PNKD (PNKD metallo-beta-lactamase domain containing)

2013-03-01  

Identity

HGNC
LOCATION
2q35
LOCUSID
ALIAS
BRP17,DYT8,FKSG19,FPD1,KIPP1184,MR-1,MR-1S,MR1,PDC,PKND1,PNKD1,R1,TAHCCP2
FUSION GENES

Other Information

Locus ID:

NCBI: 25953
MIM: 609023
HGNC: 9153
Ensembl: ENSG00000127838

Variants:

dbSNP: 25953
ClinVar: 25953
TCGA: ENSG00000127838
COSMIC: PNKD

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000127838ENST00000248451Q8N490
ENSG00000127838ENST00000258362Q8N490
ENSG00000127838ENST00000273077Q8N490
ENSG00000127838ENST00000273077A0A024R415
ENSG00000127838ENST00000436005Q8N490

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
383426062024Myofibrillogenesis Regulator-1 Regulates the Ubiquitin Lysosomal Pathway of Notch3 Intracellular Domain Through E3 Ubiquitin-Protein Ligase Itchy Homolog in the Metastasis of Non-Small Cell Lung Cancer.1
383426062024Myofibrillogenesis Regulator-1 Regulates the Ubiquitin Lysosomal Pathway of Notch3 Intracellular Domain Through E3 Ubiquitin-Protein Ligase Itchy Homolog in the Metastasis of Non-Small Cell Lung Cancer.1
288942972018The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.19
288942972018The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.19
281998442017MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase.49
281998442017MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase.49
270054242016Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.26
270054242016Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.26
251078572015A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland.3
265984942015The clinical and genetic heterogeneity of paroxysmal dyskinesias.57
251078572015A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland.3
265984942015The clinical and genetic heterogeneity of paroxysmal dyskinesias.57
250662972014Phosphorylation of myofibrillogenesis regulator-1 activates the MAPK signaling pathway and induces proliferation and migration in human breast cancer MCF7 cells.10
250662972014Phosphorylation of myofibrillogenesis regulator-1 activates the MAPK signaling pathway and induces proliferation and migration in human breast cancer MCF7 cells.10
236960302013Clinicopathological and prognostic significance of myofibrillogenesis regulator-1 protein expression in pancreatic ductal adenocarcinoma.4

Citation

Dessen P

PNKD (PNKD metallo-beta-lactamase domain containing)

Atlas Genet Cytogenet Oncol Haematol. 2013-03-01

Online version: http://atlasgeneticsoncology.org/gene/53200/img/css/template-nav.css