Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7821 to 7830 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7821
Major facilitator superfamily domain containing 8
CCMD, CLN7, SLC74A1
Neuronal ceroid lipofuscinosis, Cone-rod dystrophy, Congenital neurologic anomalies, Macular dystrophy, Microcephaly, Optic atrophy, Retinitis pigmentosa, Stargardt disease

7822
MAX dimerization protein MGA
MAD5, MXD5, POF26
Bell's palsy, Adenoid cystic carcinoma, Metabolic syndrome, Obesity, Ovarian serous carcinoma, Premature ovarian failure, Prostatic neoplasms, Diabetes mellitus type 2

7823
Maltase-glucoamylase
MG, MGA
Dilated cardiomyopathy, Tourette syndrome

7824
Maltase-glucoamylase 2 (putative)
-
Anxiety disorder, Hirschsprung disease

7825
Mitochondria localized glutamic acid rich protein
C4orf49, CESP-1, HUMMR, OSAP
Rheumatoid arthritis

7826
Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
GLCNAC-TI, GLCT1, GLYT1, GNT-1, GNT-I, GnTI, MGAT
Scoliosis, Diabetes mellitus type 2

7827
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
CDG2A, CDGS2, GLCNACTII, GNT-II, GNT2
Congenital disorder of glycosylation, Global developmental delay

7828
Beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase
GNT-III, GNT3
Attention deficit hyperactivity disorder, Autism, Schizophrenia

7829
Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A
GNT-IV, GNT-IVA, GnT-4a
Bipolar disorder, Central nervous system cancer, Congenital left-sided heart lesions, Glioblastoma, Glioma, Colorectal adenoma, Ocular sarcoidosis, Sarcoidosis

7830
Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B
GNT-IV, GNT-IVB
Major depressive disorder