NIF3L1

From Wikipedia, the free encyclopedia


NIF3 NGG1 interacting factor 3-like 1 (S. pombe)
Identifiers
Symbol(s) NIF3L1; ALS2CR1; CALS-7; MDS015
External IDs OMIM: 605778 MGI1929485 HomoloGene5881
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 60491 65102
Ensembl ENSG00000196290 ENSMUSG00000026036
Uniprot Q9GZT8 Q3V2R8
Refseq NM_021824 (mRNA)
NP_068596 (protein)
NM_022988 (mRNA)
NP_075364 (protein)
Location Chr 2: 201.46 - 201.48 Mb Chr 1: 58.39 - 58.43 Mb
Pubmed search [1] [2]

NIF3 NGG1 interacting factor 3-like 1 (S. pombe), also known as NIF3L1, 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. 
  • Tascou S, Uedelhoven J, Dixkens C, et al. (2001). "Isolation and characterization of a novel human gene, NIF3L1, and its mouse ortholog, Nif3l1, highly conserved from bacteria to mammals.". Cytogenet. Cell Genet. 90 (3-4): 330-6. PMID 11124544. 
  • Hadano S, Yanagisawa Y, Skaug J, et al. (2001). "Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.". Genomics 71 (2): 200-13. doi:10.1006/geno.2000.6392. PMID 11161814. 
  • 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. PMID 12477932. 
  • Akiyama H, Fujisawa N, Tashiro Y, et al. (2003). "The role of transcriptional corepressor Nif3l1 in early stage of neural differentiation via cooperation with Trip15/CSN2.". J. Biol. Chem. 278 (12): 10752-62. doi:10.1074/jbc.M209856200. PMID 12522100. 
  • Tascou S, Kang TW, Trappe R, et al. (2003). "Identification and characterization of NIF3L1 BP1, a novel cytoplasmic interaction partner of the NIF3L1 protein.". Biochem. Biophys. Res. Commun. 309 (2): 440-8. PMID 12951069. 
  • 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. 
  • Merla G, Howald C, Antonarakis SE, Reymond A (2005). "The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3.". Hum. Mol. Genet. 13 (14): 1505-14. doi:10.1093/hmg/ddh163. PMID 15163635. 
  • 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. 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:10.1038/nature04209. PMID 16189514. 
  • 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:10.1016/j.cell.2006.03.032. PMID 16713569.