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"
651 to 660 of 677 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

651
Guanylate cyclase activator 2B
GCAP-II, UGN
Kidney failure, Nephrotic syndrome, Psychiatric disorders, Systemic lupus erythematosus

652
Guanylyl cyclase domain containing 1
C22orf13, LLN4
Prostatic neoplasms

653
Guanylate cyclase 1 soluble subunit alpha 1
GC-S-alpha-1, GC-SA3, GCS-alpha-3, GUC1A3, GUCA3, GUCSA3, GUCY1A3, MYMY6
Adenoid cystic carcinoma, Cardiovascular disease, Ischemic heart disease, Colonic neoplasms, Coronary artery disease, Diabetic neuropathy, Hypertension, Major depressive disorder, Moyamoya disease, Myocardial infarction, Myocardial ischemia, Parkinson disease, Psoriasis, Pulmonary edema, Salivary gland neoplasms
View all (2 more)

654
Guanylate cyclase 1 soluble subunit alpha 2
GC-SA2, GUC1A2
Anxiety disorder, Autism, Breast neoplasms, Central nervous system infection, Colorectal cancer, Colorectal neoplasms, Coronary artery disease, Endometrial neoplasms, Gestational diabetes, Obesity, Parkinson disease, Schizophrenia, Scoliosis, Vascular disease

655
Guanylate cyclase 1 soluble subunit beta 1
GC-S-beta-1, GC-SB3, GUC1B3, GUCB3, GUCSB3, GUCY1B3
Colorectal cancer, Coronary artery disease, Diabetic retinopathy, Hypertension, Myocardial infarction, Osteoarthritis, Diabetes mellitus type 2, Uterine fibroid

656
Guanylate cyclase 2C
DIAR6, GC-C, GCC, GUC2C, HSER, MECIL, MUCIL, STAR
Chronic infantile diarrhea due to guanylate cyclase 2c overactivity, Colorectal neoplasms, Congenital diarrhea, Congenital secretory diarrhea, Congenital sodium diarrhea, Diarrhea, Duodenal atresia, Dysentery, Oligodendroglioma

657
Guanylate cyclase 2D, retinal
CACD, CACD1, CG-E, CORD5, CORD6, CSNB1I, CYGD, GUC1A4, GUC2D, LCA, LCA1, RCD2, RETGC-1, ROS-GC1, ROSGC, retGC
Leber congenital amaurosis, Optic atrophy, Central areolar choroidal dystrophy, Choroidal dystrophy, Choroidal sclerosis, Cone dystrophy, Cone-rod dystrophy, Congenital blindness, Macular dystrophy, Night blindness, congenital stationary, Nystagmus, Oguchi disease, Oligodendroglioma, Retinal cone dystrophy, Retinitis pigmentosa

658
Guanylate cyclase 2F, retinal
CYGF, GC-F, GUC2DL, GUC2F, RETGC-2, ROS-GC2
Basal cell carcinoma, Gallbladder disease, Non-melanoma skin carcinoma

659
GTP binding elongation factor GUF1
DEE40, EF-4, EF4, EIEE40
Developmental and epileptic encephalopathy, Insomnia, West syndrome

660
Guanylate kinase 1
GMK, MTDPS21
Coronary artery disease, Mitochondrial disease, Mitochondrial dna depletion syndrome