AutismKB 2.0

Annotation Detail for ADAMTS17


View Evidences View Variants View Annotations
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
Related Pathway Information Top
Related Diseases/Disorders Top
No data
No data
Desease Name
height
DEVELOPMENTAL
Desease Name
Height
Desease Name
Weill-Marchesani-like syndrome
Comparative Toxicogenomics Database Top
Chemical ID Chemical Name Interaction Interaction Action Publication
D016604 Aflatoxin B1 Aflatoxin B1 affects the expression of ADAMTS17 proteinaffects expression 20106945
Disease ID Disease Name Direct Evidence Inference Chemical Name Inference Score Publication
MESH:D006528 Carcinoma, Hepatocellular Aflatoxin B1 2.0012907637 12619106 21507988
MESH:D008113 Liver Neoplasms Aflatoxin B1 2.5018177683 15890375 2125692 9163691
MESH:D008114 Liver Neoplasms, Experimental Aflatoxin B1 3.048603461
MESH:D008175 Lung Neoplasms Aflatoxin B1 1.8814755239
OMIM:613195 WEILL-MARCHESANI-LIKE SYNDROME marker/mechanism
No data
Pharmacogenomics Knowledge Base Top
Drug Bank Top

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


Copyright © 2017, Center for Bioinformatics , Peking University | All Rights Reserved