AutismKB 2.0

Annotation Detail for FAM168B


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:FAM168B ( MGC87527 )
Gene Full Name: family with sequence similarity 168, member B
Band: 2q21.1
Quick LinksEntrez ID:130074; OMIM: NA; Uniprot ID:F168B_HUMAN; ENSEMBL ID: ENSG00000152102; HGNC ID: 27016
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
Related Diseases/Disorders Top
Comparative Toxicogenomics Database Top
Pharmacogenomics Knowledge Base Top
  • PharmGKB Accession:PA162387098
  • No data
    Releated disease ID Related disease Name
    PA446155Precursor Cell Lymphoblastic Leukemia-Lymphoma
    Releated drug ID Related drug Name
    PA450379mercaptopurine
    PA450428methotrexate
    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