FAM46A
From Wikipedia, the free encyclopedia
Family with sequence similarity 46, member A
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Identifiers | |||||
Symbol(s) | FAM46A; C6orf37; FLJ20037; FLJ31495; XTP11 | ||||
External IDs | MGI: 2670964 HomoloGene: 23032 | ||||
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RNA expression pattern | |||||
Orthologs | |||||
Human | Mouse | ||||
Entrez | 55603 | 212943 | |||
Ensembl | ENSG00000112773 | ENSMUSG00000032265 | |||
Uniprot | Q96IP4 | n/a | |||
Refseq | NM_017633 (mRNA) NP_060103 (protein) |
XM_135029 (mRNA) XP_135029 (protein) |
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Location | Chr 6: 82.51 - 82.52 Mb | Chr 9: 85.12 - 85.12 Mb | |||
Pubmed search | [1] | [2] |
Family with sequence similarity 46, member A, also known as FAM46A, is a human gene.[1]
[edit] References
[edit] Further reading
- Lagali PS, Kakuk LE, Griesinger IB, et al. (2002). "Identification and characterization of C6orf37, a novel candidate human retinal disease gene on chromosome 6q14.". Biochem. Biophys. Res. Commun. 293 (1): 356-65. doi: . PMID 12054608.
- 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.
- Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6.". Nature 425 (6960): 805-11. doi: . PMID 14574404.
- 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.
- Colland F, Jacq X, Trouplin V, et al. (2004). "Functional proteomics mapping of a human signaling pathway.". Genome Res. 14 (7): 1324-32. doi: . PMID 15231748.
- 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: . PMID 15489334.
- Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173-8. doi: . PMID 16189514.
- 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: . PMID 16344560.
- Cui J, Wang W, Lai MD, et al. (2006). "Identification of a novel VNTR polymorphism in C6orf37 and its association with colorectal cancer risk in Chinese population.". Clin. Chim. Acta 368 (1-2): 155-9. doi: . PMID 16545789.
- Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.". Cell 125 (4): 801-14. doi: . PMID 16713569.