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University Medical Center Groningen
Department of Genetics -
L1CAM Mutation Database
Introduction
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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.1267+4A>T
p.Leu376_Gln423del
Intron 10
Splice site
Disease-causing
n.a.
n.a.
n.a.
n.a.
Ig 4
Exon 10 skipping has been proven by cDNA sequencing
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
3
Adducted thumbs, Hydrocephalus, Mental retardation, Spastic paraplegia
Index case died before the age of 1 yr.
Jouet et al. (1995a)
References
Year
Author
Title
Journal
Volume
Pages
Weblink
1995a
Jouet et al.
New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome
Am. J. Hum. Genet.
56
1304-1314
7762552