AutismKB 2.0

Variant Details for HMCN1


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Basic Information Top
Gene Symbol:HMCN1 ( ARMD1,FBLN6,FIBL-6,FIBL6 )
Gene Full Name: hemicentin 1
Band: 1q25.3-q31.1
Quick LinksEntrez ID:83872; OMIM: 608548; Uniprot ID:HMCN1_HUMAN; ENSEMBL ID: ENSG00000143341; HGNC ID: 19194
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 1 2 1 0 0 0 4
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000728 1 1q25.3-q31.1 181099267 187997356 6898089 loss external link Bremer, 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
1 185985113 T C Sanger sequencing De Rubeis S, 2014
1 185985113 T C Fromer M, 2014
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
1 185833720 C T mosaic PASM Dou Y, 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