271
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|
|
GALNT8 antisense upstream 1 |
GALNT8-DT |
Curated: N/A
Unreviewed: N/A
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272
|
|
|
Glucosylceramidase beta 1 |
GBA, GCB, GLUC |
Curated: Parkinson disease, Brain aneurysm, Dementia, Gaucher disease, Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome, Hereditary parkinson disease, Hyperlipidemia, Pulmonary hypertension, Hypertension, Lewy body disease, Movement disorder, Thrombocytopenia
Unreviewed: Action Myoclonus-Renal Failure Syndrome, Akinesia, Alzheimer disease, Amyotrophic Lateral Sclerosis, Anemia, Anetoderma, Anorexia, Anxiety disorder, Aortic valve calcification, Aphasia, Apraxia, Arteriovenous malformations, Arthritis, Arthrogryposis multiplex congenita, Ataxia, Atopic dermatitis, Atrophy, B-Cell Lymphoma, Behavioral Variant Of Frontotemporal Dementia, Blindness, Bone Disease, Brain disease, Burkitt`s Lymphoma, Canavan Disease, Cardiovascular disease, Cerebellar hypoplasia, Cerebral Atrophy, Cerebral cortical atrophy, Charcot-Marie-Tooth Disease, Cirrhosis, Cognition disorder, Cognitive disorder, Congenital Ichthyosis, Congenital microtia, Congenital Nonbullous Ichthyosiform Erythroderma, Congestive Heart Failure, Cortical development malformation, Craniocerebral trauma, Cystic Fibrosis, Deficiency Of Pyruvate Kinase, Delirium, Delusions, Dementia With Lewy Body, Dermatologic Disorders, Developmental Delay, Developmental regression, Diarrhea, Diffuse Lymphoma, DiGeorge Syndrome, Dwarfism, Dysarthria, Dyskinetic Syndrome, Dysphagia, Dyssomnia, Dystonia, Ectropion, Endometriosis, Epileptic encephalopathy, Esotropia, Essential tremor, Fetal Gaucher Disease, Frontotemporal dementia, Gastrointestinal disease, Gaucher Disease, Gaucher Disease-Ophthalmoplegia-Cardiovascular Calcification Syndrome, Glycogen storage disease, Gm1 gangliosidosis, Heart disease, Hematologic disease, Hematologic neoplasm, Hepatocellular carcinoma, Hereditary Parkinson`s Disease, High palate, Horizontal nystagmus, Huntington disease, Hydrocephalus, Hydrops Fetalis, Hyperkeratosis, Hypersensitivity, Hypersplenism, Hypoalphalipoproteinemia, Hypoxia, Ichthyosis, Ichthyosis Congenita, Impaired Cognition, Intracranial Aneurysm, Lafora Disease, Leukopenia, Lewy Body Disease, Lipoidosis, Liver carcinoma, Liver failure, Liver Fibrosis, Liver neoplasms, Lung Diseases, Lung neoplasms, Lymphoma, Major depressive disorder, Malignant Neoplasm, Memory disorders, Mental Depression, Metabolic Syndrome, Microcephaly, Micrognathism, Microstomia, Microtia, Mitochondrial disease, Mitral Valve Stenosis, Motor delay, Movement Disorders, Multiple myeloma, Multiple system atrophy, Myelodysplastic syndrome, Myoclonic Epilepsy, Myoclonic Seizures, Neoplasms, Nervous system disease, Nervous System Disorder, Netherton syndrome, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Niemann-Pick Disease, Non-Hodgkin lymphoma, Oculocerebrorenal syndrome, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Orthostatic hypotension, Osteonecrosis, Osteopenia, Osteosclerosis, Pancytopenia, Paralysis, Parkinsonian disease, Pena Shokeir syndrome, Pericardial effusion, Progressive Supranuclear Palsy, Psychotic disorders, Pulmonary arterial hypertension, Ramsay Hunt Paralysis Syndrome, Schizophrenia, Secondary parkinson disease, Senile Dementia, Skin disease, Sleep Disorders, Speech Disorders, Sphingomyelinase deficiency, Squamous cell carcinoma, Strabismus, Supranuclear gaze palsy, Supranuclear ophthalmoplegia, Tay-Sachs Disease, Thoracic hypoplasia, Thoracolumbar scoliosis, Tremor, Trichohepatoenteric Syndrome, Trismus, Turcot syndrome
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273
|
|
|
Glucosylceramidase beta 1 like, pseudogene |
Beta-GC, GBA, GBAP, GBAP1, GC, GLUC |
Curated: N/A
Unreviewed: N/A
|
274
|
|
|
Glucosylceramidase beta 2 |
AD035, NLGase, SPG46 |
Curated: Cerebellar ataxia, Spastic paraplegia, Dilated cardiomyopathy, Hereditary spastic paraplegia, Intellectual developmental disorder, Neurodevelopmental disorder, Parkinson disease, Polyneuropathy, Diabetes mellitus type 2, complex hereditary spastic paraplegia
Unreviewed: Asthenozoospermia, Ataxia, Atopic dermatitis, Atrophy Of Corpus Callosum, Cataract, Cerebellar Ataxia, Cerebellar Ataxia With Spasticity, Cerebellar atrophy, Cerebral Atrophy, Cerebral cortical atrophy, Cystic Fibrosis, Dementia, Distal amyotrophy, Dysarthria, Dysphagia, Gaucher Disease, Glaucoma, Hearing Loss, Henoch-Schonlein Nephritis, Huntington Disease, Hypoplasia Of Corpus Callosum, Impaired Cognition, Mental Depression, Mental retardation, Neoplasms, Nervous System Disorder, Niemann-Pick Disease, Nystagmus, Peripheral axonal neuropathy, Peripheral nervous system disease, Scoliosis, Sensorimotor neuropathy, Sleep deprivation, Spastic Ataxia, Spastic Paraplegia, Spinocerebellar ataxia, Trichohepatoenteric Syndrome
|
275
|
|
|
Glucosylceramidase beta 3 (gene/pseudogene) |
CBG, CBGL1, GLUC, KLRP |
Curated: Alzheimer disease, Ankylosing spondylitis, Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Central nervous system cancer, Complex regional pain syndrome, Gastroesophageal reflux disease, Glioblastoma, Glioma, Gout, Obsessive-compulsive disorder, Psoriasis, Schizophrenia, Substance abuse, Tourette syndrome
Unreviewed: Asthma, Choroid plexus papilloma, Colorectal neoplasm, Cushing`s Syndrome, Cystic Fibrosis, Diabetes Mellitus, Gaucher Disease, Granulomatosis With Polyangiitis, Liver carcinoma, Neoplasms, Neuroblastoma, Neuroendocrine Tumors, Stomach Carcinoma, Stomach Neoplasms, Stroke
|
276
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
277
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
278
|
|
|
1,4-alpha-glucan branching enzyme 1 |
APBD, GBE, GSD4 |
Curated: Adult polyglucosan body disease, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Cervical cancer, Cutis laxa, Glycogen storage disease, Interstitial lung disease, Metabolic syndrome, Neurotic disorder, Osteogenesis imperfecta, Pena-shokeir syndrome , Polyneuropathy, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Scoliosis, Substance abuse, Diabetes mellitus type 2, Vascular dementia, glycogen storage disease due to glycogen branching enzyme deficiency
Unreviewed: Akinesia, Atrophy, Autism, B-Cell Lymphoma, Carcinogenesis, Cardiomyopathy, Carnitine palmitoyl transferase deficiency, Chylomicron Retention Disease, Cirrhosis, Congenital disorder of glycosylation, Congenital myopathy, Cytochrome-C Oxidase Deficiency, Dementia, Diabetes Mellitus, Dilated cardiomyopathy, Esophageal varix, Esophagus Neoplasm, Gerstmann-Straussler-Scheinker syndrome, Glycogen Storage Disease, Hydrops Fetalis, Hypoxia, Impaired Cognition, Leukemia, Leukodystrophy, Liver failure, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Melanoma, Mental retardation, Metabolic Diseases, Mitochondrial Diseases, Mitochondrial trifunctional protein deficiency, Multiple Pterygium Syndrome, Multiple Sclerosis, Myopathy, Neoplasms, Nervous system disease, Neurogenic bladder, Neurogenic Urinary Bladder, Neuromuscular disease, Obesity, Ovarian neoplasm, Paraplegia, Pena Shokeir syndrome, Peripheral axonal neuropathy, Polyglucosan Body Disease, Polyglucosan body myopathy, Porphyria, Portal Hypertension, Spastic Paraplegia, Spinal muscular atrophy, Spinocerebellar ataxia, Stroke, Uterine neoplasm
|
279
|
|
|
Golgi brefeldin A resistant guanine nucleotide exchange factor 1 |
ARF1GEF, CMT2GG, CMTDI2, CMTDIA |
Curated: Anterior segment dysgenesis, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Axonal neuropathy, Cannabis abuse, Congenital cataract, Charcot-marie-tooth disease, Digestive system disease, Epilepsy, Generalized epilepsy, Parkinson disease, Partial epilepsy, Uterine fibroid
Unreviewed: N/A
|
280
|
|
|
Globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group) |
A3GALNT, FS, UNQ2513 |
Curated: Breast cancer, Rheumatoid arthritis, Systemic lupus erythematosus, Venous thromboembolism
Unreviewed: Celiac disease, Malignant Neoplasm, Ovarian cancer, Ovarian diseases, Ovarian Epithelial carcinoma, Ovarian neoplasm
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