ATXN1
protein-coding gene in the species Homo sapiens
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Summary
ATXN1 is a gene[1]. ATXN1 ranks in the top 2% of gene entities by monthly Wikipedia readership (111 views/month).[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 281[4]
- Genomic start: 16299112[5], 16299343[6]
- Genomic end: 16761491[7], 16761722[8]
- Ortholog: Atxn1[9], atxn1a[10]
- Encodes: ataxin 1[11]
- Found in taxon: Homo sapiens[12]
- Chromosome: human chromosome 6[13]
- Genetic association: amyotrophic lateral sclerosis[14], spinocerebellar ataxia type 1[15]
- Strand orientation: reverse strand[16]
- Exact match: http://identifiers.org/ncbigene/6310[17]
- Cytogenetic location: 6p22.3[18]
- Expressed in: endothelial cell[19], Brodmann area 23[20], Skeletal muscle tissue of rectus abdominis[21], germinal epithelium[22], orbitofrontal cortex[23], Brodmann area 46[24], epithelium of colon[25], biceps brachii[26], Skeletal muscle tissue of biceps brachii[27], cartilage tissue[28]
Why It Matters
ATXN1 is known by 7 alternative names across languages and contexts.[29]