MEI1

MEI1
Identifiers
Aliases	MEI1, SPATA38, meiotic double-stranded break formation protein 1, HYDM3
External IDs	OMIM: 608797 MGI: 3028590 HomoloGene: 46535 GeneCards: MEI1
Gene location (Human)
Chr.	Chromosome 22 (human)[1]
End	41,799,456 bp[1]
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)[2]
End	82,011,015 bp[2]
RNA expression pattern
	Top expressed in
	bone marrow cells; ; spleen; ; appendix; ; blood; ; lymph node; ; rectum; ; monocyte; ; minor salivary gland; ; thymus; ; pancreatic ductal cell;
	Top expressed in
	otolith organ; ; utricle; ; morula; ; spermatid; ; superior frontal gyrus; ; seminiferous tubule; ; spermatocyte; ; submandibular gland; ; free upper limb; ; triceps brachii muscle;
	More reference expression data
	n/a
Orthologs
	150365
	74369
	ENSG00000167077
	ENSMUSG00000068117
	Q5TIA1; Q4G0I1
	Q9D4I2
	NM_152513
	NM_028897; NM_001310435
	NP_689726; NP_689726.3
	NP_001297364; NP_083173
	Wikidata
View/Edit Human	View/Edit Mouse

Meiotic double-stranded break formation protein 1 is a protein that in humans is encoded by the MEI1 gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000167077 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000068117 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: Meiotic double-stranded break formation protein 1". Retrieved 2017-03-25.

Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H, Sasaki Y, Ishikawa M, Lamb DJ, Matsumoto N, Birk OS, Niikawa N, Sengoku K (2006). "Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest". J. Hum. Genet. 51 (6): 533–40. doi:10.1007/s10038-006-0394-5. PMID 16683055.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.