2. Gene
  3. DHRS7B - dehydrogenase/reductase 7B Gene

DHRS7B - dehydrogenase/reductase 7B Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：脱氢酶/还原酶 7B

种属: Homo sapiens

同用名: CGI-93; SDR32C1

基因 ID: 25979 | 基因类型: protein coding

关于 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.

功能概要

该基因位于 17 号染色体上的 Smith-Magenis 综合征区域。它编码一种功能未知的蛋白质。[RefSeq 提供，2008 年 7 月]

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 基因产物(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 蛋白结构

adh_short

adh_short: short chain dehydrogenase (54 - 225)

  • 0
  • 100
  • 200
  • 300
  • 325 a.a.
蛋白主名 其他名称

dehydrogenase/reductase SDR family member 7B

dehydrogenase/reductase (SDR family) member 7B

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS03744 DHRS7B Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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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