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 677 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
GEM interacting protein
ARHGAP46
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Metabolic syndrome, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2, Depression

322
Glycosylphosphatidylinositol anchored molecule like
LY6DL
Autism, Cardiovascular disease, Hypertension, Osteoarthritis, Primary aldosteronism

323
Geminin coiled-coil domain containing
GEMC1
Alzheimer disease, Dementia, Psoriasis

324
Geminin DNA replication inhibitor
Gem, MGORS6
Hepatocellular carcinoma, Desbuquois syndrome, Ear, patella, short stature syndrome, Ear patella short stature syndrome, Meier-gorlin syndrome

325
GDP-mannose pyrophosphorylase A
AAMR
Glucocorticoid deficiency with achalasia, Intellectual disability with strabismus syndrome, Triple a syndrome

326
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

327
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

328
Guanosine monophosphate reductase 2
GMPR 2, hGMPR-II
Stomach neoplasms, Uterine fibroid

329
Guanine monophosphate synthase
GATD7
Cataract, Insomnia

330
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