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ARHGAP31

  • ARHGAP31

    • Protein-coding gene in the species Homo sapiens

    activating protein 31 is encoded in humans by the ARHGAP31 gene. It is a Cdc42/Rac1 GTPase regulator. ARHGAP31 encodes a GTPase-activating protein (GAP). A

    ARHGAP31

    ARHGAP31

    ARHGAP31

  • Adams–Oliver syndrome

    • Medical condition

    [citation needed] Six AOS genes have been identified: ARHGAP31, DOCK6, RBPJ, EOGT, NOTCH1, and DLL4. ARHGAP31 and DOCK6 are both regulatory proteins that control

    Adams–Oliver syndrome

    Adams–Oliver_syndrome

  • Ciliopathy

    • Genetic disease resulting in abnormal formation or function of cilia

    Acrofrontofacionasal dysostosis 2 239710 Adams–Oliver syndrome 100300 ARHGAP31, DOCK6, RBPJ, EOGT, NOTCH1, DLL4 Asplenia with cardiovascular anomalies

    Ciliopathy

    Ciliopathy

    Ciliopathy

  • Chromosome 3

    • Human chromosome

    ADIPOQ: adiponectin AMOTL2: encoding protein Angiomotin-like protein 2 ARHGAP31: Rho GRPase activating protein 31 BCHE: butyrylcholinesterase C3orf70 chromosome

    Chromosome 3

    Chromosome 3

    Chromosome_3

  • List of human protein-coding genes 1

    • Q9P2N2 959 ARHGAP29 HGNC:30207; Q52LW3 960 ARHGAP30 HGNC:27414; Q7Z6I6 961 ARHGAP31 HGNC:29216; Q2M1Z3 962 ARHGAP32 HGNC:17399; A7KAX9 963 ARHGAP33 HGNC:23085;

    List of human protein-coding genes 1

    List_of_human_protein-coding_genes_1

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