AutismKB 2.0

Evidence Details for ZC3H7A


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Basic Information Top
Gene Symbol:ZC3H7A ( FLJ10027,FLJ20318,ZC3H7,ZC3HDC7 )
Gene Full Name: zinc finger CCCH-type containing 7A
Band: 16p13.13
Quick LinksEntrez ID:29066; OMIM: NA; Uniprot ID:Z3H7A_HUMAN; ENSEMBL ID: ENSG00000122299; HGNC ID: 30959
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZC3H7A|29066|nucleotide
ATGTCCAATGTGTCCGAGGAGAGAAGAAAAAGGCAGCAGAACATTAAGGAAGGACTGCAGTTTATACAGTCACCGCTGTCATATCCAGGAACACAGGAGCAATAT
GCGGTATATTTGCGTGCTCTCGTGAGAAATCTTTTTAATGAAGGAAATGACGTTTATCGGGAACATGATTGGAACAACTCGATAAGCCAGTACACGGAAGCCTTG
AATATAGCTGATTATGCAAAATCTGAAGAAATTTTAATCCCCAAAGAAATAATTGAAAAACTATATATAAATCGTATTGCCTGCTATTCTAATATGGGTTTCCAT
GATAAAGTTTTGGAGGACTGCAATATAGTCCTCAGTTTAAATGCCAGTAACTGCAAAGCTCTGTATCGGAAATCTAAGGCTTTAAGTGATTTAGGAAGATACAAA
AAGGCTTACGATGCTGTAGCAAAGTGCTCCTTAGCAGTGCCTCAGGATGAGCATGTAATAAAACTAACTCAAGAACTAGCTCAGAAATTGGGATTTAAAATAAGA
AAAGCGTATGTCAGAGCTGAGCTCTCATTAAAATCAGTTCCTGGGGATGGGGCTACCAAGGCTTTGAACCATTCTGTGGAAGATATTGAGCCAGATTTATTAACT
CCAAGGCAAGAAGCAGTTCCTGTTGTCTCTTTACCGGCACCCAGTTTTTCTCATGAAGTTGGAAGTGAGCTGGCCTCAGTTCCTGTTATGCCCTTAACTTCTATT
TTGCCACTACAAGTGGAAGAGAGCGCTCTGCCATCTGCAGTGCTGGCAAATGGAGGAAAGATGCCCTTCACTATGCCAGAAGCTTTTCTAGATGATGGAGATATG
GTCCTTGGAGATGAACTAGATGACCTGCTTGATTCTGCACCTGAAACTAATGAAACTGTTATGCCGTCAGCTTTAGTCAGAGGACCCCTTCAGACAGCCAGTGTC
TCTCCTAGCATGCCCTTTTCGGCATCGCTGTTAGGAACCTTACCCATTGGTGCGAGGTATGCTCCTCCACCCTCCTTCTCAGAATTTTATCCACCTTTGACTTCA
TCCTTAGAAGATTTTTGTTCTTCTTTAAATTCATTTTCAATGAGTGAATCCAAACGAGATCTGTCCACCTCAACTTCTAGAGAGGGAACACCGCTTAACAACAGT
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>ZC3H7A|29066|protein
MSNVSEERRKRQQNIKEGLQFIQSPLSYPGTQEQYAVYLRALVRNLFNEGNDVYREHDWNNSISQYTEALNIADYAKSEEILIPKEIIEKLYINRIACYSNMGFH
DKVLEDCNIVLSLNASNCKALYRKSKALSDLGRYKKAYDAVAKCSLAVPQDEHVIKLTQELAQKLGFKIRKAYVRAELSLKSVPGDGATKALNHSVEDIEPDLLT
PRQEAVPVVSLPAPSFSHEVGSELASVPVMPLTSILPLQVEESALPSAVLANGGKMPFTMPEAFLDDGDMVLGDELDDLLDSAPETNETVMPSALVRGPLQTASV
SPSMPFSASLLGTLPIGARYAPPPSFSEFYPPLTSSLEDFCSSLNSFSMSESKRDLSTSTSREGTPLNNSNSSLLLMNGPGSLFASENFLGISSQPRNDFGNFFG
SAVTKPSSSVTPRHPLEGTHELRQACQICFVKSGPKLMDFTYHANIDHKCKKDILIGRIKNVEDKSWKKIRPRPTKTNYEGPYYICKDVAAEEECRYSGHCTFAY
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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 (1) 1 (3) 0 (0) 0 (0) 0 (1) 0 (1) 0 (0) 0 (0) 2 (6)
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
Pinto, 2010 - SNP microarray, qPCRASD - - - - 996 1287 2283
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Monaco, 2001 - microsatellite-based genomic screenPDD 152 - 152 - - - -
Lamb, 2005 - microsatellite-based genomic screenautism 207 - 207 - 420 - -
Buxbaum, 2004 USA microsatellite-based genomic screenautism 115 - 115 - - - -
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
Reference Case Number Family Number Mosaic Number Title
Krupp DR, 2017 - 2264 247 Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
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