RERGL - RERG like Gene

Homo sapiens

Gene ID: 79785 | Gene type: protein coding

About RERGL

This gene has 5 transcripts (splice variants), 157 orthologues and 35 paralogues. Broad expression in endometrium (RPKM 13.0), fat (RPKM 12.7) and 18 other tissues.

Summary

Predicted to enable G protein activity and GTP binding activity. [provided by Alliance of Genome Resources, Apr 2022]

RERGL Products(2)

mRNA	Protein	Name
NM_001286201.2	NP_001273130.1	ras-related and estrogen-regulated growth inhibitor-like protein isoform b
NM_024730.4	NP_079006.1	ras-related and estrogen-regulated growth inhibitor-like protein isoform a

RERGL Protein Structure

Ras

0
100
205 a.a.

Protein Preferred Names

Protein Names

ras-related and estrogen-regulated growth inhibitor-like protein

RERG/RAS-like

Related Diseases

Diseases

Alias

Viral Labyrinthitis

Epidemic Vertigo

Vestibular Neuronitis

Episodic Ataxia, Type 4

Episodic Ataxia Type 4	Periodic Vestibulocerebellar Ataxia
Patx	EA4
Ataxia, Periodic Vestibulocerebellar

Corneal Dystrophy, Subepithelial Mucinous

Subepithelial Mucinous Corneal Dystrophy

SMCD

Episodic Ataxia, Type 3

Episodic Ataxia Type 3	EA3
Ataxia, Episodic, With Vertigo And Tinnitus	Episodic Ataxia-Vertigo-Tinnitus-Myokymia Syndrome

Episodic Ataxia, Type 7

Episodic Ataxia Type 7

EA7

Temtamy Syndrome

TEMTYS	Craniofacial Dysmorphism With Ocular Coloboma Absent Corpus Callosum And Aortic Dilatation
Craniofacial Dysmorphism-Coloboma-Corpus Callosum Agenesis Syndrome	Dysmorphism, Corpus Callosum Agenesis And Colobomas
Temtamy-Shalash Syndrome	Mental Retardation With Or Without Craniofacial Dysmorphism, Ocular Coloboma, Or Abnormal Corpus Callosum

Episodic Ataxia, Type 5

Episodic Ataxia Type 5	EA5
Episodic Ataxia 5	Ea-5
Ataxia, Episodic, Type 5

Cantu Syndrome

Hypertrichotic Osteochondrodysplasia	Hypertrichotic Osteochondrodysplasia Cantu Type
Cantú Syndrome	Craniofaciocardioskeletal Syndrome
Hypertrichosis-Osteochondrodysplasia-Cardiomegaly Syndrome	Congenital Hypertrichosis-Acromegaloid Facial Features Spectrum
Congenital Hypertrichosis-Coarse Facial Features Spectrum	HTOCD
Osteochondrodysplasia, Hypertrichotic

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-RS11850	RERGL Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	RERGL	RGD	RGD:1560090
Bos taurus	RERGL	VGNC	VGNC:33874
Canis familiaris	RERGL	VGNC	VGNC:45479
Felis catus	RERGL	VGNC	VGNC:64575
Macaca mulatta	RERGL	VGNC	VGNC:100099
Mus musculus	RERGL	MGD	MGI:3642998

Name
Email *

	Sorry, but the email address you supplied was invalid.