). "Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes". Journal of Human Genetics. 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082. S2CID 6559289.
- Su, Bing; Xiao, Junhua; Underhill, Peter; Deka, Ranjan; Zhang, Weiling; Akey, Joshua; Huang, Wei; Shen, Di; Lu, Daru; Luo, Jingchun; Chu, Jiayou; Tan, Jiazhen; Shen, Peidong; Davis, Ron; Cavalli-Sforza, Luca; Chakraborty, Ranajit; Xiong, Momiao; Du, Ruofu; Oefner, Peter; Chen, Zhu; Jin, Li (December 1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". The American Journal of Human Genetics. 65 (6): 1718–1724. doi:10.1086/302680. PMC 1288383. PMID 10577926.
- Jing, Chen; Hui, Li; Zhen-Dong, Qin; Wen-Hong, Liu; Wei-Xiong, Lin; Rui-Xing, Yin; Li, Jin; Shang-Ling, Pan (December 2006). "Y-chromosome Genotyping and Genetic Structure of Zhuang Populations". Acta Genetica Sinica. 33 (12): 1060–1072. doi:10.1016/S0379-4172(06)60143-1. PMID 17185165.
- He, Jun-Dong; Peng, Min-Sheng; Quang, Huy Ho; Dang, Khoa Pham; Trieu, An Vu; Wu, Shi-Fang; Jin, Jie-Qiong; Murphy, Robert W.; Yao, Yong-Gang; Zhang, Ya-Ping (7 May 2012). "Patrilineal Perspective on the Austronesian Diffusion in Mainland Southeast Asia". PLOS ONE. 7 (5): e36437. Bibcode:2012PLoSO...736437H. doi:10.1371/journal.pone.0036437. PMC 3346718. PMID 22586471.
- Bing Su, Li Jin, Peter Underhill, et al. (2000), "Polynesian origins: Insights from the Y chromosome." PNAS, vol. 97, no. 15, 8225–8228.
- Cai, Xiaoyun; Qin, Zhendong; Wen, Bo; Xu, Shuhua; Wang, Yi; Lu, Yan; Wei, Lanhai; Wang, Chuanchao; Li, Shilin; Huang, Xingqiu; Jin, Li; Li, Hui (31 August 2011). "Human Migration through Bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum Revealed by Y Chromosomes". PLOS ONE. 6 (8): e24282. Bibcode:2011PLoSO...624282C. doi:10.1371/journal.pone.0024282. PMC 3164178. PMID 21904623.
- Wen, Bo (2004). "The origin of Mosuo people as revealed by mtDNA and Y chromosome variation". Science in China Series C. 47 (1): 1–10. doi:10.1360/02yc0207. PMID 15382670. S2CID 7999778.
- Peng, Min-Sheng; He, Jun-Dong; Fan, Long; Liu, Jie; Adeola, Adeniyi C; Wu, Shi-Fang; Murphy, Robert W; Yao, Yong-Gang; Zhang, Ya-Ping (August 2014). "Retrieving Y chromosomal haplogroup trees using GWAS data". European Journal of Human Genetics. 22 (8): 1046–1050. doi:10.1038/ejhg.2013.272. PMC 4350590. PMID 24281365.
- Yao X, Tang S, Bian B, Wu X, Chen G, Wang CC (April 2017). "Improved phylogenetic resolution for Y-chromosome Haplogroup O2a1c-002611". Scientific Reports. 7 (1): 1146. Bibcode:2017NatSR...7.1146Y. doi:10.1038/s41598-017-01340-z. PMC 5430735. PMID 28442769.
- "O-M159单倍群详情".
- "O-Mf22947单倍群详情".
- "O-Z25518单倍群详情".
- "O-Mf14135单倍群详情".
- "夏代东部大族祖源分析-23魔方祖源基因检测".
- Time Tree of Y-DNA haplogroup O-M175 at FamilyTreeDNA Discover
- Li, Hui; Huang, Ying; Mustavich, Laura F.; Zhang, Fan; Tan, Jing-Ze; Wang, Ling-E; Qian, Ji; Gao, Meng-He; Jin, Li (November 2007). "Y chromosomes of prehistoric people along the Yangtze River". Human Genetics. 122 (3–4): 383–388. doi:10.1007/s00439-007-0407-2. PMID 17657509. S2CID 2533393.
- "O-Mf9858单倍群详情".
- "O-F1262单倍群详情".
- "O-Mf106428单倍群详情".
- Kutanan, Wibhu; Shoocongdej, Rasmi; Srikummool, Metawee; Hübner, Alexander; Suttipai, Thanatip; Srithawong, Suparat; Kampuansai, Jatupol; Stoneking, Mark (November 2020). "Cultural variation impacts paternal and maternal genetic lineages of the Hmong-Mien and Sino-Tibetan groups from Thailand". European Journal of Human Genetics. 28 (11): 1563–1579. doi:10.1038/s41431-020-0693-x. PMC 7576213. PMID 32690935.
- "O-Mf48275单倍群详情".
- "O-F14832单倍群详情".
- "O-Y140772单倍群详情".
- "O-Z25400单倍群详情".
- "O-Mf36985单倍群详情".
- "O-Mf193618单倍群详情".
- Huang, Xiufeng; Xia, Zi-Yang; Bin, Xiaoyun; He, Guanglin; Guo, Jianxin (2022-06-30). "Genomic Insights Into the Demographic History of the Southern Chinese". Frontiers in Ecology and Evolution. Frontiers Media SA. 10. doi:10.3389/fevo.2022.853391. ISSN 2296-701X.
- Naitoh S, Kasahara-Nonaka I, Minaguchi K, Nambiar P (April 2013). "Assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree". Journal of Human Genetics. 58 (4): 195–201. doi:10.1038/jhg.2012.159. PMID 23389242.
- Wei, Lan-Hai; Yan, Shi; Teo, Yik-Ying; Huang, Yun-Zhi; Wang, Ling-Xiang; Yu, Ge; Saw, Woei-Yuh; Ong, Rick Twee-Hee; Lu, Yan; Zhang, Chao; Xu, Shu-Hua; Jin, Li; Li, Hui (5 April 2017). "Phylogeography of Y-chromosome haplogroup O3a2b2-N6 reveals patrilineal traces of Austronesian populations on the eastern coastal regions of Asia". PLOS ONE. 12 (4): e0175080. Bibcode:2017PLoSO..1275080W. doi:10.1371/journal.pone.0175080. PMC 5381892. PMID 28380021.
- Mondal, Mayukh; Casals, Ferran; Xu, Tina; Dall'Olio, Giovanni M; Pybus, Marc; Netea, Mihai G; Comas, David; Laayouni, Hafid; Li, Qibin; Majumder, Partha P; Bertranpetit, Jaume (September 2016). "Genomic analysis of Andamanese provides insights into ancient human migration into Asia and adaptation". Nature Genetics. 48 (9): 1066–1070. doi:10.1038/ng.3621. hdl:10230/34401. PMID 27455350. S2CID 205352099.
- "Y-DNA Haplogroup D-M174 and its Subclades - 2017".
Sources for conversion tables
- Capelli, Cristian; Wilson, James F.; Richards, Martin; Stumpf, Michael P.H.; et al. (February 2001). "A Predominantly Indigenous Paternal Heritage for the Austronesian-Speaking Peoples of Insular Southeast Asia and Oceania". The American Journal of Human Genetics. 68 (2): 432–443. doi:10.1086/318205. PMC 1235276. PMID 11170891.
- Hammer, Michael F.; Karafet, Tatiana M.; Redd, Alan J.; Jarjanazi, Hamdi; et al. (1 July 2001). "Hierarchical Patterns of Global Human Y-Chromosome Diversity". Molecular Biology and Evolution. 18 (7): 1189–1203. doi:10.1093/oxfordjournals.molbev.a003906. PMID 11420360.
- Jobling, Mark A.; Tyler-Smith, Chris (2000), "New uses for new haplotypes", Trends in Genetics, 16 (8): 356–62, doi:10.1016/S0168-9525(00)02057-6, PMID 10904265
- Kaladjieva, Luba; Calafell, Francesc; Jobling, Mark A; Angelicheva, Dora; et al. (February 2001). "Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages". European Journal of Human Genetics. 9 (2): 97–104. doi:10.1038/sj.ejhg.5200597. PMID 11313742. S2CID 21432405.
- Karafet, Tatiana; Xu, Liping; Du, Ruofu; Wang, William; et al. (September 2001). "Paternal Population History of East Asia: Sources, Patterns, and Microevolutionary Processes". The American Journal of Human Genetics. 69 (3): 615–628. doi:10.1086/323299. PMC 1235490. PMID 11481588.
- Semino, O.; Passarino, G; Oefner, PJ; Lin, AA; et al. (2000), "The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective", Science, 290 (5494): 1155–9, Bibcode:2000Sci...290.1155S, doi:10.1126/science.290.5494.1155, PMID 11073453
- Su, Bing; Xiao, Junhua; Underhill, Peter; Deka, Ranjan; et al. (December 1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". The American Journal of Human Genetics. 65 (6): 1718–1724. doi:10.1086/302680. PMC 1288383. PMID 10577926.
- Underhill, Peter A.; Shen, Peidong; Lin, Alice A.; Jin, Li; et al. (November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics. 26 (3): 358–361. doi:10.1038/81685. PMID 11062480. S2CID 12893406.
Further reading
- Edmondson JA (2007). Jimmy G. Harris, Somsonge Burusphat and James E. Harris (ed.). "The power of language over the past: Tai settlement and Tai linguistics in southern China and northern Vietnam" (PDF). Studies in Southeast Asian Languages and Linguistics. Bangkok, Thailand: Ek Phim Thai Co. Ltd.
- van Driem, George (2011). "Rice and the Austroasiatic and Hmong-Mien Homelands". In Enfield, N. J (ed.). Dynamics of Human Diversity (PDF). Pacific Linguistics. pp. 361–390. CiteSeerX 10.1.1.694.9991. ISBN 978-0-85883-638-9. S2CID 135246934.
- Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, Ayub Q (January 2007). "Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan". European Journal of Human Genetics. 15 (1): 121–6. doi:10.1038/sj.ejhg.5201726. PMC 2588664. PMID 17047675.
- Fornarino, Simona; Pala, Maria; Battaglia, Vincenza; Maranta, Ramona; Achilli, Alessandro; Modiano, Guido; Torroni, Antonio; Semino, Ornella; Santachiara-Benerecetti, Silvana A (December 2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation". BMC Evolutionary Biology. 9 (1): 154. doi:10.1186/1471-2148-9-154. PMC 2720951. PMID 19573232.
- Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF (May 2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research. 18 (5): 830–8. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
- Kayser M, Choi Y, van Oven M, Mona S, Brauer S, Trent RJ, et al. (July 2008). "The impact of the Austronesian expansion: evidence from mtDNA and Y chromosome diversity in the Admiralty Islands of Melanesia". Molecular Biology and Evolution. 25 (7): 1362–74. doi:10.1093/molbev/msn078. PMID 18390477.
- Kharkov, V. N.; Stepanov, V. A.; Medvedeva, O. F.; Spiridonova, M. G.; Voevoda, M. I.; Tadinova, V. N.; Puzyrev, V. P. (2007). "Gene pool differences between Northern and Southern Altaians inferred from the data on Y-chromosomal haplogroups". Russian Journal of Genetics. 43 (5): 551–562. doi:10.1134/S1022795407050110. PMID 17633562. S2CID 566825.
- Kim SH, Kim KC, Shin DJ, Jin HJ, Kwak KD, Han MS, et al. (April 2011). "High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea". Investigative Genetics. 2 (1): 10. doi:10.1186/2041-2223-2-10. PMC 3087676. PMID 21463511.
- Ratliff M (1998). "Ho Ne (She) is Hmongic: One final argument" (PDF). Linguistics of the Tibeto-Burman Area. 21 (2): 97–109.
- Rootsi S, Zhivotovsky LA, Baldovic M, Kayser M, Kutuev IA, Khusainova R, et al. (February 2007). "A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe". European Journal of Human Genetics. 15 (2): 204–11. doi:10.1038/sj.ejhg.5201748. PMID 17149388.
- Scheinfeldt L, Friedlaender F, Friedlaender J, Latham K, Koki G, Karafet T, et al. (August 2006). "Unexpected NRY chromosome variation in Northern Island Melanesia". Molecular Biology and Evolution. 23 (8): 1628–41. doi:10.1093/molbev/msl028. PMID 16754639.
- Shi H, Dong YL, Wen B, Xiao CJ, Underhill PA, Shen PD, et al. (September 2005). "Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122". American Journal of Human Genetics. 77 (3): 408–19. doi:10.1086/444436. PMC 1226206. PMID 16080116.
- Su B, Jin L, Underhill P, Martinson J, Saha N, McGarvey ST, et al. (July 2000). "Polynesian origins: insights from the Y chromosome". Proceedings of the National Academy of Sciences of the United States of America. 97 (15): 8225–8. Bibcode:2000PNAS...97.8225S. doi:10.1073/pnas.97.15.8225. PMC 26928. PMID 10899994.
- Wells RS, Yuldasheva N, Ruzibakiev R, Underhill PA, Evseeva I, Blue-Smith J, et al. (August 2001). "The Eurasian heartland: a continental perspective on Y-chromosome diversity". Proceedings of the National Academy of Sciences of the United States of America. 98 (18): 10244–9. Bibcode:2001PNAS...9810244W. doi:10.1073/pnas.171305098. PMC 56946. PMID 11526236.
- Bo W, Hong S, Ling R, Huifeng X, Kaiyuan L, Wenyi Z, et al. (February 2004). "The origin of Mosuo people as revealed by mtDNA and Y chromosome variation". Science in China Series C: Life Sciences. 47 (1): 1–10. doi:10.1360/02yc0207. PMID 15382670. S2CID 7999778.
- Xue Y, Zerjal T, Bao W, Zhu S, Shu Q, Xu J, et al. (April 2006). "Male demography in East Asia: a north-south contrast in human population expansion times". Genetics. 172 (4): 2431–9. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
External links
- Bradshaw Foundation. "Journey of Man - The Peopling of the World".
- ISOGG (2012). "Y-DNA Haplogroup O and its Subclades - 2012".
- TMC (1998). "Genetic Findings Support 'Out of Africa' Theory". Archived from the original on 2009-10-10.
- Spread of Haplogroup O, from The Genographic Project, National Geographic
- Y-DNA Phylogenetic Tree of Haplogroup O (DNAHaplogroups.org)
- Migration patterns of early Humans and the full size map
- China DNA at Family Tree DNA