Cldn14 Gene Search Result

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3 records found for search term Cldn14

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1319353	CLDN14	claudin 14	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 cont ... (more) inuous 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. The encoded protein also binds specifically to the WW domain of Yes-associated protein. Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness. It is also reported that four synonymous variants in this gene are associated with kidney stones and reduced bone mineral density. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2010]	21	36460621	36576569	Human	109	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
38637361	CLDN14-AS1	CLDN14 antisense RNA 1		21	36430325	36498526	Human		symbol , COSMIC , name , Human Proteome Map	gene, ncrna, VALIDATED [RefSeq]
155791660	LNCTSI	lncRNA TGF-beta/SMAD3 pathway interacting					Human		old_gene_symbol	gene, ncrna