PNKD

PNKD
Identifiers
AliasesPNKD, 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
External IDsOMIM: 609023; MGI: 1930773; HomoloGene: 75045; GeneCards: PNKD; OMA:PNKD - orthologs
Orthologs
SpeciesHumanMouse
Entrez

25953

56695

Ensembl

ENSG00000127838

ENSMUSG00000026179

UniProt

Q8N490

Q69ZP3

RefSeq (mRNA)

NM_022572
NM_001077399
NM_015488

NM_001039509
NM_019999
NM_025580

RefSeq (protein)

NP_001070867
NP_056303
NP_072094

NP_001034598
NP_064383
NP_079856

Location (UCSC)Chr 2: 218.27 – 218.35 MbChr 1: 74.32 – 74.39 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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).