ACO2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 22[15]
- Cytogenetic location
- 22q13.2[18]
- Encodes
- Aconitase 2[13]
- Expressed in
- right ventricle, apex of heart, myocardium of left ventricle, gastrocnemius muscle, muscle of thigh, right auricle of heart, jejunal mucosa, cardiac muscle tissue of right atrium, Skeletal muscle tissue of biceps brachii, vastus lateralis muscle[19][20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[14]
- Genetic association
- infantile cerebellar-retinal degeneration[16]
- HomoloGene ID
- 856[3]
- Strand orientation
- forward strand[17]
🏷️ Also known as
en ACO2
en aconitase 2
en ACONM
en HEL-S-284
en ICRD
en OCA8
en OPA9
uk Аконітаза-2
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000100412
- Ensembl transcript ID
- ENST00000482208, ENST00000216254, ENST00000396512, ENST00000466237, ENST00000471094, ENST00000478010, ENST00000676792, ENST00000677007, ENST00000677516, ENST00000678788, ENST00000676959, ENST00000678688, ENST00000678269, ENST00000677554, ENST00000676822, ENST00000677153, ENST00000678454, ENST00000676664, ENST00000678819, ENST00000676748, ENST00000679264, ENST00000677698, ENST00000678600, ENST00000677427, ENST00000677492, ENST00000676883, ENST00000677532, ENST00000679284, ENST00000679311, ENST00000679320, ENST00000676714, ENST00000678394
- Entrez Gene ID
- 50
- Exact match
- identifiers.org
- Freebase ID
- /m/0138k35t
- HGNC ID
- 118
- HGNC gene symbol
- ACO2
- Microsoft Academic ID (discontinued)
- 2777675208
- OMIM ID
- 100850
- RefSeq RNA ID
- NM_001098
- UMLS CUI
- C1412127
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Summary
ACO2 is a gene[1].