KCNQ5
protein-coding gene in the species Homo sapiens
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KCNQ5
Summary
KCNQ5 is a gene[1].
Key Facts
- KCNQ5's instance of is recorded as gene[2].
- KCNQ5 is a type of protein-coding gene[3].
- KCNQ5's HomoloGene ID is recorded as 28270[4].
- KCNQ5's genomic start is recorded as 72621792[5].
- KCNQ5's genomic start is recorded as 73331520[6].
- KCNQ5's genomic end is recorded as 73908574[7].
- KCNQ5's genomic end is recorded as 73198853[8].
- KCNQ5's ortholog is recorded as Kcnq5[9].
- KCNQ5's ortholog is recorded as Kcnq5[10].
- KCNQ5's ortholog is recorded as kqt-1[11].
- KCNQ5's ortholog is recorded as kcnq5a[12].
- KCNQ5's ortholog is recorded as kcnq5b[13].
- KCNQ5's encodes is recorded as Potassium voltage-gated channel subfamily Q member 5[14].
- KCNQ5's encodes is recorded as Potassium voltage-gated channel subfamily KQT member 5[15].
- KCNQ5's found in taxon is recorded as Homo sapiens[16].
- KCNQ5's chromosome is recorded as human chromosome 6[17].
- KCNQ5's genetic association is recorded as refractive error[18].
- KCNQ5's genetic association is recorded as autosomal dominant mental retardation 46[19].
- KCNQ5's strand orientation is recorded as forward strand[20].
- KCNQ5's exact match is recorded as http://identifiers.org/ncbigene/56479[21].
- KCNQ5's cytogenetic location is recorded as 6q13[22].
- KCNQ5's expressed in is recorded as endothelial cell[23].
- KCNQ5's expressed in is recorded as pons[24].
- KCNQ5's expressed in is recorded as Brodmann area 23[25].
- KCNQ5's expressed in is recorded as tibialis anterior muscle[26].