L1CAM Chromosome X

L1 cell adhesion molecule
250 variants 250 Health Risk

Upload your DNA to see your personal genotypes for variants in L1CAM.

What This Gene Does
The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of this gene results in multiple transcript variants, some of which include an alternate exon that is considered to be specific to neurons. [provided by RefSeq, May 2013]
Gene Info
Gene Group
"CD molecules|Fibronectin type III domain containing|I-set domain containing|Ig-like cell adhesion molecule family"
Locus Type
gene with protein product
Location
Xq28
Ensembl
ENSG00000198910
Associated Conditions (28)
Spastic paraplegia
Inborn genetic diseases
MASA syndrome
X-linked complicated corpus callosum dysgenesis
X-linked hydrocephalus syndrome
See cases
Hereditary spastic paraplegia
L1CAM-related disorder
Hereditary ataxia
History of neurodevelopmental disorder
L1 syndrome
Intellectual disability
Thyroid cancer
nonmedullary
1
Nonpapillary renal cell carcinoma
Muscular dystrophy
limb-girdle
autosomal recessive 23
L1CAM-related disorders
+8 more conditions
Key Variants
RS1032992615
Conflicting classifications of pathogenicity
Spastic paraplegia, Inborn genetic diseases, Spastic paraplegia
Health Risk
RS1064796541
Conflicting classifications of pathogenicity
Spastic paraplegia, Spastic paraplegia
Health Risk
RS1172761444
Conflicting classifications of pathogenicity
Spastic paraplegia, Spastic paraplegia
Health Risk
RS1206062430
Conflicting classifications of pathogenicity
Inborn genetic diseases, Spastic paraplegia, Inborn genetic diseases
Health Risk
RS1273221058
Conflicting classifications of pathogenicity
Spastic paraplegia, Inborn genetic diseases, Spastic paraplegia
Health Risk
RS1298830102
Conflicting classifications of pathogenicity
Spastic paraplegia, MASA syndrome, X-linked complicated corpus callosum dysgenesis
Health Risk
RS1372534909
Conflicting classifications of pathogenicity
See cases, Spastic paraplegia, See cases
Health Risk
RS137940405
Conflicting classifications of pathogenicity
Spastic paraplegia, Spastic paraplegia
Health Risk
RS139197516
Conflicting classifications of pathogenicity
Inborn genetic diseases, Spastic paraplegia, MASA syndrome
Health Risk
RS141213959
Conflicting classifications of pathogenicity
Inborn genetic diseases, Spastic paraplegia, Inborn genetic diseases
Health Risk
RS1424993007
Conflicting classifications of pathogenicity
Spastic paraplegia, Hereditary spastic paraplegia, Spastic paraplegia
Health Risk
RS142563956
Conflicting classifications of pathogenicity
Spastic paraplegia, L1CAM-related disorder, Spastic paraplegia
Health Risk
All Variants (250)
RSID Category Clinical Significance Conditions
RS2520970677 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS2520985267 Health Risk Pathogenic X-linked hydrocephalus syndrome, X-linked hydrocephalus syndrome
RS2520986296 Health Risk Pathogenic L1CAM-related disorder, L1CAM-related disorder
RS2520999577 Health Risk Pathogenic X-linked hydrocephalus syndrome, X-linked hydrocephalus syndrome
RS2521000590 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS2521005091 Health Risk Pathogenic
RS2521011529 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS2521016418 Health Risk Pathogenic L1CAM-related disorder, L1CAM-related disorder
RS2521024037 Health Risk Pathogenic X-linked hydrocephalus syndrome, X-linked hydrocephalus syndrome
RS2521024495 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS2521024663 Health Risk Pathogenic Spastic paraplegia, Nonpapillary renal cell carcinoma, Spastic paraplegia
RS2521043571 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS377470679 Health Risk Pathogenic
RS398123362 Health Risk Pathogenic
RS398123364 Health Risk Pathogenic
RS782178366 Health Risk Pathogenic
RS797045673 Health Risk Pathogenic X-linked complicated corpus callosum dysgenesis, X-linked hydrocephalus syndrome, L1 syndrome
RS797045674 Health Risk Pathogenic X-linked hydrocephalus syndrome, X-linked hydrocephalus syndrome
RS863224494 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS878853099 Health Risk Pathogenic
RS879253713 Health Risk Pathogenic X-linked hydrocephalus syndrome, X-linked hydrocephalus syndrome
RS879253714 Health Risk Pathogenic MASA syndrome, MASA syndrome
RS879253715 Health Risk Pathogenic X-linked hydrocephalus syndrome, X-linked hydrocephalus syndrome
RS879253717 Health Risk Pathogenic Hydrocephalus, X-linked, with congenital idiopathic intestinal pseudoobstruction
RS879253724 Health Risk Pathogenic X-linked hydrocephalus syndrome, X-linked hydrocephalus syndrome
RS886039404 Health Risk Pathogenic
RS886039407 Health Risk Pathogenic X-linked hydrocephalus syndrome, Spastic paraplegia, X-linked hydrocephalus syndrome
RS886039409 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS886039410 Health Risk Pathogenic Spastic paraplegia, Spastic paraplegia
RS886039411 Health Risk Pathogenic
RS886041704 Health Risk Pathogenic
RS1064793162 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, Spastic paraplegia
RS111247323 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, Spastic paraplegia
RS137852522 Health Risk Pathogenic/Likely pathogenic X-linked hydrocephalus syndrome, MASA syndrome, Severe hydrocephalus
RS137852526 Health Risk Pathogenic/Likely pathogenic X-linked complicated corpus callosum dysgenesis, X-linked hydrocephalus syndrome, Congenital cerebellar hypoplasia
RS1557090943 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, Spastic paraplegia
RS1557091678 Health Risk Pathogenic/Likely pathogenic L1CAM-related disorder, L1CAM-related disorders, Spastic paraplegia
RS1557092247 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, L1 syndrome, X-linked hydrocephalus syndrome
RS1569544908 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, Spastic paraplegia
RS2148491960 Health Risk Pathogenic/Likely pathogenic L1CAM-related disorder, L1 syndrome, L1CAM-related disorder
RS2148494128 Health Risk Pathogenic/Likely pathogenic MASA syndrome, X-linked hydrocephalus syndrome, MASA syndrome
RS2521002176 Health Risk Pathogenic/Likely pathogenic L1CAM-related disorder, Spastic paraplegia, L1CAM-related disorder
RS2521039402 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, Spastic paraplegia
RS367665974 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, Inborn genetic diseases, X-linked complicated corpus callosum dysgenesis
RS782553641 Health Risk Pathogenic/Likely pathogenic MASA syndrome, X-linked complicated corpus callosum dysgenesis, X-linked hydrocephalus syndrome
RS797044787 Health Risk Pathogenic/Likely pathogenic X-linked hydrocephalus syndrome, L1CAM-related disorder, Spastic paraplegia
RS875989884 Health Risk Pathogenic/Likely pathogenic X-linked hydrocephalus syndrome, L1 syndrome, X-linked hydrocephalus syndrome
RS886039405 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, L1 syndrome, MASA syndrome
RS886039406 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, L1 syndrome, Spastic paraplegia
RS886039408 Health Risk Pathogenic/Likely pathogenic Spastic paraplegia, L1 syndrome, MASA syndrome
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