SPG16
Identifiers
AliasesSPG16, SPG, spastic paraplegia 16 (complicated, X-linked recessive)
External IDsGeneCards: SPG16
Orthologs
SpeciesHumanMouse
Entrez

57760

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Ensembl

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UniProt

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a

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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 16 (complicated, X-linked recessive) is a protein that in humans is encoded by the SPG16 gene.[2]

References

  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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