Centrosomal protein 120kDa | |||||||||||||
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Identifiers | |||||||||||||
Symbols | CEP120; CCDC100; DKFZp686I06246; FLJ36090; FLJ38327 | ||||||||||||
External IDs | OMIM: 613446 MGI: 2147298 HomoloGene: 27415 GeneCards: CEP120 Gene | ||||||||||||
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Orthologs | |||||||||||||
Species | Human | Mouse | |||||||||||
Entrez | 153241 | 225523 | |||||||||||
Ensembl | ENSG00000168944 | ENSMUSG00000048799 | |||||||||||
UniProt | Q8N960 | Q7TSG1 | |||||||||||
RefSeq (mRNA) | NM_001166226.1 | NM_178686.3 | |||||||||||
RefSeq (protein) | NP_001159698.1 | NP_848801.2 | |||||||||||
Location (UCSC) | Chr 5: 122.68 – 122.76 Mb |
Chr 18: 53.84 – 53.9 Mb |
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PubMed search | [1] | [2] |
Centrosomal protein of 120 kDa (Cep120), also known as coiled-coil domain-containing protein 100, is a protein that in humans is encoded by the CEP120 gene.[1][2]
This gene encodes a protein that functions in the microtubule-dependent coupling of the nucleus and the centrosome. A similar protein in mouse plays a role in both interkinetic nuclear migration, which is a characteristic pattern of nuclear movement in neural progenitors, and in neural progenitor self-renewal. Mutations in this gene are predicted to result in neurogenic defects.[1]
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