CNTN1
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CNTN1
Summary
CNTN1 is a gene[1]. CNTN1 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2]
Key Facts
- CNTN1's instance of is recorded as gene[3].
- CNTN1 is a type of protein-coding gene[4].
- CNTN1's HomoloGene ID is recorded as 7274[5].
- CNTN1's genomic start is recorded as 41086244[6].
- CNTN1's genomic start is recorded as 40692439[7].
- CNTN1's genomic end is recorded as 41466220[8].
- CNTN1's genomic end is recorded as 41072415[9].
- CNTN1's ortholog is recorded as Cntn1[10].
- CNTN1's ortholog is recorded as Cntn1[11].
- CNTN1's ortholog is recorded as cntn1a[12].
- CNTN1's ortholog is recorded as Cont[13].
- CNTN1's encodes is recorded as contactin 1[14].
- CNTN1's encodes is recorded as Contactin-1[15].
- CNTN1's found in taxon is recorded as Homo sapiens[16].
- CNTN1's chromosome is recorded as human chromosome 12[17].
- CNTN1's genetic association is recorded as Compton-North congenital myopathy[18].
- CNTN1's strand orientation is recorded as forward strand[19].
- CNTN1's exact match is recorded as http://identifiers.org/ncbigene/1272[20].
- CNTN1's cytogenetic location is recorded as 12q12[21].
- CNTN1's expressed in is recorded as Brodmann area 23[22].
- CNTN1's expressed in is recorded as endothelial cell[23].
- CNTN1's expressed in is recorded as superior frontal gyrus[24].
- CNTN1's expressed in is recorded as postcentral gyrus[25].
- CNTN1's expressed in is recorded as entorhinal cortex[26].
- CNTN1's expressed in is recorded as prefrontal cortex[27].
Why It Matters
CNTN1 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2] CNTN1 has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] CNTN1 is known by 4 alternative names across languages and contexts.[29]