SPG14

Spastic paraplegia 14 (autosomal recessive) is a protein that in humans is encoded by the SPG14 gene.[2]

SPG14
Identifiers
Aliases	SPG14, spastic paraplegia 14 (autosomal recessive)
External IDs	GeneCards: SPG14
Orthologs
Species	Human	Mouse
Entrez	57309	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 14 (autosomal recessive)".

Further reading

• Vazza G, Zortea M, Boaretto F, Micaglio GF, Sartori V, Mostacciuolo ML (August 2000). "A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28". American Journal of Human Genetics. 67 (2): 504–9. doi:10.1086/303017. PMC 1287196. PMID 10877981.