help  | about  | cite  | software

Gene : CNTRL Homo sapiens

Name  ? centriolin Cytological Location  9q33.2
Brief Description  centriolin
Description  This gene encodes a centrosomal protein required for the centrosome to function as a microtubule organizing center. The gene product is also associated with centrosome maturation. One version of stem cell myeloproliferative disorder is the result of a reciprocal translocation between chromosomes 8 and 9, with the breakpoint associated with fibroblast growth factor receptor 1 and centrosomal protein 1. [provided by RefSeq, Jul 2008]
  • synonyms:
  • AF513978,
  • HGNC:1858,
  • CEP1,
  • OTTHUMG00000020581,
  • CEP1,
  • centrosomal protein 1,
  • uc064vkk.1,
  • NM_007018,
  • centrosomal protein 110kDa,
  • FAN,
  • CNTRL,
  • bA165P4.1,
  • CEP110,
  • CEP110
  • identifiers:
  • 11064,
  • ENSG00000119397,

Genome feature

Region: gene ? Length: 102719  
Location: 9:121074892-121177610 Cyto location: 9q33.2

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

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]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



3740 SNPs

5 Cross References

17 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results