|
191
|
|
|
Glycine N-methyltransferase |
HEL-S-182mP |
Glycine n-methyltransferase deficiency, Hepatic methionine adenosyltransferase deficiency, Hyperhomocysteinemia, Hypermethioninemia, Liver neoplasms, Liver cancer, Liver carcinoma, Non-alcoholic fatty liver disease, Prostatic neoplasms, Prostate cancer, S-adenosylhomocysteine hydrolase deficiency |
|
192
|
|
|
G-patch domain and KOW motifs |
GPATC5, GPATCH5, Mos2, Spp2, T54 |
|
|
193
|
|
|
Glutamate-cysteine ligase catalytic subunit |
CNSHA7, GCL, GCS, GLCL, GLCLC |
Anemia, Benign prostatic hyperplasia, Coronary vessel anomalies, Dermatitis, Developmental delay, Disorder of amino acid metabolism, Dysarthria, Dyslexia, Enzymopathy, Gamma-glutamylcysteine synthetase deficiency, Glutamate-cysteine ligase deficiency, Hypertension, Inherited errors of amino acid metabolism, Lung carcinoma, Lung neoplasms, Lung cancer, Mental retardation, Microangiopathic hemolytic anemia, Myocardial infarction, Myocardial ischemia, Myopathy, Nervous system diseases, Polyneuropathy, Psychosis, Schizophrenia, Spinocerebellar degenerationView all (11 more) |
|
194
|
|
|
Glutamate-cysteine ligase modifier subunit |
GLCLR |
|
|
195
|
|
|
Glycine decarboxylase |
GCE, GCE1, GCSP, HYGN1 |
Agenesis of corpus callosum, Asthma, Epilepsy, Epileptic encephalopathy, Glycine encephalopathy, Hyperglycinemia, Hyperglycinuria, Mental retardation, Nonketotic hyperglycinemia, Obesity, Osteosarcoma |
|
196
|
|
|
GLE1 RNA export mediator |
CAAHC, CAAHD, GLE1L, LCCS, LCCS1, hGLE1 |
Amniotic bands, Amyotrophic lateral sclerosis, Anterior horn cell disease, Anxiety disorder, Arthrogryposis multiplex congenita, Arthrogryposis-anterior horn cell disease syndrome, Congenital clubfoot, Pulmonary hypoplasia, Cryptorchidism, Dwarfism, Dysarthria, Dysmorphic features, High palate, Laryngospasm, Lethal arthrogryposis with anterior horn cell disease, Lethal congenital contracture syndrome, Mental depression, Micrognathism, Mood swings, Motor delay, Multiple congenital anomalies, Myopia, Neck webbing, Pena shokeir syndrome, Peripheral axonal neuropathy, Ptosis, Respiratory failure, Scoliosis, Vertical talusView all (14 more) |
|
197
|
|
|
Golgi integral membrane protein 4 |
GIMPC, GOLPH4, GPP130, P138 |
|
|
198
|
|
|
Golgi glycoprotein 1 |
CFR-1, ESL-1, MG-160, MG160 |
|
|
199
|
|
|
GLI family zinc finger 1 |
GLI, PAPA8, PPD1 |
Cubitus valgus, Atrial septal defect, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Cryptorchidism, Diffuse lymphoma, Ellis-van creveld syndrome, Epispadias, Gastrointestinal stromal tumor, Hypodontia, Hypospadias, Leukemia, Liver carcinoma, Mental retardation, Microdontia, Micromelia, Nail diseases, Nail dysplasia, Nervous system diseases, Polydactyly, Polydactyly of toes, Promyelocytic leukemia, Situs inversus, Strabismus, Ventricular septal defectView all (11 more) |
|
200
|
|
|
GLI family zinc finger 2 |
CJS, HPE9, PHS2, THP1, THP2 |
Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Arrhinencephaly, Asthma, Basal cell neoplasm, Carcinoma, Choanal atresia, Cleft palate and bilateral cleft lip, Congenital coloboma of iris, Congenital hypoplasia of penis, Cryptorchidism, Culler-jones syndrome, Cyclocephaly, Developmental delay, Duodenal atresia, Dwarfism, Dysmorphic features, Ectopic anterior pituitary gland, Fused incisors, Gastrointestinal stromal tumor, Hemangioma, Holoprosencephaly, Hydrocephalus, Hypoglycemia, Hypogonadism, Hypogonadotropic hypogonadism, Hypopituitarism, Hypoplasia of the maxilla, Hypoplasia of the optic nerve, Hypothyroidism, Isolated somatotropin deficiency, Lobar holoprosencephaly, Macrotia, Mental retardation, Microcephaly, Microform holoprosencephaly, Microphthalmos, Midline interhemispheric variant of holoprosencephaly, Multiple congenital anomalies, Osteopenia, Osteoporosis of vertebrae, Panhypopituitarism, Partial agenesis of corpus callosum, Penis agenesis, Pituitary dwarfism, Pituitary hormone deficiency, Polydactyly, Promyelocytic leukemia, Renal agenesis, Scoliosis, Semilobar holoprosencephaly, Septo-optic dysplasia, Septopreoptic holoprosencephaly, Skin cancer, Skin neoplasms, Somatotropin deficiency, Strabismus, Syndromic microphthalmia, Tetralogy of fallot, Postaxial hand polydactylyView all (46 more) |
