MIDN (midnolin)

2014-08-01  

Identity

HGNC
LOCATION
19p13.3
LOCUSID
ALIAS
Stx
FUSION GENES

Other Information

Locus ID:

NCBI: 90007
MIM: 606700
HGNC: 16298
Ensembl: ENSG00000167470

Variants:

dbSNP: 90007
ClinVar: 90007
TCGA: ENSG00000167470
COSMIC: MIDN

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000167470ENST00000300952Q504T8
ENSG00000167470ENST00000586757K7END3
ENSG00000167470ENST00000586843K7EN89
ENSG00000167470ENST00000591446Q504T8

Expression (GTEx)

0
50
100
150

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
368585662023Structural Variants of Midnolin, a Genetic Risk Factor for Parkinson's Disease, in a Yamagata Cohort.1
376163432023The midnolin-proteasome pathway catches proteins for ubiquitination-independent degradation.13
368585662023Structural Variants of Midnolin, a Genetic Risk Factor for Parkinson's Disease, in a Yamagata Cohort.1
376163432023The midnolin-proteasome pathway catches proteins for ubiquitination-independent degradation.13
315886912019Midnolin is a confirmed genetic risk factor for Parkinson's disease.6
315886912019Midnolin is a confirmed genetic risk factor for Parkinson's disease.6
287249632017Midnolin is a novel regulator of parkin expression and is associated with Parkinson's Disease.14
287249632017Midnolin is a novel regulator of parkin expression and is associated with Parkinson's Disease.14
241871342013Identification of the ubiquitin-like domain of midnolin as a new glucokinase interaction partner.22
241871342013Identification of the ubiquitin-like domain of midnolin as a new glucokinase interaction partner.22

Citation

Dessen P

MIDN (midnolin)

Atlas Genet Cytogenet Oncol Haematol. 2014-08-01

Online version: http://atlasgeneticsoncology.org/gene/54458/favicon/gene-fusions/?id=54458