CNTN5
protein-coding gene in the species Homo sapiens
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CNTN5
Summary
CNTN5 is a gene[1].
Key Facts
- CNTN5's instance of is recorded as gene[2].
- CNTN5 is a type of protein-coding gene[3].
- CNTN5's HomoloGene ID is recorded as 28447[4].
- CNTN5's genomic start is recorded as 98891683[5].
- CNTN5's genomic start is recorded as 99020949[6].
- CNTN5's genomic end is recorded as 100358885[7].
- CNTN5's genomic end is recorded as 100229616[8].
- CNTN5's ortholog is recorded as Cntn5[9].
- CNTN5's ortholog is recorded as Cntn5[10].
- CNTN5's ortholog is recorded as cntn5[11].
- CNTN5's ortholog is recorded as Cont[12].
- CNTN5's encodes is recorded as Contactin 5[13].
- CNTN5's found in taxon is recorded as Homo sapiens[14].
- CNTN5's chromosome is recorded as human chromosome 11[15].
- CNTN5's genetic association is recorded as myopia[16].
- CNTN5's genetic association is recorded as smallpox[17].
- CNTN5's strand orientation is recorded as forward strand[18].
- CNTN5's exact match is recorded as http://identifiers.org/ncbigene/53942[19].
- CNTN5's cytogenetic location is recorded as 11q22.1[20].
- CNTN5's expressed in is recorded as gonad[21].
- CNTN5's expressed in is recorded as islet of Langerhans[22].
- CNTN5's expressed in is recorded as testicle[23].
- CNTN5's expressed in is recorded as primary visual cortex[24].
- CNTN5's expressed in is recorded as prefrontal cortex[25].
- CNTN5's expressed in is recorded as Brodmann area 23[26].