AutismKB 2.0

Evidence Details for ZNF862


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Basic Information Top
Gene Symbol:ZNF862 ( FLJ30362,KIAA0543 )
Gene Full Name: zinc finger protein 862
Band: 7q36.1
Quick LinksEntrez ID:643641; OMIM: NA; Uniprot ID:ZN862_HUMAN; ENSEMBL ID: ENSG00000106479; HGNC ID: 34519
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZNF862|643641|nucleotide
ATGGAGCCCAGAGAGTCGGGGAAGGCTCCTGTGACGTTTGATGACATCACTGTGTACTTACTCCAGGAGGAATGGGTGCTGCTGAGCCAGCAACAGAAGGAGCTC
TGTGGTTCCAACAAGCTGGTGGCACCACTGGGACCAACTGTTGCCAATCCTGAGCTGTTCCGCAAGTTCGGACGAGGGCCAGAGCCATGGCTTGGCAGCGTCCAG
GGCCAGAGGAGCCTTCTGGAGCATCACCCAGGAAAAAAACAGATGGGCTACATGGGAGAAATGGAGGTGCAAGGTCCCACCAGGGAGAGTGGACAGTCCCTCCCG
CCTCAGAAGAAAGCCTACCTTTCCCACCTCAGTACAGGCAGTGGACACATCGAGGGAGACTGGGCCGGAAGAAACAGGAAACTTCTGAAGCCCCGGTCCATCCAG
AAGTCGTGGTTTGTGCAGTTTCCGTGGCTGATCATGAATGAGGAGCAGACGGCTCTGTTCTGCTCTGCTTGCCGAGAATACCCCTCCATCAGGGACAAACGGTCA
AGACTAATAGAAGGTTATACAGGACCATTCAAGGTGGAGACTCTCAAATACCACGCGAAGAGCAAGGCCCACATGTTCTGTGTCAATGCCTTGGCAGCGAGGGAC
CCCATCTGGGCAGCCCGGTTCCGGAGCATCAGAGACCCACCTGGAGATGTTCTGGCCAGCCCGGAGCCGCTCTTCACTGCAGATTGCCCCATATTCTACCCCCCA
GGGCCTCTGGGAGGATTTGATAGCATGGCTGAGCTCCTGCCAAGTTCAAGAGCTGAACTAGAGGACCCTGGGGGGGATGGAGCAATTCCTGCAATGTATCTAGAC
TGCATTTCAGATTTGAGGCAAAAAGAAATCACTGATGGCATCCACAGCTCCTCAGACATTAATATTTTATATAATGATGCAGTAGAATCCTGCATTCAGGACCCT
TCTGCAGAGGGGCTGTCGGAGGAGGTTCCTGTGGTGTTTGAGGAGCTGCCGGTGGTGTTCGAGGATGTGGCAGTGTATTTCACCCGGGAGGAGTGGGGCATGCTA
GACAAGCGGCAGAAGGAGCTGTACAGAGACGTGATGCGGATGAACTACGAGCTGTTGGCATCCTTGGGACCTGCCGCTGCCAAGCCAGACTTGATCTCCAAACTG
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>ZNF862|643641|protein
MEPRESGKAPVTFDDITVYLLQEEWVLLSQQQKELCGSNKLVAPLGPTVANPELFRKFGRGPEPWLGSVQGQRSLLEHHPGKKQMGYMGEMEVQGPTRESGQSLP
PQKKAYLSHLSTGSGHIEGDWAGRNRKLLKPRSIQKSWFVQFPWLIMNEEQTALFCSACREYPSIRDKRSRLIEGYTGPFKVETLKYHAKSKAHMFCVNALAARD
PIWAARFRSIRDPPGDVLASPEPLFTADCPIFYPPGPLGGFDSMAELLPSSRAELEDPGGDGAIPAMYLDCISDLRQKEITDGIHSSSDINILYNDAVESCIQDP
SAEGLSEEVPVVFEELPVVFEDVAVYFTREEWGMLDKRQKELYRDVMRMNYELLASLGPAAAKPDLISKLERRAAPWIKDPNGPKWGKGRPPGNKKMVAVREADT
QASAADSALLPGSPVEARASCCSSSICEEGDGPRRIKRTYRPRSIQRSWFGQFPWLVIDPKETKLFCSACIERPNLHDKSSRLVRGYTGPFKVETLKYHEVSKAH
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Evidence summary Top

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Evidences Syndromic Gene GWAS CNV Linkage Association Expression NGS de novo NGS Mosaic NGS Other Low-Scale Gene Studies Total
Score (No. of Studies) No 0 (0) 0 (1) 1 (2) 0 (0) 0 (0) 0 (1) 0 (1) 0 (0) 0 (0) 2 (5)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Pinto, 2010 - SNP microarray, qPCRASD - - - - 996 1287 2283
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Liu, 2001 USA microsatellite-based genomic screenautism, ASD 110 - 110 - - - -
Molloy, 2005 USA microsatellite-based genomic screenASD 34 - 34 - - - -
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference Case Number Family Number de novo Number Title
Iossifov I, 2014 2508 - 1194 The contribution of de novo coding mutations to autism spectrum disorder.
NGS Mosaic SNV Studies Top
Reference Case Number Family Number Mosaic Number Title
Lim ET, 2017 - 5947 376 Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
NGS Other Studies Top
Low Scale Gene Studies Top

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  (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