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Revision as of 21:00, 6 June 2016
This article needs more links to other articles to help integrate it into the encyclopedia. (December 2013) |
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | ATL1, AD-FSP, FSP1, GBP3, HSN1D, SPG3, SPG3A, atlastin1, Atlastin, atlastin GTPase 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 606439; MGI: 1921241; HomoloGene: 9302; GeneCards: ATL1; OMA:ATL1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Atlastin, or Atlastin-1, is a protein that in humans is encoded by the ATL1 gene.[5][6][7]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000198513 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000021066 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J (Jan 1994). "Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q". Nat Genet. 5 (2): 163–7. doi:10.1038/ng1093-163. PMID 8252041.
- ^ Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G (Feb 1995). "Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity". Am J Hum Genet. 56 (1): 183–7. PMC 1801298. PMID 7825576.
- ^ "Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)".
External links
Further reading