Atlastin

From Wikipedia, the free encyclopedia
  (Redirected from ATL1)
Jump to: navigation, search
ATL1
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases ATL1, AD-FSP, FSP1, GBP3, HSN1D, SPG3, SPG3A, atlastin1, Atlastin, atlastin GTPase 1
External IDs MGI: 1921241 HomoloGene: 9302 GeneCards: ATL1
Gene location (Human)
Chromosome 14 (human)
Chr. Chromosome 14 (human)[1]
Chromosome 14 (human)
Genomic location for ATL1
Genomic location for ATL1
Band 14q22.1 Start 50,532,509 bp[1]
End 50,633,068 bp[1]
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_181598
NM_001127713
NM_015915

NM_178628

RefSeq (protein)

NP_001121185
NP_056999
NP_853629

NP_848743

Location (UCSC) Chr 14: 50.53 – 50.63 Mb Chr 14: 69.89 – 69.97 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Atlastin, or Atlastin-1, is a protein that in humans is encoded by the ATL1 gene.[5][6][7]


References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000198513 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000021066 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". 
  4. ^ "Mouse PubMed Reference:". 
  5. ^ 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. PMID 8252041. doi:10.1038/ng1093-163. 
  6. ^ 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 1801298Freely accessible. PMID 7825576. 
  7. ^ "Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)". 

External links[edit]

Further reading[edit]