651
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|
|
Glia maturation factor beta |
GMF |
Curated: N/A
Unreviewed: Alzheimer disease, Chorea, Diabetic retinopathy, Encephalitis, Glioblastoma, Lymphatic metastasis, Neoplasms, Nervous system disease, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy, Schizophrenia, Sleep deprivation, Thymoma, Uterine disease, Uterine neoplasm
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652
|
|
|
Glia maturation factor beta pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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653
|
|
|
Glia maturation factor gamma |
GMF-GAMMA |
Curated: Dyslexia, Lung cancer
Unreviewed: Bile duct neoplasms, Breast neoplasm, Cardiovascular Diseases, Colorectal Cancer, Coronary Arteriosclerosis, Glioblastoma, Glioma, Kidney disease, Lung neoplasms, Lymphatic metastasis, Melanoma, Metabolic Diseases, Myeloid leukemia, Myocardial Ischemia, Ovarian cancer, Ovarian Epithelial carcinoma, Pancreatic neoplasm, Prostatic neoplasm, Renal cell carcinoma, Squamous cell carcinoma, Testicular germ cell tumor, Testicular neoplasm, Triple negative breast cancer
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654
|
|
|
GEM interacting protein |
ARHGAP46 |
Curated: Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Metabolic syndrome, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2, Depression
Unreviewed: Cerebral hemorrhage, Impaired Cognition, Mental Depression
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655
|
|
|
Glycosylphosphatidylinositol anchored molecule like |
LY6DL |
Curated: Autism, Cardiovascular disease, Hypertension, Osteoarthritis, Primary aldosteronism
Unreviewed: Cardiovascular Diseases, Colorectal Cancer, Congenital adrenal hyperplasia, Corticosterone Methyl Oxidase Deficiency, Esophageal Carcinoma, Esophagus Neoplasm, Glioblastoma, Hyperaldosteronism, Lung carcinoma, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Malignant Neoplasm
|
656
|
|
|
Geminin coiled-coil domain containing |
GEMC1 |
Curated: Alzheimer disease, Dementia, Psoriasis
Unreviewed: Brain disease, Congenital Hydrocephalus, Developmental disability, Schizophrenia, Sclerosing Cholangitis
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657
|
|
|
Geminin DNA replication inhibitor |
Gem, MGORS6 |
Curated: Hepatocellular carcinoma, Desbuquois syndrome, Ear, patella, short stature syndrome, Meier-gorlin syndrome, meier-gorlin syndrome 6
Unreviewed: Adrenocortical carcinoma, Age-related macular degeneration, Amyloid Nephropathy, Amyloidosis, Amyotrophic Lateral Sclerosis, Aneuploidy, Ankylosing Spondylitis, Anotia, Aplastic anemia, Arthritis, Asthenozoospermia, Astrocytoma, Autism, Autism Spectrum Disorder, Autoimmune Diseases, Autoimmune hepatitis, Behcet Syndrome, Bile duct carcinoma, Birdshot Chorioretinopathy, Bladder carcinoma, Bladder Neoplasm, Bone marrow failure syndrome, Brachydactyly, Breast aplasia, Breast Cancer, Breast Carcinoma, Breast neoplasm, Burkitt`s Lymphoma, Camptodactyly of fingers, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Celiac disease, Cervical Intraepithelial Neoplasia, Cholangiocarcinoma, Chronic obstructive pulmonary disease, Cirrhosis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Common Variable Immunodeficiency, Complete Atrioventricular Block, Congenital diarrhea, Congenital Exomphalos, Congenital Hypoplasia Of Penis, Coronary Syndrome, Craniosynostosis, Crohn Disease, Cryptorchidism, Dermatitis, Dermatologic Disorders, Developmental Delay, Diabetes Mellitus, Diffuse Lymphoma, Down Syndrome, Dwarfism, Ear Diseases, Ear-Patella-Short Stature Syndrome, Eclampsia, Eczema, Endometrial stromal sarcoma, Entropion, Epispadias, Frontal bossing, Gaucher Disease, Glioblastoma, Graft-Vs-Host Disease, Graves Disease, Hashimoto Disease, Hearing Loss, Hematologic Neoplasms, Hodgkin Disease, Hodgkin Lymphoma, Huntington disease, Hypertension, Hypertrophy Of Clitoris, Hypoplasia of the maxilla, Hypospadias, Immune System Diseases, Immune Thrombocytopenic Purpura, Immunologic Deficiency Syndromes, Inflammatory Bowel Disease, Ischemic Stroke, Isolated Somatotropin Deficiency, Kaposi Sarcoma, Kidney Disease, Kidney Failure, Laryngeal Carcinoma, Leiomyosarcoma, Leprosy, Leukemia, Leukopenia, Lip and Oral Cavity Carcinoma, Lipodystrophy, Liver Cancer, Liver carcinoma, Liver Cirrhosis, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lupus Erythematosus, Lupus Vulgaris, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Lymphoproliferative Disorder, Lymphoproliferative Disorder Of Natural Killer Cells, Malignant Neoplasm, Malignant neoplasm of mouth, Mammary Neoplasms, Mandibular aplasia, Mantle Cell Lymphoma, Meier-Gorlin Syndrome, Melanoma, Mental retardation, Microcephaly, Micrognathism, Microstomia, Microtia, Migraine, Miller Dieker Syndrome, Miscarriage, Monocytic Leukemia, Motor delay, Mouth neoplasm, Mucinous Adenocarcinoma, Multiple myeloma, Multiple Sclerosis, MUNGAN SYNDROME, Muscular dystrophy, Myelodysplastic Syndrome, Myeloid Leukemia, Myeloproliferative disorder, Myotonic dystrophy, Nasopharyngeal Carcinoma, Neoplasms, Neuroblastoma, Neurodegenerative Disorders, Neurofibroma, Neutropenia, Obesity, Oral Ulcer, Osteoarthritis, Ovarian diseases, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Pancytopenia, Panic disorder, Papilloma, Paroxysmal nocturnal hemoglobinuria, Pemphigus Foliaceus, Pemphigus Vulgaris, Periodontal Diseases, Periodontitis, Pituitary dwarfism, Posteriorly Rotated Ear, Prostate cancer, Prostatic neoplasm, Pseudohyperkalemia Cardiff, Psoriasis, Psoriasis vulgaris, Psoriatic Arthritis, Rectal Carcinoma, Renal Carcinoma, Renal cell carcinoma, Respiratory Failure, Rheumatoid arthritis, Scleroderma, Seckel Syndrome, Septicemia, Skin cancer, Somatotropin Deficiency, Specific Learning Disorder, Spondyloarthritis, Squamous cell carcinoma, Stenosis Of External Auditory Canal, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Stroke, Submucosal cleft palate, Syndactyly, Syndromic microphthalmia, T-Cell Lymphoma, Teratoma, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Tracheomalacia, Trichohepatoenteric Syndrome, Triple negative breast cancer, Triple Negative Breast Neoplasms, Ulcerative colitis, Uranostaphyloschisis, Urinary bladder cancer, Urinary bladder neoplasms, Urothelial Carcinoma, Uterine disease, Uveitis, Uveomeningoencephalitic Syndrome
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658
|
|
|
GDP-mannose pyrophosphorylase A |
AAMR |
Curated: Glucocorticoid deficiency with achalasia, Intellectual disability with strabismus syndrome, Triple a syndrome, alacrima, achalasia, and intellectual disability syndrome
Unreviewed: Achalasia, Alacrima, Alacrima, Achalasia, And Mental Retardation Syndrome, Autonomic nervous system disease, Congenital Coloboma Of Iris, Congenital disorder of glycosylation, Developmental Delay, Developmental disability, Developmental regression, Down Syndrome, Dwarfism, Dysphagia, Esophageal achalasia, Glucocorticoid Deficiency With Achalasia, Hearing Loss, Hypopituitarism, Intellectual developmental disorder, Mental retardation, Microcephaly, Optic Atrophy, Palmoplantar keratoderma, Stomach neoplasms, Triple A Syndrome
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659
|
|
|
GDP-mannose pyrophosphorylase B |
LGMDR19, MDDGA14, MDDGB14, MDDGC14 |
Curated: Alzheimer disease, Limb girdle muscular dystrophy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital myasthenic syndrome, Congenital myopathy, Global developmental delay, Muscle eye brain disease, Muscular dystrophy, Myasthenic syndrome, Walker-warburg syndrome, myopathy caused by variation in GMPPB
Unreviewed: Agenesis Of Corpus Callosum, alpha-Dystroglycanopathy, Arthrogryposis, Autism, Cardiomyopathy, Cataract, Centronuclear Myopathy, Cerebellar Hypoplasia, Cerebral cortical atrophy, Cobblestone Lissencephaly, Congenital disorder of glycosylation, Congenital Keratoglobus, Congenital Meningocele, Congenital Muscular Dystrophy With Cerebellar Involvement, Congenital Muscular Dystrophy With Intellectual Disability, Congenital Muscular Dystrophy-Dystroglycanopathy With Brain And Eye Anomalies, Congenital Muscular Dystrophy-Dystroglycanopathy With Mental Retardation, Congenital Myasthenic Syndromes With Glycosylation Defect, Congenital ocular coloboma, Cryptorchidism, Developmental Delay, Epilepsy, Esotropia, Fabry disease, Facial paralysis, Facioscapulohumeral muscular dystrophy, Fukuyama Type Congenital Muscular Dystrophy, Generalized epilepsy, Glaucoma, Glioblastoma, Hearing Loss, Hemiplegia/hemiparesis, High palate, Holoprosencephaly, Hydrocephalus, Hypoplasia Of Corpus Callosum, Hypoplasia Of The Optic Nerve, Impaired Cognition, Lambert-Eaton Myasthenic Syndrome, Limb Muscle Atrophy, Limb-Girdle Muscular Dystrophy, Limb-Girdle Muscular Dystrophy-Dystroglycanopathy, Macroglossia, Mental retardation, Metabolic Myopathy, Microcephaly, Microphthalmos, Motor delay, Multiple Congenital Anomalies, Muscle Eye Brain Disease, Muscular Dystrophy-Dystroglycanopathy, Myasthenia Gravis, Myasthenic Syndrome, Myopathy, Myopia, Neuronal Heterotopia, Nystagmus, Occipital Encephalocele, Optic Atrophy, Penis Agenesis, Polymicrogyria, Ptosis, Respiratory Failure, Retinal Detachment, Retinitis Pigmentosa, Scoliosis, Speech Disorders, Strabismus, Walker-Warburg Congenital Muscular Dystrophy
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660
|
|
|
Guanosine monophosphate reductase |
GMPR 1, GMPR1, hGMPR-I |
Curated: Alzheimer disease, Juvenile arthritis, Central nervous system cancer, Glioblastoma, Glioma, Hypertrophic cardiomyopathy, Juvenile idiopathic arthritis, Major depressive disorder, Oligoarticular juvenile idiopathic arthritis
Unreviewed: Arthritis, Hyperoxaluria, Melanoma, Mental Depression, Mitochondrial disease, Myeloid leukemia, Polyarthritis, Rheumatoid Factor Positive, Seronegative polyarthritis, Still Disease
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