POF1B
From Wikipedia, the free encyclopedia
Premature ovarian failure, 1B
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Identifiers | ||||||||
Symbol(s) | POF1B; POF; FLJ22792 | |||||||
External IDs | OMIM: 300603 MGI: 1916943 HomoloGene: 11785 | |||||||
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RNA expression pattern | ||||||||
Orthologs | ||||||||
Human | Mouse | |||||||
Entrez | 79983 | 69693 | ||||||
Ensembl | ENSG00000124429 | ENSMUSG00000034607 | ||||||
Uniprot | Q8WVV4 | Q8R4R8 | ||||||
Refseq | NM_024921 (mRNA) NP_079197 (protein) |
NM_181579 (mRNA) NP_853557 (protein) |
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Location | Chr X: 84.42 - 84.52 Mb | Chr X: 108.76 - 108.82 Mb | ||||||
Pubmed search | [1] | [2] |
Premature ovarian failure, 1B, also known as POF1B, is a human gene.[1]
[edit] References
[edit] Further reading
- Bione S, Toniolo D (2001). "X chromosome genes and premature ovarian failure.". Semin. Reprod. Med. 18 (1): 51-7. PMID 11299520.
- 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.
- 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.
- Bione S, Rizzolio F, Sala C, et al. (2005). "Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B.". Hum. Reprod. 19 (12): 2759-66. doi: . PMID 15459172.
- 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.
- Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature 434 (7031): 325-37. doi: . PMID 15772651.
- Lacombe A, Lee H, Zahed L, et al. (2006). "Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.". Am. J. Hum. Genet. 79 (1): 113-9. doi: . PMID 16773570.