{{Rsnum
|rsid=312262792
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AAAC)
|geno3=(AAAC;AAAC)
|Gene=SPG11
|position=44563296
|Gene_s=EIF3J,SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TGTTT
|CHROM=15
|CLNACC=RCV000034265.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44855494_44855495insGTTT
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|Disease=Spastic paraplegia 11
|FwdALT=AACA
|REF=T
|RSPOS=44855494
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=312262792
|GENEINFO=SPG11:80208; EIF3J:8669
|GENE_ID=80208; 8669
|GENE_NAME=SPG11; EIF3J
}}{{PMID Auto
|PMID=18717728
|Title=Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11).
}}