181
|
|
|
Potassium voltage-gated channel subfamily Q member 5 |
Kv7.5, MRD46 |
Curated: Angioedema, Nonsyndromic intellectual disability, Cataract, Central nervous system cancer, Obstructive pulmonary disease, Color vision deficiency, Eye disease, Glioblastoma, Glioma, Global developmental delay, Hyperopia, Insomnia, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Myopia, Periodontitis, Primary angle closure glaucoma, Proliferative diabetic retinopathy, Schizophrenia, Diabetes mellitus type 2
Unreviewed: Amyotrophic lateral sclerosis, Asthma, Atrial Fibrillation, Autism, Benign Epilepsy, Brain disease, Colorectal Cancer, Colorectal neoplasm, Cone-rod dystrophy, Congenital diaphragmatic hernia, Convulsions, Craniosynostosis, Developmental and epileptic encephalopathy, Developmental Delay, Developmental disability, Diarrhea, Epilepsy, Epileptic encephalopathy, Generalized epilepsy, Hypertension, Hypokalemic Periodic Paralysis, Irritable Bowel Syndrome, Mental Depression, Mental retardation, Morgagni diaphragmatic hernia, Multiple myeloma, Multiple sclerosis, Myeloid leukemia, Non-Syndromic Intellectual Disability, Posterolateral diaphragmatic hernia
|
182
|
|
|
KCNQ5 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
183
|
|
|
KCNQ5 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
184
|
|
|
KCNQ5 intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
|
185
|
|
|
Potassium channel regulator |
DLTET |
Curated: N/A
Unreviewed: Autoimmune polyendocrine syndrome type 1, Congenital Chromosomal Disease, Gastrointestinal stromal tumor, Liver carcinoma, Lymphocytic Leukemia, Lymphoma, Multiple myeloma, Neoplasms, Prostatic neoplasm, Prostatic Neoplasms
|
186
|
|
|
Potassium voltage-gated channel modifier subfamily S member 1 |
Kv9.1, hKv9.1 |
Curated: Bipolar disorder, Depression
Unreviewed: Anxiety Disorder, Intracranial hypertension, Major depressive disorder, Osteoporosis, Sensory neuropathy
|
187
|
|
|
Potassium voltage-gated channel modifier subfamily S member 2 |
KV9.2 |
Curated: N/A
Unreviewed: Tremor
|
188
|
|
|
Potassium voltage-gated channel modifier subfamily S member 3 |
KV9.3 |
Curated: Amyotrophic lateral sclerosis, Autism, Breast cancer, Obstructive pulmonary disease, Colorectal cancer, Conotruncal cardiac defect, Coronary artery disease, Gout, Ovarian epithelial cancer, Colorectal adenoma, Multinodular goiter, Oligodendroglioma, Ovarian cancer, Parkinson disease, Peptic ulcer disease, Schizophrenia, Scoliosis, Diabetes mellitus type 2
Unreviewed: Asthma, Impaired Cognition, Lung disease, Pulmonary arterial hypertension
|
189
|
|
|
Potassium sodium-activated channel subfamily T member 1 |
DEE14, EIEE14, ENFL5, KCa4.1, KNa1.1, SLACK, Slo2.2, bA100C15.2 |
Curated: Nocturnal frontal lobe epilepsy, Childhood-onset epilepsy syndrome, Color vision deficiency, Colorectal cancer, Developmental and epileptic encephalopathy, Developmental disability, Partial epilepsy, Epilepsy of infancy with migrating focal seizures, Frontal lobe epilepsy, Rolandic epilepsy, Gastrointestinal disease, Hydrocephalus, Malignant migrating partial seizures of infancy, Neurodevelopmental disorder, Schizophrenia, Scoliosis
Unreviewed: Amygdalo-Hippocampal Epilepsy, Amyotrophic Lateral Sclerosis, Atherosclerosis, Benign Occipital Epilepsy, Brain disease, Brugada syndrome, Cardiac arrhythmias, Cerebral cortical atrophy, Congenital abnormalities, Congestive Heart Failure, Cortical development malformation, Cyanosis, Demyelinating diseases, Development Disorder, Developmental regression, Digestive Epilepsy, Dilated cardiomyopathy, Dystonia, Epilepsy, Epileptic encephalopathy, Facial dysmorphism, Focal Epilepsy, Fragile X Syndrome, Generalized epilepsy, Heart disease, Heart Failure, Histiocytic medullary reticulosis, Hypoplasia Of Corpus Callosum, Impaired Cognition, Infantile spasms, Leukoencephalopathy, Mental Depression, Mental retardation, Microcephaly, Migrating Partial Seizures In Infancy, Movement disorder, Movement Disorders, Myoclonic epilepsy, Nocturnal Epilepsy, Panayiotopoulos Syndrome, Precocious puberty, Psychotic disorders, Quadriplegia, Rhinencephalic Epilepsy, Seizure, Seizures, Spasms X-Linked, Status Epilepticus, Subclinical Seizure, West Syndrome
|
190
|
|
|
Potassium sodium-activated channel subfamily T member 2 |
DEE57, EIEE57, KCa4.2, KNa1.2, SLICK, SLO2.1 |
Curated: Atrophic macular degeneration, Color vision deficiency, Developmental and epileptic encephalopathy, Macular degeneration, Major depressive disorder, Scoliosis, Age-related macular degeneration, complex neurodevelopmental disorder
Unreviewed: Absence Seizure, Breast Cancer, Developmental Delay, Developmental regression, Epilepsy, Epileptic encephalopathy, Exudative Macular Degeneration, Geographic Atrophy, Hypoplasia Of Corpus Callosum, Lennox-Gastaut Syndrome, Melanoma, Myoclonic Seizures, West Syndrome
|