Sft2 domain containing 2

SFT2D2
Identifiers
Aliases	SFT2D2, UNQ512, dJ747L4.C1.2, SFT2 domain containing 2
External IDs	MGI: 1917362 HomoloGene: 27069 GeneCards: SFT2D2
Gene location (Human)
Chr.	Chromosome 1 (human)[1]
End	168,253,021 bp[1]
Gene location (Mouse)
Chr.	Chromosome 1 (mouse)[2]
End	165,022,007 bp[2]
RNA expression pattern
	Top expressed in
	sperm; ; gums; ; nipple; ; superficial temporal artery; ; human penis; ; visceral pleura; ; cavity of mouth; ; germinal epithelium; ; renal medulla; ; synovial joint;
	Top expressed in
	submandibular gland; ; median eminence; ; sciatic nerve; ; parotid gland; ; lacrimal gland; ; epithelium of stomach; ; stria vascularis; ; iris; ; molar; ; ciliary body;
	More reference expression data
	n/a
Gene ontology
Molecular function	molecular function;
Cellular component	integral component of membrane; extracellular exosome; membrane;
Biological process	protein transport; vesicle-mediated transport; transport; biological process;
	Sources:Amigo / QuickGO
Orthologs
	375035
	108735
	ENSG00000213064
	ENSMUSG00000040848
	O95562
	Q8VD57
	NM_199344
	NM_145512
	NP_955376
	NP_663487
	Wikidata
View/Edit Human	View/Edit Mouse

SFT2 domain containing 2 is a protein that in humans is encoded by the SFT2D2 gene.[5]

References

GRCh38: Ensembl release 89: ENSG00000213064 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000040848 - 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: SFT2 domain containing 2". Retrieved 2018-10-17.

Cheung CL, Chan BY, Chan V, Ikegawa S, Kou I, Ngai H, Smith D, Luk KD, Huang QY, Mori S, Sham PC, Kung AW (February 2009). "Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation". Hum. Mol. Genet. 18 (4): 679–687. doi:10.1093/hmg/ddn397. PMID 19064610.

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