{{Rsnum
|rsid=200079802
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=EIF3J
|position=44563302
|Gene_s=EIF3J,SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=15
|CLNACC=RCV000001174.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44855500C>G
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1210; 610844.0007
|Disease=Spastic paraplegia 11
|FwdALT=G
|FwdREF=C
|GENEINFO=SPG11:80208; EIF3J:8669
|GENE_ID=80208; 8669
|GENE_NAME=SPG11; EIF3J
|REF=C
|RSPOS=44855500
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=200079802
}}{{PMID Auto
|PMID=19194956
|Title=SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
}}