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University Medical Center Groningen
Department of Genetics -
L1CAM Mutation Database
Introduction
Database
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Mutations
Protein domains
References
Mutation Details
DNA change
Protein change
Exon/intron
Type
Reported classification
Bateman
SIFT
PolyPhen
Conserved
Protein domain
Remarks
LOVD ID
c.466C>G
p.Ser156X
Exon 5
Nonsense
Disease-causing
n.a.
n.a.
n.a.
n.a.
Ig 2
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
2
(Dys)agenesis corpus callosum, Hydrocephalus, Mental retardation
Index case died at the age of 12 yrs. Patient 2 died shortly after birth.
Graf et al. (2000)
References
Year
Author
Title
Journal
Volume
Pages
Weblink
2000
Graf et al.
Diffusion-weighted magnetic resonance imaging in boys with neural cell adhesion molecule L1 mutations and congenital hydrocephalus
Ann. Neurol.
47
113-117
10632110