Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5131 to 5140 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5131
Guided entry of tail-anchored proteins factor 4
C7orf20, CDG2Y, CEE, CGI-20, TRC35
Congenital disorder of glycosylation

5132
Glial fibrillary acidic protein
ALXDRD
Alexander disease, Amyotrophic lateral sclerosis, Autism, Bipolar disorder, Neuronal ceroid lipofuscinosis, Ciliary dyskinesia, Major depressive disorder, Epilepsy, Hyperalgesia, Metachromatic leukodystrophy, Lewy body disease, Motor neuron disease, Nervous system disease, Non-neoplastic peripheral nervous system disease, Parkinson disease
View all (6 more)

5133
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

5134
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

5135
Growth factor independent 1B transcriptional repressor
BDPLT17, ZNF163B
Macrothrombocytopenia, Bipolar disorder, Platelet-type bleeding disorder, Graves ophthalmopathy, Myeloproliferative disorder, Prostate cancer, Thrombasthenia-thrombocytopenia, Thrombocytopenia

5136
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

5137
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

5138
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

5139
Gfo/Idh/MocA-like oxidoreductase domain containing 2
-
Androgenetic alopecia

5140
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