DHRS7B - dehydrogenase/reductase 7B Gene

Also Known as CGI-93; SDR32C1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 25979

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

adh_short: short chain dehydrogenase (54 - 225)

  • 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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS03744 DHRS7B Human Pre-designed siRNA Set A Pre-designed Set / 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
Others DHRS7B NCBI