Gene

otoa

ID
ZDB-GENE-100922-124
Name
otoancorin
Symbol
otoa Nomenclature History
Previous Names
  • si:dkey-71b5.7
Type
protein_coding_gene
Location
Chr: 16 Mapping Details/Browsers
Description
Predicted to be involved in cell-matrix adhesion. Predicted to localize to cell surface. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 22. Orthologous to human OTOA (otoancorin).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
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 otoa Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive nonsyndromic deafness 22 Alliance Deafness, autosomal recessive 22 607039
Associated With otoa Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR048992 Stereocilin, LRR domain
Family IPR010335 Mesothelin
Family IPR026664 Stereocilin-related
Domain Details Per Protein
Protein Length Mesothelin Stereocilin, LRR domain Stereocilin-related
UniProtKB:A0A8M6Z1A9 656
UniProtKB:E7EXK7 1214
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