CTNNA2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 2[14]
- Cytogenetic location
- 2p12[17]
- Encodes
- Catenin alpha 2, Catenin alpha-2[11][12]
- Expressed in
- frontal pole, Brodmann area 46, superior frontal gyrus, postcentral gyrus, lateral nuclear group of thalamus, Brodmann area 10, corpus epididymis, dorsolateral prefrontal cortex, orbitofrontal cortex, sperm[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- Alzheimer's disease[15]
- HomoloGene ID
- 68394[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en CAP-R
en CAPR
en catenin alpha 2
en CDCBM9
en CT114
en CTNNA2
en CTNR
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000066032
- Ensembl transcript ID
- ENST00000629316, ENST00000343114, ENST00000361291, ENST00000402739, ENST00000409266, ENST00000409550, ENST00000409971, ENST00000451966, ENST00000465616, ENST00000466387, ENST00000467488, ENST00000467892, ENST00000493024, ENST00000496251, ENST00000496558, ENST00000497804, ENST00000508970, ENST00000540488, ENST00000541047
- Entrez Gene ID
- 1496
- Exact match
- identifiers.org
- Freebase ID
- /m/02kfgff
- HGNC ID
- 2510
- HGNC gene symbol
- CTNNA2
- OMIM ID
- 114025
- PDB structure ID
- 6DUW
- RefSeq RNA ID
- XM_011532557, NM_001164883, NM_001282597, NM_001282598, NM_001282599, NM_001282600, NM_004389, XM_011532556, NM_001320810, XM_017003403, XM_017003405, XM_024452714, XM_024452715, NM_001399737, XM_047443447
- UMLS CUI
- C1413796
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Summary
CTNNA2 is a gene[1].