OCLN

GENERAL INFORMATION

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Gene name

OCLN

Gene description

Occludin

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Predicted secreted proteins
Transporters

Predicted localization

Membrane,Secreted

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (thyroid gland)
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and membranous expression in selected tissues, most abundant in gastrointestinal tract, kidney, urinary bladder and endometrium.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 5 antibodies.
HPA005933 , CAB013075 , CAB068212 , CAB068213 , CAB068214
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Gallbladder

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (thyroid gland)

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

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Gene name

OCLN (HGNC Symbol)

Synonyms

PPP1R115

Description

Occludin (HGNC Symbol)

Entrez gene summary

This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011]

Chromosome

5

Cytoband

q13.2

Chromosome location (bp)

69492292 - 69558104

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000197822 (version 78.38)

Entrez gene

100506658

UniProt

Q16625 (UniProt - Evidence at protein level)

neXtProt

NX_Q16625

Antibodypedia

OCLN antibodies


PROTEIN BROWSER

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ENST00000355237
 
ENST00000396442
 
ENST00000538151
 
 
 
 


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)

OCLN-001 ENSP00000347379
ENST00000355237
Q16625
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Show » Show » 522 59.1 No 4
OCLN-002 ENSP00000379719
ENST00000396442
Q16625
Show all »
Show » Show » 522 59.1 No 4
OCLN-201 ENSP00000445940
ENST00000538151
Q16625
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Show » Show » 271 31.6 Yes 0