Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
5241 to 5250 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

5241
Geminin DNA replication inhibitor
Gem, MGORS6
Hepatocellular carcinoma, Desbuquois syndrome, Ear, patella, short stature syndrome, Ear patella short stature syndrome, Meier-gorlin syndrome

5242
GDP-mannose pyrophosphorylase A
AAMR
Glucocorticoid deficiency with achalasia, Intellectual disability with strabismus syndrome, Triple a syndrome

5243
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

5244
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

5245
Guanosine monophosphate reductase 2
GMPR 2, hGMPR-II
Stomach neoplasms, Uterine fibroid

5246
Guanine monophosphate synthase
GATD7
Cataract, Insomnia

5247
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

5248
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)

5249
G protein subunit alpha 13
G13, HG1N
Burkitt lymphoma, Hypertension

5250
G protein subunit alpha 14
HG1I
Anastomosing haemangioma, Bipolar disorder, Cerebrofacial arteriovenous metameric syndrome, Scoliosis, Myopia