CLDN19

GENERAL INFORMATION

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Gene name

CLDN19

Gene description

Claudin 19

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (kidney, placenta)
GTEx:Tissue enriched (kidney)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (kidney, placenta)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (kidney)

Organ

Expression



GENE INFORMATION

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Gene name

CLDN19

Synonyms

Description

Claudin 19 (HGNC Symbol)

Entrez gene summary

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]

Chromosome

1

Cytoband

p34.2

Chromosome location (bp)

42733093 - 42740254

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000164007 (version 78.38)

Entrez gene

149461

UniProt

Q8N6F1 (UniProt - Evidence at protein level)

neXtProt

NX_Q8N6F1

Antibodypedia

CLDN19 antibodies


PROTEIN BROWSER

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ENST00000296387
 
ENST00000372539
 
ENST00000539749
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CLDN19-001 ENSP00000296387
ENST00000296387
Q8N6F1
Show all »
Show » Show » 224 23.2 No 4
CLDN19-002 ENSP00000361617
ENST00000372539
Q8N6F1
Show all »
Show » Show » 211 22.1 No 4
CLDN19-201 ENSP00000443229
ENST00000539749
Q8N6F1
Show all »
Show » Show » 218 22.7 No 3