CEP85L
CEP85L, for "Centrosomal Protein 85kDa-Like"[1] is a gene which encodes a protein that has been identified as a breast cancer antigen. Nothing more is known of its function at this time. Three transcript variants encoding different isoforms have been found for this gene. It has been shown to be related to the QT interval in GWAS studies.[2]
| Centrosomal Protein 85kDa-Like | |
|---|---|
| Identifiers | |
| Symbol | CEP85L |
| OMIM | 618865 |
| Other data | |
| Locus | Chr. 6 q22.31 |
Pathology
Mutations of the CEP85L gene were associated with posterior predominant lissencephaly in a 2020 study,[3] added under #618873 in the OMIM catalogue, where it received the name of lissencephaly 10.
See also
- Centrosome - the product of the gene localizes in the centrosome
Sources
- Database, GeneCards Human Gene. "CEP85L Gene - GeneCards | CE85L Protein | CE85L Antibody". www.genecards.org.
- Chambers JC, Zhao J, Terracciano CM, Bezzina CR, Zhang W, Kaba R, et al. (February 2010). "Genetic variation in SCN10A influences cardiac conduction". Nature Genetics. 42 (2): 149–52. doi:10.1038/ng.516. PMID 20062061. S2CID 39153818.
- Tsai MH, Muir AM, Wang WJ, Kang YN, Yang KC, Chao NH, et al. (April 2020). "Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly". Neuron. 106 (2): 237–245.e8. doi:10.1016/j.neuron.2020.01.027. PMC 7357395. PMID 32097630.
- Kodani, Andrew; Kenny, Connor; Lai, Abbe; Gonzalez, Dilenny M.; Stronge, Edward; Sejourne, Gabrielle M.; Isacco, Laura; Partlow, Jennifer N.; O'Donnell, Anne; McWalter, Kirsty; Byrne, Alicia B. (22 April 2020). "Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5". Neuron. 106 (2): 246–255.e6. doi:10.1016/j.neuron.2020.01.030. ISSN 1097-4199. PMC 7255387. PMID 32097629.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.