AutismKB 2.0

Evidence Details for ADAMTS17


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Basic Information Top
Gene Symbol:ADAMTS17 ( FLJ16363,FLJ32769 )
Gene Full Name: ADAM metallopeptidase with thrombospondin type 1 motif, 17
Band: 15q26.3
Quick LinksEntrez ID:170691; OMIM: 607511; Uniprot ID:ATS17_HUMAN; ENSEMBL ID: ENSG00000140470; HGNC ID: 17109
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ADAMTS17|170691|nucleotide
ATGTGTGACGGCGCCCTGCTGCCTCCGCTCGTCCTGCCCGTGCTGCTGCTGCTGGTTTGGGGACTGGACCCGGGCACAGCTGTCGGCGACGCGGCGGCCGACGTG
GAGGTGGTGCTCCCGTGGCGGGTGCGCCCCGACGACGTGCACCTGCCGCCGCTGCCCGCAGCCCCCGGGCCCCGACGGCGGCGACGCCCCCGCACGCCCCCAGCC
GCCCCGCGCGCCCGGCCCGGAGAGCGCGCCCTGCTGCTGCACCTGCCGGCCTTCGGGCGCGACCTGTACCTTCAGCTGCGCCGCGACCTGCGCTTCCTGTCCCGA
GGCTTCGAGGTGGAGGAGGCGGGCGCGGCCCGGCGCCGCGGCCGCCCCGCCGAGCTGTGCTTCTACTCGGGCCGTGTGCTCGGCCACCCCGGCTCCCTCGTCTCG
CTCAGCGCCTGCGGCGCCGCCGGCGGCCTGGTTGGCCTCATTCAGCTTGGGCAGGAGCAGGTGCTAATCCAGCCCCTCAACAACTCCCAGGGCCCATTCAGTGGA
CGAGAACATCTGATCAGGCGCAAATGGTCCTTGACCCCCAGCCCTTCTGCTGAGGCCCAGAGACCTGAGCAGCTCTGCAAGGTTCTAACAGAAAAGAAGAAGCCG
ACGTGGGGCAGGCCTTCGCGGGACTGGCGGGAGCGGAGGAACGCTATCCGGCTCACCAGCGAGCACACGGTGGAGACCCTGGTGGTGGCCGACGCCGACATGGTG
CAGTACCACGGGGCCGAGGCCGCCCAGAGGTTCATCCTGACCGTCATGAACATGGTATACAATATGTTTCAGCACCAGAGCCTGGGGATTAAAATTAACATTCAA
GTGACCAAGCTTGTCCTGCTACGACAACGTCCCGCTAAGTTGTCCATTGGGCACCATGGTGAGCGGTCCCTGGAGAGCTTCTGTCACTGGCAGAACGAGGAGTAT
GGAGGAGCGCGATACCTCGGCAATAACCAGGTTCCCGGCGGGAAGGACGACCCGCCCCTGGTGGATGCTGCCGTGTTTGTGACCAGGACAGATTTCTGTGTACAC
AAGGATGAACCGTGTGACACTGTTGGAATTGCTTACTTAGGAGGTGTGTGCAGTGCTAAGAGGAAGTGTGTGCTTGCCGAAGACAATGGTCTCAATTTGGCCTTT
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>ADAMTS17|170691|protein
MCDGALLPPLVLPVLLLLVWGLDPGTAVGDAAADVEVVLPWRVRPDDVHLPPLPAAPGPRRRRRPRTPPAAPRARPGERALLLHLPAFGRDLYLQLRRDLRFLSR
GFEVEEAGAARRRGRPAELCFYSGRVLGHPGSLVSLSACGAAGGLVGLIQLGQEQVLIQPLNNSQGPFSGREHLIRRKWSLTPSPSAEAQRPEQLCKVLTEKKKP
TWGRPSRDWRERRNAIRLTSEHTVETLVVADADMVQYHGAEAAQRFILTVMNMVYNMFQHQSLGIKINIQVTKLVLLRQRPAKLSIGHHGERSLESFCHWQNEEY
GGARYLGNNQVPGGKDDPPLVDAAVFVTRTDFCVHKDEPCDTVGIAYLGGVCSAKRKCVLAEDNGLNLAFTIAHELGHNLGMNHDDDHSSCAGRSHIMSGEWVKG
RNPSDLSWSSCSRDDLENFLKSKVSTCLLVTDPRSQHTVRLPHKLPGMHYSANEQCQILFGMNATFCRNMEHLMCAGLWCLVEGDTSCKTKLDPPLDGTECGADK
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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 (1) 0 (0) 0 (0) 0 (0) 2 (3)
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
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
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