{{Rsnum
|rsid=202247811
|Chromosome=4
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=CEP135
|position=55965785
|Gene_s=CEP135
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=4
|CLNACC=RCV000024354.2
|CLNALLE=1
|CLNDBN=Primary autosomal recessive microcephaly 8
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK9587:CN128714:614673:2512
|CLNHGVS=NC_000004.11:g.56831951delC
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611423.0001
|Disease=Primary autosomal recessive microcephaly 8
|FwdREF=C
|GENEINFO=CEP135:9662
|GENE_ID=9662
|GENE_NAME=CEP135
|REF=TC
|RSPOS=56831950
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050268000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=202247811
}}{{PMID Auto
|PMID=22521416
|Title=A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function.
|OA=1
}}