AutismKB 2.0

Variant Details for SLCO1C1


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Basic Information Top
Gene Symbol:SLCO1C1 ( OATP-F,OATP1,OATP14,OATP1C1,OATPF,OATPRP5,SLC21A14 )
Gene Full Name: solute carrier organic anion transporter family, member 1C1
Band: 12p12.2
Quick LinksEntrez ID:53919; OMIM: 613389; Uniprot ID:SO1C1_HUMAN; ENSEMBL ID: ENSG00000139155; HGNC ID: 13819
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 2 1 0 0 0 6
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0004299 12 12p11.22-p12.3 17015267 29997799 12982532 loss external link Sanders, 2011
AutCNV0003966 12 12p12.2 20899503 21006495 106992 loss external link Levy, 2011
AutCNV0003831 12 12p12.3-p11.22 17016260 29990846 12974586 loss external link Levy, 2011
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
12 20890190 G T p.Arg393Met Sanger sequencingneutral0.0905 Sanders SJ, 2012
12 20864352 A R Sanger sequencing O'Roak BJ, 2012
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
12 20890190 G T 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
No related data!




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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