Sequence Detail

ID/Version

Q9ET38 Q8R4B7 (UniProt | EBI)

Last sequence update: 2004-05-24
Last annotation update: 2024-07-24

Sequence description from provider

RecName: Full=Claudin-19 {ECO:0000303|PubMed:19706394};

Provider

SWISS-PROT

Sequence

Polypeptide 224 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	Cldn19	claudin 19	49	104	3	9

Sequence references in MGI

J:99659 Miyamoto T, et al., Tight junctions in Schwann cells of peripheral myelinated axons: a lesson from claudin-19-deficient mice. J Cell Biol. 2005 May 9;169(3):527-38
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:153096 Hou J, et al., Claudin-16 and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium. Proc Natl Acad Sci U S A. 2009 Sep 8;106(36):15350-5
J:239545 Milatz S, et al., Mosaic expression of claudins in thick ascending limbs of Henle results in spatial separation of paracellular Na+ and Mg2+ transport. Proc Natl Acad Sci U S A. 2017 Jan 10;114(2):E219-E227
J:245332 Saitoh Y, et al., Tight junctions. Structural insight into tight junction disassembly by Clostridium perfringens enterotoxin. Science. 2015 Feb 13;347(6223):775-8
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:352406 Wang SB, et al., Disease-associated mutations of claudin-19 disrupt retinal neurogenesis and visual function. Commun Biol. 2019;2:113