{{Rsnum
|rsid=312262720
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AT)
|geno3=(AT;AT)
|Gene=SPG11
|position=44657230
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=15
|CLNACC=RCV000001171.3
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44949428_44949429delAT
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1210; 610844.0004
|Disease=Spastic paraplegia 11
|FwdREF=AT
|REF=CAT
|RSPOS=44949427
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=312262720
|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=17717710
|Title=SPG11: a consistent clinical phenotype in a family with homozygous spatacsin truncating mutation.
}}

{{PMID Auto
|PMID=18067136
|Title=Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.
}}

{{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=18835492
|Title=Novel mutations of the SPG11 gene in hereditary 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.
}}