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PNKD, PNKD metallo-beta-lactamase domain containing

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PNKD, PNKD metallo-beta-lactamase domain containing

  • This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

  • Gene Synonyms (probable hydrolase PNKD, PNKD, MBL domain containing, brain protein 17, myofibrillogenesis regulator 1, trans-activated by hepatitis C virus core protein 2, BRP17, DYT8, FKSG19, FPD1, KIPP1184, MR-1, MR-1S, MR1, PDC, PKND1, PNKD1, R1, TAHCCP2,)
  • NCBI Gene ID: 25953
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A024R415
    UNIPROT ID#>>Q8N490
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

PNKD metallo-beta-lactamase domain containing interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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