help  | about  | cite  | software

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:
  • HGNC:1568,
  • KBTBD14,
  • BTBD20,
  • Z46967,
  • KBTBD14,
  • BTBD20,
  • OTTHUMG00000019901,
  • NM_005893,
  • uc003zzb.5,
  • CCIN
  • identifiers:
  • 881,
  • ENSG00000185972,
  • CCIN

Genome feature

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


Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

Homologue Displayer

Gene --> Orthologues

Interactions

Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

28 SN Ps

5 Cross References

13 Data Sets

41 Homologues

0 Located Features

97 Rna Seq Results