| PNKD | 
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| Identifiers | 
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| Aliases | PNKD, BRP17, DYT8, FPD1, KIPP1184, MR-1, MR1, PDC, PKND1, TAHCCP2, FKSG19, paroxysmal nonkinesigenic dyskinesia, PNKD1, MBL domain containing, MR-1S, PNKD metallo-beta-lactamase domain containing, R1 | 
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| External IDs | OMIM: 609023; MGI: 1930773; HomoloGene: 75045; GeneCards: PNKD; OMA:PNKD - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 1 (mouse) | 
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 |  |  | Band | 1|1 C3 | Start | 74,324,089 bp | 
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 | End | 74,392,853 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | right uterine tube
 right lobe of liver
 mucosa of transverse colon
 right lobe of thyroid gland
 left lobe of thyroid gland
 Brodmann area 9
 right frontal lobe
 prefrontal cortex
 cingulate gyrus
 anterior cingulate cortex
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 | | Top expressed in |  | pontine nuclei
 superior colliculus
 yolk sac
 CA3 field
 right kidney
 perirhinal cortex
 Medulla Oblongata
 central gray substance of midbrain
 primary visual cortex
 entorhinal cortex
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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PNKD is the abbreviation for a human neurological movement disorder  paroxysmal nonkinesiogenic dyskinesia. Like many other human genetics disorders, PNKD also refers to the disease, the disease gene and the encoded protein. (PNKD) is a protein that in humans is encoded by the PNKD gene. Alternative splicing results in the transcription of three isoforms.  The mouse ortholog is called brain protein 17 (Brp17).