AutismKB 2.0

Annotation Detail for KIRREL3


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Basic Information Top
Gene Symbol:KIRREL3 ( KIAA1867,KIRRE,MGC126824,MGC126850,MRD4,NEPH2,PRO4502 )
Gene Full Name: kin of IRRE like 3 (Drosophila)
Band: 11q24.2
Quick LinksEntrez ID:84623; OMIM: 607761; Uniprot ID:KIRR3_HUMAN; ENSEMBL ID: ENSG00000149571; HGNC ID: 23204
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
No data
No data
Pathway IDPathway Name
Interactions of the immunoglobulin superfamily (IgSF) member proteins
No data
No data
No data
Related Diseases/Disorders Top
No data
No data
Desease Name
protein quantitative trait loci
PSYCH
PHARMACOGENOMIC
Attention deficit hyperactivity disorder and conduct disorder
response to antipsychotic treatment
Desease Name
Response to antipsychotic treatment
Protein quantitative trait loci
Attention deficit hyperactivity disorder and conduct disorder
Desease Name
Mental retardation, autosomal dominant 4
Comparative Toxicogenomics Database Top
Chemical ID Chemical Name Interaction Interaction Action Publication
C025643 vinclozolin vinclozolin affects the expression of KIRREL3 mRNAaffects expression 19015723
Disease ID Disease Name Direct Evidence Inference Chemical Name Inference Score Publication
MESH:D001008 Anxiety Disorders vinclozolin 4.1019015723
MESH:D003456 Cryptorchidism vinclozolin 5.1314966744
MESH:D030342 Genetic Diseases, Inborn vinclozolin 6.0216973722
MESH:D005832 Genital Diseases, Male vinclozolin 6.7216417039
MESH:D007248 Infertility, Male vinclozolin 3.3816467254
MESH:D007984 Leydig Cell Tumor vinclozolin 5.8216417039
OMIM:612581 MENTAL RETARDATION, AUTOSOMAL DOMINANT 4 marker/mechanism
MESH:D011297 Prenatal Exposure Delayed Effects vinclozolin 4.9819015723 18220299 18042343
MESH:D011469 Prostatic Diseases vinclozolin 6.0218220299
MESH:D011472 Prostatitis vinclozolin 6.0218629315
Pathway ID Pathway Name
REACT:23853 Interactions of the immunoglobulin superfamily (IgSF) member proteins
Pharmacogenomics Knowledge Base Top
  • PharmGKB Accession:PA134958283
  • No data
    Releated disease ID Related disease Name
    PA447197Attention Deficit Disorder with Hyperactivity
    No data
    Drug Bank Top

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    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