1101
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Glutamate ionotropic receptor NMDA type subunit 1 |
DEE101, GluN1, MRD8, NDHMSD, NDHMSR, NMD-R1, NMDA1, NMDAR1, NR1, hNR1 |
Curated: Autism, Nonsyndromic intellectual disability, Bilateral generalized polymicrogyria, Bipolar disorder, Ischemic stroke, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Rolandic epilepsy, Hemimegalencephaly, Hyperalgesia, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Psychotic disorders, Trigeminal neuralgia, complex neurodevelopmental disorder
Unreviewed: N/A
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1102
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Glutamate ionotropic receptor NMDA type subunit 2A |
EPND, FESD, GluN2A, LKS, NMDAR2A, NR2A |
Curated: Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Kidney disease, Colorectal neoplasms, Neurodevelopmental disorder, Continuous spike and wave during slow wave sleep syndrome, Continuous spike and wave during sleep syndrome, Vascular dementia, Bipolar depression, Major depressive disorder, Developmental and epileptic encephalopathy, Partial epilepsy, Epilepsy, Familial temporal lobe epilepsy, Focal epilepsy with speech disorder and impaired intellectual development, Pyridoxine dependent epilepsy, Rolandic epilepsy, Global developmental delay, Huntington disease, Hypertension, Intellectual developmental disorder, Language development disorders, Melanoma, Mood disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Schizophrenia, Scoliosis, Substance abuse, Tourette syndrome, complex neurodevelopmental disorder
Unreviewed: Absence Seizure, Agnosia, Alzheimer disease, Amyotrophic Lateral Sclerosis, Anxiety Disorder, Aphasia, Apraxia, Ataxia, Atrophy, Attention Deficit Hyperactivity Disorder, Auditory processing disorder, Autism spectrum disorder, Autoimmune Diseases, Basal cell carcinoma, Benign Rolandic Epilepsy, Bilateral convulsive seizures, Bipolar Disorder, Brain disease, Brunner syndrome, Cerebral Infarction, Cerebral Ischemia, Cirrhosis, Cognition disorder, Colorectal Cancer, Colorectal Neoplasms, Congenital abnormalities, Congenital adrenal hyperplasia, Congenital heart defects, Congenital Microcephaly, Continuous spike and waves during slow sleep, Cortical development malformation, Cortical Dysplasia, Delirium, Developmental Delay, Developmental disability, Diabetes, Diabetes Mellitus, Diastrophic dysplasia, Dwarfism, Dysarthria, Dyskinetic Syndrome, Dyslalia, Dysphasia, Epilepsy, Focal, With Speech Disorder And With Or Without Mental Retardation, Epileptic encephalopathy, Epileptic Encephalopathy And Intellectual Disability, Fabry disease, Febrile seizures, Focal cortical dysplasia, Focal Seizures, Fragile X Syndrome, Ganglioglioma, Hemifacial seizures, Huntington Disease, Hyperhomocysteinemia, Hypoplasia Of Corpus Callosum, Hypotension, Impaired Cognition, Infantile Spasms, Irritable Bowel Syndrome, Ischemic Stroke, Landau-Kleffner Syndrome, Language Development Disorders, Language Disorders, Laryngospasm, Liver Cirrhosis, Lung disease, Lupus Erythematosus, Lupus Vulgaris, Malignant Neoplasm, Manic Disorder, Mental Depression, Mental Disorders, Mental retardation, Migraine, Mixed Anxiety And Depressive Disorder, Mood Disorder, Mood swings, Movement disorder, Movement Disorders, Multiple polyposis syndrome, Multiple sclerosis, Myeloproliferative disorder, Myoclonic dystonia, Myoclonic epilepsy, Nasopharyngeal Carcinoma, Neoplasms, Nervous System Disorder, Neurodegenerative disorder, Neurodevelopmental Disorders, Neuropsychiatric Systemic Lupus Erythematosus, Nonorganic Psychosis, Obesity, Osteoglosphonic dysplasia, Papillary thyroid cancer, Paraneoplastic syndrome, Parkinson disease, Peripheral Neuropathy, Periventricular leukomalacia, Psychosis, Rheumatoid arthritis, Rolandic Epilepsy, Rolandic Epilepsy-Speech Dyspraxia Syndrome, Salaam Seizures, Seizure, Seizures, Septicemia, Sleep Apnea, Specific Learning Disorder, Speech Delay, Speech Disorders, Spherocytosis, Spinal Muscular Atrophy, Squamous cell carcinoma, Status Epilepticus, Stereotypy, Stress Disorder, Stroke, Trigeminal neuralgia, West Syndrome
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1103
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Glutamate ionotropic receptor NMDA type subunit 2B |
DEE27, EIEE27, GluN2B, MRD6, NMDAR2B, NR2B, NR3, hNR3 |
Curated: Alzheimer disease, Astigmatism, Autism, Nonsyndromic intellectual disability, Barrett esophagus, Behcet disease, Bipolar disorder, Cerebral palsy, Obstructive airway disease, Color vision deficiency, Colorectal cancer, Neurodevelopmental disorder, Craniosynostosis, Bipolar depression, Major depressive disorder, Developmental and epileptic encephalopathy, Developmental delay, Developmental disability, Epilepsy, Global developmental delay, Huntington disease, Hyperalgesia, Hypotension, Intellectual developmental disorder, Keratoconus, Non-specific syndromic intellectual disability, Dental caries, Schizophrenia, Scoliosis, Intellectual disability, Squamous cell carcinoma, Testicular disease, Urinary bladder cancer, West syndrome, complex neurodevelopmental disorder
Unreviewed: Agenesis Of Corpus Callosum, Amnesia, Amyloidosis, Androgen insensitivity syndrome, Anorexia, Anxiety Disorder, Aplasia Cutis Congenita, Arthritis, Attention Deficit Hyperactivity Disorder, Auditory perceptual disorder, Autism spectrum disorder, Basal ganglia disease, Behavior Disorders, Bipolar Disorder, Brain disease, Brain Neoplasms, Breast neoplasm, Brunner syndrome, Carcinoma, Catatonia, Central nervous system disease, Cholangiocarcinoma, Cirrhosis, CNS Disorder, Cognition disorder, Cognitive disorder, Colorectal Cancer, Colorectal neoplasm, Congenital Epicanthus, Cortical development malformation, Cortical Dysplasia, Delirium, Dementia, Development Disorder, Developmental Delay, Developmental dyslexia, Developmental regression, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetic Neuralgia, Disruptive, impulse control, and conduct disorders, Dyskinetic Syndrome, Dyslexia, Dysphagia, Epileptic encephalopathy, Esophageal neoplasm, Esophagus Neoplasm, Fabry disease, Febrile seizures, Focal cortical dysplasia, Glaucoma, Glioma, Huntington Disease, Hyperkinesia, Hyperplasia, Hypothyroidism, Impaired Cognition, Impulse control disorder, Infantile Spasms, Intestinal disease, Iron overload, Irritable Bowel Syndrome, Ischemic Stroke, Lafora disease, Language development disorders, Language Disorders, Learning Disorders, Leukemia, Liver Cirrhosis, Lung carcinoma, Lupus Erythematosus, Macrotia, Macular dystrophy, Malformation of cortical development, Malignant Bone Neoplasm, Meleda Disease, Memory Disorders, Mental Depression, Mental Disorders, Mental retardation, Microcephaly, Migraine, Mood Disorder, Movement Disorders, Multiple Sclerosis, Myoclonic Astatic Epilepsy, Neoplasms, Nervous System Disorder, Neurodegenerative disorder, Neurodegenerative Disorders, Neurodevelopmental Disorders, Neuropsychiatric Systemic Lupus Erythematosus, Neuroticism, Night blindness, congenital stationary, Non-Syndromic Intellectual Disability, Nonorganic Psychosis, Noonan Syndrome, Obsessive-Compulsive Disorder, Open angle glaucoma, Osteoarthritis, Osteoglosphonic dysplasia, Paraneoplastic syndrome, Parkinson disease, Partial epilepsy, Peripheral Neuropathy, Psychosis, Pulmonary arterial hypertension, Renal cell carcinoma, Rett Syndrome, Sarcoma, Seizures, Senile Dementia, Septicemia, Smith-Magenis Syndrome, Spasms Syndrome, Status Epilepticus, Stomach Carcinoma, Stomach Neoplasms, Stroke, Subarachnoid hemorrhage, Synophrys, Temporal lobe epilepsy, Thyroid disease, Tourette Syndrome, Visual disorder, West Syndrome
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1104
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Glutamate ionotropic receptor NMDA type subunit 2C |
GluN2C, NMDAR2C, NR2C |
Curated: Alzheimer disease, Auditory neuropathy with optic atrophy, Hyperopia, Schizophrenia
Unreviewed: Bipolar disorder, Cerebral Infarction, Epilepsy, Ischemic Stroke, Mental Disorders, Neoplasms, Parkinson disease, Sleep disorder, Tuberous Sclerosis
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1105
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Glutamate ionotropic receptor NMDA type subunit 2D |
DEE46, EB11, EIEE46, GluN2D, NMDAR2D, NR2D |
Curated: Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Endometriosis, Non-specific syndromic intellectual disability, Schizophrenia, complex neurodevelopmental disorder
Unreviewed: Alzheimer disease, Anhedonia, Attention Deficit Hyperactivity Disorder, Autism, Brain disease, Breast Cancer, Breast neoplasm, Central Visual Impairment, Cerebral Atrophy, Coronary artery disease, Developmental Delay, Developmental regression, Dwarfism, Dyskinetic Syndrome, Dysphagia, Epilepsy, Epileptic encephalopathy, Gastroesophageal Reflux Disease, Herpetic keratitis, Hypodontia, Impaired Cognition, Major depressive disorder, Malignant Neoplasm, Mental Depression, Mental Disorders, Mental retardation, Microcephaly, Nervous System Disorder, Neurodegenerative Disorders, Non-Specifi Epileptic Encephalopathy, Nystagmus, Optic Atrophy, Parkinson disease, Ptosis, Shared Paranoid Disorder, Status Epilepticus, Stomach neoplasms, Triple negative breast cancer, Tropical spastic paraparesis
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1106
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Glutamate ionotropic receptor NMDA type subunit 3A |
GluN3A, NMDAR-L, NMDAR3A, NR3A |
Curated: Bipolar disorder, Coronary aneurysm, Erectile dysfunction, Interstitial lung disease, Metabolic syndrome, Obesity, Schizophrenia, Diabetes mellitus type 2
Unreviewed: Aural Atresia, Congenital, Autoimmune Diseases, Bipolar Disorder, Cerebral palsy, Congenital disorder of glycosylation, Congenital macrodactylia, Coronary Aneurysm, Delirium, Erectile Dysfunction, Huntington Disease, Intellectual developmental disorder, Kawasaki disease, Nervous System Disorder, Osteonecrosis, Periventricular leukomalacia
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1107
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Glutamate ionotropic receptor NMDA type subunit 3B |
GluN3B, NR3B |
Curated: Alzheimer disease, Dementia, Neurodevelopmental disorder
Unreviewed: Amyotrophic Lateral Sclerosis, Breast Cancer, Breast Carcinoma, Epilepsy, Melanoma, Prostatic neoplasm, Schizophrenia
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1108
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Glutamate ionotropic receptor NMDA type subunit associated protein 1 |
HNRGW, LFG1, NMDARA1, TMBIM3 |
Curated: N/A
Unreviewed: Alzheimer disease, Arthritis, Celiac disease, Cerebral Ischemia, Dyslipidemias, Huntington Disease, Ischemic Stroke, Major depressive disorder, Osteoarthritis, Osteoarthritis Of Hip, Schizophrenia, Stomach Carcinoma, Stomach Neoplasms, Stroke, Transient Ischemic Attack
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1109
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Glutamate receptor interacting protein 1 |
FRASRS3, GRIP |
Curated: Alzheimer disease, Autoimmune thrombocytopenic purpura, Cryptophthalmos syndrome, Fraser syndrome, Intellectual developmental disorder, Lymphoid leukemia, Multiple myeloma, fraser syndrome 3
Unreviewed: N/A
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1110
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Glutamate receptor interacting protein 2 |
- |
Curated: Breast cancer, Estrogen-receptor negative breast cancer, Scoliosis, Stroke
Unreviewed: Breast neoplasm, Diabetes mellitus, type 2, Squamous cell carcinoma
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