RAB3GAP1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 2[13]
- Cytogenetic location
- 2q21.3[16]
- Expressed in
- hair follicle, Brodmann area 23, secondary oocyte, endothelial cell, middle temporal gyrus, visceral pleura, tibia, pars reticulata, parietal pleura, entorhinal cortex[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- Warburg micro syndrome[14]
- HomoloGene ID
- 45617[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en MARTS2
en P130
en RAB3GAP
en RAB3GAP1
en RAB3GAP130
en RAB3 GTPase activating protein catalytic subunit 1
en WARBM1
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000115839
- Ensembl transcript ID
- ENST00000539493, ENST00000264158, ENST00000425393, ENST00000442034, ENST00000487003, ENST00000489858, ENST00000497080, ENST00000687630, ENST00000685874, ENST00000690785, ENST00000684914, ENST00000691339, ENST00000689187, ENST00000690208, ENST00000686403, ENST00000691478, ENST00000685967, ENST00000686114, ENST00000689880, ENST00000687199, ENST00000693554, ENST00000685652, ENST00000688182, ENST00000692993, ENST00000688088
- Entrez Gene ID
- 22930
- Exact match
- identifiers.org
- Freebase ID
- /m/03g_z2z
- HGNC ID
- 17063
- HGNC gene symbol
- RAB3GAP1
- OMIM ID
- 602536
- RefSeq RNA ID
- XM_011510825, NM_001172435, NM_012233, XM_011510823, XR_001738674, XM_047443732
- UMLS CUI
- C1826756
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Summary
RAB3GAP1 is a gene[1].