cabp4

ID

ZDB-GENE-081104-291

Name

calcium binding protein 4

Symbol

cabp4 Nomenclature History

Previous Names

cabp4a (1)
si:ch73-56f16.1

Type

protein_coding_gene

Location

Chr: 8 Mapping Details/Browsers

Genome Assembly

GRCz12tu

Annotation Status

Unknown

Description

Predicted to enable calcium channel regulator activity. Predicted to be involved in phototransduction and visual perception. Is expressed in retinal photoreceptor layer. Human ortholog(s) of this gene implicated in congenital stationary night blindness. Orthologous to human CABP4 (calcium binding protein 4).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

2 figures from 2 publications

Cross-Species Comparison

High Throughput Data

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Daniocell

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 cabp4 Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
		Cone-rod synaptic disorder, congenital nonprogressive	610427

Associated With cabp4 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	Additional Resources	Length
UniProtKB:A0A8M9QIQ8	InterPro	268
UniProtKB:A0A8M2BEY0	InterPro	228
UniProtKB:A0A286Y9G4	InterPro	229
UniProtKB:A0A8M9QDW6	InterPro	267
UniProtKB:A0A8M3B1U9	InterPro	118
UniProtKB:A0AC58G8F0	InterPro	118
UniProtKB:A0AC58G8F8	InterPro	118