AutismKB 2.0

Evidence Details for WDR55


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:WDR55 ( FLJ20195,FLJ21702 )
Gene Full Name: WD repeat domain 55
Band: 5q31.3
Quick LinksEntrez ID:54853; OMIM: NA; Uniprot ID:WDR55_HUMAN; ENSEMBL ID: ENSG00000120314; HGNC ID: 25971
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>WDR55|54853|nucleotide
ATGGACCGCACTTGTGAGGAGAGGCCCGCTGAGGATGGGAGCGACGAGGAGGACCCAGACTCCATGGAAGCCCCAACCCGGATCCGGGACACTCCGGAAGACATC
GTGCTGGAAGCTCCGGCTAGTGGGCTGGCGTTCCATCCGGCCCGTGACCTACTGGCTGCAGGGGACGTGGACGGGGACGTGTTCGTCTTTTCCTACTCTTGCCAA
GAGGGAGAAACCAAGGAGCTCTGGTCATCAGGTCACCATCTCAAGGCCTGCCGAGCTGTGGCCTTCTCTGAAGATGGGCAGAAGCTCATTACTGTCTCCAAGGAC
AAAGCCATCCATGTTCTAGATGTGGAGCAGGGCCAACTGGAAAGACGTGTTTCCAAGGCTCATGGTGCCCCCATCAATAGTCTTCTGCTGGTGGATGAGAATGTT
CTGGCCACTGGGGATGACACAGGTGGTATCCGTCTCTGGGACCAGCGGAAGGAGGGCCCCTTAATGGATATGAGGCAACATGAAGAGTACATCGCAGACATGGCT
CTGGATCCAGCCAAAAAGCTGCTGCTGACAGCCAGCGGGGATGGCTGCCTTGGCATCTTCAACATTAAGAGGCGTCGGTTTGAGCTGCTCTCAGAACCTCAGTCT
GGGGACCTGACCTCTGTCACTCTCATGAAATGGGGGAAGAAGGTAGCCTGTGGCTCCAGTGAAGGTACCATCTACCTCTTCAATTGGAATGGCTTTGGGGCCACA
AGTGACCGCTTTGCCCTGAGAGCTGAATCTATCGACTGCATGGTTCCAGTCACCGAGAGTCTGCTGTGTACTGGCTCCACTGATGGAGTCATCAGGGCTGTGAAC
ATCCTACCGAACCGAGTGGTGGGCAGTGTGGGCCAGCACACTGGGGAGCCTGTGGAGGAGCTGGCCCTCTCCCACTGTGGCCGCTTCCTGGCCAGTAGTGGCCAT
GACCAGCGCCTCAAGTTTTGGGACATGGCCCAGCTGCGAGCTGTGGTGGTGGATGACTACCGTCGGCGCAAAAAAAAGGGAGGACCACTGCGGGCTCTGAGCAGC
AAGACTTGGAGCACCGATGACTTCTTCGCAGGACTGAGGGAAGAGGGAGAAGACTCCATGGCTCAGGAAGAAAAGGAGGAGACTGGGGATGACAGTGACTGA
Show »

>WDR55|54853|protein
MDRTCEERPAEDGSDEEDPDSMEAPTRIRDTPEDIVLEAPASGLAFHPARDLLAAGDVDGDVFVFSYSCQEGETKELWSSGHHLKACRAVAFSEDGQKLITVSKD
KAIHVLDVEQGQLERRVSKAHGAPINSLLLVDENVLATGDDTGGIRLWDQRKEGPLMDMRQHEEYIADMALDPAKKLLLTASGDGCLGIFNIKRRRFELLSEPQS
GDLTSVTLMKWGKKVACGSSEGTIYLFNWNGFGATSDRFALRAESIDCMVPVTESLLCTGSTDGVIRAVNILPNRVVGSVGQHTGEPVEELALSHCGRFLASSGH
DQRLKFWDMAQLRAVVVDDYRRRKKKGGPLRALSSKTWSTDDFFAGLREEGEDSMAQEEKEETGDDSD

Show »

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) 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
Iossifov I, 2012 - 343 50 De novo gene disruptions in children on the autistic spectrum.
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.

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