Gene: CDH13 (cadherin 13, H-cadherin (heart))  Homo sapiens

Symbol: CDH13
Name: cadherin 13, H-cadherin (heart)
Description: This gene encodes a member of the cadherin superfamily. The encoded protein is localized to the surface of the cell membrane and is anchored by a GPI moiety, rather than by a transmembrane domain. The protein lacks the cytoplasmic domain characteristic of other cadherins, and so is not thought to be a cell-cell adhesion glycoprotein. This protein acts as a negative regulator of axon growth during neural differentiation. It also protects vascular endothelial cells from apoptosis due to oxidative stress, and is associated with resistance to atherosclerosis. The gene is hypermethylated in many types of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2011]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: cadherin 13; cadherin-13; CDHH; H-cadherin; heart cadherin; heart-cadherin; P105; P105; T-cad; T-cadherin; truncated cadherin; truncated-cadherin
Orthologs: Mus musculus : Cdh13 (cadherin 13)  MGI
Rattus norvegicus : Cdh13 (cadherin 13)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11683,666,649 - 84,836,402+NCBI
Human Genome Assembly HuRef1668,413,614 - 69,581,731+NCBI
Human Genome Assembly GRCh371682,660,399 - 83,830,215+NCBI
Human Genome Assembly Build 361681,218,079 - 82,387,702+NCBI
Human Cytogenetic Map16q23.3 NCBI
Human Genome Assembly1681,218,078 - 82,387,698 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on CDH13
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 734374
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2013-04-23
Status: ACTIVE