Gene: CLDN4 (claudin 4)  Homo sapiens

Symbol: CLDN4
Name: claudin 4
Description: This gene encodes an integral membrane protein, which belongs to the claudin family. The protein is a component of tight junction strands and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: claudin-4; Clostridium perfringens enterotoxin receptor 1; CPE-R; CPE-receptor; CPER; CPETR; CPETR1; hCPE-R; OTTHUMP00000160507; OTTHUMP00000211778; WBSCR8; Williams-Beuren syndrome chromosomal region 8 protein
Orthologs: Mus musculus : Cldn4 (claudin 4)  MGI
Rattus norvegicus : Cldn4 (claudin 4)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_1776,770,253 - 76,772,075+NCBI
Human Alternate Assembly CRA_TCAGchr7v2772,578,265 - 72,580,087+NCBI
Human Genome Assembly HuRef769,128,478 - 69,130,300+NCBI
Human Genome Assembly GRCh37773,245,193 - 73,247,015+NCBI
Human Genome Assembly Build 36772,883,129 - 72,884,951+NCBI
Human Cytogenetic Map7q11.23 NCBI
Human Genome Assembly772,689,843 - 72,691,665 NCBI
Model

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


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway 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 CLDN4
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1317413
Created: 2005-01-12
Species: Homo sapiens
Last Modified: 2013-04-23
Status: ACTIVE