G2Cdb::Allele report

Mutation type
MI

Altered genes (1)

Gene Symbol Species Description
G00001881 L1CAM Homo sapiens L1 cell adhesion molecule

Diseases (1)

Disease Description Nervous effect
D00000198 Epilepsy (autosomal dominant partial with auditory features) Y

Literature (1)

Pubmed - other

© G2C 2014. The Genes to Cognition Programme received funding from The Wellcome Trust and the EU FP7 Framework Programmes:
EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).

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