291
|
|
|
Glutamate ionotropic receptor kainate type subunit 3 |
EAA5, GLR7, GLUR7, GluK3, GluR7a |
|
292
|
|
|
Glutamate ionotropic receptor kainate type subunit 4 |
EAA1, GRIK, GluK4, GluK4-2, KA1 |
|
293
|
|
|
Glutamate ionotropic receptor kainate type subunit 5 |
EAA2, GRIK2, GluK5, KA2 |
|
294
|
|
|
Glutamate ionotropic receptor NMDA type subunit 1 |
DEE101, GluN1, MRD8, NDHMSD, NDHMSR, NMD-R1, NMDA1, NMDAR1, NR1, hNR1 |
Autism, Bipolar disorder, Cerebral atrophy, Developmental delay, Dyskinetic syndrome, Dysmorphic features, Epilepsy, Epileptic encephalopathy, Febrile seizures, Frontal bossing, Hypoplasia of corpus callosum, Mental retardation, Movement disorders, Neurodevelopmental disorder with hyperkinetic movements without seizures, Neurodevelopmental disorder with or without hyperkinetic movements and seizures, Non-syndromic intellectual disability, Polymicrogyria, Psychosis, Schizoaffective disorder, Schizophreniform disorders, Scoliosis, Strabismus, Trigeminal neuralgiaView all (8 more) |
295
|
|
|
Glutamate ionotropic receptor NMDA type subunit 2A |
EPND, FESD, GluN2A, LKS, NMDAR2A, NR2A |
Absence seizure, Agnosia, Anxiety disorder, Aphasia, Apraxia, Attention deficit hyperactivity disorder, Auditory processing disorder, Autism, Benign rolandic epilepsy, Bilateral convulsive seizures, Bipolar disorder, Colorectal cancer, Colorectal neoplasms, Congenital microcephaly, Continuous spike and waves during slow sleep, Developmental delay, Dwarfism, Dysarthria, Dyslalia, Dysphasia, Epilepsy, Epilepsy, focal, with speech disorder and with or without mental retardation, Epileptic encephalopathy and intellectual disability, Febrile seizures, Focal seizures, Hemifacial seizures, Hypoplasia of corpus callosum, Mental retardation, Landau-kleffner syndrome, Language development disorders, Laryngospasm, Manic disorder, Melanoma, Mental depression, Migraine, Mood disorder, Mood swings, Rolandic epilepsy, Rolandic epilepsy-speech dyspraxia syndrome, Salaam seizures, Schizophrenia, Seizure, Sleep apnea, Specific learning disorder, Speech delay, Speech disorders, StereotypyView all (32 more) |
296
|
|
|
Glutamate ionotropic receptor NMDA type subunit 2B |
DEE27, EIEE27, GluN2B, MRD6, NMDAR2B, NR2B, NR3, hNR3 |
Astigmatism, Autism spectrum disorder, Autism, Bipolar disorder, Congenital epicanthus, Craniosynostosis, Developmental delay, Developmental regression, Dyskinetic syndrome, Dysphagia, Epilepsy, Epileptic encephalopathy, Impaired cognition, Mental retardation, Leukemia, Macrotia, Mental depression, Neurodevelopmental disorders, Non-syndromic intellectual disability, Schizophrenia, Scoliosis, Spasms syndrome, Synophrys, West syndromeView all (9 more) |
297
|
|
|
Glutamate ionotropic receptor NMDA type subunit 2C |
GluN2C, NMDAR2C, NR2C |
|
298
|
|
|
Glutamate ionotropic receptor NMDA type subunit 2D |
DEE46, EB11, EIEE46, GluN2D, NMDAR2D, NR2D |
Attention deficit hyperactivity disorder, Autism, Breast cancer, Central visual impairment, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Dysphagia, Endometriosis, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Mental retardation, Microcephaly, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Schizophrenia, Status epilepticusView all (7 more) |
299
|
|
|
Glutamate metabotropic receptor 1 |
GPRC1A, MGLU1, MGLUR1, PPP1R85, SCA44, SCAR13 |
Spinocerebellar ataxia, Attention deficit hyperactivity disorder, Cerebellar atrophy, Chondromyxoid fibroma, Colorectal cancer, Congenital cerebellar ataxia, Developmental delay, Dwarfism, Dysarthria, Dysphagia, Epilepsy, Esotropia, Fibroma, Fibromatosis, Grand mal status epilepticus, Horizontal nystagmus, Mental depression, Mental retardation, Minimal brain dysfunction, Motor delay, Myxofibroma, Neoplasms of bone tissue, Nonconvulsive status epilepticus, Petit mal status, Polyneuropathy, Ptosis, Schizophrenia, Status epilepticusView all (13 more) |
300
|
|
|
Glutamate metabotropic receptor 2 |
GLUR2, GPRC1B, MGLUR2, mGlu2 |
|