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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.523+6T>G
none
Intron 5
Intronic variation
Non disease-causing
n.a.
n.a.
n.a.
n.a.
n.a.
Proven, no influence on RNA splicing
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
1
Adducted thumbs, Hirschsprung's disease, Hydrocephalus, Mental retardation
Hofstra et al. (2002)
References
Year
Author
Title
Journal
Volume
Pages
Weblink
2002
Hofstra et al.
Hirschsprung disease and L1CAM: is the disturbed sex ratio caused by L1CAM mutations?
J. Med. Genet
39
el 1
11897831
2004
Okamoto et al.
Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM
J Hum Genet
49
334-337
15148591