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Gene : CCIN Homo sapiens

Name  ? calicin Cytological Location  9p13.3
Brief Description  calicin
Description  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]
  • synonyms:
  • NM_005893,
  • KBTBD14,
  • CCIN,
  • OTTHUMG00000019901,
  • HGNC:1568,
  • KBTBD14,
  • Z46967,
  • BTBD20,
  • uc003zzb.5,
  • BTBD20
  • identifiers:
  • 881,
  • ENSG00000185972,
  • CCIN

Genome feature

Region: gene ? Length: 1947  
Location: 9:36169388-36171334 Cyto location: 9p13.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

28 SN Ps

5 Cross References

15 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results