AutismKB 2.0

Evidence Details for WDR59


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Basic Information Top
Gene Symbol:WDR59 ( FLJ12270,MGC11230 )
Gene Full Name: WD repeat domain 59
Band: 16q23.1
Quick LinksEntrez ID:79726; OMIM: NA; Uniprot ID:WDR59_HUMAN; ENSEMBL ID: ENSG00000103091; HGNC ID: 25706
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>WDR59|79726|nucleotide
ATGGCGGCGCGATGGAGCAGCGAAAACGTGGTTGTAGAGTTCCGTGACTCCCAGGCAACTGCGATGTCTGTGGACTGTCTTGGGCAGCATGCAGTGCTTTCTGGC
CGCAGATTCTTATACATCGTCAATCTAGATGCCCCTTTCGAAGGTCACCGAAAGATCTCTCGCCAGAGCAAATGGGACATTGGAGCTGTGCAGTGGAATCCTCAT
GACAGCTTTGCACACTATTTTGCGGCTTCGAGTAACCAACGAGTAGACCTTTACAAGTGGAAAGACGGCAGTGGGGAAGTTGGCACAACCTTACAAGGCCACACT
CGTGTCATCAGCGACTTGGACTGGGCGGTGTTTGAGCCTGACCTCCTGGTTACCAGCTCTGTGGACACCTACATCTACATTTGGGATATCAAAGACACAAGGAAA
CCTACTGTTGCACTGTCTGCTGTTGCGGGTGCCTCCCAGGTCAAATGGAATAAAAAAAATGCTAACTGCCTTGCCACCAGCCATGACGGCGATGTGCGGATATGG
GATAAGAGGAAACCCAGTACAGCAGTGGAATATCTAGCCGCCCACCTCTCCAAAATCCATGGCCTGGACTGGCACCCAGACAGCGAGCACATTCTTGCTACCTCC
AGTCAAGACAATTCTGTGAAGTTCTGGGATTACCGCCAGCCTCGGAAATACCTCAATATTCTTCCTTGCCAGGTGCCTGTCTGGAAGGCCAGATACACACCTTTC
AGCAATGGATTGGTGACTGTGATGGTTCCCCAGCTGCGGAGGGAAAACAGCCTTCTCCTGTGGAATGTCTTTGACTTGAACACCCCAGTCCACACCTTCGTGGGG
CATGATGATGTGGTCCTGGAGTTCCAGTGGAGGAAGCAGAAGGAAGGGTCCAAGGACTATCAACTGGTGACGTGGTCCCGGGATCAGACCTTGAGAATGTGGCGG
GTGGATTCCCAGATGCAGAGGCTTTGTGCAAATGACATATTAGATGGTGTTGATGAGTTCATTGAGAGTATTTCCCTTCTGCCGGAACCTGAGAAGACCCTGCAC
ACTGAAGATACAGATCACCAGCACACTGCAAGCCATGGGGAGGAAGAAGCCCTAAAAGAAGATCCCCCTAGAAATCTCCTGGAAGAGAGGAAATCAGATCAACTG
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>WDR59|79726|protein
MAARWSSENVVVEFRDSQATAMSVDCLGQHAVLSGRRFLYIVNLDAPFEGHRKISRQSKWDIGAVQWNPHDSFAHYFAASSNQRVDLYKWKDGSGEVGTTLQGHT
RVISDLDWAVFEPDLLVTSSVDTYIYIWDIKDTRKPTVALSAVAGASQVKWNKKNANCLATSHDGDVRIWDKRKPSTAVEYLAAHLSKIHGLDWHPDSEHILATS
SQDNSVKFWDYRQPRKYLNILPCQVPVWKARYTPFSNGLVTVMVPQLRRENSLLLWNVFDLNTPVHTFVGHDDVVLEFQWRKQKEGSKDYQLVTWSRDQTLRMWR
VDSQMQRLCANDILDGVDEFIESISLLPEPEKTLHTEDTDHQHTASHGEEEALKEDPPRNLLEERKSDQLGLPQTLQQEFSLINVQIRNVNVEMDAADRSCTVSV
HCSNHRVKMLVKFPAQYPNNAAPSFQFINPTTITSTMKAKLLKILKDTALQKVKRGQSCLEPCLRQLVSCLESFVNQEDSASSNPFALPNSVTPPLPTFARVTTA
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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 (0) 0 (0) (0)
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
Reference Case Number Family Number de novo Number Title
Chen R, 2017 107 116 128 Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in aut
NGS Mosaic SNV Studies Top
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