PNKD PNKD metallo-beta-lactamase domain containing [ Homo sapiens (human) ] - Gene - Data resources

25953

PNKD PNKD metallo-beta-lactamase domain containing [ Homo sapiens (human) ]
Source: NCBI Gene (ID 25953)

Symbol: PNKD

Full name: PNKD metallo-beta-lactamase domain containing

Gene type: protein coding

RefSeq status: REVIEWED

Also known as: BRP17; DYT8; FKSG19; FPD1; KIPP1184; MR-1; MR-1S; MR1; PDC; PKND1; PNKD1; R1; TAHCCP2

Summary: 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]

Expression: Ubiquitous expression in prostate (RPKM 19.3), kidney (RPKM 16.6) and 25 other tissues

Orthologs: mouse

Gene size: 76275bp

Exon count: 12