Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7831 to 7840 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7831
MGAT4 family member C
GNTIVH, HGNT-IV-H
Astrocytoma, Atherosclerosis, Attention deficit hyperactivity disorder, Bell's palsy, Central nervous system cancer, Conotruncal cardiac defect, Glioblastoma, Glioma, Major depressive disorder, Small vessel stroke, Substance abuse

7832
MGAT4 family member D
GnT1IP
Central nervous system cancer, Glioblastoma, Glioma

7833
Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase
GNT-V, GNT-VA, MGAT5A, glcNAc-T V
Asthma, Attention deficit hyperactivity disorder, Breast cancer, Basal cell carcinoma, Lymphocytic leukemia, Colorectal cancer, Diverticular disease, Gestational diabetes, Gout, Multiple sclerosis, Open angle glaucoma, Osteoarthritis, Prostate cancer, Schizophrenia, Substance abuse
View all (4 more)

7834
Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
GnT-IX, GnT-VB
Autism, Colorectal cancer, Emphysema, Endometrial neoplasms, Hypotension, Polycystic ovary syndrome, Post-traumatic stress disorder

7835
Monoglyceride lipase
HU-K5, HUK5, MAGL, MGL
Bipolar disorder, Central nervous system cancer, Color vision deficiency, Glioblastoma, Glioma, Liver cirrhosis, Oligodendroglioma, Osteoporosis, Pelvic organ prolapse, Prostate cancer, Schizophrenia, Uterine prolapse

7836
Mitochondrial genome maintenance exonuclease 1
C20orf72, DDK1, MTDPS11, bA504H3.4
Alzheimer disease, Mitochondrial disease, Mitochondrial dna depletion syndrome, Ophthalmoplegia

7837
O-6-methylguanine-DNA methyltransferase
-
Alzheimer disease, Anorexia nervosa, Eczema, Brain neoplasms, Carpal tunnel syndrome, Central nervous system cancer, Crohn disease, Dementia, Eating disorder, Esophageal squamous cell carcinoma, Melanoma, Generalized anxiety disorder, Giant cell glioblastoma, Glioblastoma, Glioma
View all (15 more)

7838
Matrix Gla protein
GIG36, MGLAP, NTI
Aortic valve disease, Arteriosclerosis, Bicuspid aortic valve, Carcinoma, Desbuquois syndrome, Myocardial infarction, Osteoarthritis, Spondyloepiphyseal dysplasia, Uremia, Varicose veins, Vascular calcification

7839
Microsomal glutathione S-transferase 1
GST12, MGST, MGST-I, PMAN
Asthma, Barrett esophagus, Bell's palsy, Breast cancer, Degenerative disorder, Dementia, Esophageal adenocarcinoma, Insomnia, Large artery stroke, Colorectal adenoma, Neurodegenerative disorder, Scoliosis, Tourette syndrome

7840
Microsomal glutathione S-transferase 2
GST2, MGST-II
Color vision deficiency, Vesicoureteral reflux