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SPG23

SPG23
Identifiers
AliasesSPG23, spastic paraplegia 23 (autosomal recessive)
External IDsGeneCards: SPG23
Orthologs
DatabasesNCBI: entry
SpeciesHumanMouse
Entrez

353293

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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
View/Edit Human

Spastic paraplegia 23 (SPG autosomal recessive)[2] is a 25cM gene locus at 1q24-q32.[3] A genome-wide linkage screen has associated this locus with a type of hereditary spastic paraplegia (HSP).[4]

References

  1. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. ^ "Entrez Gene: Spastic paraplegia 23 (autosomal recessive)".
  3. ^ "SPG23 Symbol Report | HUGO Gene Nomenclature Committee". www.genenames.org. Archived from the original on 2017-09-29. Retrieved 2017-09-29.
  4. ^ Blumen SC, Bevan S, Abu-Mouch S, Negus D, Kahana M, Inzelberg R, Mazarib A, Mahamid A, Carasso RL, Slor H, Withers D, Nisipeanu P, Navon R, Reid E (December 2003). "A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32". Annals of Neurology. 54 (6): 796–803. doi:10.1002/ana.10768. PMID 14681889. S2CID 12631177.

Further reading

  • Blumen SC, Bevan S, Abu-Mouch S, Negus D, Kahana M, Inzelberg R, Mazarib A, Mahamid A, Carasso RL, Slor H, Withers D, Nisipeanu P, Navon R, Reid E (December 2003). "A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32". Annals of Neurology. 54 (6): 796–803. doi:10.1002/ana.10768. PMID 14681889. S2CID 12631177.


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