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Gene

oclna

ID
ZDB-GENE-040426-2685
Name
occludin a
Symbol
oclna Nomenclature History
Previous Names
  • ocln (1)
  • wu:fd23h10
  • wu:fi13c01
  • zgc:113992 (1)
  • zgc:56359
Type
protein_coding_gene
Location
Chr: 10 Mapping Details/Browsers
Description
Predicted to act upstream of or within bicellular tight junction assembly. Predicted to be located in bicellular tight junction and plasma membrane. Predicted to be integral component of membrane. Is expressed in several structures, including EVL; digestive system; musculature system; pleuroperitoneal region; and sensory system. Human ortholog(s) of this gene implicated in Crohn's disease and pseudo-TORCH syndrome 1. Orthologous to human OCLN (occludin).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
19 figures from 8 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
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 oclna Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
pseudo-TORCH syndrome 1 Alliance Pseudo-TORCH syndrome 1 251290
Associated With oclna Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR008253 Marvel domain
Domain IPR010844 Occludin homology domain
Family IPR002958 Occludin
Family IPR031176 ELL/occludin family
Domain Details Per Protein
Protein Length ELL/occludin family Marvel domain Occludin Occludin homology domain
UniProtKB:Q4KM13 492
UniProtKB:Q7ZUE7 492
UniProtKB:F1R799 491
UniProtKB:Q6NX99 500
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