FAM167A

FAM167A
Identifiers
Aliases	FAM167A, C8orf13, D8S265, family with sequence similarity 167 member A, DIORA-1
External IDs	OMIM: 610085; MGI: 3606565; HomoloGene: 14243; GeneCards: FAM167A; OMA:FAM167A - orthologs
Gene location (Human)
Chr.	Chromosome 8 (human)
End	11,475,908 bp
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)
End	63,702,947 bp
RNA expression pattern
	Top expressed in
	stromal cell of endometrium; ; islet of Langerhans; ; secondary oocyte; ; skin of arm; ; thyroid gland; ; left lobe of thyroid gland; ; right lobe of thyroid gland; ; Amygdala; ; gonad; ; cingulate gyrus;
	Top expressed in
	fourth ventricle; ; choroid plexus of fourth ventricle; ; molar; ; choroidal fissure; ; lip; ; secondary oocyte; ; skin of abdomen; ; body of femur; ; primary oocyte; ; lumbar spinal ganglion;
	More reference expression data
	n/a
Orthologs
	83648
	219148
	ENSG00000154319
	ENSMUSG00000035095
	Q96KS9
	Q6P1G6
	NM_053279
	NM_177628
	NP_444509
	NP_808296
	Wikidata
View/Edit Human	View/Edit Mouse

Family with sequence similarity 167, member A is a protein in humans that is encoded by the FAM167A gene located on chromosome 8. FAM167A and its paralogs are protein encoding genes containing the conserved domain DUF3259, a protein of unknown function. FAM167A has many orthologs in which the domain of unknown function is highly conserved.