MIDN (midnolin)

2014-08-01  

Identity

HGNC
MIDN
LOCATION
19p13.3
LOCUSID
90007
ALIAS
Stx
FUSION GENES
Show Gene Fusions

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
Adipose - Subcutaneous
Adipose - Visceral
Adrenal Gland
Artery - Aorta
Artery - Tibial
Bladder
Brain - Amygdala
Brain - Anterior cingulate cortex
Brain - Caudate
Brain - Cerebellar Hemisphere
Brain - Cerebellum
Brain - Cortex
Brain - Frontal Cortex
Brain - Hippocampus
Brain - Hypothalamus
Brain - Nucleus accumbens
Brain - Putamen
Brain - Spinal cord
Brain - Substantia nigra
Breast - Mammary Tissue
Cells - Cultured fibroblasts
Cells - EBV - transformed lymphocytes
Cervix - Ectocervix
Cervix - Endocervix
Colon - Sigmoid
Colon - Transverse
Esophagus - Gastroesophageal Junction
Esophagus - Mucosa
Esophagus - Muscularis
Fallopian Tube
Heart - Atrial Appendage
Heart - Left Ventricle
Kidney - Cortex
Kidney - Medulla
Liver
Lung
Minor Salivary Gland
Muscle - Skeletal
Nerve - Tibial
Ovary
Pancreas
Pituitary
Prostate
Skin - Not Sun Exposed
Skin - Sun Exposed
Small Intestine - Terminal Ileum
Spleen
Stomach
Testis
Thyroid
Uterus
Vagina
Whole Blood

Protein levels (Protein atlas)

Not detected
Low
Medium
High
cerebral cortex
cerebellum
hippocampus
caudate
thyroid gland
parathyroid gland
adrenal gland
nasopharynx
bronchus
lung
oral mucosa
salivary gland
esophagus
stomach 1
stomach 2
duodenum
small intestine
colon
rectum
liver
gallbladder
pancreas
kidney
urinary bladder
testis
epididymis
seminal vesicle
prostate
vagina
ovary
fallopian tube
endometrium 1
endometrium 2
cervix, uterine
placenta
breast
heart muscle
smooth muscle
skeletal muscle
soft tissue 1
soft tissue 2
adipose tissue
skin 1
skin 2
appendix
spleen
lymph node
tonsil
bone marrow

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/haematological-explorer/gene-fusions/?id=54458