CLDN11 Chromosome 3

Claudin 11
1 variant 1 Health Risk

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What This Gene Does
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]
Gene Info
Gene Group
"Claudins|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
3q26.2
Ensembl
ENSG00000013297
Associated Conditions (3)
Leukodystrophy
hypomyelinating
22
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS2108249442 Health Risk Pathogenic Leukodystrophy, hypomyelinating, 22
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