Disease-gene associations mined from literature

Literature associating CNTN2 and cortical dysplasia-focal epilepsy syndrome

CNTN2 [ENSP00000330633]

Transient axonal glycoprotein 1; In conjunction with another transmembrane protein, CNTNAP2, contributes to the organization of axonal domains at nodes of Ranvier by maintaining voltage-gated potassium channels at the juxtaparanodal region. May be involved in cell adhesion; Fibronectin type III domain containing

Synonyms:  CNTN2,  CNTN2p,  hCNTN2,  A0A024R9B4,  Q02246 ...

Linkouts:  STRING  Pharos  UniProt  OMIM