Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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149461 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Claudin 19 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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CLDN19 |
SynonymsGene synonyms aliases
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HOMG5 |
ChromosomeChromosome number
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1 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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1p34.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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 |
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Sequence |
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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.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Hypertension |
Hypertensive disease |
rs13306026, rs13333226 |
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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 |
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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 |
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Nystagmus |
Nystagmus |
rs137852207, rs137852208, rs1928435502, rs137852209, rs137852210, rs1929191668, rs137852211, rs137852212, rs2124209414, rs387906720, rs387906721, rs1602791884, rs786205896 |
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Rod-cone dystrophy |
Rod-Cone Dystrophy |
rs267606641, rs199476133, rs193302849, rs777668842, rs775518991, rs752300607, rs142759730, rs756225251, rs536742386, rs1588830568, rs778907433 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Astigmatism |
Astigmatism |
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Coloboma of macula |
Hereditary macular coloboma |
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Congenital exomphalos |
Congenital exomphalos |
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Fundus coloboma |
Fundus coloboma |
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Hypomagnesemia renal, with ocular involvement |
Hypomagnesemia 5, Renal, with Ocular Involvement |
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17033971 |
Medullary nephrocalcinosis |
Medullary nephrocalcinosis |
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Meier blumberg imahorn syndrome |
Meier Blumberg Imahorn syndrome |
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17033971 |
Nephrocalcinosis |
Nephrocalcinosis |
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28893421 |
Nephrolithiasis |
Nephrolithiasis |
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28893421 |
Hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement |
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement |
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Retinal coloboma |
Coloboma of the Retina |
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Strabismus |
Strabismus |
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