ALS2

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Amiotrofna lateralna skleroya 2 (juvenilna)
Identifikatori
SimboliALS2; ALS2CR6; ALSJ; IAHSP; PLSJ
Vanjski IDOMIM606352 MGI1921268 HomoloGene23264 GeneCards: ALS2 Gene
Pregled RNK izražavanja
PBB GE ALS2 gnf1h00370 at tn.png
podaci
Ortolozi
VrstaČovekMiš
Entrez5767974018
EnsemblENSG00000003393ENSMUSG00000026024
UniProtQ96Q42Q920R0
Ref. Sekv. (iRNK)NM_001135745NM_001159948
Ref. Sekv. (protein)NP_001129217NP_001153420
Lokacija (UCSC)Chr 2:
202.57 - 202.65 Mb
Chr 1:
59.16 - 59.24 Mb
PubMed pretraga[1][2]

Alsin je protein koji je kod čoveka kodiran ALS2 genom.[1][2] ALS2 ortolozi[3] su identifikovani kod svih sisara kod kojih su kompletni genomski pododaci dostupni.

Vidi još[uredi - уреди | uredi izvor]

Reference[uredi - уреди | uredi izvor]

  1. Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE (Oct 2001). "A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2". Nat Genet 29 (2): 166–73. PMID 11586298. doi:10.1038/ng1001-166.  Check date values in: |date= (help)
  2. "Entrez Gene: ALS2 amyotrophic lateral sclerosis 2 (juvenile)". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57679. 
  3. "OrthoMaM phylogenetic marker: ALS2 coding sequence". http://www.orthomam.univ-montp2.fr/orthomam/data/cds/detailMarkers/ENSG00000003393_ALS2.xml. 

Literatura[uredi - уреди | uredi izvor]

  • Hadano S (2002). "[Causative genes for familial amyotrophic lateral sclerosis]". Seikagaku 74 (6): 483–9. PMID 12138710. 
  • Nakajima D; Okazaki N; Yamakawa H et al. (2003). "Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones". DNA Res. 9 (3): 99–106. PMID 12168954. doi:10.1093/dnares/9.3.99. 
  • Hadano S; Nichol K; Brinkman RR et al. (1999). "A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34". Genomics 55 (1): 106–12. PMID 9889004. doi:10.1006/geno.1998.5637. 
  • Hosler BA; Sapp PC; Berger R et al. (2000). "Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33". Neurogenetics 2 (1): 34–42. PMID 9933298. doi:10.1007/s100480050049. 
  • Nagase T; Kikuno R; Nakayama M et al. (2001). "Prediction of the coding sequences of unidentified human genes. XVIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Res. 7 (4): 273–81. PMID 10997877. doi:10.1093/dnares/7.4.271. 
  • Yang Y; Hentati A; Deng HX et al. (2001). "The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis". Nat. Genet. 29 (2): 160–5. PMID 11586297. doi:10.1038/ng1001-160. 
  • Birkenhäger R; Otto E; Schürmann MJ et al. (2001). "Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure". Nat. Genet. 29 (3): 310–4. PMID 11687798. doi:10.1038/ng752. 
  • Eymard-Pierre E; Lesca G; Dollet S et al. (2002). "Infantile-Onset Ascending Hereditary Spastic Paralysis Is Associated with Mutations in the Alsin Gene". Am. J. Hum. Genet. 71 (3): 518–27. PMC 379189. PMID 12145748. doi:10.1086/342359. 
  • 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. PMC 139241. PMID 12477932. doi:10.1073/pnas.242603899. 
  • Lesca G; Eymard-Pierre E; Santorelli FM et al. (2004). "Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families". Neurology 60 (4): 674–82. PMID 12601111. doi:10.1212/01.wnl.0000048207.28790.25. 
  • Otomo A; Hadano S; Okada T et al. (2003). "ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamics". Hum. Mol. Genet. 12 (14): 1671–87. PMID 12837691. doi:10.1093/hmg/ddg184. 
  • Nagano I; Murakami T; Shiote M et al. (2003). "Single-nucleotide polymorphisms in uncoding regions of ALS2 gene of Japanese patients with autosomal-recessive amyotrophic lateral sclerosis". Neurol. Res. 25 (5): 505–9. PMID 12866199. doi:10.1179/016164103101201733. 
  • Devon RS; Helm JR; Rouleau GA et al. (2004). "The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings". Clin. Genet. 64 (3): 210–5. PMID 12919135. doi:10.1034/j.1399-0004.2003.00138.x. 
  • Yamanaka K; Vande Velde C; Eymard-Pierre E et al. (2004). "Unstable mutants in the peripheral endosomal membrane component ALS2 cause early-onset motor neuron disease". Proc. Natl. Acad. Sci. U.S.A. 100 (26): 16041–6. PMC 307689. PMID 14668431. doi:10.1073/pnas.2635267100. 
  • Hand CK; Devon RS; Gros-Louis F et al. (2004). "Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis". Arch. Neurol. 60 (12): 1768–71. PMID 14676054. doi:10.1001/archneur.60.12.1768. 
  • 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. PMID 14702039. doi:10.1038/ng1285. 
  • Kanekura K; Hashimoto Y; Niikura T et al. (2004). "Alsin, the product of ALS2 gene, suppresses SOD1 mutant neurotoxicity through RhoGEF domain by interacting with SOD1 mutants". J. Biol. Chem. 279 (18): 19247–56. PMID 14970233. doi:10.1074/jbc.M313236200. 

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