AutismKB 2.0

Evidence Details for ZNF213


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:ZNF213 ( CR53,ZKSCAN21 )
Gene Full Name: zinc finger protein 213
Band: 16p13.3
Quick LinksEntrez ID:7760; OMIM: 608387; Uniprot ID:ZN213_HUMAN; ENSEMBL ID: ENSG00000085644; HGNC ID: 13005
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZNF213|7760|nucleotide
ATGGCAGCCCCCTTGGAGGCCCAGGACCAGGCCCCTGGGGAGGGAGAAGGGCTTCTGATTGTGAAAGTGGAAGATTCCTCCTGGGAACAGGAATCTGCCCAGCAT
GAGGATGGCAGGGATTCCGAAGCCTGCCGCCAGCGCTTCCGGCAATTCTGCTACGGGGATGTGCATGGGCCTCATGAGGCCTTCAGCCAGCTCTGGGAGCTCTGC
TGCCGCTGGCTGCGGCCCGAGCTGCGTACCAAGGAGCAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTCCTGACAGTGCTGCCAGGGGAGATCCAGGGCTGGGTG
CGTGAGCAGCACCCGGGAAGCGGTGAGGAGGCTGTCGCCTTGGTGGAGGACCTACAGAAGCAGCCAGTGAAAGCCTGGCGACAGGATGTGCCCTCGGAGGAGGCG
GAACCCGAGGCTGCAGGCCGGGGATCCCAGGCCACGGGGCCTCCCCCGACGGTGGGGGCACGGAGGCGGCCGTCTGTTCCCCAGGAGCAGCACAGCCATAGCGCC
CAGCCTCCTGCTCTTCTTAAAGAGGGTCGTCCCGGAGAGACGACGGACACCTGCTTTGTCTCTGGGGTCCATGGACCTGTGGCATTGGGAGACATCCCATTCTAT
TTCTCCCGGGAAGAATGGGGCACCCTGGACCCTGCTCAGCGGGATCTCTTCTGGGACATAAAGCGGGAGAACTCCCGGAACACCACCCTGGGTTTTGGGCTCAAA
GGCCAAAGTGAGAAGTCCCTGCTGCAGGAGATGGTGCCGGTGGTGCCAGGCCAGACAGGCAGCGACGTGACTGTGTCCTGGAGCCCCGAGGAGGCTGAGGCCTGG
GAGAGCGAGAACCGGCCGAGGGCGGCCCTGGGCCCAGTGGTGGGCGCGCGACGGGGGCGGCCACCCACTCGCCGGCGCCAGTTCCGGGACCTGGCAGCCGAGAAG
CCGCACAGCTGCGGGCAGTGTGGAAAGCGCTTCCGCTGGGGCTCGGACCTGGCGCGGCACCAGCGCACGCACACGGGCGAGAAGCCACACAAGTGCCCTGAGTGC
GACAAGAGCTTCCGCAGCTCCTCGGACCTGGTGCGCCACCAAGGCGTGCACACGGGCGAGAAGCCCTTCTCCTGTTCCGAGTGCGGCAAGAGCTTCAGCCGCAGC
Show »

>ZNF213|7760|protein
MAAPLEAQDQAPGEGEGLLIVKVEDSSWEQESAQHEDGRDSEACRQRFRQFCYGDVHGPHEAFSQLWELCCRWLRPELRTKEQILELLVLEQFLTVLPGEIQGWV
REQHPGSGEEAVALVEDLQKQPVKAWRQDVPSEEAEPEAAGRGSQATGPPPTVGARRRPSVPQEQHSHSAQPPALLKEGRPGETTDTCFVSGVHGPVALGDIPFY
FSREEWGTLDPAQRDLFWDIKRENSRNTTLGFGLKGQSEKSLLQEMVPVVPGQTGSDVTVSWSPEEAEAWESENRPRAALGPVVGARRGRPPTRRRQFRDLAAEK
PHSCGQCGKRFRWGSDLARHQRTHTGEKPHKCPECDKSFRSSSDLVRHQGVHTGEKPFSCSECGKSFSRSAYLADHQRIHTGEKPFGCSDCGKSFSLRSYLLDHR
RVHTGERPFGCGECDKSFKQRAHLIAHQSLHAKMAQPVG
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 (1) 1 (2) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (4)
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
Gai, 2011 AGRE SNP microarray--autism - - - - 1224 3801 5025
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Buxbaum, 2004 USA microsatellite-based genomic screenautism 115 - 115 - - - -
Lauritsen, 2006 Faroe Islands microsatellite-based genomic screenautism - - - - 12 44 56
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
Sanders SJ, 2012 - 238 172 De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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