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SPG16

From Wikipedia, the free encyclopedia
SPG16
Identifiers
AliasesSPG16, SPG, spastic paraplegia 16 (complicated, X-linked recessive)
External IDsGeneCards: SPG16; OMA:SPG16 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

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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 16 (complicated, X-linked recessive) is a protein that in humans is encoded by the SPG16 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 16 (complicated, X-linked recessive)".

Further reading

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