Entity Details

Primary name CLD19_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8N6F1
EntryNameCLD19_HUMAN
FullNameClaudin-19
TaxID9606
Evidenceevidence at protein level
Length224
SequenceStatuscomplete
DateCreated2003-01-17
DateModified2021-06-02

Ontological Relatives

GenesCLDN19

GO terms

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GOName
GO:0001934 positive regulation of protein phosphorylation
GO:0005198 structural molecule activity
GO:0005634 nucleus
GO:0005886 plasma membrane
GO:0005923 bicellular tight junction
GO:0007155 cell adhesion
GO:0007601 visual perception
GO:0008285 negative regulation of cell population proliferation
GO:0010628 positive regulation of gene expression
GO:0010629 negative regulation of gene expression
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
GO:0016338 calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules
GO:0019227 neuronal action potential propagation
GO:0030336 negative regulation of cell migration
GO:0031532 actin cytoskeleton reorganization
GO:0042802 identical protein binding
GO:0043296 apical junction complex
GO:0048471 perinuclear region of cytoplasm
GO:0050896 response to stimulus
GO:0061045 negative regulation of wound healing
GO:0070830 bicellular tight junction assembly
GO:0150111 regulation of transepithelial transport
GO:1901890 positive regulation of cell junction assembly

Subcellular Location

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Subcellular Location
Cell junction
Cell membrane

Domains

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DomainNameCategoryType
IPR004031 PMP-22/EMP/MP20/Claudin superfamilyFamilyFamily
IPR006187 ClaudinFamilyFamily
IPR017974 Claudin, conserved siteSiteConserved site

Diseases

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Disease IDSourceNameDescription
248190 OMIMHypomagnesemia 5, renal, with or without ocular involvement (HOMG5)A progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. The renal phenotype is virtually undistinguishable from that of patients with HOMG3. The disease is caused by variants affecting the gene represented in this entry.

Interactions

65 interactions

InteractorPartnerSourcesPublicationsLink
CLD19_HUMANCLD16_HUMANDIP, MINT19706394 22373575 details
CLD19_HUMANSRPK2_HUMANBioGRID, IntAct23602568 details
CLD19_HUMANGGT7_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANK1H1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSTOM_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANM4A4A_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANT106C_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANHG2A_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANPKHB2_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANTNF14_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANKELL_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANDHB13_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANT4S18_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCLC14_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANLRC25_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANTM248_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANIL3RA_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANAQP9_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANMUC1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSUSD3_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANMO2R1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANFCGRN_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANBT2A1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSAR1A_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANGP161_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSGPL1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANPDZ1I_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSCRB2_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSLAF6_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANTM52B_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANFKBP7_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANAQP6_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANFNDC9_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANLRC4C_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANGORAB_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCLRN1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANFCGR1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCD53_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSACA1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANICAM3_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANF209A_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANLAPM5_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSYNE4_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANMFF_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANKRT34_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCRTP1_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANSTML3_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCXCR3_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANM4A14_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCLC2D_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANBIK_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANB2L13_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCXA8_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANGPX8_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANTMM80_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANKI2L3_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANS35C2_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANERGI3_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANINGR2_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANNTCP_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANPVR_HUMANBioGRID, IntAct32296183 details
CLD19_HUMANCREB3_HUMANBioGRID, IntAct25910212 details
CLD19_HUMANPK2L1_HUMANBioGRID, IntAct25910212 details
CLD19_HUMANCLD18_HUMANDIP19706394 details
CLD19_HUMANBSCL2_HUMANBioGRID32296183 details