Contactin-associated protein-like 2, partial [Cuculus canorus]

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Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case-control association study reveals potential biomarkers. [Mol Biol Rep. 2024]
Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case-control association study reveals potential biomarkers.
Ul Mudassir B, Agha Z. Mol Biol Rep. 2024 Feb 5; 51(1):276. Epub 2024 Feb 5.
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants. [Epilepsia Open. 2024]
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants.
Panza N, Bianchini C, Cetica V, Balestrini S, Barba C, Ferrari AR, Mei D, Parmeggiani L, Parrini E, Guerrini R. Epilepsia Open. 2024 Feb; 9(1):417-423. Epub 2023 Dec 15.
Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder. [Hum Genet. 2023]
Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder.
D'Onofrio G, Accogli A, Severino M, Caliskan H, Kokotović T, Blazekovic A, Jercic KG, Markovic S, Zigman T, Goran K, et al. Hum Genet. 2023 Jul; 142(7):909-925. Epub 2023 May 14.

RefSeq protein
See the reference protein sequence for contactin-associated protein-like 2 (XP_009566762.1).

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Protein