Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 84665
MIM: 608517
HGNC: 23246
Ensembl: ENSG00000138347
Variants:
dbSNP: 84665
ClinVar: 84665
TCGA: ENSG00000138347
COSMIC: MYPN
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 31133047 | 2019 | Congenital myopathy with hanging big toe due to homozygous myopalladin (MYPN) mutation. | 8 |
| 31133047 | 2019 | Congenital myopathy with hanging big toe due to homozygous myopalladin (MYPN) mutation. | 8 |
| 28017374 | 2017 | Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy. | 39 |
| 28220527 | 2017 | Recessive MYPN mutations cause cap myopathy with occasional nemaline rods. | 15 |
| 28427417 | 2017 | Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome. | 14 |
| 28017374 | 2017 | Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy. | 39 |
| 28220527 | 2017 | Recessive MYPN mutations cause cap myopathy with occasional nemaline rods. | 15 |
| 28427417 | 2017 | Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome. | 14 |
| 25541130 | 2014 | Disturbance in Z-disk mechanosensitive proteins induced by a persistent mutant myopalladin causes familial restrictive cardiomyopathy. | 25 |
| 25541130 | 2014 | Disturbance in Z-disk mechanosensitive proteins induced by a persistent mutant myopalladin causes familial restrictive cardiomyopathy. | 25 |
| 22892539 | 2013 | Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy. | 18 |
| 22892539 | 2013 | Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy. | 18 |
| 22286171 | 2012 | Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. | 42 |
| 22286171 | 2012 | Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. | 42 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
Citation
Dessen P
MYPN (myopalladin)
Atlas Genet Cytogenet Oncol Haematol. 2003-12-01
Online version: http://atlasgeneticsoncology.org/gene/41486/mypn
