SLC2A4RG - SLC2A4 regulator Gene

Also Known as GEF; HDBP1; HDBP-1; Si-1-2; Si-1-2-19

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 56731

About 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.

Summary

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 Products (1)

mRNA Protein Name
NM_020062.4 NP_064446.2 SLC2A4 regulator

Gene Ontology

  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence References Source
enables DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
10825161 GOA
Biological Process GO Annotation Evidence References Source
involved in regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
10825161 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

SLC2A4 regulator

  • GLUT4 enhancer factor

Related Diseases

Diseases Alias
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
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-RS13173 SLC2A4RG Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source 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
Others SLC2A4RG NCBI