AutismKB 2.0

Evidence Details for ZNF721


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Basic Information Top
Gene Symbol:ZNF721 ( FLJ11452,KIAA1982 )
Gene Full Name: zinc finger protein 721
Band: 4p16.3
Quick LinksEntrez ID:170960; OMIM: NA; Uniprot ID:D9N162_HUMAN; ENSEMBL ID: ENSG00000246238; HGNC ID: 29425
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZNF721|170960|nucleotide
ATGTTGGAGAACTACAGAAACCTGGTCTCCCTAGCTATGTGTTCTCATTTCACCCAAGACTTTTTGCCAGTGCAGGGGATAGAAGATTCATTCCACAAACTTATA
CTGAGAAGATATGAGAAATGTGGGCATGATAATTTACAATTAAGGAAAGGCTGTAAAAGTATGAACGTGTGTAAAGTGCAGAAGGGAGTTTATAATGGAATTAAT
AAATGCTTGTCAAATACTCAGAGCAAAATATTTCAATGTAATGCACGTGTCAAAGTTTTTAGTAAATTTGCAAATTCAAACAAAGATAAGACAAGACATACTGGA
GAGAAACACTTTAAATGTAACGAATGTGGCAAGTCATTTCAGAAGTTCTCAGACCTAACTCAACATAAAGGAATTCATGCTGGAGAGAAACCCTACACTTGTGAA
GAACGTGGCAAAGACTTTGGATGGTACACAGACCTGAATCAACACAAGAAAATTCATACTGGAGAGAAACCTTACAAATGTGAAGAATGTGGCAAAGCCTTTAAT
AGGTCAACAAACCTTACTGCACATAAGAGAATTCACAACAGAGAGAAAGCTTACACAGGTGAAGATCGTGACAGAGCCTTTGGATGGTCCACAAACCTGAATGAA
TATAAGAAAATTCATACTGGAGATAAACCCTACAAATGTAAAGAATGTGGGAAAGCCTTTATGCATTCCTCACACCTGAATAAACATGAGAAAATTCATACTGGA
GAGAAACCCTACAAATGTAAGGAATGTGGCAAAGTCATTTCCTCATCCTCAAGCTTTGCTAAACATAAGAGGATTCATACTGGCGAGAAACCCTTTAAATGTTTA
GAATGTGGTAAAGCCTTTAATATTTCCACAACCCTTACTAAACATAGGAGAATTCATACTGGAGAGAAACCCTACACATGTGAAGTATGTGGCAAAGCCTTTAGA
CAGTCCGCAAACCTTTATGTACATAGGAGAATTCATACTGGAGAGAAACCCTACACATGTGGAGAATGTGGCAAAACCTTTAGACAGTCCGCAAACCTTTACGTA
CATAGGAGAATTCATACTGGAGAGAAACCTTACAAATGCGAAGACTGTGGCAAAGCCTTTGGACGGTACACAGCCCTGAATCAACACAAGAAAATTCATACTGGA
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>ZNF721|170960|protein
MLENYRNLVSLAMCSHFTQDFLPVQGIEDSFHKLILRRYEKCGHDNLQLRKGCKSMNVCKVQKGVYNGINKCLSNTQSKIFQCNARVKVFSKFANSNKDKTRHTG
EKHFKCNECGKSFQKFSDLTQHKGIHAGEKPYTCEERGKDFGWYTDLNQHKKIHTGEKPYKCEECGKAFNRSTNLTAHKRIHNREKAYTGEDRDRAFGWSTNLNE
YKKIHTGDKPYKCKECGKAFMHSSHLNKHEKIHTGEKPYKCKECGKVISSSSSFAKHKRIHTGEKPFKCLECGKAFNISTTLTKHRRIHTGEKPYTCEVCGKAFR
QSANLYVHRRIHTGEKPYTCGECGKTFRQSANLYVHRRIHTGEKPYKCEDCGKAFGRYTALNQHKKIHTGEKPYKCEECGKAFNSSTNLTAHKRIHTREKPYTCE
DRGRAFGLSTNLNEYKKIHTGDKPYKCKECGKAFIHSLHLNKHEKIHTGKKPYKCKQCGKVITSSSSFAKHKRIHTGEKPFECLECGKAFTSSTTLTKHRRIHTG
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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 (3) 1 (1) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (5)
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
Szatmari, 2007 Europe, North America SNP microarrayASD 1491 - - - - - 0
Pinto, 2010 - SNP microarray, qPCRASD - - - - 996 1287 2283
Sanders, 2011 Simons Simplex Collection SNP microarray--ASD 1127 1127 - - - - -
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Bailey, 1998 - microsatellite-based genomic screenPDD 99 - 99 - - - -
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
Michaelson JJ, 2012 - 10 565 Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
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