KIAA1109
From Wikipedia, the free encyclopedia
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KIAA1109
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| Identifiers | |||||||||||
| Symbol(s) | KIAA1109; DKFZp781P0474; FSA; MGC110967 | ||||||||||
| External IDs | HomoloGene: 52105 | ||||||||||
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| RNA expression pattern | |||||||||||
| Orthologs | |||||||||||
| Human | Mouse | ||||||||||
| Entrez | 84162 | 665732 | |||||||||
| Ensembl | ENSG00000138688 | n/a | |||||||||
| Refseq | XM_371706 (mRNA) XP_371706 (protein) |
XM_622891 (mRNA) XP_622891 (protein) |
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| Location | Chr 4: 123.39 - 123.5 Mb | n/a | |||||||||
| Pubmed search | [1] | [2] | |||||||||
KIAA1109, also known as KIAA1109, is a human gene.[1]
[edit] References
[edit] 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. PMID 8125298.
- 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. PMID 9373149.
- Kikuno R, Nagase T, Ishikawa K, et al. (1999). "Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.". DNA Res. 6 (3): 197–205. PMID 10470851.
- Nagase T, Kikuno R, Ishikawa KI, et al. (2000). "Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro.". DNA Res. 7 (1): 65–73. PMID 10718198.
- 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:. 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:. PMID 14702039.
- Kuo MT, Wei Y, Yang X, et al. (2006). "Association of fragile site-associated (FSA) gene expression with epithelial differentiation and tumor development.". Biochem. Biophys. Res. Commun. 340 (3): 887–93. doi:. PMID 16386706.
- Wei Y, Lin-Lee YC, Yang X, et al. (2006). "Molecular cloning of Chinese hamster 1q31 chromosomal fragile site DNA that is important to mdr1 gene amplification reveals a novel gene whose expression is associated with spermatocyte and adipocyte differentiation.". Gene 372: 44–52. doi:. PMID 16545529.
- van Heel DA, Franke L, Hunt KA, et al. (2007). "A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.". Nat. Genet. 39 (7): 827–9. doi:. PMID 17558408.

