ALS2
Template:PBB Alsin is a protein that in humans is encoded by the ALS2 gene.[1][2] ALS2 orthologs [3] have been identified in all mammals for which complete genome data are available.
See also
References
- ^ 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 (2001). "A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2". Nat Genet. 29 (2): 166–73. doi:10.1038/ng1001-166. PMID 11586298.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: ALS2 amyotrophic lateral sclerosis 2 (juvenile)".
- ^ "OrthoMaM phylogenetic marker: ALS2 coding sequence".
Further reading
- 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. doi:10.1093/dnares/9.3.99. PMID 12168954.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1006/geno.1998.5637. PMID 9889004.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1007/s100480050049. PMID 9933298.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1093/dnares/7.4.271. PMID 10997877.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1038/ng1001-160. PMID 11586297.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1038/ng752. PMID 11687798.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1086/342359. PMC 379189. PMID 12145748.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. PMC 139241. PMID 12477932.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1093/hmg/ddg184. PMID 12837691.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1179/016164103101201733. PMID 12866199.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1034/j.1399-0004.2003.00138.x. PMID 12919135.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1073/pnas.2635267100. PMC 307689. PMID 14668431.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1001/archneur.60.12.1768. PMID 14676054.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1074/jbc.M313236200. PMID 14970233.
{{cite journal}}: Unknown parameter|author-separator=ignored (help)CS1 maint: unflagged free DOI (link)
External links
- GeneReviews/NCBI/NIH/UW entry on ALS2-Related Disorders
- OMIM entries on ALS2-Related Disorders
- Genetics Home Reference- US National Library of Medicine®
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