DHRS7B

DHRS7B
Identifiers
Aliases	DHRS7B, SDR32C1, CGI-93, dehydrogenase/reductase (SDR family) member 7B, dehydrogenase/reductase 7B
External IDs	OMIM: 616160; MGI: 2384931; HomoloGene: 41044; GeneCards: DHRS7B; OMA:DHRS7B - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	21,193,265 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	60,751,021 bp
RNA expression pattern
	Top expressed in
	muscle of thigh; ; olfactory zone of nasal mucosa; ; gastrocnemius muscle; ; mucosa of transverse colon; ; apex of heart; ; triceps brachii muscle; ; Achilles tendon; ; left ventricle; ; left testis; ; bronchial epithelial cell;
	Top expressed in
	Ileal epithelium; ; spermatocyte; ; brown adipose tissue; ; yolk sac; ; right kidney; ; lactiferous gland; ; duodenum; ; jejunum; ; intercostal muscle; ; proximal tubule;
	More reference expression data
	n/a
Gene ontology
Molecular function	oxidoreductase activity; molecular function;
Cellular component	integral component of membrane; endoplasmic reticulum membrane; membrane; endoplasmic reticulum;
Biological process	biological process; ether lipid biosynthetic process; neutrophil differentiation; macromolecule metabolic process;
	Sources:Amigo / QuickGO
Orthologs
	25979
	216820
	ENSG00000109016
	ENSMUSG00000042569
	Q6IAN0
	Q99J47
	NM_015510; NM_001330159
	NM_001172112; NM_145428
	NP_001317088; NP_056325
	NP_001165583; NP_663403
	Wikidata
View/Edit Human	View/Edit Mouse

Dehydrogenase/reductase (SDR family) member 7B is an enzyme encoded by the DHRS7B gene in humans, found on chromosome 17p11.2. DHRS7B encodes a protein that is predicted to function in steroid hormone regulation. A deletion in the chromosomal region 17p11.2 has been associated with Smith-Magenis Syndrome, a genetic developmental disorder.