|
191
|
|
|
Glycine N-methyltransferase |
HEL-S-182mP |
Hepatocellular carcinoma, Persistent hepatitis, S-adenosylhomocysteine hydrolase deficiency, Glycine n-methyltransferase deficiency, Hepatic methionine adenosyltransferase deficiency, Hepatitis, Hyperhomocysteinemia, Liver neoplasm, Nonalcoholic fatty liver disease, Peroxisome biogenesis disorder, Prostatic neoplasm |
|
192
|
|
|
G-patch domain and KOW motifs |
GPATC5, GPATCH5, Mos2, Spp2, T54 |
|
|
193
|
|
|
Glutamate-cysteine ligase catalytic subunit |
CNSHA7, GCL, GCS, GLCL, GLCLC |
Amino acid metabolism disorder, Congenital nonspherocytic hemolytic anemia, Hemolytic anemia, Non-small-cell lung carcinoma, Contact dermatitis, Coronary vessel anomalies, Cystic fibrosis, Diabetes mellitus type 2, Hereditary hemolytic anemia, Hypertension, Lung cancer, Lung neoplasms, Microphthalmos, Myocardial infarction, Myocardial ischemia, Ovarian serous carcinoma, SchizophreniaView all (2 more) |
|
194
|
|
|
Glutamate-cysteine ligase modifier subunit |
GLCLR |
|
|
195
|
|
|
Glycine decarboxylase |
GCE, GCE1, GCSP, HYGN1 |
Asthma, Astrocytoma, Glycine encephalopathy, Generalized epilepsy, Global developmental delay, Hyperglycemia, Neurodevelopmental disorders, Obesity, Osteosarcoma, Retinitis pigmentosa, Severe acute respiratory syndrome |
|
196
|
|
|
GLE1 RNA export mediator |
CAAHC, CAAHD, GLE1L, LCCS, LCCS1, hGLE1 |
|
|
197
|
|
|
Golgi integral membrane protein 4 |
GIMPC, GOLPH4, GPP130, P138 |
Barrett esophagus, Diabetic retinopathy, Digestive system disease, Epilepsy, Esophageal adenocarcinoma, Generalized epilepsy, Hypertension, Oligodendroglioma, Partial epilepsy, Proliferative diabetic retinopathy, Psychiatric disorders |
|
198
|
|
|
Golgi glycoprotein 1 |
CFR-1, ESL-1, MG-160, MG160 |
|
|
199
|
|
|
GLI family zinc finger 1 |
GLI, PAPA8, PPD1 |
Bardet-biedl syndrome, Hepatocellular carcinoma, Ellis-van creveld syndrome, Gastrointestinal stromal tumor, Gout, Insomnia, Promyelocytic leukemia, Diffuse large b-cell lymphoma, Non-neoplastic peripheral nervous system disease, Premature ovarian failure, Peripheral nervous system disease, Peripheral neuropathy, Polydactyly, Postaxial polydactyly, Urinary tract infection |
|
200
|
|
|
GLI family zinc finger 2 |
CJS, HPE9, PHS2, THP1, THP2 |
Alzheimer disease, Androgenetic alopecia, Cerebral arteriovenous malformations, Asthma, Bardet-biedl syndrome, Basal cell nevus syndrome, Breast cancer, Basal cell carcinoma, Coloboma, Combined pituitary hormone deficiency, Congenital arteriovenous malformation, Craniosynostosis, Dementia, Desbuquois syndrome, Developmental disability, Erectile dysfunction, Exostoses, Facial dysmorphism syndrome, Gastrointestinal stromal tumor, Holoprosencephaly, Intellectual developmental disorder, Promyelocytic leukemia, Male infertility single gene azoospermia, Microform holoprosencephaly, Syntelencephaly, Oligodendroglioma, Pituitary stalk interruption syndrome, Postaxial polydactyly–anterior pituitary anomalies–facial dysmorphism syndrome, Prostate cancer, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Severe acute respiratory syndrome, Skin neoplasm, Diabetes mellitus, type 2, White sutton syndromeView all (20 more) |
