AutismKB 2.0

Evidence Details for ZNF398


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Basic Information Top
Gene Symbol:ZNF398 ( KIAA1339,P51,P71,ZER6 )
Gene Full Name: zinc finger protein 398
Band: 7q35
Quick LinksEntrez ID:57541; OMIM: NA; Uniprot ID:ZN398_HUMAN; ENSEMBL ID: ENSG00000197024; HGNC ID: 18373
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZNF398|57541|nucleotide
ATGAAGGGCAACTACGAGTCTCTCATCTCCATGGATTATGCTATAAATCAACCTGATGTCTTATCTCAGATTCAACCAGAAGGGGAACATAATACAGAGGACCAG
GCAGGGCCAGAGGAAAGTGAGATTCCCACAGACCCCAGTGAAGAGCCTGGTATTTCAACATCAGATATTCTGTCTTGGATTAAACAAGAAGAAGAGCCTCAGGTT
GGGGCCCCACCGGAGTCCAAGGAGAGTGACGTGTACAAAAGCACTTATGCTGATGAAGAGCTTGTCATCAAAGCTGAAGGCCTTGCTAGATCCTCGTTGTGCCCT
GAGGTTCCAGTCCCTTTCTCTTCTCCACCAGCAGCAGCAAAGGATGCTTTTTCAGATGTGGCTTTCAAAAGCCAGCAGTCTACATCCATGACACCTTTTGGACGT
CCAGCCACTGACCTGCCTGAAGCCTCTGAGGGACAAGTGACTTTTACTCAGTTGGGTAGCTATCCCCTCCCACCTCCAGTTGGCGAGCAGGTGTTCTCATGCCAC
CACTGTGGCAAGAATCTCAGCCAAGACATGTTGCTGACCCACCAATGTAGCCATGCTACTGAGCACCCCTTACCCTGTGCCCAGTGCCCTAAGCACTTTACTCCA
CAGGCGGACCTCAGCAGCACCTCCCAGGACCATGCCAGCGAGACACCCCCCACCTGCCCACACTGTGCCAGGACTTTTACTCACCCATCAAGACTTACCTACCAT
CTTCGGGTCCATAACAGCACTGAGCGTCCTTTCCCCTGTCCTGATTGCCCCAAGCGCTTTGCTGACCAGGCTCGACTCACCAGCCACCGGAGAGCTCATGCAAGC
GAAAGGCCCTTCCGCTGTGCCCAGTGCGGCAGGAGCTTCAGCTTGAAAATCAGCCTCCTGCTCCACCAGCGGGGTCATGCACAAGAGCGCCCTTTCTCCTGCCCT
CAGTGTGGCATTGACTTCAACGGCCACTCGGCCCTGATCCGCCACCAGATGATCCACACAGGCGAGCGTCCTTACCCCTGCACTGACTGCAGTAAGAGCTTCATG
CGCAAGGAGCACCTGCTGAACCACCGGCGGCTGCACACAGGCGAGCGGCCCTTCAGTTGTCCTCACTGTGGCAAGAGCTTCATCCGCAAGCACCACCTAATGAAA
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>ZNF398|57541|protein
MKGNYESLISMDYAINQPDVLSQIQPEGEHNTEDQAGPEESEIPTDPSEEPGISTSDILSWIKQEEEPQVGAPPESKESDVYKSTYADEELVIKAEGLARSSLCP
EVPVPFSSPPAAAKDAFSDVAFKSQQSTSMTPFGRPATDLPEASEGQVTFTQLGSYPLPPPVGEQVFSCHHCGKNLSQDMLLTHQCSHATEHPLPCAQCPKHFTP
QADLSSTSQDHASETPPTCPHCARTFTHPSRLTYHLRVHNSTERPFPCPDCPKRFADQARLTSHRRAHASERPFRCAQCGRSFSLKISLLLHQRGHAQERPFSCP
QCGIDFNGHSALIRHQMIHTGERPYPCTDCSKSFMRKEHLLNHRRLHTGERPFSCPHCGKSFIRKHHLMKHQRIHTGERPYPCSYCGRSFRYKQTLKDHLRSGHN
GGCGGDSDPSGQPPNPPGPLITGLETSGLGVNTEGLETNQWYGEGSGGGVL
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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 (0) 1 (2) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (3)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Liu, 2001 USA microsatellite-based genomic screenautism, ASD 110 - 110 - - - -
Molloy, 2005 USA microsatellite-based genomic screenASD 34 - 34 - - - -
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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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