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"
321 to 330 of 674 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
Geminin coiled-coil domain containing
GEMC1
Alzheimer disease, Dementia, Psoriasis

322
Geminin DNA replication inhibitor
Gem, MGORS6
Hepatocellular carcinoma, Desbuquois syndrome, Ear, patella, short stature syndrome, Ear patella short stature syndrome, Meier-gorlin syndrome

323
GDP-mannose pyrophosphorylase A
AAMR
Glucocorticoid deficiency with achalasia, Intellectual disability with strabismus syndrome, Triple a syndrome

324
GDP-mannose pyrophosphorylase B
LGMDR19, MDDGA14, MDDGB14, MDDGC14
Alzheimer disease, Limb girdle muscular dystrophy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital myasthenic syndrome, Congenital myopathy, Global developmental delay, Muscle eye brain disease, Muscular dystrophy, Myasthenic syndrome, Walker-warburg syndrome

325
Guanosine monophosphate reductase
GMPR 1, GMPR1, hGMPR-I
Alzheimer disease, Juvenile arthritis, Central nervous system cancer, Glioblastoma, Glioma, Hypertrophic cardiomyopathy, Juvenile idiopathic arthritis, Major depressive disorder, Oligoarticular juvenile idiopathic arthritis

326
Guanosine monophosphate reductase 2
GMPR 2, hGMPR-II
Stomach neoplasms, Uterine fibroid

327
Guanine monophosphate synthase
GATD7
Cataract, Insomnia

328
G protein subunit alpha 11
FBH, FBH2, FHH2, GNA-11, HG1K, HHC2, HYPOC2
Anastomosing haemangioma, Hypocalcemia, Calcium metabolism disorders, Capillary malformation, Congenital venous anomaly, Congenital heart defects, Congenital hemangioma, Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi, Cutis marmorata telangiectatica congenita, Hypocalciuric hypercalcemia, Congenital heart defect, Melanoma, Schwartz-jampel syndrome, Uveal melanoma

329
G protein subunit alpha 12
HG1M1, NNX3, RMP, gep
Ankylosing spondylitis, Atrial fibrillation, Bipolar disorder, Ulcerative colitis, Obstructive pulmonary disease, Colorectal cancer, Congenital cardiovascular anomaly, Crohn disease, Dementia, Hypertension, Hypothyroidism, Inflammatory bowel disease, Insomnia, Major depressive disorder, Myocardial ischemia
View all (10 more)

330
G protein subunit alpha 13
G13, HG1N
Burkitt lymphoma, Hypertension