Version 5.4
Homo sapiens Gene: CABP4
Summary
InnateDB Gene IDBG-60464.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CABP4
Gene Name calcium binding protein 4
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000175544
Encoded Proteins
IDBP-60466
calcium binding protein 4
IDBP-379463
calcium binding protein 4
IDBP-584219
calcium binding protein 4
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. [provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:67452406-67460313
Strand Forward strand
Band q13.2
Transcripts
ENST00000325656 ENSP00000324960
ENST00000438189 ENSP00000401555
ENST00000538060
ENST00000542025
ENST00000545040
ENST00000542233
ENST00000545777 ENSP00000439145
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005509 calcium ion binding
Biological Process
GO:0007165 signal transduction
GO:0007601 visual perception
GO:0007602 phototransduction
GO:0008594 photoreceptor cell morphogenesis
GO:0046549 retinal cone cell development
GO:0060040 retinal bipolar neuron differentiation
Cellular Component
GO:0005576 extracellular region
GO:0005829 cytosol
GO:0043195 terminal bouton
GO:0045202 synapse
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
ENSMUSG00000024842
View Gene Order
ENSBTAG00000004785
Not yet available
Cross-References
SwissProt P57796
TrEMBL A0A024R5K4 F5H3E8
UniProt Splice Variant
Entrez Gene 57010
UniGene Hs.143036 Hs.616957 Hs.691167 Hs.734577
RefSeq NM_001300895 NM_145200 XM_005274114 XM_005274115
HUGO HGNC:1386
OMIM 608965
CCDS CCDS73333 CCDS8166
HPRD
IMGT
EMBL AC005849 AP003419 AY039217 BC033167 CH471076
GenPept AAH33167 AAK83462 EAW74628 EAW74629 EAW74630
RNA Seq Atlas 57010

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca