KCTD7
protein-coding gene in the species Homo sapiens
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KCTD7
Summary
KCTD7 is a gene[1].
Key Facts
- KCTD7's instance of is recorded as gene[2].
- KCTD7 is a type of protein-coding gene[3].
- KCTD7's HomoloGene ID is recorded as 17687[4].
- KCTD7's genomic start is recorded as 66093868[5].
- KCTD7's genomic start is recorded as 66628881[6].
- KCTD7's genomic end is recorded as 66276446[7].
- KCTD7's genomic end is recorded as 66649067[8].
- KCTD7's ortholog is recorded as Kctd7[9].
- KCTD7's ortholog is recorded as Kctd7[10].
- KCTD7's ortholog is recorded as kctd7[11].
- KCTD7's encodes is recorded as Potassium channel tetramerization domain containing 7[12].
- KCTD7's encodes is recorded as Potassium channel tetramerisation domain containing 7, isoform CRA_b[13].
- KCTD7's found in taxon is recorded as Homo sapiens[14].
- KCTD7's chromosome is recorded as human chromosome 7[15].
- KCTD7's genetic association is recorded as progressive myoclonic epilepsy type 3[16].
- KCTD7's strand orientation is recorded as forward strand[17].
- KCTD7's exact match is recorded as http://identifiers.org/ncbigene/154881[18].
- KCTD7's cytogenetic location is recorded as 7q11.21[19].
- KCTD7's expressed in is recorded as ganglionic eminence[20].
- KCTD7's expressed in is recorded as C1 segment[21].
- KCTD7's expressed in is recorded as middle frontal gyrus[22].
- KCTD7's expressed in is recorded as ventricular zone[23].
- KCTD7's expressed in is recorded as stromal cell of endometrium[24].
- KCTD7's expressed in is recorded as buccal mucosa cell[25].
- KCTD7's expressed in is recorded as substantia nigra[26].