AutismKB 2.0

Evidence Details for ZDHHC1


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Basic Information Top
Gene Symbol:ZDHHC1 ( C16orf1,HSU90653,ZNF377 )
Gene Full Name: zinc finger, DHHC-type containing 1
Band: 16q22.1
Quick LinksEntrez ID:29800; OMIM: NA; Uniprot ID:ZDHC1_HUMAN; ENSEMBL ID: ENSG00000159714; HGNC ID: 17916
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZDHHC1|29800|nucleotide
ATGTACAAGATGAACATCTGCAACAAGCCCTCCAACAAGACGGCCCCTGAGAAGAGTGTGTGGACGGCACCGGCACAGCCCAGCGGACCCTCCCCTGAGCTGCAG
GGCCAGCGATCCCGCCGGAATGGGTGGAGCTGGCCCCCTCACCCGCTCCAGATTGTGGCCTGGCTGCTGTACCTCTTCTTTGCTGTGATCGGCTTTGGGATCCTT
GTTCCCCTCCTGCCTCACCACTGGGTGCCCGCTGGCTACGCTTGCATGGGCGCCATCTTTGCTGGCCACCTTGTGGTGCACCTGACCGCCGTCTCCATCGATCCA
GCAGATGCCAACGTGCGGGACAAGAGCTATGCGGGGCCCCTGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACTGCAACTTGTGCAAC
GTGGATGTGAGCGCTCGCTCCAAGCACTGCAGCGCCTGCAACAAGTGCGTGTGCGGTTTCGACCACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAAC
TACCGGCTCTTTCTACACAGTGTTGCATCCGCTTTACTGGGCGTCCTGCTCCTGGTGCTGGTGGCCACATATGTCTTCGTGGAGTTCTTTGTCAACCCCATGCGT
CTGCGCACCAACCGACACTTTGAAGTCCTGAAGAATCACACGGATGTGTGGTTCGTGTTCCTGCCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCCATCCTGGCC
CTGGCCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACCTGCTCTGCTTCCACATTTATCTCATGTGGCACAAGCTCACCACCTATGAG
TACATCGTGCAGCACCGCCCACCACAGGAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGGCCCATTCAGGAGATGGAGTTCTACATG
CGGACCTTCAGACATATGCGCCCAGAGCCCCCTGGCCAGGCCGGGCCAGCAGCAGTGAATGCCAAACACTCTCGCCCTGCCTCCCCGGATCCGACCCCAGGTAGG
AGGGACTGTGCTGGGCCTCCGGTCCAGGTGGAGTGGGATAGAAAGAAGCCTCTACCCTGGCGCTCGCCTCTGCTTCTTTTGGCGATGTGGGGCCCTCAGGCTCCC
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>ZDHHC1|29800|protein
MYKMNICNKPSNKTAPEKSVWTAPAQPSGPSPELQGQRSRRNGWSWPPHPLQIVAWLLYLFFAVIGFGILVPLLPHHWVPAGYACMGAIFAGHLVVHLTAVSIDP
ADANVRDKSYAGPLPIFNRSQHAHVIEDLHCNLCNVDVSARSKHCSACNKCVCGFDHHCKWLNNCVGERNYRLFLHSVASALLGVLLLVLVATYVFVEFFVNPMR
LRTNRHFEVLKNHTDVWFVFLPAAPVETQAPAILALAALLILLGLLSTALLGHLLCFHIYLMWHKLTTYEYIVQHRPPQEAKGVHRELESCPPKMRPIQEMEFYM
RTFRHMRPEPPGQAGPAAVNAKHSRPASPDPTPGRRDCAGPPVQVEWDRKKPLPWRSPLLLLAMWGPQAPPCLCRKRGRGACIKCERLRPRIRRRGLGPPAAAPA
RRRIPRTPALCTPLALPAPTTRRRQSPWTRFQWRRRAWAAPLWPPRGAGADSPRWRGRRVRPPFS
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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 (2) 0 (0) 0 (0) 0 (0) 0 (2) 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
Wassink, 2001 USA Chromosomal analysis of G-bandautism - - - - 278 - 278
Bucan, 2009 USA SNP microarrayautism, ASD 912 - 912 - - 1488 1488
Linkage Studies Top
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
Neale BM, 2012 175 175 173 Patterns and rates of exonic de novo mutations in autism spectrum disorders.
De Rubeis S, 2014 2270 - 1702 Synaptic, transcriptional and chromatin genes disrupted in autism
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