Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "G"
191 to 200 of 677 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
Growth factor, augmenter of liver regeneration
ALR, ERV1, HERV1, HPO, HPO1, HPO2, HSS, MMCHD, MPMCD
Congenital cataract hearing loss developmental delay syndrome, Kidney failure, Liver failure, Mitochondrial disease

192
Growth factor independent 1 transcriptional repressor
GFI-1, GFI1A, SCN2, ZNF163
Spinocerebellar ataxia, Severe congenital neutropenia, Gastro-entero-pancreatic neuroendocrine tumor, Myeloid leukemia, Multiple sclerosis, Neutropenia, nonimmune chronic idiopathic, adult, Obstructive sleep apnea syndrome, Peripheral neuropathy, Prostate cancer, Rheumatoid arthritis, Congenital neutropenia, Systemic lupus erythematosus, Diabetes mellitus type 2

193
Growth factor independent 1B transcriptional repressor
BDPLT17, ZNF163B
Macrothrombocytopenia, Bipolar disorder, Platelet-type bleeding disorder, Graves ophthalmopathy, Myeloproliferative disorder, Prostate cancer, Thrombasthenia-thrombocytopenia, Thrombocytopenia

194
G elongation factor mitochondrial 1
COXPD1, EFG, EFG1, EFGM, EGF1, GFM, hEFG1, mtEF-G1
Combined oxidative phosphorylation deficiency, Developmental regression, Hepatoencephalopathy due to combined oxidative phosphorylation defect, Leigh syndrome

195
GTP dependent ribosome recycling factor mitochondrial 2
EF-G2mt, EFG2, MRRF2, MST027, MSTP027, RRF, RRF2, RRF2mt, hEFG2, mEF-G 2
Combined oxidative phosphorylation deficiency, Leigh syndrome, Mitochondrial disease, Sandhoff disease

196
Gfo/Idh/MocA-like oxidoreductase domain containing 1
ADG-90, C6orf114
Breast cancer, Cardiovascular disease, Ischemic heart disease, Coronary artery disease, Gout, Hypertension, Myocardial ischemia, Oropharyngeal cancer

197
Gfo/Idh/MocA-like oxidoreductase domain containing 2
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Androgenetic alopecia

198
Glutamine--fructose-6-phosphate transaminase 1
CMS12, CMSTA1, GFA, GFAT, GFAT 1, GFAT1, GFAT1m, GFPT, GFPT1L, MSLG
Alzheimer disease, Atrial fibrillation, Congenital myasthenic syndrome, Myasthenic syndrome, Myopathy, Obesity, Osteoarthritis, Small vessel stroke

199
Glutamine-fructose-6-phosphate transaminase 2
GFAT, GFAT 2, GFAT2
Colorectal cancer, Diabetes mellitus type 2, Parkinson disease

200
GDNF family receptor alpha 1
GDNFR, GDNFR-alpha-1, GDNFRA, GFR-ALPHA-1, GFRalpha-1, RET1L, RETL1, RHDA4, TRNR1
Color vision deficiency, Renal agenesis, Epilepsy, Hirschsprung disease, Huntington disease, Liver cirrhosis, Migraine, Schizophrenia, Scoliosis, Uveal melanoma