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Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
Centriolin is a protein that in humans is encoded by the CNTRL gene. It was previously known as CEP110.[5][6]
CNTRL | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | CNTRL, CEP1, CEP110, FAN, bA165P4.1, centriolin | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 605496; MGI: 1889576; HomoloGene: 38260; GeneCards: CNTRL; OMA:CNTRL - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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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.[6]
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