AutismKB 2.0

Evidence Details for ERI3


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Basic Information Top
Gene Symbol:ERI3 ( FLJ22943,MGC2683,PINT1,PRNPIP )
Gene Full Name: ERI1 exoribonuclease family member 3
Band: 1p34.1
Quick LinksEntrez ID:79033; OMIM: 609917; Uniprot ID:ERI3_HUMAN; ENSEMBL ID: ENSG00000117419; HGNC ID: 17276
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ERI3|79033|nucleotide
ATGGCGACAGCCTCTCCCGCTGCTGACGGGGGGCGGGGGCGGCCCTGGGAAGGAGGGCTGGTCTCCTGGCCCCCCGCCCCTCCCCTTACTCTCCCCTGGACTTGG
ATGGGCCCGAGTTGGGGGCAACACCCCGGGCATTGGGGCTTTCCAGCTCTCACAGAACCTTCAGCATCCCCAGCTGCCGGTCTTGGCATCTTCGAAGTAAGGAGA
GTTTTAGATGCTTCTGGATGTTCAATGCTAGCACCTTTACAGACTGGAGCAGCTCGATTTTCTTCGTATTTACTTTCAAGAGCAAGAAAAGTGCTGGGCTCCCAC
TTATTTTCTCCCTGTGGTGTTCCGGAGTTCTGCTCCATATCCACCAGAAAGCTGGCGGCCCACGGCTTTGGCGCATCCATGGCGGCAATGGTGTCCTTCCCTCCC
CAGAGGTATCACTACTTTTTAGTGCTGGACTTTGAGGCCACGTGCGACAAGCCACAGATTCATCCTCAGGAAATCATCGAGTTCCCCATCCTAAAGCTAAATGGC
CGGACCATGGAGATTGAGTCTACCTTTCACATGTATGTCCAGCCTGTAGTCCATCCACAGCTTACCCCATTCTGTACAGAGCTCACCGGGATTATTCAAGCCATG
GTGGATGGTCAGCCAAGCCTGCAGCAAGTGCTGGAGAGGGTCGATGAATGGATGGCGAAGGAAGGCCTCTTAGATCCAAACGTCAAGTCAATTTTTGTCACCTGT
GGAGACTGGGACTTAAAAGTCATGCTCCCAGGCCAGTGCCAGTACTTGGGCTTGCCAGTGGCGGATTACTTCAAGCAGTGGATTAATCTGAAAAAGGCTTACAGC
TTCGCCATGGGCTGCTGGCCCAAGAATGGACTTCTAGACATGAACAAGGGCCTCAGCCTGCAACACATAGGCCGGCCCCACAGCGGCATTGACGACTGCAAGAAC
ATTGCCAACATCATGAAGACACTCGCCTATCGAGGCTTCATCTTCAAGCAGACATCGAAGCCGTTCTGA

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>ERI3|79033|protein
MATASPAADGGRGRPWEGGLVSWPPAPPLTLPWTWMGPSWGQHPGHWGFPALTEPSASPAAGLGIFEVRRVLDASGCSMLAPLQTGAARFSSYLLSRARKVLGSH
LFSPCGVPEFCSISTRKLAAHGFGASMAAMVSFPPQRYHYFLVLDFEATCDKPQIHPQEIIEFPILKLNGRTMEIESTFHMYVQPVVHPQLTPFCTELTGIIQAM
VDGQPSLQQVLERVDEWMAKEGLLDPNVKSIFVTCGDWDLKVMLPGQCQYLGLPVADYFKQWINLKKAYSFAMGCWPKNGLLDMNKGLSLQHIGRPHSGIDDCKN
IANIMKTLAYRGFIFKQTSKPF

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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 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (1)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference Source Platform ADI-R ADOS Diagnosis Family Affected Validation Method
Total Simplex Multiplex
Doan RN, 2016 - ---ASD - - - - -
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