Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "M"
401 to 410 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

401
Mitochondrial contact site and cristae organizing system subunit 10
C1orf151, MINOS1, MIO10, Mic10
Hyperthyroidism, Hypothyroidism, Multinodular goiter, Thyroid disease, Toxic nodular goiter, Vascular dementia

402
MICOS10-NBL1 readthrough
C1orf151-NBL1, DAN, DAND1, MINOS1-NBL1, NBL1
Bronchopulmonary dysplasia

403
Mitochondrial contact site and cristae organizing system subunit 13
C19orf70, MIC12, MIC13, P117, QIL1
3-methylglutaconic aciduria, Combined oxidative phosphorylation deficiency, Mitochondrial disease

404
Mitochondrial calcium uptake 1
CALC, CBARA1, EFHA3, MPXPS, ara CALC
Atrial fibrillation, Basal ganglia disease, Congenital neurologic anomalies, Learning disorders, Mitochondrial disease, Movement disorder, Myopathy, Neurodevelopmental disorder, Sarcoidosis

405
Mitochondrial calcium uptake 2
1110008L20Rik, EFHA1, hMICU3
Atrial fibrillation, Mitochondrial disease

406
Mitochondrial calcium uptake 3
EFHA2, hMICU3
Obstructive pulmonary disease

407
Midline 1
BBBG1, FXY, GBBB, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY
Alzheimer disease, Clinodactyly, Congenital esophageal anomaly, Dandy-walker syndrome, X-linked opitz syndrome

408
Midline 2
FXY2, MRX101, RNF60, TRIM1, XLID101
Esophageal atresia, Intellectual developmental disorder, x-linked, X-linked intellectual disability

409
Mitotic deacetylase associated SANT domain protein
C14orf117, C14orf43, ELMSAN1, LSR68, c14_5541
Cardiac embolism, Cardioembolic stroke, Multiple sclerosis

410
Midnolin
Stx
Long qt syndrome, Nephrotic syndrome