Homo sapiens coiled-coil domain containing 88C (CCDC88C), RefSeqGene o - Nucleotide

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CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. [Clin Genet. 2024]
CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation.
Chen YJ, Wang WJ, Zou DF, Luo JX, Jin PY, Jin L, Liu XR, Liao WP, Li B, Chen YJ, et al. Clin Genet. 2024 Apr; 105(4):397-405. Epub 2024 Jan 3.
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.
A Novel c.3636-4 A>G Mutation in the CCDC88C Plays a Causative Role in Familial Spinocerebellar Ataxia. [Hum Hered. 2023]
A Novel c.3636-4 A>G Mutation in the CCDC88C Plays a Causative Role in Familial Spinocerebellar Ataxia.
Chai S, Liu D, Liu Y, Sang M. Hum Hered. 2023; 88(1):91-97. Epub 2023 Oct 27.

RefSeq alternative splicing
See 9 reference mRNA sequence splice variants for the CCDC88C gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.