CDH3

GENERAL INFORMATION

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Gene name

CDH3

Gene description

Cadherin 3, type 1, P-cadherin (placental)

Protein class

Disease related genes
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (skin)
GTEx:Tissue enhanced (ovary)

Protein evidence

Evidence at protein level

Protein localization

Membranous expression in most glandular cells and surface epithelium.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA001767 , CAB002487
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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

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 (skin)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (ovary)

Organ

Expression



GENE INFORMATION

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Gene name

CDH3 (HGNC Symbol)

Synonyms

CDHP, PCAD

Description

Cadherin 3, type 1, P-cadherin (placental) (HGNC Symbol)

Entrez gene summary

This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. This gene is located in a six-cadherin cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. In addition, aberrant expression of this protein is observed in cervical adenocarcinomas. Mutations in this gene have been associated with congential hypotrichosis with juvenile macular dystrophy. [provided by RefSeq, Jul 2008]

Chromosome

16

Cytoband

q22.1

Chromosome location (bp)

68636189 - 68722616

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000062038 (version 78.38)

Entrez gene

1001

UniProt

P22223 (UniProt - Evidence at protein level)

neXtProt

NX_P22223

Antibodypedia

CDH3 antibodies


PROTEIN BROWSER

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ENST00000264012
 
ENST00000429102
 
ENST00000568292
 
ENST00000569080
 
 
 
 


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)

CDH3-001 ENSP00000264012
ENST00000264012
P22223
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Show » Show » 829 91.4 Yes 1
CDH3-002 ENSP00000398485
ENST00000429102
P22223
Show all »
Show » Show » 784 86.6 Yes 1
CDH3-005 ENSP00000463364
ENST00000568292
Show » Show » 155 17.3 No 1
CDH3-010 ENSP00000463415
ENST00000569080
J3QL75
Show all »
Show » 81 9.1 No 0