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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:
  • uc064vkk.1,
  • CEP110,
  • NM_007018,
  • FAN,
  • CEP1,
  • centrosomal protein 110kDa,
  • CEP110,
  • AF513978,
  • OTTHUMG00000020581,
  • CNTRL,
  • bA165P4.1,
  • centrosomal protein 1,
  • HGNC:1858,
  • CEP1
  • identifiers:
  • 11064,
  • ENSG00000119397,
  • CNTRL

Genome feature

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


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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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

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

3753 SN Ps

5 Cross References

17 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results