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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.3457+3A>T
p.?
Intron 25
RNA splicing defect
Disease-causing
n.a.
n.a.
n.a.
n.a.
n.a.
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
Unknown
Hydrocephalus, Mental retardation
Hubner et al (2004)
References
Year
Author
Title
Journal
Volume
Pages
Weblink
2004
Hubner et al
Intronic mutations in the L1CAM gene may cause X-linked hydrocephalus by aberrant splicing
Hum Mutat
23(5)
526
15108295