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CLDN19 (claudin 19)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
149461
Gene nameGene Name - the full gene name approved by the HGNC.
Claudin 19
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
CLDN19
SynonymsGene synonyms aliases
HOMG5
ChromosomeChromosome number
1
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p34.2
SummarySummary of gene provided in NCBI Entrez Gene.
The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia rena
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs118203979 C>T Pathogenic Missense variant, coding sequence variant
rs118203980 G>A,C Pathogenic Stop gained, missense variant, coding sequence variant
rs118203981 A>C,G Pathogenic Missense variant, coding sequence variant
rs145591298 C>T Likely-pathogenic Coding sequence variant, synonymous variant, missense variant
rs1557551678 C>A Pathogenic Coding sequence variant, missense variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT518276 hsa-miR-4438 PAR-CLIP 23446348
MIRT518277 hsa-miR-6746-3p PAR-CLIP 23446348
MIRT518275 hsa-miR-4537 PAR-CLIP 23446348
MIRT518274 hsa-miR-5095 PAR-CLIP 23446348
MIRT518273 hsa-miR-7151-3p PAR-CLIP 23446348
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001934 Process Positive regulation of protein phosphorylation IMP 27593915
GO:0005198 Function Structural molecule activity IEA
GO:0005634 Component Nucleus IEA
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005923 Component Bicellular tight junction IBA 21873635
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q8N6F1
Protein name Claudin-19
Protein function Forms paracellular channels: coassembles with CLDN16 into tight junction strands with cation-selective channels through the strands, conveying epithelial permeability in a process known as paracellular tight junction permeability (PubMed:1818845
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00822 PMP22_Claudin
4 182
PMP-22/EMP/MP20/Claudin family
Family
Sequence
Sequence length 224
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
  Virion - Hepatitis viruses
Cell adhesion molecules
Tight junction
Leukocyte transendothelial migration
Pathogenic Escherichia coli infection
Hepatitis C
 
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Hypertension Hypertensive disease rs13306026, rs13333226
Hypomagnesemia Hypomagnesemia 2, renal, HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT rs118203979, rs118203980, rs118203981, rs104893720, rs104893721, rs104893722, rs104893723, rs104893724, rs104893725, rs104893727, rs104893728, rs104893729, rs104893730, rs104893731, rs104893732, rs121908543, rs121909379, rs28936387, rs28936388, rs755560627, rs121909380, rs1347239469, rs121909382, rs121909383, rs2144723103, rs121909384, rs121909385, rs267607050, rs121918067, rs387906880, rs371443644, rs786205909, rs786205910, rs794726858, rs138977195, rs568513106, rs185927948, rs886041108, rs201255508, rs374163823, rs147901432, rs199974259, rs13306668, rs200697179, rs200817545, rs140012781, rs202114767, rs749098014, rs373899077, rs1553809654, rs201555148, rs140551719, rs775931992, rs771701344, rs199849117, rs1555499234, rs759801838, rs1555499151, rs1555501632, rs765256758, rs1253995767, rs138308105, rs1557551678, rs779160677, rs752101663, rs759426055, rs1563974797, rs759377924, rs1366655422, rs754378340, rs34803727, rs370175770, rs1557785499, rs1557785503, rs781629728, rs1570980551, rs768527231, rs201945662, rs145337602, rs1596890176, rs139743444, rs780299444, rs1596883431, rs751409326, rs1274973729, rs146158333, rs747139582, rs753523115, rs148038173, rs374182921, rs761242621, rs751959432, rs1577430815, rs758035631, rs369360334, rs374055486, rs750710315, rs770513014, rs758683818, rs746818109, rs747249619, rs771326058, rs746623621, rs781209989, rs772241737 17033971, 27530400, 500385
Kidney disease Kidney Diseases, Chronic Kidney Diseases rs74315342, rs749740335, rs757649673, rs112417755, rs35138315
Myopia Myopia, Severe myopia rs387907109, rs146936371, rs587776903, rs786205127, rs398122836, rs199624584, rs587777625, rs786205216, rs758872875, rs764211125, rs1135402746, rs765658563, rs1555941129, rs1555941116, rs199923805, rs782555528, rs1554862601, rs1586620121, rs1387950081, rs2051026773, rs1422332023
Unknown
Disease name Disease term dbSNP ID References
Astigmatism Astigmatism
Coloboma of macula Hereditary macular coloboma
Congenital exomphalos Congenital exomphalos
Fundus coloboma Fundus coloboma

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