CLDN1 Chromosome 3

Claudin 1
10 variants 10 Health Risk

Upload your DNA to see your personal genotypes for variants in CLDN1.

What This Gene Does
Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. Loss of function mutations result in neonatal ichthyosis-sclerosing cholangitis syndrome. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Claudins
Locus Type
gene with protein product
Location
3q28
Ensembl
ENSG00000163347
Associated Conditions (3)
CLDN1-related disorder
Inborn genetic diseases
Neonatal ichthyosis-sclerosing cholangitis syndrome
Key Variants
All Variants (10)
RSID Category Clinical Significance Conditions
RS145197251 Health Risk Conflicting classifications of pathogenicity CLDN1-related disorder, CLDN1-related disorder
RS200926144 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373516096 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS377184401 Health Risk Conflicting classifications of pathogenicity
RS1402621591 Health Risk Likely pathogenic Neonatal ichthyosis-sclerosing cholangitis syndrome, Neonatal ichthyosis-sclerosing cholangitis syndrome
RS1716943798 Health Risk Pathogenic
RS773766654 Health Risk Pathogenic Neonatal ichthyosis-sclerosing cholangitis syndrome, Neonatal ichthyosis-sclerosing cholangitis syndrome
RS864309516 Health Risk Pathogenic Neonatal ichthyosis-sclerosing cholangitis syndrome, Neonatal ichthyosis-sclerosing cholangitis syndrome
RS864309517 Health Risk Pathogenic Neonatal ichthyosis-sclerosing cholangitis syndrome, Neonatal ichthyosis-sclerosing cholangitis syndrome
RS752054405 Health Risk Pathogenic/Likely pathogenic
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