401
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Glial fibrillary acidic protein |
ALXDRD |
Curated: Alexander disease, Amyotrophic lateral sclerosis, Autism, Bipolar disorder, Neuronal ceroid lipofuscinosis, Ciliary dyskinesia, Major depressive disorder, Epilepsy, Hyperalgesia, Metachromatic leukodystrophy, Lewy body disease, Motor neuron disease, Nervous system disease, Non-neoplastic peripheral nervous system disease, Parkinson disease, Peripheral nervous system disease, Peripheral neuropathy, Schizophrenia, Scoliosis, Trigeminal neuralgia, Depression
Unreviewed: Adenocarcinoma, Adrenocortical carcinoma, Agenesis Of Corpus Callosum, Akinesia, Alexander Disease, alpha-Thalassemia Mental Retardation Syndrome, X-Linked, Alzheimer disease, Amyloidosis, Amyotrophic Lateral Sclerosis, Amyotrophic Lateral Sclerosis With Dementia, Anaplastic Oligodendroglioma, Anemia, Anorexia, Anxiety Disorder, Aplasia Cutis Congenita, Arrhythmogenic right ventricular cardiomyopathy, Arthritis, Astrocytoma, Ataxia, Atrophy, Atrophy of the spinal cord, Autism spectrum disorder, Autoimmune Diabetes, Autoimmune Diseases, Autonomic Central Nervous System Diseases, B-Cell Lymphoma, Bardet-Biedl Syndrome, Benign Neoplasm, Bipolar Disorder, Borderline personality disorder, Brain disease, Brain edema, Brain injuries, Brain Neoplasms, Brain Stem Glioma, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchopulmonary Dysplasia, CADASIL Syndrome, Calcinosis, Carcinoma, Cardiomyopathy, Catalepsy, Central Nervous System Neoplasms, Cerebellar Ataxia, Cerebral amyloid angiopathy, Cerebral Infarction, Cerebral Ischemia, Cerebral palsy, Cerebrovascular Occlusion, Chondrosarcoma, Chordoma, CNS Disorder, Cognition disorder, Cognitive disorder, Colorectal Cancer, Colorectal Neoplasms, Cone-rod dystrophy, Congenital glucose-galactose malabsorption, Congenital heart defects, Congestive Heart Failure, Corneal Diseases, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Creutzfeldt-Jakob disease, Crohn disease, Cyst, Delirium, Dementia, Demyelinating Diseases, Dental caries, Dermatologic Disorders, Developmental disability, Developmental regression, Diabetes, Diabetes Mellitus, Diabetic Ketoacidosis, Diabetic Retinopathy, Diffuse Intrinsic Pontine Glioma, Digeorge syndrome, Down Syndrome, Dysautonomia, Dyskinetic Syndrome, Dystonia, Encephalitis, Ependymoma, Epidermolysis Bullosa Simplex, Epilepsia Partialis Continua, Epileptic encephalopathy, Epiretinal Membrane, Ewing sarcoma, Extraskeletal myxoid chondrosarcoma, Fanconi Anemia, Fatal Insomnia, Fibrosarcoma, Fleck Corneal Dystrophy, Focal cortical dysplasia, Fraser syndrome, Friedreich Ataxia, Frontotemporal dementia, Ganglioglioma, Ganglioneuroma, Gastrinoma, Gastroparesis, Gaucher disease, Gemistocytic Astrocytoma, Geographic Atrophy, Giant axonal neuropathy, Glaucoma, Glioblastoma, Glioma, Gliosarcoma, Graves ophthalmopathy, Guillain-Barre Syndrome, Harlequin Ichthyosis, Heart Failure, Hemimegalencephaly, Hepatitis c, Hepatocellular adenoma, Hepatocellular carcinoma, Hepatolenticular degeneration, Hereditary spastic paraplegia, Huntington Disease, Hydrocephalus, Hypercholesterolemia, Hyperglycemia, Hyperhomocysteinemia, Hyperkinesia, Hypertension, Hypothyroidism, Hypoxia, Hypoxic-Ischemic Encephalopathy, Impaired Cognition, Infantile spasms, Intellectual developmental disorder, Intestinal Diseases, Intestinal Pseudoobstruction, Intraventricular Meningioma, Irritable bowel syndrome, Ischemic Stroke, Lafora Disease, Lateral Sclerosis, Leber congenital amaurosis, Leukodystrophy, Leukoencephalopathy, Leukoplakia, Lewy Body Disease, Liver carcinoma, Liver failure, Liver Fibrosis, Lung carcinoma, Lung Neoplasms, Machado-Joseph Disease, Macrocephaly, Macular degeneration, Malignant Bone Neoplasm, Malignant Neoplasm, Medulloblastoma, Megalencephalic Leukoencephalopathy With Subcortical Cysts, Melanoma, Membranous glomerulonephritis, Memory disorders, Meningioma, Meningomyelocele, Mental Depression, Mental Disorders, Mental retardation, Metabolic Syndrome, Mitral Valve Stenosis, Mixed Oligodendroglioma-Astrocytoma, Mood Disorder, Motor Neuron Disease, Mouth disease, Mucopolysaccharidosis, Multiple Endocrine Neoplasia, Multiple polyposis syndrome, Multiple Sclerosis, Myelodysplastic Syndrome, Myeloid leukemia, Myeloproliferative disorder, Myeloproliferative Disorder with Eosinophilia, Myocardial Infarction, Myocardial Ischemia, Myofibrillar myopathy, Myopathy, Nasopharyngeal Carcinoma, Neoplasms, Nervous System Diseases, Nervous System Disorder, Neurilemmoma, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Neurodevelopmental Disorders, Neuroectodermal Tumors, Neurofibromatosis, Neuromyelitis Optica, Neuronal Ceroid Lipofuscinosis, Niemann-Pick Disease, Obesity, Ocular Hypertension, Oculocutaneous albinism, Oligodendroglioma, Open angle glaucoma, Optic Nerve Glioma, Optic Neuritis, Osteosarcoma, Papillary Meningioma, Papilledema, Peripheral Neuropathy, Persistent Hyperplastic Primary Vitreous, Phenylketonuria, Pica, Pigmentary Disorder, Reticulate, With Systemic Manifestations, Pituitary neoplasm, Pleomorphic Xanthoastrocytoma, Postnatal asphyxia, Progeria, Progressive Supranuclear Palsy, Proliferative Diabetic Retinopathy, Proliferative Vitreoretinopathy, Prostate cancer, Prostatic neoplasm, Psychiatric disorders, Psychosis, Retinal Detachment, Retinal Diseases, Retinoblastoma, Retinopathy, Rett Syndrome, Rhabdoid tumor predisposition syndrome, Rheumatoid arthritis, Russell-Silver Syndrome, Sarcoma, Schilder disease, Sclerosing Cholangitis, Seizures, Senile Dementia, Senile Plaques, Septicemia, Spastic Paraplegia, Sphingomyelinase deficiency, Spina Bifida, Spina Bifida Cystica, Spinal Cord Neoplasms, Spinal Muscular Atrophy, Spinocerebellar Ataxia, Status Epilepticus, Stress Disorder, Stroke, Subarachnoid hemorrhage, Supratentorial Neoplasm, Tauopathies, Temporal lobe epilepsy, Tuberous Sclerosis, Tuberous sclerosis complex, Ulcerative colitis, Urinary bladder diseases, Uveal Melanoma, Vitreoretinopathy, Vulval varices
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402
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|
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Growth factor, augmenter of liver regeneration |
ALR, ERV1, HERV1, HPO, HPO1, HPO2, HSS, MMCHD, MPMCD |
Curated: Congenital cataract hearing loss developmental delay syndrome, Kidney failure, Liver failure, Mitochondrial disease
Unreviewed: Acute Kidney Insufficiency, Amyotrophic lateral sclerosis, Ankylosing Spondylitis, Anorexia, Arteriosclerosis, Arthritis, Atherosclerosis, Autoimmune Diseases, Carcinogenesis, Cardiomyopathy, Cataract, Cholangiocarcinoma, Cirrhosis, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Congenital Cataract-Progressive Muscular Hypotonia-Hearing Loss-Developmental Delay Syndrome, Congenital diaphragmatic hernia, Cytochrome c oxidase deficiency, Developmental Delay, Developmental disability, Diabetes, Diabetes Mellitus, Diabetic Ketoacidosis, Diabetic Retinopathy, Eosinophilia, Epilepsy, Fatty Liver, Hearing Loss, Hematologic neoplasm, Hematologic Neoplasms, Hermaphroditism, Hodgkin Disease, Hodgkin Lymphoma, Hyperglycemia, Hypoplasia Of Corpus Callosum, Kearns Sayre Syndrome, Kidney Failure, Kidney neoplasm, Liver carcinoma, Liver Cirrhosis, Liver Fibrosis, Lung Cancer, Lung carcinoma, Lung Diseases, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Malignant Neoplasm, Mental Depression, Mental retardation, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial Respiratory Chain Deficiencies, Multiple myeloma, Myeloid leukemia, Myopathy, Myopathy, Mitochondrial With Congenital Cataract, Hearing Loss, And Developmental Delay, Neoplasms, Nephropathy with Pretibial Epidermolysis Bullosa and Deafness, Nervous System Diseases, Neurodegenerative Disorders, Obesity, Osteosarcoma, Pancreatitis, Peripheral Neuropathy, Peritoneal Fibrosis, Polycystic kidney disease, Proliferative Diabetic Retinopathy, Ptosis, Rotary nystagmus, Schwartz-Jampel Syndrome, Spastic paraplegia, Stevens-Johnson Syndrome, Visceral neuropathy
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403
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Growth factor independent 1 transcriptional repressor |
GFI-1, GFI1A, SCN2, ZNF163 |
Curated: Spinocerebellar ataxia, Severe congenital neutropenia, Gastro-entero-pancreatic neuroendocrine tumor, Myeloid leukemia, Multiple sclerosis, Neutropenia, nonimmune chronic idiopathic, adult, Obstructive sleep apnea syndrome, Peripheral neuropathy, Prostate cancer, Rheumatoid arthritis, Congenital neutropenia, Systemic lupus erythematosus, Diabetes mellitus type 2
Unreviewed: Abetalipoproteinemia, Agammaglobulinemia, Aphthous Ulcer, Aplastic anemia, Atherosclerosis, Attention Deficit Hyperactivity Disorder, Autoimmune Diseases, Bone Disease, Breast neoplasm, Carcinoma, Cardiomyopathy, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Colorectal Cancer, Colorectal neoplasm, Congenital Neutropenia, Cyclic neutropenia, Digestive system neuroendocrine neoplasm, Eosinophilia, Erythroblastic Leukemia, Esophageal squamous cell carcinoma, Gingivitis, Glaucoma, Hemangioma, Hematological Disease, Hyperoxia, Hypertrophic cardiomyopathy, Hypohidrotic ectodermal dysplasia, Hypohidrotic Ectodermal Dysplasia, X-Linked, Hypoxia, Laryngeal neoplasm, Leukemia, Leukopenia, Liver neoplasms, Lung Cancer, Lung carcinoma, Lupus Erythematosus, Lupus Vulgaris, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Lymphoma, Lymphopenia, Malignant Neoplasm, Medulloblastoma, Miller Dieker Syndrome, Monocytic Leukemia, Monocytosis, Multiple myeloma, Multiple Sclerosis, Myelodysplasia, Myelodysplastic Syndrome, Myeloid Leukemia, Myeloproliferative disorder, Neoplasms, Neutropenia, Obesity, Oral Ulcer, Osteopenia, Osteoporosis, Periodontitis, Pharyngitis, Promyelocytic leukemia, Prostatic Neoplasms, Pyoderma Gangrenosum, Reticular dysgenesis, Rhinitis, Sepsis, Specific Granule Deficiency, Spinocerebellar Ataxia, Syndromic microphthalmia, T-Cell Lymphoma/Leukemia, Wiskott-Aldrich Syndrome
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404
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Growth factor independent 1B transcriptional repressor |
BDPLT17, ZNF163B |
Curated: Macrothrombocytopenia, Bipolar disorder, Platelet-type bleeding disorder, Graves ophthalmopathy, Myeloproliferative disorder, Prostate cancer, Thrombasthenia-thrombocytopenia, Thrombocytopenia, platelet-type bleeding disorder 17
Unreviewed: Aplastic anemia, Arthrogryposis, Renal Dysfunction, And Cholestasis, Blast phase chronic myelogenous leukemia, Blood Coagulation Disorders, Budd-Chiari syndrome, Carcinogenesis, Colorectal Cancer, Erythroblastic Leukemia, Gray Platelet Syndrome, Hematologic neoplasm, Hematological Disease, Hemorrhage, Hepatic Vein Thrombosis, Hereditary neuropathy with liability to pressure palsies, Immune System Diseases, Immune Thrombocytopenic Purpura, Leukemia, Lung carcinoma, Lymphocytic Leukemia, Lymphoma, Malignant Neoplasm, Medulloblastoma, Megakaryocytic Leukemia, Monocytic Leukemia, Myelodysplasia, Myelodysplastic Syndrome, Myelofibrosis, Myeloid Leukemia, Platelet Alpha-Granule Deficiency, Platelet disorder, Platelet Storage Pool Deficiency, SEBASTIAN SYNDROME, Storage Pool Disease Of Platelets, T-Cell Lymphoma, Teratoma, Thrombasthenia, Von willebrand disorder
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405
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G elongation factor mitochondrial 1 |
COXPD1, EFG, EFG1, EFGM, EGF1, GFM, hEFG1, mtEF-G1 |
Curated: Combined oxidative phosphorylation deficiency, Developmental regression, Hepatoencephalopathy due to combined oxidative phosphorylation defect, Leigh syndrome
Unreviewed: Adenoma, Alzheimer disease, Arteriosclerosis, Atherosclerosis, Basal ganglia cysts, Biliary Tract Cancer, Biliary tract neoplasms, Blindness, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Brooke-Spiegler Syndrome, Cataract, Cervix carcinoma, Cholestasis, Chondrosarcoma, Combined Oxidative Phosphorylation Deficiency, Congenital disorder of glycosylation, Craniosynostosis, Endometriosis, Epilepsy, Epileptic encephalopathy, Factor vii deficiency, Glioblastoma, Hemophilia b, Hepatoencephalopathy, Huntington disease, Hypoplasia Of Corpus Callosum, Intellectual developmental disorder, Leigh Syndrome, Liver disease, Liver failure, Lung Cancer, Lung carcinoma, Metabolic syndrome, Microcephaly, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial encephalopathy, Motor delay, Myelodysplastic syndrome, Myelomonocytic Leukemia, Necrotizing encephalomyelopathy, Neoplasms, Neurodegenerative disorder, Nystagmus, Oxidative Phosphorylation Deficiency, Parkinson disease, Polymicrogyria, SEBASTIAN SYNDROME, Seizures, Skin Lesion, Venous thromboembolism
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406
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GTP dependent ribosome recycling factor mitochondrial 2 |
EF-G2mt, EFG2, MRRF2, MST027, MSTP027, RRF, RRF2, RRF2mt, hEFG2, mEF-G 2 |
Curated: Combined oxidative phosphorylation deficiency, Leigh syndrome, Mitochondrial disease, Sandhoff disease
Unreviewed: Arthrogryposis multiplex congenita, Combined Oxidative Phosphorylation Deficiency, Cytochrome-C Oxidase Deficiency, Developmental Delay, Developmental disability, Developmental regression, Diabetes mellitus, type 1, Dysarthria, Leigh Syndrome, MELAS Syndrome, Microcephaly, Mitochondrial Diseases, Mitochondrial trifunctional protein deficiency, Myopathy, Necrotizing encephalomyelopathy
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407
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|
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- |
- |
Curated: N/A
Unreviewed: N/A
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408
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|
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Gfo/Idh/MocA-like oxidoreductase domain containing 1 |
ADG-90, C6orf114 |
Curated: Breast cancer, Cardiovascular disease, Ischemic heart disease, Coronary artery disease, Gout, Hypertension, Myocardial ischemia, Oropharyngeal cancer
Unreviewed: Glioblastoma, Myocardial infarction, Renal Carcinoma, Renal cell carcinoma
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409
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|
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GFOD1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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410
|
|
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Gfo/Idh/MocA-like oxidoreductase domain containing 2 |
- |
Curated: Androgenetic alopecia
Unreviewed: Hypercholesterolemia, Panic disorder
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