AutismKB 2.0

Evidence Details for ZNF774


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Basic Information Top
Gene Symbol:ZNF774 ( MGC75360 )
Gene Full Name: zinc finger protein 774
Band: 15q26.1
Quick LinksEntrez ID:342132; OMIM: NA; Uniprot ID:ZN774_HUMAN; ENSEMBL ID: ENSG00000196391; HGNC ID: 33108
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZNF774|342132|nucleotide
ATGTGGCTGGGGACTTCAGGGAAGAGTGGGTTACCTGGACACTGCTTAGAGAATCCTCTCCAGGAATGCCACCCAGCACAGTTAGAAGAATGGGCTCTCAAAGGA
ATTTCCAGGCCTAGTGTAATCTCCCAGCCGGAGCAGAAAGAAGAGCCATGGGTCCTACCACTCCAAAACTTTGAGGCGAGGAAGATCCCGAGGGAAAGCCACACA
GACTGTGAGCATCAGGTGGCAAAGCTCAATCAGGACAATTCTGAAACAGCAGAACAATGTGGAACATCCTCAGAAAGGACCAATAAAGATCTTTCTCATACTCTT
AGTTGGGGAGGAAACTGGGAGCAAGGCCTAGAATTAGAAGGGCAACATGGAACCCTTCCAGGAGAGGGCCAGCTGGAGTCCTTTTCACAGGAGAGGGATTTAAAC
AAGCTCCTGGATGGATATGTAGGAGAGAAGCCTATGTGTGCAGAATGCGGGAAAAGCTTTAACCAGAGTTCCTATCTCATAAGACACCTAAGAACCCACACTGGC
GAGAGGCCCTATACGTGCATTGAGTGTGGGAAAGGCTTCAAACAGAGCTCAGACCTTGTCACCCATCGCAGAACACACACAGGAGAGAAGCCCTACCAATGCAAG
GGGTGTGAGAAGAAATTCAGCGACAGCTCAACACTCATCAAACATCAGAGAACCCACACAGGGGAGAGACCCTATGAGTGCCCAGAGTGTGGAAAGACTTTTGGG
CGGAAGCCACACCTCATAATGCACCAAAGAACCCACACAGGCGAGAAGCCCTACGCGTGCCTGGAATGTCACAAAAGCTTCAGTCGAAGCTCAAATTTCATCACT
CACCAGAGGACCCACACAGGGGTGAAGCCTTACAGGTGTAATGACTGTGGGGAGAGTTTTAGCCAGAGCTCGGATTTGATTAAGCACCAACGAACCCACACGGGA
GAACGGCCCTTCAAATGCCCGGAGTGCGGGAAGGGCTTCAGAGATAGTTCTCATTTTGTAGCTCACATGAGCACTCATTCAGGAGAGAGGCCTTTCAGTTGTCCT
GACTGCCACAAAAGCTTCAGTCAGAGCTCACATTTGGTCACGCACCAAAGAACACACACAGGTGAGAGACCTTTTAAGTGCGAAAACTGTGGGAAAGGATTCGCC
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>ZNF774|342132|protein
MWLGTSGKSGLPGHCLENPLQECHPAQLEEWALKGISRPSVISQPEQKEEPWVLPLQNFEARKIPRESHTDCEHQVAKLNQDNSETAEQCGTSSERTNKDLSHTL
SWGGNWEQGLELEGQHGTLPGEGQLESFSQERDLNKLLDGYVGEKPMCAECGKSFNQSSYLIRHLRTHTGERPYTCIECGKGFKQSSDLVTHRRTHTGEKPYQCK
GCEKKFSDSSTLIKHQRTHTGERPYECPECGKTFGRKPHLIMHQRTHTGEKPYACLECHKSFSRSSNFITHQRTHTGVKPYRCNDCGESFSQSSDLIKHQRTHTG
ERPFKCPECGKGFRDSSHFVAHMSTHSGERPFSCPDCHKSFSQSSHLVTHQRTHTGERPFKCENCGKGFADSSALIKHQRIHTGERPYKCGECGKSFNQSSHFIT
HQRIHLGDRPYRCPECGKTFNQRSHFLTHQRTHTGEKPFHCSKCNKSFRQKAHLLCHQNTHLI
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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) 1 (3) 1 (1) 0 (0) 0 (0) 2 (2) 0 (0) 1 (1) 0 (0) 32 (7)
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
Bonati, 2005 - FISHautism - - - - 1 - 1
Szatmari, 2007 Europe, North America SNP microarrayASD 1491 - - - - - 0
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
Risch, 1999 USA microsatellite-based genomic screenPDD 90 - 90 - - - -
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
De Rubeis S, 2014 2270 - 1702 Synaptic, transcriptional and chromatin genes disrupted in autism
Fromer M, 2014 - - 94 De novo mutations in schizophrenia implicate synaptic networks.
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference Source Platform ADI-R ADOS Diagnosis Family Affected Validation Method
Total Simplex Multiplex
Yuen RK, 2015 - Complete Genomics ASD 85 - 85 170 Sanger sequencing
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