LITAF
From Wikipedia, the free encyclopedia
Lipopolysaccharide-induced TNF factor
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Identifiers | |||||||||||
Symbol(s) | LITAF; CMT1C; FLJ38636; MGC116698; MGC116700; MGC116701; MGC125274; MGC125275; MGC125276; PIG7; SIMPLE; TP53I7 | ||||||||||
External IDs | OMIM: 603795 MGI: 1929512 HomoloGene: 37974 | ||||||||||
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RNA expression pattern | |||||||||||
Orthologs | |||||||||||
Human | Mouse | ||||||||||
Entrez | 9516 | 56722 | |||||||||
Ensembl | ENSG00000189067 | ENSMUSG00000022500 | |||||||||
Uniprot | Q99732 | Q9JLJ0 | |||||||||
Refseq | NM_004862 (mRNA) NP_004853 (protein) |
NM_019980 (mRNA) NP_064364 (protein) |
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Location | Chr 16: 11.55 - 11.59 Mb | Chr 16: 10.87 - 10.91 Mb | |||||||||
Pubmed search | [1] | [2] |
Lipopolysaccharide-induced TNF factor, also known as LITAF, is a human gene.[1]
[edit] References
[edit] Further reading
- Polyak K, Xia Y, Zweier JL, et al. (1997). "A model for p53-induced apoptosis.". Nature 389 (6648): 300–5. doi: . PMID 9305847.
- Myokai F, Takashiba S, Lebo R, Amar S (1999). "A novel lipopolysaccharide-induced transcription factor regulating tumor necrosis factor alpha gene expression: molecular cloning, sequencing, characterization, and chromosomal assignment.". Proc. Natl. Acad. Sci. U.S.A. 96 (8): 4518–23. PMID 10200294.
- Jolliffe CN, Harvey KF, Haines BP, et al. (2001). "Identification of multiple proteins expressed in murine embryos as binding partners for the WW domains of the ubiquitin-protein ligase Nedd4.". Biochem. J. 351 Pt 3: 557–65. PMID 11042109.
- Moriwaki Y, Begum NA, Kobayashi M, et al. (2001). "Mycobacterium bovis Bacillus Calmette-Guerin and its cell wall complex induce a novel lysosomal membrane protein, SIMPLE, that bridges the missing link between lipopolysaccharide and p53-inducible gene, LITAF(PIG7), and estrogen-inducible gene, EET-1.". J. Biol. Chem. 276 (25): 23065–76. doi: . PMID 11274176.
- Street VA, Goldy JD, Golden AS, et al. (2002). "Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies.". Am. J. Hum. Genet. 70 (1): 244–50. PMID 11713717.
- 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.
- Street VA, Bennett CL, Goldy JD, et al. (2003). "Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.". Neurology 60 (1): 22–6. PMID 12525712.
- Matsuda A, Suzuki Y, Honda G, et al. (2003). "Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways.". Oncogene 22 (21): 3307–18. doi: . PMID 12761501.
- Street VA, Bennett CL, Bird TD, Chance PF (2004). "New gene for CMT.". J. Peripher. Nerv. Syst. 8 (4): 206. PMID 14641644.
- 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.
- Ludes-Meyers JH, Kil H, Bednarek AK, et al. (2004). "WWOX binds the specific proline-rich ligand PPXY: identification of candidate interacting proteins.". Oncogene 23 (29): 5049–55. doi: . PMID 15064722.
- Bennett CL, Shirk AJ, Huynh HM, et al. (2004). "SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve.". Ann. Neurol. 55 (5): 713–20. doi: . PMID 15122712.
- Matsumura Y, Matsumura Y, Nishigori C, et al. (2004). "PIG7/LITAF gene mutation and overexpression of its gene product in extramammary Paget's disease.". Int. J. Cancer 111 (2): 218–23. doi: . PMID 15197774.
- 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.
- Saifi GM, Szigeti K, Wiszniewski W, et al. (2006). "SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation.". Hum. Mutat. 25 (4): 372–83. doi: . PMID 15776429.
- Meggouh F, de Visser M, Arts WF, et al. (2005). "Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease.". Ann. Neurol. 57 (4): 589–91. doi: . PMID 15786462.
- Tang X, Marciano DL, Leeman SE, Amar S (2005). "LPS induces the interaction of a transcription factor, LPS-induced TNF-alpha factor, and STAT6(B) with effects on multiple cytokines.". Proc. Natl. Acad. Sci. U.S.A. 102 (14): 5132–7. doi: . PMID 15793005.
- Beauvais K, Furby A, Latour P (2006). "Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.". Neuromuscul. Disord. 16 (1): 14–8. doi: . PMID 16373087.
- Latour P, Gonnaud PM, Ollagnon E, et al. (2006). "SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations.". J. Peripher. Nerv. Syst. 11 (2): 148–55. doi: . PMID 16787513.
- Stucchi A, Reed K, O'Brien M, et al. (2007). "A new transcription factor that regulates TNF-alpha gene expression, LITAF, is increased in intestinal tissues from patients with CD and UC.". Inflamm. Bowel Dis. 12 (7): 581–7. doi: . PMID 16804395.