RAB3GAP2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[13]
- Cytogenetic location
- 1q41[18]
- Expressed in
- Epithelium of choroid plexus, lateral nuclear group of thalamus, spinal ganglia, pericardium, trigeminal ganglion, pons, Brodmann area 46, cardia, beta cell, endothelial cell[19][20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- cataract-intellectual disability-hypogonadism syndrome, Warburg micro syndrome 2, Warburg micro syndrome[14][15][16]
- HomoloGene ID
- 40842[3]
- Strand orientation
- reverse strand[17]
🏷️ Also known as
en MARTS1
en p150
en RAB3-GAP150
en RAB3GAP150
en RAB3GAP2
en RAB3 GTPase activating non-catalytic protein subunit 2
en SPG69
en WARBM2
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000118873
- Ensembl transcript ID
- ENST00000491305, ENST00000237724, ENST00000358951, ENST00000462353, ENST00000474178, ENST00000474966, ENST00000475769, ENST00000478976, ENST00000484658, ENST00000491005, ENST00000690824, ENST00000689820, ENST00000693602, ENST00000687065, ENST00000690315, ENST00000685286, ENST00000693454, ENST00000684982, ENST00000688904, ENST00000692208, ENST00000692813, ENST00000692972, ENST00000688035, ENST00000686381, ENST00000690379, ENST00000691862, ENST00000691661, ENST00000690373, ENST00000685664, ENST00000688281, ENST00000687394, ENST00000687647
- Entrez Gene ID
- 25782
- Exact match
- identifiers.org
- Freebase ID
- /m/03hm2k2
- HGNC ID
- 17168
- HGNC gene symbol
- RAB3GAP2
- OMIM ID
- 609275
- RefSeq RNA ID
- NM_012414
- UMLS CUI
- C1826757
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