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SPG9

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SPG9
Identifiers
AliasesSPG9, spastic paraplegia 9 (autosomal dominant)
External IDsGeneCards: SPG9; OMA:SPG9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

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

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  1. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. ^ "Entrez Gene: Spastic paraplegia 9 (autosomal dominant)".

Further reading

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