GIT2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 12[13]
- Cytogenetic location
- 12q24.11[16]
- Encodes
- GIT ArfGAP 2[11]
- Expressed in
- monocyte, middle temporal gyrus, Brodmann area 23, granulocyte, right hemisphere of cerebellum, blood, body of pancreas, visceral pleura, spleen, bone marrow[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- metabolic disease[14]
- HomoloGene ID
- 41336[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en CAT-2
en CAT2
en GIT2
en GIT ArfGAP 2
en PKL
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000139436
- Ensembl transcript ID
- ENST00000553118, ENST00000320063, ENST00000355312, ENST00000361006, ENST00000457474, ENST00000546613, ENST00000547267, ENST00000547694, ENST00000547815, ENST00000548000, ENST00000548643, ENST00000548655, ENST00000549999, ENST00000550186, ENST00000550480, ENST00000551209, ENST00000551455, ENST00000551721, ENST00000552978
- Entrez Gene ID
- 9815
- Exact match
- identifiers.org
- Freebase ID
- /m/03gx62f
- HGNC ID
- 4273
- HGNC gene symbol
- GIT2
- OMIM ID
- 608564
- RefSeq RNA ID
- NM_001135213, NM_001135214, NM_014776, NM_057169, NM_057170, NM_139201, XM_005253997, XM_006719707, XM_006719708, XM_006719709, XM_006719712, XM_006719713, XM_017020258, XM_017020261, NM_001330153, NM_001330154, XM_047429922, XM_047429923, XM_047429924, XM_047429925, XM_047429926, XM_047429927, XM_047429928
- UMLS CUI
- C1333677
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