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CLDN19
HPA
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  • CLDN19
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

CLDN19
Synonyms
Gene descriptioni

Full gene name according to HGNC.

Claudin 19
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Disease related genes
Human disease related genes
Potential drug targets
Transporters
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Membrane
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 1
Cytoband p34.2
Chromosome location (bp) 42733093 - 42740254
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

3
Ensembl ENSG00000164007 (version 109)
Entrez gene 149461
HGNC HGNC:2040
UniProt Q8N6F1 (UniProt - Evidence at protein level)
neXtProt NX_Q8N6F1
GeneCards CLDN19
Antibodypedia CLDN19 antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

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 1, 2. Involved in the maintenance of ion gradients along the nephron. In the thick ascending limb (TAL) of Henle's loop, facilitates sodium paracellular permeability from the interstitial compartment to the lumen, contributing to the lumen-positive transepithelial potential that drives paracellular magnesium and calcium reabsorption (By similarity) 3, 4. Forms paracellular barriers on its own. In the peripheral nervous system, represents a major constituent of the tight junctions in Schwann cells and contributes to electrical sealing. During retinal neurogenesis, may regulate the barrier properties of tight junctions in retinal pigment epithelium, required for proper retinal tissue differentiation and vision (By similarity) 5, 6.... show less
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

Sensory transduction, Vision
Ligand (UniProt)i

Keywords assigned by UniProt to proteins because they bind, are associated with, or whose activity is dependent of some molecule.

Magnesium
Gene summary (Entrez)i

Useful information about the gene from Entrez

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 renal with ocular involvement (HOMGO). HOMGO is 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. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
CLDN19-201
ENSP00000296387
ENST00000296387
Q8N6F1
[Direct mapping] Claudin-19
Show all
Transporters
   Transporter channels and pores
Predicted membrane proteins
   Prediction method-based
   Membrane proteins predicted by MDM
   MEMSAT3 predicted membrane proteins
   MEMSAT-SVM predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   # TM segments-based
   4TM proteins predicted by MDM
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Other congenital disorders of metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
   DeepTMHMM predicted membrane proteins
Show all
GO:0001934 [positive regulation of protein phosphorylation]
GO:0005198 [structural molecule activity]
GO:0005634 [nucleus]
GO:0005737 [cytoplasm]
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:0016020 [membrane]
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:0030054 [cell junction]
GO:0030336 [negative regulation of cell migration]
GO:0031532 [actin cytoskeleton reorganization]
GO:0042802 [identical protein binding]
GO:0043296 [apical junction complex]
GO:0043297 [apical junction assembly]
GO:0048471 [perinuclear region of cytoplasm]
GO:0050896 [response to stimulus]
GO:0061045 [negative regulation of wound healing]
GO:0070161 [anchoring junction]
GO:0070830 [bicellular tight junction assembly]
GO:0120193 [tight junction organization]
GO:0150111 [regulation of transepithelial transport]
GO:1901890 [positive regulation of cell junction assembly]
Show all
224 aa
23.2 kDa
No 4
CLDN19-202
ENSP00000361617
ENST00000372539
Q8N6F1
[Direct mapping] Claudin-19
Show all
Transporters
   Transporter channels and pores
Predicted membrane proteins
   Prediction method-based
   Membrane proteins predicted by MDM
   MEMSAT3 predicted membrane proteins
   MEMSAT-SVM predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   # TM segments-based
   4TM proteins predicted by MDM
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Other congenital disorders of metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
   DeepTMHMM predicted membrane proteins
Show all
GO:0001934 [positive regulation of protein phosphorylation]
GO:0005198 [structural molecule activity]
GO:0005515 [protein binding]
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:0016020 [membrane]
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: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:0070161 [anchoring junction]
GO:0070830 [bicellular tight junction assembly]
GO:0150111 [regulation of transepithelial transport]
GO:1901890 [positive regulation of cell junction assembly]
Show all
211 aa
22.1 kDa
No 4
CLDN19-203
ENSP00000443229
ENST00000539749
Q8N6F1
[Direct mapping] Claudin-19
Show all
Transporters
   Transporter channels and pores
Predicted membrane proteins
   Prediction method-based
   Membrane proteins predicted by MDM
   MEMSAT3 predicted membrane proteins
   MEMSAT-SVM predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   # TM segments-based
   3TM proteins predicted by MDM
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Other congenital disorders of metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
   DeepTMHMM predicted membrane proteins
Show all
GO:0001934 [positive regulation of protein phosphorylation]
GO:0005198 [structural molecule activity]
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:0016020 [membrane]
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: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:0070161 [anchoring junction]
GO:0070830 [bicellular tight junction assembly]
GO:0150111 [regulation of transepithelial transport]
GO:1901890 [positive regulation of cell junction assembly]
Show all
218 aa
22.7 kDa
No 3

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