5341
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|
|
Glypican 6 |
OMIMD1 |
Alzheimer disease, Astrocytoma, Attention deficit hyperactivity disorder, Omodysplasia, Bipolar disorder, Central nervous system cancer, Colorectal cancer, Craniofacial abnormalities, Desbuquois syndrome, Glioblastoma, Glioma, Glomerulonephritis, Insomnia, Congenital anomaly of limb, Major depressive disorder, Metabolic syndrome, Nervous system disease, Neurotic disorder, Nonalcoholic fatty liver disease, Obesity, Osteoporosis, Pelvic organ prolapse, Peripheral neuropathy, Schizophrenia, Secondary parkinson disease, Diabetes mellitus type 2View all (11 more) |
5342
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|
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Glycerophosphocholine phosphodiesterase 1 |
EDI3, GDE5, GDPD6, PREI4 |
|
5343
|
|
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Glycerol-3-phosphate dehydrogenase 1 |
GPD-C, GPDH-C, HTGTI |
|
5344
|
|
|
Glycerol-3-phosphate dehydrogenase 1 like |
GPD1-L |
|
5345
|
|
|
Glycerol-3-phosphate dehydrogenase 2 |
GDH2, GPDM, mGDH, mGPDH |
|
5346
|
|
|
G protein-coupled estrogen receptor 1 |
CEPR, CMKRL2, DRY12, FEG-1, GPCR-Br, GPER, GPR30, LERGU, LERGU2, LyGPR, mER |
|
5347
|
|
|
Glycoprotein hormone subunit alpha 2 |
A2, GPA2, ZSIG51 |
|
5348
|
|
|
Gephyrin |
GEPH, GPH, GPHRYN, HKPX1, MOCODC |
Anxiety disorder, Arachnoid cysts, Eczema, Cerebral palsy, Color vision deficiency, Neurodevelopmental disorder, Cone-rod dystrophy, Glycosylphosphatidylinositol biosynthesis defect, Hereditary hyperekplexia, Hyperekplexia, Hyperexplexia hereditary, Intellectual developmental disorder, Leber congenital amaurosis, Promyelocytic leukemia, Macular dystrophy, Major depressive disorder, Non-specific syndromic intellectual disability, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome, Rett syndrome, Schizophrenia, Scoliosis, Stargardt diseaseView all (9 more) |
5349
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|
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Glucose-6-phosphate isomerase |
AMF, CNSHA4, GNPI, NLK, PGI, PHI, SA-36, SA36 |
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5350
|
|
|
Glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 |
GPI-HBP1, HYPL1D |
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