Gene

cldn11b

ID
ZDB-GENE-010328-13
Name
claudin 11b
Symbol
cldn11b Nomenclature History
Previous Names
  • cldn11
  • fb97c11
  • wu:fb97c11 (1)
Type
protein_coding_gene
Location
Chr: 24 Mapping Details/Browsers
Description
Predicted to have structural molecule activity. Predicted to localize to bicellular tight junction; integral component of membrane; and plasma membrane. Is expressed in several structures, including digestive system; eye; gonad; heart; and kidney. Orthologous to human CLDN11 (claudin 11).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
7 figures from 3 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With cldn11b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hypomyelinating leukodystrophy 22 Alliance Leukodystrophy, hypomyelinating, 22 619328
Associated With cldn11b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR017974 Claudin, conserved site
Family IPR006187 Claudin
Domain Details Per Protein
Protein Length Claudin Claudin, conserved site
UniProtKB:A4QNU3 256
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations