AutismKB 2.0

Variant Details for NFIB


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Basic Information Top
Gene Symbol:NFIB ( HMGIC/NFIB,NFI-RED,NFIB2,NFIB3 )
Gene Full Name: nuclear factor I/B
Band: 9p23-p22.3
Quick LinksEntrez ID:4781; OMIM: 600728; Uniprot ID:NFIB_HUMAN; ENSEMBL ID: ENSG00000147862; HGNC ID: 7785
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 2 2 1 0 0 0 5
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000086 9 9p22.3-23 11621200 14491300 2870100 gain external link Szatmari, 2007
AutCNV0000084 9 9p13.3-24.3 249391 33926500 33677109 gain external link Szatmari, 2007
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
9 14150143 C T PCR or Sanger sequencing Iossifov I, 2014
0 Redin C, 2017
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
9 14307297 G A High-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