CNTN1
protein-coding gene in the species Homo sapiens
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Summary
CNTN1 is a gene[1].
Key Facts
- Subclass of: protein-coding gene[2]
- HomoloGene ID: 7274[3]
- Genomic start: 41086244[4], 40692439[5]
- Genomic end: 41466220[6], 41072415[7]
- Ortholog: Cntn1[8], cntn1a[9], Cont[10]
- Encodes: contactin 1[11], Contactin-1[12]
- Found in taxon: Homo sapiens[13]
- Chromosome: human chromosome 12[14]
- Genetic association: Compton-North congenital myopathy[15]
- Strand orientation: forward strand[16]
- Cytogenetic location: 12q12[17]
- Expressed in: Brodmann area 23[18], endothelial cell[19], superior frontal gyrus[20], postcentral gyrus[21], entorhinal cortex[22], prefrontal cortex[23], cerebellar cortex[24], primary visual cortex[25], amygdala[26], cerebellar hemisphere[27]