KCTD7
protein-coding gene in the species Homo sapiens
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Summary
KCTD7 is a gene[1]. KCTD7 is a type of protein-coding gene[2].
Key Facts
- HomoloGene ID: 17687[3]
- Genomic start: 66093868[4], 66628881[5]
- Genomic end: 66276446[6], 66649067[7]
- Ortholog: Kctd7[8]
- Encodes: Potassium channel tetramerization domain containing 7[9], Potassium channel tetramerisation domain containing 7, isoform CRA_b[10]
- Found in taxon: Homo sapiens[11]
- Chromosome: human chromosome 7[12]
- Genetic association: progressive myoclonic epilepsy type 3[13]
- Strand orientation: forward strand[14]
- Cytogenetic location: 7q11.21[15]
- Expressed in: ganglionic eminence[16], C1 segment[17], middle frontal gyrus[18], ventricular zone[19], stromal cell of endometrium[20], buccal mucosa cell[21], substantia nigra[22], Brodmann area 10[23], tendon of biceps brachii[24], nucleus accumbens[25]