FAM170B (gene)

FAM170B
Identifiers
Aliases	FAM170B, C10orf73, family with sequence similarity 170 member B
External IDs	MGI: 2145650 HomoloGene: 19055 GeneCards: FAM170B
Gene location (Human)
Chr.	Chromosome 10 (human)
End	49,134,021 bp
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)
End	32,558,746 bp
RNA expression pattern
	Top expressed in
	blood; ; duodenum; ; human musculoskeletal system; ; muscular system; ; muscle of leg; ; lower leg; ; gastrocnemius muscle; ; smooth muscle tissue; ; renal cortex; ; tibial nerve;
	Top expressed in
	spermatid; ; seminiferous tubule; ; ascending aorta; ; aortic valve; ; supraoptic nucleus; ; spermatocyte; ; Paneth cell; ; cumulus cell; ; left lobe of liver; ; abdominal wall;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding;
Cellular component	acrosomal vesicle; outer acrosomal membrane; membrane; cytoplasmic vesicle;
Biological process	positive regulation of acrosome reaction; regulation of fertilization;
	Sources:Amigo / QuickGO
Orthologs
	170370
	105511
	ENSG00000172538
	ENSMUSG00000078127
	A6NMN3
	E9PXT9
	NM_001164484
	NM_001164485
	NP_001157956
	NP_001157957
	Wikidata
View/Edit Human	View/Edit Mouse

Family with sequence similarity 170 member B is a protein that in humans is encoded by the FAM170B gene. ^[5]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000172538 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000078127 - 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: Family with sequence similarity 170 member B". Retrieved 2016-06-24.