Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
5061 to 5070 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

5061
Glutamine amidotransferase class 1 domain containing 1
FERRY5, Fy-5, PDDC1
Fuchs endothelial dystrophy

5062
Glutamine amidotransferase class 1 domain containing 3
C21orf33, ES1, GATD3A, GATD3B, GT335, HES1, KNPH, KNPI
Ankylosing spondylitis, Anophthalmia/microphthalmia-esophageal atresia syndrome, Celiac disease, Crohn disease, Inflammatory bowel disease, Psoriasis, Sclerosing cholangitis, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

5063
Glycine amidinotransferase
AGAT, AT, CCDS3, FRTS, FRTS1, RFS
Agat deficiency, Arginine-glycine amidinotransferase deficiency, Carcinoma, Cerebral creatine deficiency syndrome, Kidney disease, Congestive heart failure, De toni-debre-fanconi syndrome, Fanconi renotubular syndrome, Fanconi syndrome, Heart failure, Kidney failure, Lennox-gastaut syndrome, Myocardial ischemia, Necrosis

5064
Glucosylceramidase beta 1
GBA, GCB, GLUC
Parkinson disease, Brain aneurysm, Dementia, Gaucher disease, Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome, Hereditary parkinson disease, Hyperlipidemia, Pulmonary hypertension, Hypertension, Lewy body disease, Movement disorder, Thrombocytopenia

5065
Glucosylceramidase beta 2
AD035, NLGase, SPG46
Cerebellar ataxia, Spastic paraplegia, Dilated cardiomyopathy, Hereditary spastic paraplegia, Intellectual developmental disorder, Neurodevelopmental disorder, Parkinson disease, Polyneuropathy, Diabetes mellitus type 2

5066
Glucosylceramidase beta 3 (gene/pseudogene)
CBG, CBGL1, GLUC, KLRP
Alzheimer disease, Ankylosing spondylitis, Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Central nervous system cancer, Complex regional pain syndrome, Gastroesophageal reflux disease, Glioblastoma, Glioma, Gout, Obsessive-compulsive disorder, Psoriasis, Schizophrenia, Substance abuse, Tourette syndrome

5067
1,4-alpha-glucan branching enzyme 1
APBD, GBE, GSD4
Adult polyglucosan body disease, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Cervical cancer, Cutis laxa, Glycogen storage disease, Interstitial lung disease, Metabolic syndrome, Neurotic disorder, Osteogenesis imperfecta, Pena-shokeir syndrome , Polyneuropathy, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Scoliosis, Substance abuse
View all (2 more)

5068
Golgi brefeldin A resistant guanine nucleotide exchange factor 1
ARF1GEF, CMT2GG, CMTDI2, CMTDIA
Anterior segment dysgenesis, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Axonal neuropathy, Cannabis abuse, Congenital cataract, Charcot-marie-tooth disease, Digestive system disease, Epilepsy, Generalized epilepsy, Parkinson disease, Partial epilepsy, Uterine fibroid

5069
Globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group)
A3GALNT, FS, UNQ2513
Breast cancer, Rheumatoid arthritis, Systemic lupus erythematosus, Venous thromboembolism

5070
Guanylate binding protein 2
-
Liver cirrhosis, Myocardial ischemia