AutismKB 2.0

Variant Details for CCPG1


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Basic Information Top
Gene Symbol:CCPG1 ( CPR8,FLJ60574,KIAA1254 )
Gene Full Name: cell cycle progression 1
Band: 15q21.3
Quick LinksEntrez ID:9236; OMIM: 611326; Uniprot ID:CCPG1_HUMAN; ENSEMBL ID: ENSG00000214882; HGNC ID: 24227
Relate to Another Database: SFARIGene; denovo-db
Variant Statistic Top

Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. Chromosome coordinates: hg19
Genetic Category CNVs/SVs de novo Mutations Mosaics SNVs NGS Other Mutations Low-Scale Gene Mutations Linkage Regions Total
Number 3 0 1 0 0 3 7
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000110 15 15q21.2-26.3 51558408 102352477 50794069 gain external link Szatmari, 2007
AutCNV0000028 15 15q21.2-26.3 51558408 102352477 50794069 gain external link Szatmari, 2007
AutCNV0000686 15 15q21.3 53312708 58012708 4700000 loss external link Berkel, 2010
NGS de novo Mutations Top
iFish (integrated Functional inference of SNVs in human) is based on gene/gene family customized models to classify missense mutations.
Chr Pos Ref Alt Coding AA Validated Method iFish Prediction iFish Probability Reference
No related data!
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
15 55651891 G A Low-confidence mosaics Resequencing Lim ET, 2017
NGS Other Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
No related data!
Low-Scale Gene Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
No related data!
Linkage Regions Top
Linkage Name Band Chr Marker LOD NPL P Value Reference
AutLD0000137 15q21.3 15 D15S998/D15S198 - - 0.00276 Lauritsen, 2006
AutLD0000157 15q21.2-q22.1 15 rs11856 5.31 - - Allen-Brady, 2010
AutLD0000158 15q21.1-q22.2 15 rs383902 1.49 - - Allen-Brady, 2010




Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018