SPG9

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

SPG9
Identifiers
Aliases	SPG9, spastic paraplegia 9 (autosomal dominant)
External IDs	GeneCards: SPG9
Orthologs
Species	Human	Mouse
Entrez	9193	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	[1]	n/a
Wikidata
View/Edit Human

References

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

• 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.