G2Cdb::Search

Search results for: L1CAM

Disease (18)

Disease Description Nervous effect
D00000166 Schizophrenia Y
D00000176 MASA syndrome Y
D00000188 Spastic paraplegia (X-linked complicated) Y
D00000189 Spastic paraplegia (X-linked) Y
D00000197 Epilepsy (autosomal dominant lateral temporal) Y
D00000198 Epilepsy (autosomal dominant partial with auditory features) Y
D00000201 Epilepsy (partial with auditory features) Y
D00000202 Epilepsy (temporal lobe) Y
D00000207 Hereditary motor and sensory neuropathy Y
D00000211 Spastic paraplegia Y
D00000215 Hydrocephalus Y
D00000216 L1 syndrome Y
D00000217 X-linked hydrocephalus Y
D00000218 Hydrocephalus-stenosis of the aqueduct of Sylvius Y
D00000271 Nephrogenic diabetes insipidus N
D00000290 Hirschsprung's disease N
D00000292 Duplex kidneys N
D00000323 CRASH syndrome Y

Gene (4)

Gene Symbol Species Description
G00000632 L1cam Mus musculus L1 cell adhesion molecule
G00001881 L1CAM Homo sapiens L1 cell adhesion molecule
G00002845 Chl1 Mus musculus cell adhesion molecule with homology to L1CAM
G00005835 CHL1 Homo sapiens cell adhesion molecule with homology to L1CAM (close homolog of L1)
© 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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