SYNPO2
protein-coding gene in the species Homo sapiens
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Summary
SYNPO2 is a gene[1]. SYNPO2 is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 15400[4]
- Genomic start: 118850688[5], 119809996[6]
- Genomic end: 119061247[7], 119982402[8]
- Ortholog: Synpo2[9]
- Encodes: Synaptopodin 2[10]
- Found in taxon: Homo sapiens[11]
- Chromosome: human chromosome 4[12]
- Genetic association: amyotrophic lateral sclerosis[13]
- Strand orientation: forward strand[14]
- Exact match: http://identifiers.org/ncbigene/171024[15]
- Cytogenetic location: 4q26[16]
- Expressed in: saphenous vein[17], tail of epididymis[18], seminal vesicula[19], Skeletal muscle tissue of rectus abdominis[20], Skeletal muscle tissue of biceps brachii[21], nipple[22], urethra[23], body of tongue[24], superficial temporal artery[25], pericardium[26]