Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "G"
171 to 180 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

171
Growth hormone releasing hormone receptor
GHRFR, GRFR, IGHD1B, IGHD4
Desbuquois syndrome, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Schizophrenia, Scoliosis, Sheehan syndrome

172
Growth hormone secretagogue receptor
GHDP, GHS-R1a, GHSR-1a
Desbuquois syndrome, Digestive system neoplasm, Growth hormone insensitivity syndrome, Obesity, Pseudohypoparathyroidism

173
Gastric inhibitory polypeptide
-
Anorexia, Coronary artery disease, Diabetes mellitus type 2, Diabetic neuropathy, Hypertension, Hyperlipidemia, Insomnia, Metabolic syndrome, Myocardial infarction, Obesity, Prostate cancer, Diabetes mellitus, type 2

174
Gastric inhibitory polypeptide receptor
PGQTL2
Alzheimer disease, Bladder calculus, Body weight, Breast cancer, Non-small-cell lung carcinoma, Cardiovascular disease, Cervical cancer, Cholecystolithiasis, Coronary artery disease, Diabetes mellitus, Diabetic retinopathy, Estrogen-receptor negative breast cancer, Gallstones, Heart failure, Metabolic syndrome
View all (8 more)

175
Gap junction protein alpha 1
AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL, HLHS1, HSS, ODDD, PPKCA
Anhedonia, Cardiac arrhythmias, Atrial fibrillation, Atrioventricular septal defect, Autism, Palmoplantar keratoderma with congenital alopecia, Breast neoplasm, Cardiac arrhythmia, Obstructive pulmonary disease, Congenital heart disease, Coronary aneurysm, Craniometaphyseal dysplasia, Syndactyly, Desbuquois syndrome, Erythrokeratodermia variabilis
View all (18 more)

176
G protein-coupled receptor 160
GPCR1, GPCR150
Psoriasis, Testicular carcinoma

177
Gap junction protein alpha 3
CTRCT14, CX46, CZP3
Cataract, Congenital cataract, Congenital cataract facial dysmorphism neuropathy syndrome, Posterior subcapsular cataract

178
Gap junction protein alpha 4
CX37
Ischemic heart disease, Coronary artery disease, Hemangiosarcoma, Hypertension, Liver cirrhosis, Myocardial infarction, Myocardial ischemia

179
Gap junction protein alpha 5
ATFB11, CX40
Atrial fibrillation, Atrial flutter, Atrial standstill, Cardioembolic stroke, Chromosome 1q21.1 deletion syndrome, Congenital heart disease, Gout, Heart disease, Hereditary atrial fibrillation, Hypertension, Hypertrophic cardiomyopathy, Interstitial lung disease, Parkinson disease, Scoliosis, Wolff-parkinson-white syndrome

180
Gap junction protein alpha 8
CAE, CAE1, CTRCT1, CX50, CZP1, MP70
Anterior segment mesenchymal dysgenesis, Atrial fibrillation, Atrial flutter, Cardioembolic stroke, Cataract, Cataract-microcornea syndrome, Congenital cataract, Chromosome 1q21.1 deletion syndrome, Gout, Microphthalmos, Schizophrenia, Scoliosis