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University Medical Center Groningen
Department of Genetics -
L1CAM Mutation Database
Introduction
Database
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Mutations
Protein domains
References
Reference details
Author
Year
Journal
Pages
Volume
Title
Weblink
Parisi et al
2002
Am J med Genet A
51-56
108
Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease?
11857550
Mutations mentioned in reference
Protein Domain
Exon/Intron
DNA Change
Protein Change
Type
Reported Classification
Details
LOVD ID
Fn 2
Exon 18
c.2254G>A
p.Val752Met
Missense
Disease-causing
Details
Patients
Family
# Affected relatives
DNA change
Protein change
Exon/Intron
Clinical features
Remarks
1
1
c.2254G>A
p.Val752Met
Exon 18
(Dys)agenesis corpus callosum, Adducted thumbs, Hirschsprung's disease, Hydrocephalus, Hypotonia
> 2 yrs