DHRS7B - dehydrogenase/reductase 7B Gene

Homo sapiens

Also known as CGI-93; SDR32C1

Gene ID: 25979 | Gene type: protein coding

About DHRS7B

Cytogenetic location: 17p11.2 Genomic coordinates (GRCh38): 17:21,126,964-21,191,420 (from NCBI)

This gene has 10 transcripts (splice variants), 215 orthologues and 13 paralogues. Ubiquitous expression in testis (RPKM 7.1), thyroid (RPKM 6.1) and 25 other tissues.

Summary

This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]

DHRS7B Products(6)

mRNA	Protein	Name
NM_001330159.3	NP_001317088.1	dehydrogenase/reductase SDR family member 7B isoform 2
NM_001393657.1	NP_001380586.1	dehydrogenase/reductase SDR family member 7B isoform 4
NM_001393658.1	NP_001380587.1	dehydrogenase/reductase SDR family member 7B isoform 5
NM_001393659.1	NP_001380588.1	dehydrogenase/reductase SDR family member 7B isoform 6
NM_001393660.1	NP_001380589.1	dehydrogenase/reductase SDR family member 7B isoform 7
NM_015510.5	NP_056325.2	dehydrogenase/reductase SDR family member 7B isoform 1

DHRS7B Protein Structure

adh_short

0
100
200
300
325 a.a.

Protein Preferred Names

Protein Names

dehydrogenase/reductase SDR family member 7B

dehydrogenase/reductase (SDR family) member 7B

Related Diseases

Diseases

Alias

Cortisone Reductase Deficiency 2

CORTRD2

Partial Fetal Alcohol Syndrome

Cortisone Reductase Deficiency

11-Alpha Beta-Hydroxysteroid Dehydrogenase Type I Deficiency Of	Cortrd
Hsd 11b1 Deficiency

Smith-Magenis Syndrome

SMS	Chromosome 17p11.2 Deletion Syndrome
17p11.2 Microdeletion Syndrome	17p11.2 Monosomy
Chromosome 17p Deletion Syndrome	Del(17)
P11.2	17p- Syndrome
Deletion 17p Syndrome	Partial Monosomy 17p

Alcohol-Related Birth Defects

Arbd	Alcohol-Related Birth Defect
Alcohol Related Birth Defect	Fetal Alcohol Syndrome

Rhizomelic Chondrodysplasia Punctata

Chondrodysplasia Punctata, Rhizomelic	Rcdp
Chondrodysplasia Punctata, Rhizomelic Form	Rcp
Chondrodysplasia Punctata Rhizomelic

Peroxisomal Biogenesis Disorder

Zellweger Spectrum Disorders	Peroxisome Biogenesis Disorder-Zellweger Syndrome Spectrum
Disorders Of Peroxisome Biogenesis	Zellweger Spectrum
Zellweger Syndrome Spectrum	Peroxisomal Biogenesis Disorders
Pbd, Zss	Pbd-Zsd
Pbd-Zss	Pbd-Zellweger Spectrum Disorder
Peroxisomal Biogenesis Disorders, Zellweger Syndrome Spectrum	Peroxisome Biogenesis Disorder
Peroxisome Biogenesis Disorder Spectrum	Peroxisome Biogenesis Disorders
Zellweger Spectrum Disorder	Hyperpipecolic Acidaemia

Zellweger Syndrome

Cerebrohepatorenal Syndrome	Zellweger Leukodystrophy
Zs	Congenital Iron Overload
Chr	Zws
Severe Pbd-Zsd	Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS03744	DHRS7B Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	DHRS7B	VGNC	VGNC:71701
Canis familiaris	DHRS7B	VGNC	VGNC:54295
Mus musculus	DHRS7B	MGD	MGI:2384931
Rattus norvegicus	DHRS7B	RGD	RGD:1311243
Felis catus	DHRS7B	VGNC	VGNC:61472
Bos taurus	DHRS7B	VGNC	VGNC:28044

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