CNTRL
Sign in to saveAlso known as CEP1, CEP110, FAN, bA165P4.1, centriolin
Centriolin is a protein that in humans is encoded by the CNTRL gene. It was previously known as CEP110.
Gene data
CNTRL- Name
- centriolin
- Type
- protein-coding
- Position
- 121,074,660–121,177,786 (+)
- Aliases
- CEP1, CEP110, FAN, bA165P4.1
- Ensembl
- ENSG00000119397
- RefSeq RNA
- NM_001330762.2, NM_001369892.1, NM_001369893.1, NM_001369894.1, NM_001369895.1
- RefSeq protein
- NP_001317691.1, NP_001356821.1, NP_001356822.1, NP_001356823.1, NP_001356824.1
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].
Gene Ontology
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
centriolin
- Symbol
- CNTRL
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 9:121,074,660-121,177,786
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 38260
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/11064
- genomic end
- 121177729
- genomic start
- 121074660
- chromosome
- human chromosome 9
- cytogenetic location
- 9q33.2
- expressed in
- monocyte
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- References
- External links
- Further reading
Centriolin is a protein that in humans is encoded by the CNTRL gene. It was previously known as CEP110.
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 centriolin.
Excerpted from Wikipedia’s “CNTRL” article, available under the CC BY-SA 4.0 licence.