{{Rsnum
|rsid=118203963
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SPG11
|position=44573652
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SPG11
}}{{omim
|id=610844
|rsnum=118203963
|variant=0001
}}{{ClinVar
|rsid=118203963
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=44865850
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SPG11:80208
|GENE_NAME=SPG11
|GENE_ID=80208
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.44865850G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1210; 610844.0001
|CLNSIG=5
|CLNCUI=C1858479
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|Disease=Spastic paraplegia 11
|CLNACC=RCV000001168.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
}}{{PMID Auto
|PMID=17322883
|Title=Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
}}

{{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=18332254
|Title=Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
}}

{{PMID Auto
|PMID=18663179
|Title=SPG11 compound mutations in spastic paraparesis 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.
}}