RecName: Full=Probable hydrolase PNKD; AltName: Full=Myofibrillogenesi - Protein

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The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. [Mol Psychiatry. 2018]
The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.
Sun N, Nasello C, Deng L, Wang N, Zhang Y, Xu Z, Song Z, Kwan K, King RA, Pang ZP, et al. Mol Psychiatry. 2018 Jun; 23(6):1487-1495. Epub 2017 Sep 12.
A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland. [Brain Res. 2015]
A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland.
Liang S, Yu X, Zhang S, Tai J. Brain Res. 2015 Jan 21; 1595:120-6. Epub 2014 Aug 5.
Clinicopathological and prognostic significance of myofibrillogenesis regulator-1 protein expression in pancreatic ductal adenocarcinoma. [Tumour Biol. 2013]
Clinicopathological and prognostic significance of myofibrillogenesis regulator-1 protein expression in pancreatic ductal adenocarcinoma.
Zhao CY, Guo ZJ, Dai SM, Zhang Y, Zhou JJ. Tumour Biol. 2013 Oct; 34(5):2983-7. Epub 2013 May 22.

RefSeq genomic sequence
See the genomic reference sequence for the PNKD gene (NG_017060.1).

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Q8N490 [Domain Mapping of Disease Mut...]
Q8N490
Domain Mapping of Disease Mutations
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