SPG23

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

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]

AliasesSPG23, spastic paraplegia 23 (autosomal recessive)
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SPG23
Identifiers
AliasesSPG23, spastic paraplegia 23 (autosomal recessive)
External IDsGeneCards: SPG23; OMA:SPG23 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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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