{{Rsnum
|rsid=312262716
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;ATATT)
|geno3=(ATATT;ATATT)
|Gene=SPG11
|position=44659213
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000001169.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44951411_44951415delAATAT
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1210; 610844.0002
|Disease=Spastic paraplegia 11
|FwdREF=ATATT
|REF=AAATAT
|RSPOS=44951410
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=312262716
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
}}{{PMID Auto
|PMID=17322883
|Title=Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
}}

{{PMID Auto
|PMID=19105190
|Title=Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
}}