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 677 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

391
Golgi transport 1A
CGI-141, GOT1, GOT1B, HMFN1187, YMR292W, hGOT1b
Melanoma

392
Gon-4 like
GON-4, GON4, LTMS, YARP
Atrial fibrillation, Breast cancer, Gastric cancer, Gout, Intellectual developmental disorder, Neurodevelopmental disorder

393
GON7 subunit of KEOPS complex
C14orf142, PNAS-127
Galloway-mowat syndrome

394
Golgi associated PDZ and coiled-coil motif containing
CAL, FIG, GOPC1, PIST, dJ94G16.2
Astrocytoma, Atrial fibrillation, Tourette syndrome, Male infertility globozoospermia, Melanoma

395
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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396
Golgi reassembly stacking protein 2
GOLPH6, GRASP55, GRS2, p59
Scoliosis

397
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

398
Glutamic-oxaloacetic transaminase 1
AST, AST1, ASTQTL1, GIG18, SGOT, cAspAT, cCAT
Amyloidosis, Amyotrophic lateral sclerosis, Hearing loss, Liver cirrhosis, Peripheral arterial disease, Scoliosis, Transient ischemic attack

399
Glutamic-oxaloacetic transaminase 2
DEE82, KAT4, KATIV, KYAT4, mitAAT
Developmental and epileptic encephalopathy

400
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