Gene

cabp2a

ID
ZDB-GENE-050913-25
Name
calcium binding protein 2a
Symbol
cabp2a Nomenclature History
Previous Names
  • zgc:112300 (1)
Type
protein_coding_gene
Location
Chr: 1 Mapping Details/Browsers
Description
Predicted to have calcium ion binding activity. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 93. Is expressed in notochord and retinal inner nuclear layer. Orthologous to human CABP2 (calcium binding protein 2).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Di Donato 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 cabp2a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive nonsyndromic deafness 93 Alliance Deafness, autosomal recessive 93 614899
Associated With cabp2a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Binding_site IPR018247 EF-Hand 1, calcium-binding site
Domain IPR002048 EF-hand domain
Family IPR043582 Calcium binding protein 1/2/4/5
Homologous_superfamily IPR011992 EF-hand domain pair
Domain Details Per Protein
Protein Length Calcium binding protein 1/2/4/5 EF-Hand 1, calcium-binding site EF-hand domain EF-hand domain pair
UniProtKB:A0A8M3B2R3 233
UniProtKB:A0A0R4IU57 236
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