Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "G"
201 to 210 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
GLI family zinc finger 3
ACLS, GCPS, GLI3-190, GLI3FL, PAP-A, PAPA, PAPA1, PAPB, PHS, PPDIV
Acrocallosal syndrome, Asthma, Blepharoptosis, Tibial hemimelia, Craniosynostosis, Crohn disease, Desbuquois syndrome, Emphysema, Gastrointestinal stromal tumor, Glaucoma, Global developmental delay, Inflammatory bowel disease, Ovarian epithelial cancer, Migraine, Multiple sclerosis
View all (14 more)

202
Glyoxalase I
GLOD1, GLYI, HEL-S-74
Anxiety disorder, Autism, Bipolar disorder, Major depressive disorder, Diabetes mellitus type 2, Diabetic retinopathy, Esophageal squamous cell carcinoma, Insomnia, Kidney failure, Melanoma, Depression, Schizophrenia, Tuberculosis, Vascular disease

203
Glucagon like peptide 1 receptor
GLP-1, GLP-1-R, GLP-1R
Colorectal cancer, Diabetes mellitus, Diabetes mellitus type 2, Heart failure, Hyperplasia, Hypertension, Obesity, Diabetes mellitus, type 1, Diabetes mellitus, type 2

204
Glycine receptor alpha 1
HKPX1, STHE
Central nervous system cancer, Dystonia, Glioblastoma, Glioma, Hereditary hyperekplexia, Hyperekplexia, Hyperexplexia hereditary, Scoliosis, Diabetes mellitus, type 2

205
Glycine receptor alpha 2
GLR, MRXSP
Intellectual developmental disorder, x-linked, Severe acute respiratory syndrome

206
Glycine receptor beta
HKPX2
Hereditary hyperekplexia, Hyperekplexia, Hyperexplexia hereditary

207
Glutaminase
AAD20, CASGID, DEE71, EIEE71, GAC, GAM, GDPAG, GLS1, KGA
Eczema, B-cell acute lymphoblastic leukemia, Casgid syndrome, Coronary artery disease, Crohn disease, Developmental and epileptic encephalopathy, Epilepsy, Generalized epilepsy, Global developmental delay, Hypertension, Inflammatory bowel disease, Liver cirrhosis, Myositis, Glutaminase deficiency, Osteoarthritis
View all (6 more)

208
Glutamate dehydrogenase 1
GDH, GDH1, GLUD, hGDH1
Congenital microcephaly, Gout, Hyperammonemia, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Hyperinsulinism-hyperammonemia syndrome, Hypoglycemia

209
Glutamate dehydrogenase 2
GDH2, GLUDP1
Male infertility single gene azoospermia, Hereditary parkinson disease

210
Glutamate-ammonia ligase
DEE116, GLNS, GS, PIG43, PIG59
Alzheimer disease, Brain disease, Hepatocellular carcinoma, Congenital brain dysgenesis due to glutamine synthetase deficiency, Major depressive disorder, Developmental and epileptic encephalopathy, Heart disease, Hepatic encephalopathy, Huntington disease, Liver neoplasm, Depression, Mood disorder, Obesity, Psychotic disorders, Schizophrenia