Contactin 2 (axonal) [Homo sapiens]

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Gene-gene interaction network analysis indicates CNTN2 is a candidate gene for idiopathic generalized epilepsy. [Neurogenetics. 2024]
Gene-gene interaction network analysis indicates CNTN2 is a candidate gene for idiopathic generalized epilepsy.
Lin ZJ, He JW, Zhu SY, Xue LH, Zheng JF, Zheng LQ, Huang BX, Chen GZ, Lin PX. Neurogenetics. 2024 Apr; 25(2):131-139. Epub 2024 Mar 9.
Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families. [Front Genet. 2023]
Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families.
Abdulkareem AA, Zaman Q, Khan H, Khan S, Rehman G, Tariq N, Ahmad M, Owais M, Najumuddin, Muthaffar OY, et al. Front Genet. 2023; 14:1185065. Epub 2023 Jun 8.
Routine Diagnostics Confirm Novel Neurodevelopmental Disorders. [Genes (Basel). 2022]
Routine Diagnostics Confirm Novel Neurodevelopmental Disorders.
Jauss RT, Schließke S, Abou Jamra R. Genes (Basel). 2022 Dec 7; 13(12). Epub 2022 Dec 7.

RefSeq genomic sequence
See the genomic reference sequence for the CNTN2 gene (NG_033845.1).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the CNTN2 gene.

Nucleotide
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Protein