CCDC28B
| Coiled-coil domain containing 28B | |||||||||||||
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| Identifiers | |||||||||||||
| Symbols | CCDC28B ; RP4-622L5.5 | ||||||||||||
| External IDs | OMIM: 610162 MGI: 1913514 HomoloGene: 11509 GeneCards: CCDC28B Gene | ||||||||||||
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| RNA expression pattern | |||||||||||||
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| More reference expression data | |||||||||||||
| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 79140 | 66264 | |||||||||||
| Ensembl | ENSG00000160050 | ENSMUSG00000028795 | |||||||||||
| UniProt | Q9BUN5 | Q8CEG5 | |||||||||||
| RefSeq (mRNA) | NM_001301011 | NM_025455 | |||||||||||
| RefSeq (protein) | NP_001287940 | NP_079731 | |||||||||||
| Location (UCSC) |
Chr 1: 32.2 – 32.21 Mb |
Chr 4: 129.62 – 129.62 Mb | |||||||||||
| PubMed search | |||||||||||||
Coiled-coil domain-containing protein 28B is a protein that in humans is encoded by the CCDC28B gene.[1][2]
The product of this gene localizes to centrosomes and basal bodies. It interacts and colocalizes with several proteins associated with Bardet-Biedl syndrome (BBS).[2]
References
- ↑ Badano JL, Leitch CC, Ansley SJ, May-Simera H, Lawson S, Lewis RA, Beales PL, Dietz HC, Fisher S, Katsanis N (Jan 2006). "Dissection of epistasis in oligogenic Bardet-Biedl syndrome". Nature 439 (7074): 326–30. doi:10.1038/nature04370. PMID 16327777.
- 1 2 "Entrez Gene: CCDC28B coiled-coil domain containing 28B".
Further reading
- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K; et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Kimura K, Wakamatsu A, Suzuki Y; et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
- Gregory SG, Barlow KF, McLay KE; et al. (2006). "The DNA sequence and biological annotation of human chromosome 1.". Nature 441 (7091): 315–21. doi:10.1038/nature04727. PMID 16710414.
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