SPG9

SPG9
Identifiers
AliasesSPG9, spastic paraplegia 9 (autosomal dominant)
External IDsGeneCards: SPG9
Orthologs
SpeciesHumanMouse
Entrez

9193

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed search[1]n/a
Wikidata
View/Edit Human

Spastic paraplegia 9 (autosomal dominant) is a protein that in humans is encoded by the SPG9 gene.[2]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "Entrez Gene: Spastic paraplegia 9 (autosomal dominant)".

Further reading

  • Seri M, Cusano R, Forabosco P, Cinti R, Caroli F, Picco P, Bini R, Morra VB, De Michele G, Lerone M, Silengo M, Pela I, Borrone C, Romeo G, Devoto M (February 1999). "Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy". American Journal of Human Genetics. 64 (2): 586–93. doi:10.1086/302241. PMC 1377769. PMID 9973297.


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