1. Gene
  2. RRAGC - Ras related GTP binding C Gene

RRAGC - Ras related GTP binding C Gene

Homo sapiens

Also known as GTR2; RAGC; TIB929

Gene ID: 64121 | Gene type: protein coding

About RRAGC

Cytogenetic location: 1p34.3 Genomic coordinates (GRCh38): 1:38,838,198-38,859,772 (from NCBI)

This gene has 4 transcripts (splice variants), 268 orthologues and 3 paralogues. Ubiquitous expression in fat (RPKM 23.8), placenta (RPKM 15.8) and 25 other tissues.

Summary

This gene encodes a member of the GTR/RAG GTP-binding protein family. The encoded protein is a monomeric guanine nucleotide-binding protein which forms a heterodimer with RRAGA and RRAGB and is primarily localized to the cytoplasm. The encoded protein promotes intracellular localization of the mTOR complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]

RRAGC Products(2)

mRNA Protein Name
NM_001271851.2 NP_001258780.1 ras-related GTP-binding protein C isoform 2
NM_022157.4 NP_071440.1 ras-related GTP-binding protein C isoform 1

RRAGC Protein Structure

Gtr1_RagA

Gtr1_RagA: Gtr1/RagA G protein conserved region (63 - 289)

  • 0
  • 100
  • 200
  • 300
  • 399 a.a.
Protein Preferred Names Protein Names

ras-related GTP-binding protein C

GTPase-interacting protein 2

Related Diseases

Diseases Alias
Birt-Hogg-Dube Syndrome

Hornstein-Knickenberg Syndrome

Fibrofolliculomas With Trichodiscomas And Acrochordons

BHD

Birt-Hogg-Dubé Syndrome

Multiple Fibrofolliculoma Familial

Bhd Syndrome

Birt Hogg Dube Syndrome

Hornstein-Birt-Hogg-Dubé Syndrome

Multiple Fibrofolliculomas

Retinitis Pigmentosa 60

RP60

Retinitis Pigmentosa, Type 60

Familial Renal Oncocytoma
Dilated Cardiomyopathy

Familial Dilated Cardiomyopathy

Primary Dilated Cardiomyopathy

Idiopathic Dilated Cardiomyopathy

Congestive Cardiomyopathy

Idiopathic Dilation Cardiomyopathy

Primary Familial Dilated Cardiomyopathy

Cardiomyopathy, Dilated

DCM

Cardiomyopathy, Familial Dilated

Dilated Cardiomyopathy, Familial

Hypokinetic Dilated Cardiomyopathy, Familial

Familial Idiopathic Cardiomyopathy

Fdc

Cardiomyopathy, Familial Idiopathic

Idiopathic Cardiomegaly

Dilated Congestive Cardiomyopathy

Chronic Dilated Cardiomyopathy

Ccm - [Congestive Cardiomyopathy]

Cocm - [Congestive Cardiomyopathy]

Dcm - [Dilated Cardiomyopathy]

Dilated-Hypokinetic Cardiomyopathy

Congestive Idiopathic Cardiomyopathy

Primary Idiopathic Dilated Cardiomyopathy

Fanconi Anemia, Complementation Group C

Fanconi Anemia Complementation Group C

FANCC

Facc

Fac

Fa3

Fanconi Pancytopenia Type 3

Fanconi Pancytopenia, Type 3

Faces Syndrome

Facial Features , Anorexia, Cachexia, Eye And Skin Anomalies

Friedman-Goodman Syndrome

Abnormality Of The Face

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

Orthologs Information

Species Symbol Source ID
Canis familiaris RRAGC VGNC VGNC:45756
Mus musculus RRAGC MGD MGI:1858751
Rattus norvegicus RRAGC RGD RGD:1311760
Bos taurus RRAGC VGNC VGNC:34160
Macaca mulatta RRAGC VGNC VGNC:77060
Felis catus RRAGC VGNC VGNC:64769