{{Rsnum
|rsid=312262770
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=SPG11
|position=44583911
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=15
|CLNACC=RCV000034228.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44876109delA
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|Disease=Spastic paraplegia 11
|FwdREF=T
|REF=TA
|RSPOS=44876108
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=312262770
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
}}{{PMID Auto
|PMID=18079167
|Title=Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
}}

{{PMID Auto
|PMID=18337587
|Title=SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia.
|OA=1
}}