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
241871342013Identification of the ubiquitin-like domain of midnolin as a new glucokinase interaction partner.13
287249632017Midnolin is a novel regulator of parkin expression and is associated with Parkinson's Disease.4

Citation

Dessen P

MIDN (midnolin)

Atlas Genet Cytogenet Oncol Haematol. 2014-08-01

Online version: http://atlasgeneticsoncology.org/gene/54458/midn