Homo sapiens Gene: CCIN
Summary
InnateDB Gene IDBG-64896.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CCIN
Gene Name calicin
Synonyms BTBD20; KBTBD14
Species Homo sapiens
Ensembl Gene ENSG00000185972
Encoded Proteins
calicin
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is a basic protein of the sperm head cytoskeleton. This protein contains kelch repeats and a BTB/POZ domain and is necessary for normal morphology during sperm differentiation. This gene is intronless. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 9:36169394-36171334
Strand Forward strand
Band p13.3
Transcripts
ENST00000335119 ENSP00000334996
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0007275 multicellular organismal development
GO:0007283 spermatogenesis
GO:0030154 cell differentiation
Cellular Component
GO:0005634 nucleus
GO:0033150 cytoskeletal calyx
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q13939
TrEMBL Q8WX35
UniProt Splice Variant
Entrez Gene 881
UniGene Hs.115460
RefSeq NM_005893
HUGO HGNC:1568
OMIM 603960
CCDS CCDS6599
HPRD
IMGT
EMBL AF333334 AK313763 CH471071 Z46967
GenPept AAK20829 BAG36501 CAA87088 EAW58313 EAW58314
RNA Seq Atlas 881