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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.1756C>T
p.Gln586X
Exon 14
Nonsense
Disease-causing
n.a.
n.a.
n.a.
n.a.
Ig 6
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
2
Adducted thumbs, Hydrocephalus, Mental retardation, Spastic paraplegia
Died before the age of 1 yr: 1/2
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