Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5571 to 5580 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5571
Guanylate cyclase 1 soluble subunit alpha 2
GC-SA2, GUC1A2
Anxiety disorder, Autism, Breast neoplasms, Colorectal cancer, Colorectal neoplasms, Coronary artery disease, Endometrial neoplasms, Gestational diabetes, Obesity, Parkinson disease, Schizophrenia, Scoliosis, Vascular disease

5572
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

5573
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, Duodenal atresia, Oligodendroglioma

5574
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

5575
Guanylate cyclase 2F, retinal
CYGF, GC-F, GUC2DL, GUC2F, RETGC-2, ROS-GC2
Basal cell carcinoma, Gallbladder disease, Non-melanoma skin carcinoma

5576
GTP binding elongation factor GUF1
DEE40, EF-4, EF4, EIEE40
Developmental and epileptic encephalopathy, Insomnia, West syndrome

5577
Guanylate kinase 1
GMK, MTDPS21
Coronary artery disease, Mitochondrial disease, Mitochondrial dna depletion syndrome

5578
GULP PTB domain containing engulfment adaptor 1
CED-6, CED6, GULP
Schizophrenia, Thyroid disease, Uterine fibroid

5579
Glucuronidase beta
BG, MPS7
Alzheimer disease, Autism, Desbuquois syndrome, Non-immune hydrops fetalis, Mucopolysaccharidosis, Nervous system disease, Proteinuria

5580
GVQW motif containing 3
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Asthma