PFN1
protein-coding gene in the species Homo sapiens
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Summary
PFN1 is a gene[1]. PFN1 ranks in the top 2% of gene entities by monthly Wikipedia readership (60 views/month).[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 3684[4]
- Genomic start: 4945652[5], 4848947[6]
- Genomic end: 4949061[7], 4852356[8]
- Ortholog: Pfn1[9]
- Encodes: Profilin 1[10]
- Found in taxon: Homo sapiens[11]
- Chromosome: human chromosome 17[12]
- Genetic association: amyotrophic lateral sclerosis type 18[13]
- Strand orientation: reverse strand[14]
- Exact match: http://identifiers.org/ncbigene/5216[15]
- Cytogenetic location: 17p13.2[16]
- Expressed in: granulocyte[17], mucosa of transverse colon[18], muscle layer of sigmoid colon[19], mucosa of ileum[20], monocyte[21], thoracic aorta[22], ascending aorta[23], stromal cell of endometrium[24], Descending thoracic aorta[25], left coronary artery[26]
Why It Matters
PFN1 is known by 5 alternative names across languages and contexts.[27]