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  2. RAB2A - RAB2A, member RAS oncogene family Gene

RAB2A - RAB2A, member RAS oncogene family Gene

Homo sapiens

Also known as LHX; RAB2

Gene ID: 5862 | Gene type: protein coding

About RAB2A

Cytogenetic location: 8q12.1-q12.2 Genomic coordinates (GRCh38): 8:60,516,910-60,623,644 (from NCBI)

This gene has 12 transcripts (splice variants), 209 orthologues and 68 paralogues. Ubiquitous expression in brain (RPKM 44.0), thyroid (RPKM 43.9) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the Rab family, members of which are small molecular weight guanosine triphosphatases (GTPases) that contain highly conserved domains involved in GTP binding and hydrolysis. The Rabs are membrane-bound proteins, involved in vesicular fusion and trafficking. This protein is a resident of pre-Golgi intermediates, and is required for protein transport from the endoplasmic reticulum (ER) to the Golgi complex. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

RAB2A Products(2)

mRNA Protein Name
NM_001242644.1 NP_001229573.1 ras-related protein Rab-2A isoform b
NM_002865.3 NP_002856.1 ras-related protein Rab-2A isoform a
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables GDP binding IDA
IDA: Inferred from direct assay
16034420 GOA
enables GTP binding IDA
IDA: Inferred from direct assay
16034420 GOA
enables GTPase activity IDA
IDA: Inferred from direct assay
16034420 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence Reference Source
involved in Golgi organization IMP
IMP: Inferred from mutant phenotype
17684057 GOA
NOT involved in endoplasmic reticulum to Golgi vesicle-mediated transport IMP
IMP: Inferred from mutant phenotype
17684057 GOA
involved in macroautophagy IMP
IMP: Inferred from mutant phenotype
28483915 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

RAB2A Protein Structure

Ras

Ras: Ras family (8 - 168)

  • 0
  • 100
  • 200
  • 212 a.a.
Protein Preferred Names Protein Names

ras-related protein Rab-2A

RAB2, member RAS oncogene family

RAB2A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
RAB2A P61019 ICA1 Homo sapiens Q05084 25416956
Intra
RAB2A P61019 ICA1 Homo sapiens Q05084 29892012
Intra
RAB2A P61019 ICA1 Homo sapiens Q05084 25416956
Intra
RAB2A P61019 FAM114A2 Homo sapiens Q9NRY5 32296183
Intra
RAB2A P61019 FAM114A2 Homo sapiens Q9NRY5 32296183
Intra
RAB2A P61019 FAM114A2 Homo sapiens Q9NRY5 32296183
Intra
RAB2A P61019 FRMD1 Homo sapiens Q8N878 32296183
Intra
RAB2A P61019 TBC1D25 Homo sapiens Q3MII6 32296183
Intra
RAB2A P61019 TBC1D25 Homo sapiens Q3MII6 32296183
Intra
RAB2A P61019 TBC1D25 Homo sapiens Q3MII6 32296183
Intra
RAB2A P61019 CCDC125 Homo sapiens Q86Z20 32296183
Intra
RAB2A P61019 CCDC125 Homo sapiens Q86Z20 32296183
Intra
RAB2A P61019 CCDC125 Homo sapiens Q86Z20 32296183
Intra
RAB2A P61019 PMAIP1 Homo sapiens Q13794-2 32296183
Intra
RAB2A P61019 GARIN1A Homo sapiens Q6NXP2-2 32296183
Intra
RAB2A P61019 GARIN1A Homo sapiens Q6NXP2-2 32296183
Intra
RAB2A P61019 GARIN1A Homo sapiens Q6NXP2-2 32296183
Intra
RAB2A P61019 GARIN4 Homo sapiens Q8IYT1 32296183
Intra
RAB2A P61019 GARIN4 Homo sapiens Q8IYT1 32296183
Intra
RAB2A P61019 GARIN4 Homo sapiens Q8IYT1 32296183
Intra
RAB2A P61019 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
RAB2A P61019 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
RAB2A P61019 BLZF1 Homo sapiens Q9H2G9 31515488
Intra
RAB2A P61019 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
RAB2A P61019 FAM114A1 Homo sapiens Q8IWE2 31515488
Intra
RAB2A P61019 FAM114A1 Homo sapiens Q8IWE2 25416956
Intra
RAB2A P61019 FAM114A1 Homo sapiens Q8IWE2 32296183
Intra
RAB2A P61019 FAM114A1 Homo sapiens Q8IWE2 25416956
Intra
RAB2A P61019 FAM114A1 Homo sapiens Q8IWE2 32296183
Intra
RAB2A P61019 FAM114A1 Homo sapiens Q8IWE2 25416956
Intra
RAB2A P61019 FAM114A1 Homo sapiens Q8IWE2 32296183
Intra
RAB2A P61019 TRIM7 Homo sapiens Q9C029 32296183
Intra
RAB2A P61019 TRIM7 Homo sapiens Q9C029 32296183
Intra
RAB2A P61019 TRIM7 Homo sapiens Q9C029 32296183
Intra
RAB2A P61019 CFL2 Homo sapiens Q9Y281 32296183
Intra
RAB2A P61019 GOLGA2 Homo sapiens Q08379 32296183
Intra
RAB2A P61019 GOLGA2 Homo sapiens Q08379 25416956
Intra
RAB2A P61019 GOLGA2 Homo sapiens Q08379 32296183
Intra
RAB2A P61019 GOLGA2 Homo sapiens Q08379 32296183
Intra
RAB2A P61019 GOLGA2 Homo sapiens Q08379 25416956
Intra
RAB2A P61019 TMEM70 Homo sapiens Q9BUB7 32296183
Intra
RAB2A P61019 STAMBPL1 Homo sapiens Q96FJ0 25416956
Intra
RAB2A P61019 STAMBPL1 Homo sapiens Q96FJ0 32296183
Intra
RAB2A P61019 STAMBPL1 Homo sapiens Q96FJ0 32296183
Intra
RAB2A P61019 STAMBPL1 Homo sapiens Q96FJ0 32296183
Intra
RAB2A P61019 STAMBPL1 Homo sapiens Q96FJ0
Y2H
21516116
Intra
RAB2A P61019 HES6 Homo sapiens Q96HZ4 32296183
Intra
RAB2A P61019 GARIN6 Homo sapiens Q8NEG0 32296183
Intra
RAB2A P61019 GARIN6 Homo sapiens Q8NEG0 32296183
Intra
RAB2A P61019 GARIN6 Homo sapiens Q8NEG0 16189514
Intra
RAB2A P61019 GARIN6 Homo sapiens Q8NEG0 25416956
Intra
RAB2A P61019 GARIN6 Homo sapiens Q8NEG0 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Warburg Micro Syndrome 1

Warburg Micro Syndrome

Micro Syndrome

Warbm

WARBM1

Warburg Sjo Fledelius Syndrome

Warburg-Sjo-Fledelius Syndrome

Micro Syndrome 1

Microcephaly, Microcornea, Congenital Cataract, Intellectual Disability, Optic Atrophy And Hypogenitalism

Lipoblastoma
Sezary'S Disease

Sezary Syndrome

Sézary Syndrome

Sezary'S Lymphoma

Sezary Disease

Sezary Erythroderma

Sezary Lymphoma

Chronic Salpingo-Oophoritis

Chronic Salpingitis And Oophoritis

Chronic Salpingitis/Oophoritis

Warburg Micro Syndrome 3

WARBM3

Micro Syndrome 3

Warburg Micro Syndrome 2

WARBM2

Micro Syndrome 2

Smith-Mccort Dysplasia 1

Smith-Mccort Dysplasia

SMC1

Smc

Smith Mccort Dysplasia

Smith-Mccort Dwarfism

Warburg Micro Syndrome 4

WARBM4

Micro Syndrome 4

Salpingo-Oophoritis

Tubo-Ovarian Inflammatory Disease

Salpingitis/Oophoritis

Suppurative Salpingo Oophoritis

Tubo-Ovarian Inflammation

Tubo-Ovarian Inflammatory Disorder

Purulent Salpingo Oophoritis

Septic Salpingo Oophoritis

Salpingo-Ovaritis

Inflammation Oviduct

Ruptured Salpingo Oophoritis

Pyosalpinx Rupture

Dyggve-Melchior-Clausen Disease

Dyggve-Melchior-Clausen Syndrome

DMC

Dmc Disease

Pseudo-Morquio Disease Type I

Dmc Syndrome

Duane Retraction Syndrome

Stilling-Turk-Duane Syndrome

Duane'S Syndrome

Duane Syndrome

Isolated Duane Retraction Syndrome

Co-Contractive Retraction Syndrome

Duane Anomaly, Isolated

Ocular Retraction Syndrome

Drs

Durs

Cleft Palate, Isolated

Cleft Palate

Isolated Cleft Palate

CPI

Cp

Palatoschisis

Cleft Palate Isolated

Uranostaphyloschisis

Congenital Fissure Of Palate

Cleft Of Secondary Palate

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
Bos taurus RAB2A VGNC VGNC:33637
Canis familiaris RAB2A VGNC VGNC:45271
Macaca mulatta RAB2A VGNC VGNC:81529
Felis catus RAB2A VGNC VGNC:97587
Mus musculus RAB2A MGD MGI:1928750
Rattus norvegicus RAB2A RGD RGD:68323
Others RAB2A NCBI