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SPG9

Genetic element in the species Homo sapiens From Wikipedia, the free encyclopedia

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

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

9193

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Ensembl

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UniProt

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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
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