| 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).