Medical Knowledge Cockpit cortical dysplasia-focal epilepsy syndrome

CNTNAP2

Somatic tumors

glioma, melanoma

Tumor types germline

Cancer Syndrom

Translocation partner

Name

contactin associated protein like 2

Chromosome banding

7q35-q36.1

Cancer molecular gen.

Mutation type

Mis

Other syndrome disease

CNTNAP2

• A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
• Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders