{{Rsnum
|rsid=312262717
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=SPG11
|position=44659104
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=15
|CLNACC=RCV000034244.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44951302delA
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|Disease=Spastic paraplegia 11
|FwdREF=T
|REF=CA
|RSPOS=44951301
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=312262717
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
}}{{PMID Auto
|PMID=19194956
|Title=SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
}}