AutismKB 2.0

Annotation Detail for PCNT


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Basic Information Top
Gene Symbol:PCNT ( KEN,MOPD2,PCN,PCNT2,PCNTB,PCTN2,SCKL4 )
Gene Full Name: pericentrin
Band: 21q22.3
Quick LinksEntrez ID:5116; OMIM: 605925; Uniprot ID:PCNT_HUMAN; ENSEMBL ID: ENSG00000160299; HGNC ID: 16068
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
No data
No data
Pathway IDPathway Name
Cell Cycle, Mitotic
No data
No data
Pathway IDPathway Name
500383Loss of proteins required for interphase microtubule organization from the centrosome
500384Loss of Nlp from mitotic centrosomes
Related Diseases/Disorders Top
No data
Desease IDDesease Name
1831Prostate cancer
1848Embryoma
2045Bipolar disorder
No data
No data
Desease Name
Microcephalic osteodysplastic primordial dwarfism, type II
Comparative Toxicogenomics Database Top
No data
Disease ID Disease Name Direct Evidence Inference Chemical Name Inference Score Publication
OMIM:210720 MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II marker/mechanism
MESH:C537533 Seckel syndrome 1 marker/mechanism 18157127
MESH:C537534 Seckel syndrome 2 marker/mechanism 18174396
Pathway ID Pathway Name
REACT:152 Cell Cycle, Mitotic
Pharmacogenomics Knowledge Base Top
  • PharmGKB Accession:PA33079
    • No data
    Releated disease ID Related disease Name
    PA162372626Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)
    No data
    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


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