BTB/POZ domain-containing protein KCTD3 isoform 2 [Homo sapiens]

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Phenotypic characterization of KCTD3-related developmental epileptic encephalopathy. [Clin Genet. 2018]
Phenotypic characterization of KCTD3-related developmental epileptic encephalopathy.
Faqeih EA, Almannai M, Saleh MM, AlWadei AH, Samman MM, Alkuraya FS. Clin Genet. 2018 May; 93(5):1081-1086. Epub 2018 Mar 15.
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. [Neurogenetics. 2010]
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.
Poot M, Beyer V, Schwaab I, Damatova N, Van't Slot R, Prothero J, Holder SE, Haaf T. Neurogenetics. 2010 Feb; 11(1):81-9. Epub 2009 Jul 7.
Up-regulation of hyperpolarization-activated cyclic nucleotide-gated channel 3 (HCN3) by specific interaction with K+ channel tetramerization domain-containing protein 3 (KCTD3). [J Biol Chem. 2013]
Up-regulation of hyperpolarization-activated cyclic nucleotide-gated channel 3 (HCN3) by specific interaction with K+ channel tetramerization domain-containing protein 3 (KCTD3).
Cao-Ehlker X, Zong X, Hammelmann V, Gruner C, Fenske S, Michalakis S, Wahl-Schott C, Biel M. J Biol Chem. 2013 Mar 15; 288(11):7580-7589. Epub 2013 Feb 4.

RefSeq genomic sequence
See the genomic reference sequence for the KCTD3 gene (NG_047148.1).
RefSeq mRNA
See reference mRNA sequence for the KCTD3 gene (NM_001319294.2).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the KCTD3 gene.

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