CTNND2

GENERAL INFORMATION

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Gene name

CTNND2

Gene description

Catenin (cadherin-associated protein), delta 2

Protein class

Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

7
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (cerebral cortex)
GTEx:Group enriched (cerebellum, cerebral cortex, hippocampus)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and nuclear expression mainly in the CNS.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Presumed off target binding observed and disregarded.

Data reliability

Supportive based on 2 antibodies.
HPA015077 , CAB037339
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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

Lateral ventricle

Lymph node

Liver

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 enriched (cerebral cortex)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (cerebellum, cerebral cortex, hippocampus)

Organ

Expression



GENE INFORMATION

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Gene name

CTNND2 (HGNC Symbol)

Synonyms

GT24, NPRAP

Description

Catenin (cadherin-associated protein), delta 2 (HGNC Symbol)

Entrez gene summary

This gene encodes an adhesive junction associated protein of the armadillo/beta-catenin superfamily and is implicated in brain and eye development and cancer formation. The protein encoded by this gene promotes the disruption of E-cadherin based adherens junction to favor cell spreading upon stimulation by hepatocyte growth factor. This gene is overexpressed in prostate adenocarcinomas and is associated with decreased expression of tumor suppressor E-cadherin in this tissue. This gene resides in a region of the short arm of chromosome 5 that is deleted in Cri du Chat syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]

Chromosome

5

Cytoband

p15.2

Chromosome location (bp)

10971840 - 11904043

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000169862 (version 78.38)

Entrez gene

1501

UniProt

Q9UQB3 (UniProt - Evidence at protein level)

neXtProt

NX_Q9UQB3

Antibodypedia

CTNND2 antibodies


PROTEIN BROWSER

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ENST00000304623
 
ENST00000458100
 
ENST00000502551
 
ENST00000503622
 
ENST00000508761
 
ENST00000511377
 
ENST00000513598
 
 
 
 


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)

CTNND2-001 ENSP00000307134
ENST00000304623
Q9UQB3
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Show » Show » 1225 132.7 No 0
CTNND2-004 ENSP00000426887
ENST00000503622
B4DRK2
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Show » Show » 888 98 No 0
CTNND2-005 ENSP00000426510
ENST00000511377
E7EPC8
Show all »
Show » Show » 1134 123.1 No 0
CTNND2-008 ENSP00000424296
ENST00000508761
D6RBA8
Show all »
Show » Show » 169 18.4 No 0
CTNND2-009 ENSP00000422389
ENST00000502551
D6RC65
Show all »
Show » Show » 209 22.7 No 0
CTNND2-012 ENSP00000426625
ENST00000513598
D6RF55
Show all »
Show » Show » 181 18.9 No 0
CTNND2-201 ENSP00000391155
ENST00000458100
Show » Show » 320 35.8 No 0