Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7881 to 7890 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7881
Myo-inositol oxygenase
ALDRL6
Hearing loss, Kidney disease

7882
Major intrinsic protein of lens fiber
AQP0, CTRCT15, LIM1, MIP26, MP26
Cataract, Congenital cataract, Congenital total cataract, Lamellar cataract, Nuclear cataract, Posterior polar cataract, Sutural cataract, Microphthalmos, Nystagmus, Posterior subcapsular cataract, Diabetes mellitus type 2

7883
Mitochondrial intermediate peptidase
COXPD31, HMIP, MIP
Cardiomyopathy, Combined oxidative phosphorylation deficiency, Left ventricular disease, Lung cancer, Mitochondrial disease, Squamous cell carcinoma, Venous thromboembolism

7884
Mirror-image polydactyly 1
CCDC193
Gout, Nephrolithiasis, Parkinson disease, Polydactyly, Prostate cancer, Urolithiasis

7885
MIS18 binding protein 1
C14orf106, HSA242977, KNL2, M18BP1
Prostate cancer

7886
Mitochondrial sheath formation associated
Kastor, Polluks, SPTY2D1-AS1, SPTY2D1OS
Central nervous system cancer, Glioblastoma, Glioma

7887
MISP family member 3
-
Iga nephropathy

7888
Microtubule interacting and trafficking domain containing 1
-
Hearing impairment, Lipoyltransferase deficiency

7889
Melanocyte inducing transcription factor
CMM8, COMMAD, MI, MITF-A, WS2, WS2A, bHLHe32
Isolated sensorineural deafness, Renal cell carcinoma, Cataract, Chagas cardiomyopathy, Clear cell papillary renal cell carcinoma, Commissural facial cleft, Congenital ear anomaly, Congenital sensorineural hearing loss, Coronary artery disease, Melanoma, Deafness, Dyslexia, Gout, Hearing impairment, Hypertrophic cardiomyopathy
View all (11 more)

7890
Mix paired-like homeobox
MILD1, MIX, MIXL
Astrocytoma