81
|
|
|
Potassium voltage-gated channel subfamily C member 1 |
EPM7, KV3.1, KV4, NGK2 |
Curated: Neurodevelopmental disorder, Progressive myoclonic epilepsy, Non-specific syndromic intellectual disability, progressive myoclonus epilepsy, complex neurodevelopmental disorder
Unreviewed: Action Myoclonus-Renal Failure Syndrome, Alzheimer disease, Ataxia, Attention Deficit Hyperactivity Disorder, Congenital abnormalities, Dentatorubral Pallidoluysian Atrophy, Developmental Delay, Developmental regression, Dysarthria, Epilepsy, Epileptic encephalopathy, Inclusion-Body Disease, Intellectual developmental disorder, Long qt syndrome, May-White Syndrome, Mental retardation, Myoclonic Epilepsy, Myoclonic Seizures, Progressive Myoclonic Epilepsy, Seizure, Seizures, Seminoma
|
82
|
|
|
Potassium voltage-gated channel subfamily C member 2 |
DEE103, KV3.2 |
Curated: Attention deficit hyperactivity disorder, Developmental and epileptic encephalopathy, Neurotic disorder, Obesity, Schizophrenia, Scoliosis, Spondylosis, Substance abuse, Vascular dementia, genetic developmental and epileptic encephalopathy
Unreviewed: Absence epilepsy, Autism, Childhood obesity, Diabetes, Diabetes Mellitus, Epilepsy, Episodic ataxia, Generalized epilepsy, Glioma, Partial epilepsy, Seizures
|
83
|
|
|
Potassium voltage-gated channel subfamily C member 3 |
KSHIIID, KV3.3, SCA13 |
Curated: Spinocerebellar ataxia, spinocerebellar ataxia type 13
Unreviewed: Ataxia, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar diseases, Cognition disorder, Development Disorder, Developmental Delay, Developmental disability, Dwarfism, Dysarthria, Dysphagia, Epilepsy, Friedreich Ataxia, Intellectual developmental disorder, Mental retardation, Motor delay, Nervous System Disorder, Neurodegenerative Disorders, Nystagmus, Optic Atrophy, Spinocerebellar Ataxia, Upgaze palsy
|
84
|
|
|
Potassium voltage-gated channel subfamily C member 4 |
C1orf30, HKSHIIIC, KSHIIIC, KV3.4 |
Curated: Temporal lobe epilepsy, Oropharyngeal cancer, Upper aerodigestive tract neoplasm
Unreviewed: Autism, Diabetes Mellitus, Epilepsy, Malignant Neoplasm Of Lateral Wall Of Oropharynx, Malignant Neoplasm Of Oropharynx, Malignant tumor of posterior wall of oropharynx, Mason type diabetes, Oropharyngeal Carcinoma, SeSAME Syndrome
|
85
|
|
|
KCNC4 divergent transcript |
KCNC4-AS1, LINC02586 |
Curated: N/A
Unreviewed: N/A
|
86
|
|
|
Potassium voltage-gated channel subfamily D member 1 |
KV4.1 |
Curated: N/A
Unreviewed: Growth disorder, Infertility, Nonobstructive azoospermia, Stomach neoplasms
|
87
|
|
|
Potassium voltage-gated channel subfamily D member 2 |
KV4.2, RK5 |
Curated: Androgenetic alopecia, Eczema, Attention deficit hyperactivity disorder, Cholangiocarcinoma, Neurodevelopmental disorder, Myoclonic encephalopathy, Insomnia, Non-specific syndromic intellectual disability, Prostate cancer, Substance abuse, Uterine fibroid, KCND2-related neurodevelopmental disorder with or without seizures
Unreviewed: Atrial fibrillation, Autism, Brugada Syndrome, Cerebral Infarction, Epilepsy, Glioblastoma, Glioma, Liver carcinoma, Long QT Syndrome, Lymphoma, Major depressive disorder, Paroxysmal atrial fibrillation, Seizures, Stomach Carcinoma, Stomach Neoplasms
|
88
|
|
|
Potassium voltage-gated channel subfamily D member 3 |
BRGDA9, KCND3L, KCND3S, KSHIVB, KV4.3, SCA19, SCA22 |
Curated: Atrial fibrillation, Breast cancer, Brugada syndrome, Cardiac arrhythmia, Ectopic rhythm, Hereditary ataxia, Intellectual developmental disorder, Neurodevelopmental disorder, Prostate cancer, Spinocerebellar ataxia, Diabetes mellitus type 2
Unreviewed: Amelogenesis Imperfecta, Apraxia, Asthma, Ataxia, Atherosclerosis, Atrial Fibrillation, Atrial flutter, Atrioventricular block, Attention deficit hyperactivity disorder, Autism, Blood coagulation disorder, Brain disease, Brugada Syndrome, Bundle Branch Block, Cardiac arrhythmias, Cardiac conduction disease, Cerebellar Ataxia, Cerebellar atrophy, Chronobiology disorder, Cognition disorder, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Congestive Heart Failure, Developmental and epileptic encephalopathy, Developmental disability, Diabetes Mellitus, Dysarthria, Dyslipidemias, Dysphagia, Dystonia, Epilepsy, Episodic ataxia, Esophagus Neoplasm, Heart Failure, Hypertension, Impaired Cognition, Keratoconus, Long QT Syndrome, Mental retardation, Microvascular angina, Multiple myeloma, Myoclonic Epilepsy, Neurodegenerative disorder, Neurodegenerative Disorders, Nystagmus, Osteoporosis, Parkinson disease, Paroxysmal atrial fibrillation, Paroxysmal ventricular fibrillation, Paroxysmal ventricular tachycardia, Renal cell carcinoma, Secondary parkinson disease, Seizures, Sick Sinus Syndrome, Sinus Node Dysfunction, Spinocerebellar Ataxia, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Supraventricular tachycardia, Trifascicular block, Ventricular Fibrillation, Ventricular tachycardia, Visual disorder
|
89
|
|
|
KCND3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
90
|
|
|
KCND3 intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
|