RERGL - RERG like Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79785

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

Ras: Ras family (19 - 173)

  • 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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS11850 RERGL Human Pre-designed siRNA Set A Pre-designed Set / 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
Others RERGL NCBI