Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8181 to 8190 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8181
Mitochondrial translational initiation factor 3
IF3mt
Color vision deficiency, Metabolic syndrome, Diabetes mellitus type 2

8182
Myotubularin 1
CNM, CNMX, MTMX, XLMTM
Alzheimer disease, Centronuclear myopathy, Congenital fiber type disproportion myopathy, Congenital structural myopathy, Myopathy, Neurodevelopmental disorder, Post-traumatic stress disorder, Spastic paraplegia, X-linked centronuclear myopathy, X-linked myotubular myopathy

8183
Myotubularin related protein 10
-
Huntington disease, Interstitial nephritis

8184
Myotubularin related protein 11
CRA
Androgenetic alopecia, Breast cancer, Carpal tunnel syndrome, Obstructive pulmonary disease, Open angle glaucoma, Scoliosis

8185
Myotubularin related protein 14
C3orf29
Alzheimer disease, Centronuclear myopathy, Epithelial ovarian carcinoma, Congenital structural myopathy

8186
Myotubularin related protein 2
CMT4B, CMT4B1
Alzheimer disease, Cannabis abuse, Charcot-marie-tooth disease, Demyelinating hereditary motor and sensory neuropathy

8187
Myotubularin related protein 3
FYVE-DSP1, ZFYVE10
Alzheimer disease, Brain aneurysm, Breast cancer, Cataract, Obstructive pulmonary disease, Color vision deficiency, Dental caries, Iga nephropathy, Lung cancer, Squamous cell carcinoma, Diabetes mellitus type 2

8188
Myotubularin related protein 4
FYVE-DSP2, ZFYVE11
Dental caries, Mesothelioma, Uterine fibroid

8189
Myotubularin related protein 7
-
Creutzfeldt-jakob disease, Insomnia, Obesity, Spermatocele

8190
Myotubularin related protein 8
-
Kleine-levin syndrome