Homo sapiens potassium channel tetramerization domain containing 7 (KC - Nucleotide

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KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature. [Epilepsia. 2024]
KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature.
Yoganathan S, Whitney R, Thomas M, Danda S, Chettali AM, Prasad AN, Farhan SMK, AlSowat D, Abukhaled M, Aldhalaan H, et al. Epilepsia. 2024 Mar; 65(3):709-724. Epub 2024 Jan 17.
KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses. [Sci Adv. 2022]
KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses.
Wang Y, Cao X, Liu P, Zeng W, Peng R, Shi Q, Feng K, Zhang P, Sun H, Wang C, et al. Sci Adv. 2022 Aug 5; 8(31):eabm5578. Epub 2022 Aug 3.
KCTD7-related progressive myoclonic epilepsy: report of three Indian families and review of literature. [Clin Dysmorphol. 2022]
KCTD7-related progressive myoclonic epilepsy: report of three Indian families and review of literature.
Narayanan DL, Somashekar PH, Majethia P, Shukla A. Clin Dysmorphol. 2022 Jan 1; 31(1):6-10.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the KCTD7 gene (NM_001167961.2).
RefSeq protein product
See the reference protein sequence for BTB/POZ domain-containing protein KCTD7 isoform 1 (NP_694578.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide