2. Gene
  3. SLC2A4RG - SLC2A4 regulator Gene

SLC2A4RG - SLC2A4 regulator Gene

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

中文名称：SLC2A4 稳压器

种属: Homo sapiens

同用名: GEF; HDBP1; HDBP-1; Si-1-2; Si-1-2-19

基因 ID: 56731 | 基因类型: protein coding

关于 SLC2A4RG

Cytogenetic location: 20q13.33 Genomic coordinates (GRCh38): 20:63,739,776-63,744,050 (from NCBI)

This gene has 8 transcripts (splice variants), 103 orthologues and 2 paralogues. Ubiquitous expression in fat (RPKM 45.9), kidney (RPKM 36.7) and 25 other tissues.

功能概要

该基因编码的蛋白质是参与溶质载体家族 2 成员 4 基因激活的核转录因子。编码的蛋白质与另一种转录因子、肌细胞增强因子 2 相互作用，以激活该基因的转录。[RefSeq 提供，2008 年 7 月]

The protein encoded by this gene is a nuclear transcription factor involved in the activation of the solute carrier family 2 member 4 gene. The encoded protein interacts with another transcription factor, myocyte enhancer factor 2, to activate transcription of this gene. [provided by RefSeq, Jul 2008]

SLC2A4RG 基因产物(1)

mRNA Protein Name
NM_020062.4 NP_064446.2 SLC2A4 regulator
蛋白主名 其他名称

SLC2A4 regulator

GLUT4 enhancer factor

关联疾病

疾病名称 别名
Huntington Disease

Huntington'S Disease

Huntington Chorea

Huntington'S Chorea

HD

Huntington Chronic Progressive Hereditary Chorea

Juvenile Huntington Disease

Chronic Progressive Chorea

Chronic Progressive Hereditary Chorea

Hc - [Huntington Chorea]

Hereditary Chorea

Progressive Hereditary Chorea
Hematocele Of Tunica Vaginalis Testis

Hematocele

Male Hematocele
Leukoencephalopathy With Vanishing White Matter

Cree Leukoencephalopathy

Vanishing White Matter Disease

Ovarioleukodystrophy

Vanishing White Matter Leukodystrophy

Childhood Ataxia With Central Nervous System Hypomyelinization

Cach

Cach Syndrome

Myelinosis Centralis Diffusa

VWM

Cle

Childhood Ataxia With Central Nervous System Hypomyelination

Childhood Ataxia With Diffuse Central Nervous System Hypomyelination

Cach/Vwm

Cach/Vwm Syndrome

Childhood Ataxia With Central Nervous System Hypomyelination/Vanishing White Matter

Cree Leukoencehalopathy

Late Infantile Cach Syndrome

Juvenile Or Adult Cach Syndrome

Congenital Or Early Infantile Cach Syndrome

Leukodystrophy With Vanishing White Matter
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-RS13173 SLC2A4RG 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 SLC2A4RG VGNC VGNC:77490
Bos taurus SLC2A4RG VGNC VGNC:57026
Canis familiaris SLC2A4RG VGNC VGNC:46342
Rattus norvegicus SLC2A4RG RGD RGD:41152591
Felis catus SLC2A4RG VGNC VGNC:65304
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