AutismKB 2.0

Variant Details for EPB41L1


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:EPB41L1 ( 4.1N,DKFZp686H17242,KIAA0338,MGC11072 )
Gene Full Name: erythrocyte membrane protein band 4.1-like 1
Band: 20q11.23
Quick LinksEntrez ID:2036; OMIM: 602879; Uniprot ID:E41L1_HUMAN; ENSEMBL ID: ENSG00000088367; HGNC ID: 3378
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 1 1 0 0 1 4
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0004378 20 20q11.1-q11.23 29637396 35710453 6073057 gain external link Sanders, 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
20 34765932 A G deleterious0.9995 Chen R, 2017
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
20 34773214 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
AutLD0000147 20q11.21-13.12 20 - - 5.56 - Allen-Brady, 2008




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