SLC2A4RG - SLC2A4 regulator Gene

Homo sapiens

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

Gene ID: 56731 | Gene type: protein coding

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

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13173	SLC2A4RG Human Pre-designed siRNA Set A	Pre-designed Sets	/	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

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