CLDN19

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Claudin-19 is a protein that in humans is encoded by the CLDN19 gene.[5] It belongs to the group of claudins. Claudin-19 has been implicated in magnesium transport.[6][7]

Quick facts Available structures, PDB ...
CLDN19
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCLDN19, HOMG5, claudin 19
External IDsOMIM: 610036; MGI: 3033992; HomoloGene: 17528; GeneCards: CLDN19; OMA:CLDN19 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_148960
NM_001123395
NM_001185117

NM_001038590
NM_153105

RefSeq (protein)

NP_001116867
NP_001172046
NP_683763

NP_001033679
NP_694745

Location (UCSC)Chr 1: 42.73 – 42.74 MbChr 4: 119.11 – 119.12 Mb
PubMed search[3][4]
Wikidata
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Claudins, such as CLDN19, are transmembrane proteins found at tight junctions. Tight junctions form barriers that control the passage of ions and molecules across an epithelial sheet and the movement of proteins and lipids between apical and basolateral domains of epithelial cells (Lee et al., 2006).[supplied by OMIM][5]

References

Further reading

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