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"
391 to 400 of 674 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

391
GON7 subunit of KEOPS complex
C14orf142, PNAS-127
Galloway-mowat syndrome

392
Golgi associated PDZ and coiled-coil motif containing
CAL, FIG, GOPC1, PIST, dJ94G16.2
Astrocytoma, Atrial fibrillation, Tourette syndrome, Male infertility globozoospermia, Melanoma

393
Golgin, RAB6 interacting
GO, NTKLBP1, SCYL1BP1
Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Atrial flutter, Bone fragility with contractures, arterial rupture, and deafness, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Congenital skin anomaly, Dementia, Desbuquois syndrome, Larsen syndrome, Osteoporosis, Osteoporosis-pseudoglioma syndrome, Skin abnormalities
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394
Golgi reassembly stacking protein 2
GOLPH6, GRASP55, GRS2, p59
Scoliosis

395
Golgi SNAP receptor complex member 2
Bos1, EPM6, GS27, MYOS
Atrial fibrillation, Atrial flutter, Bladder exstrophy, Cardioembolic stroke, Cardiovascular disease, Congenital heart disease, Coronary artery disease, Deafness, Progressive myoclonic epilepsy, Heart failure, Hypertension, Idiopathic pulmonary fibrosis, Myocardial infarction, Orofacial cleft, Stroke

396
Glutamic-oxaloacetic transaminase 1
AST, AST1, ASTQTL1, GIG18, SGOT, cAspAT, cCAT
Amyloidosis, Amyotrophic lateral sclerosis, Hearing loss, Peripheral arterial disease, Scoliosis, Transient ischemic attack

397
Glutamic-oxaloacetic transaminase 2
DEE82, KAT4, KATIV, KYAT4, mitAAT
Developmental and epileptic encephalopathy

398
Glycoprotein Ib platelet subunit alpha
BDPLT1, BDPLT3, BSS, CD42B, CD42b-alpha, DBPLT3, GP1B, GPIbA, GPIbalpha, VWDP
Macrothrombocytopenia, Bernard-soulier syndrome, Hypertension, Myocardial infarction, Thrombocytopenia, Thrombosis, Von willebrand disorder

399
Glycoprotein Ib platelet subunit beta
BDPLT1, BS, CD42C, GPIBB, GPIbbeta
22q11.2 deletion syndrome, Juvenile arthritis, Macrothrombocytopenia, Bernard-soulier syndrome, Color vision deficiency, Congenital heart defects, Craniofacial abnormalities, Digeorge syndrome, Congenital heart defect, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Polycystic ovary syndrome, Rheumatoid arthritis, Thrombocytopenia

400
Glycoprotein 2
ZAP75
Body weight, Coronary artery disease, Diabetes mellitus type 2, Metabolic syndrome, Diabetes mellitus type 1