Genesⓘ

Dataset:
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
Involutional depression, Involutional paraphrenia, Mental depression, Psychosis

112
Galactosamine (N-acetyl)-6-sulfatase
GALNAC6S, GAS, GalN6S, MPS4A
Cervical myelopathy, Colorectal cancer, Dysmorphic features, Galns deficiency, Macrostomia, Malocclusion, Mucopolysaccharidosis, Osteoporosis, Scoliosis

113
Polypeptide N-acetylgalactosaminyltransferase 1
GALNAC-T1
Development disorder

114
Polypeptide N-acetylgalactosaminyltransferase 2
CDG2T, GalNAc-T2
Coronary artery disease, Coronary heart disease, Leukemia, Metabolic syndrome, Schizophrenia

115
Polypeptide N-acetylgalactosaminyltransferase 3
GalNAc-T3, HFTC, HFTC1, HHS
Angioid streaks, Dental enamel hypoplasia, Dental pulp stone, Hyperostosis, Hyperphosphatemia, Hyperphosphatemic tumoral calcinosis, Nephrocalcinosis, Prostatic neoplasms, Prostate cancer, Taurodontism, Tumoral calcinosis

116
Galactose-1-phosphate uridylyltransferase
-
Anemia, Apraxia, Cataract, Cirrhosis, Deficiency of galactokinase, Dysarthria, Galactosemia, Hypoglycemia, Hypogonadism, Liver failure, Mental retardation, Osteoporosis, Premature menopause, Udpglucose 4-epimerase deficiency disease

117
Guanidinoacetate N-methyltransferase
CCDS2, HEL-S-20, PIG2, TP53I2
Autism, Clonic seizures, Creatine deficiency, Developmental delay, Disorder of amino acid metabolism, Dyscognitive seizures, Guanidinoacetate methyltransferase deficiency, Hypotonic seizures, Inherited errors of amino acid metabolism, Mental retardation, Jacksonian seizure, Myoclonic seizures, Seizure

118
Growth associated protein 43
B-50, GAP-43, PP46
Bipolar disorder, Colonic neoplasms, Dysthymic disorder, Grand mal status epilepticus, Hirschsprung disease, Hodgkin disease, Huntington disease, Mental depression, Mood disorder, Nonconvulsive status epilepticus, Petit mal status, Schizophrenia, Status epilepticus

119
Glyceraldehyde-3-phosphate dehydrogenase
G3PD, GAPD, HEL-S-162eP
Arthritis, Carcinoma, Colorectal cancer, Colorectal neoplasms, Coronary syndrome, Esophagus neoplasm, Liver carcinoma, Lung adenocarcinoma, Mouth neoplasms, Malignant neoplasm of mouth, Osteoarthrosis deformans, Osteoporosis

120
GRB10 interacting GYF protein 2
GYF2, PARK11, PERQ2, PERQ3, TNRC15
Akinesia, Anxiety disorder, Cerebral cortical atrophy, Coronary artery disease, Dementia, Development disorder, Dyskinetic syndrome, Dysphagia, Dyssomnia, Hereditary parkinson`s disease, Leber congenital amaurosis, Mental depression, Neurodevelopmental disorders, Schizophrenia, Sleep disorders
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