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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.2858T>G
p.Leu953Arg
Exon 21
Missense
Disease-causing
Key residue
Not tolerated
Probably damaging
Moderately
Fn 4
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
2
Adducted thumbs, Hydrocephalus, Spastic paraplegia
Kanemura et al (2006)
References
Year
Author
Title
Journal
Volume
Pages
Weblink
2006
Kanemura et al
Molecular mechanisms and neuroimaging criteria for severe L1 syndrome with X-linked hydrocephalus
J Neurosurg: Pediatrics
105
403-412
17328266