Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "G"
111 to 120 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

111
Galanin receptor 1
GALNR, GALNR1
Alzheimer disease, Atrophic macular degeneration, Behcet disease, Dementia, Major depressive disorder, Iga nephropathy, Obesity, Orofacial cleft

112
Galactosamine (N-acetyl)-6-sulfatase
GALNAC6S, GAS, GalN6S, MPS4A
Atypical femoral fracture, Autism, Desbuquois syndrome, Mucopolysaccharidosis, Skeletal dysplasia

113
Polypeptide N-acetylgalactosaminyltransferase 1
GALNAC-T1
Autism, Color vision deficiency, Eosinophilia

114
Polypeptide N-acetylgalactosaminyltransferase 2
CDG2T, GalNAc-T2
Alzheimer disease, Atherosclerosis, Congenital disorder of glycosylation, Coronary artery disease, Dementia, Desbuquois syndrome, Hyperlipidemia, Lipoprotein lipase deficiency, Fatty liver, Insomnia, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Psoriasis, Schizophrenia
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115
Polypeptide N-acetylgalactosaminyltransferase 3
GalNAc-T3, HFTC, HFTC1, HHS
Attention deficit hyperactivity disorder, Autism, Calcinosis, Calcium metabolism disorders, Colorectal cancer, Desbuquois syndrome, Endometrial neoplasm, Hyperphosphatemic tumoral calcinosis, Hypercalcemic tumoral calcinosis, Osteoporosis, Ovarian neoplasm, Prostatic neoplasm, Tumoral calcinosis, Diabetes mellitus, type 2

116
Galactose-1-phosphate uridylyltransferase
-
Asthma, Udp-glucose-hexose-1-phosphate uridylyltransferase, Galactosemia, Premature ovarian failure

117
Guanidinoacetate N-methyltransferase
CCDS2, HEL-S-20, PIG2, TP53I2
Amino acid metabolism disorder, Cerebral creatine deficiency syndrome, Congenital neurologic anomalies , Guanidinoacetate methyltransferase deficiency, Intellectual developmental disorder, Hereditary parkinson disease, Seizures

118
Growth associated protein 43
B-50, GAP-43, PP46
Bipolar disorder, Colonic neoplasm, Major depressive disorder, Human immunodeficiency virus infection, Depression, Metabolic syndrome, Mood disorder, Proliferative diabetic retinopathy, Schizophrenia, Status epilepticus, Diabetes mellitus, type 1, Diabetes mellitus, type 2

119
Glyceraldehyde-3-phosphate dehydrogenase
G3PD, GAPD, HEL-S-162eP
Alzheimer disease, Hepatocellular carcinoma, Squamous cell carcinoma, Colorectal neoplasm, Esophageal neoplasm, Hypoxia, Microcephaly, Mouth neoplasm, Necrosis, Osteoarthritis, Osteoporosis, Parkinson disease

120
GRB10 interacting GYF protein 2
GYF2, PARK11, PERQ2, PERQ3, TNRC15
Anorexia nervosa, Anxiety disorder, Asthma, Attention deficit hyperactivity disorder, Autism, Coronary artery disease, Gastroesophageal reflux disease, Hereditary parkinson disease, Leber congenital amaurosis, Major depressive disorder, Myocardial infarction, Nasal polyp, Neurodevelopmental disorders, Obesity, Parkinson disease
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