Gene

cldn19

ID
ZDB-GENE-050417-242
Name
claudin 19
Symbol
cldn19 Nomenclature History
Previous Names
  • zgc:112141
Type
protein_coding_gene
Location
Chr: 11 Mapping Details/Browsers
Description
Predicted to have structural molecule activity. Predicted to localize to bicellular tight junction; integral component of membrane; and plasma membrane. Human ortholog(s) of this gene implicated in renal hypomagnesemia 5 with ocular involvement. Orthologous to human CLDN19 (claudin 19).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Baltzegar et al., 2013
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 cldn19 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
renal hypomagnesemia 5 with ocular involvement Alliance Hypomagnesemia 5, renal, with ocular involvement 248190
Associated With cldn19 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 IPR004031 PMP-22/EMP/MP20/Claudin
Family IPR006187 Claudin
Domain Details Per Protein
Protein Length Claudin Claudin, conserved site PMP-22/EMP/MP20/Claudin
UniProtKB:A0A8M6Z120 218
UniProtKB:A0A8M6Z925 222
UniProtKB:Q567D5 209
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA cldn19-201 (1) Havana 1457 nt
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