Sequence Detail

ID/Version

Q9Z0S5 Q9D7Z0 Q9D8A6 (UniProt | EBI)

Last sequence update: 2002-05-10
Last annotation update: 2024-07-24

Sequence description from provider

RecName: Full=Claudin-15 {ECO:0000303|PubMed:37100833};

Provider

SWISS-PROT

Sequence

Polypeptide 227 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Cldn15	claudin 15	15	103	4	6

Sequence references in MGI

J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:135596 Tamura A, et al., Megaintestine in claudin-15-deficient mice. Gastroenterology. 2008 Feb;134(2):523-34
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89
J:330151 Wada M, et al., Loss of claudins 2 and 15 from mice causes defects in paracellular Na+ flow and nutrient transport in gut and leads to death from malnutrition. Gastroenterology. 2013 Feb;144(2):369-380
J:335204 Hempstock W, et al., The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine. Sci Rep. 2023 Apr 26;13(1):6799
J:335329 Tamura A, et al., Loss of claudin-15, but not claudin-2, causes Na+ deficiency and glucose malabsorption in mouse small intestine. Gastroenterology. 2011 Mar;140(3):913-23