AutismKB 2.0

Evidence Details for WDR3


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Basic Information Top
Gene Symbol:WDR3 ( FLJ12796 )
Gene Full Name: WD repeat domain 3
Band: 1p12
Quick LinksEntrez ID:10885; OMIM: 604737; Uniprot ID:WDR3_HUMAN; ENSEMBL ID: ENSG00000065183; HGNC ID: 12755
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>WDR3|10885|nucleotide
ATGGGGCTCACCAAGCAGTACCTACGCTATGTTGCTAGTGCGGTCTTTGGCGTTATCGGCAGCCAAAAAGGTAATATTGTCTTTGTGACACTTCGTGGTGAGAAA
GGACGTTATGTGGCAGTACCAGCTTGTGAACACGTTTTCATCTGGGACTTAAGGAAAGGAGAGAAGATTCTTATCCTTCAGGGGCTTAAACAAGAAGTTACTTGC
TTATGCCCCTCCCCAGATGGGCTACACTTAGCTGTTGGGTATGAGGATGGGTCGATCCGAATCTTCAGTCTCCTGAGTGGGGAAGGAAATGTGACCTTCAATGGT
CACAAAGCAGCTATCACTACCTTGAAGTATGATCAGCTAGGAGGCAGACTGGCATCTGGGTCCAAGGACACAGATATTATTGTATGGGATGTGATCAATGAAAGT
GGTCTGTACCGTCTAAAGGGGCACAAGGATGCCATCACACAAGCATTGTTTCTACGAGAAAAGAACCTGCTAGTTACTAGTGGGAAAGATACCATGGTGAAATGG
TGGGACCTTGATACTCAGCACTGCTTTAAAACAATGGTTGGCCACCGGACTGAGGTATGGGGGTTGGTTCTGTTGTCAGAAGAAAAGCGACTCATCACTGGGGCC
TCAGACAGTGAACTGAGGGTATGGGACATAGCTTATCTGCAAGAGATTGAAGACCCGGAAGAACCAGACCCCAAGAAAATCAAAGGATCTTCTCCTGGAATACAA
GATACTCTTGAGGCAGAGGATGGTGCCTTTGAGACGGATGAAGCCCCTGAGGATCGAATCCTTTCATGCAGAAAAGCTGGTTCCATAATGCGGGAAGGAAGAGAC
AGAGTTGTAAACCTTGCAGTCGACAAGACAGGCAGGATTCTTGCTTGCCATGGAACTGACTCTGTGCTAGAATTGTTTTGTATCCTTTCCAAAAAGGAAATTCAG
AAGAAAATGGATAAGAAGATGAAGAAAGCTAGAAAGAAAGCAAAATTACATTCTAGCAAAGGAGAGGAGGAAGATCCTGAGGTTAATGTTGAAATGAGTCTGCAA
GATGAAATCCAGCGGGTGACTAATATAAAAACTTCTGCCAAAATCAAGTCCTTTGACTTGATTCATTCACCTCACGGAGAGTTAAAGGCTGTCTTCCTGCTGCAG
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>WDR3|10885|protein
MGLTKQYLRYVASAVFGVIGSQKGNIVFVTLRGEKGRYVAVPACEHVFIWDLRKGEKILILQGLKQEVTCLCPSPDGLHLAVGYEDGSIRIFSLLSGEGNVTFNG
HKAAITTLKYDQLGGRLASGSKDTDIIVWDVINESGLYRLKGHKDAITQALFLREKNLLVTSGKDTMVKWWDLDTQHCFKTMVGHRTEVWGLVLLSEEKRLITGA
SDSELRVWDIAYLQEIEDPEEPDPKKIKGSSPGIQDTLEAEDGAFETDEAPEDRILSCRKAGSIMREGRDRVVNLAVDKTGRILACHGTDSVLELFCILSKKEIQ
KKMDKKMKKARKKAKLHSSKGEEEDPEVNVEMSLQDEIQRVTNIKTSAKIKSFDLIHSPHGELKAVFLLQNNLVELYSLNPSLPTPQPVRTSRITIGGHRSDVRT
LSFSSDNIAVLSAAADSIKIWNRSTLQCIRTMTCEYALCSFFVPGDRQVVIGTKTGKLQLYDLASGNLLETIDAHDGALWSMSLSPDQRGFVTGGADKSVKFWDF
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Evidence summary Top

Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
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) 1 (1) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 3 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Risch, 1999 USA microsatellite-based genomic screenPDD 90 - 90 - - - -
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 1
Reference Source Tissue #Subjects
(% Women)
ADI-R ADOS Endo- pheno Diagnosis Normal Controls
(% Women)
Fold Change Up/ Down P/Q value
Gregg, 2008_2 mixed lymphoblastoid cell lines 17
(11.76%)
autism with early onset autism 12
(25.00%)
1.571 Up 0.0403
  • Platform: U133 Plus 2.0 GeneChip (Affymetrix,Santa Clara, CA, USA)
  • ProbeSet: 218882_s_at
  • RefSeq_ID/ EST: NM_006784
  • GEO_ID: GSE6575
  • Statistic Method: a stringent 1.5-fold unpaired t test with Benjamini
Proteomics Studies:0
Reference Source Tissue Platform #Subjects
(% Women)
ADI-R ADOS Diagnosis Normal Controls(% Women)
No Evidence.
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.

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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