141
|
|
|
Potassium calcium-activated channel subfamily M regulatory beta subunit 1 |
BKbeta1, K(VCA)beta, SLO-BETA, hbeta1, hslo-beta, k(VCA)beta-1, slo-beta-1 |
|
142
|
|
|
Potassium calcium-activated channel subfamily N member 1 |
KCa2.1, SK1, SKCA1, hSK1 |
|
143
|
|
|
Potassium calcium-activated channel subfamily N member 2 |
DYT34, KCa2.2, NEDMAB, SK2, SKCA2, SKCa 2, hSK2 |
|
144
|
|
|
Potassium calcium-activated channel subfamily N member 3 |
KCa2.3, SK3, SKCA3, ZLS3, hSK3 |
|
145
|
|
|
Potassium calcium-activated channel subfamily N member 4 |
DHS2, IK, IK1, IKCA1, KCA4, KCa3.1, SK4, SKCa4, hIK1, hIKCa1, hKCa4, hSK4 |
|
146
|
|
|
Potassium voltage-gated channel subfamily Q member 1 |
ATFB1, ATFB3, JLNS1, KCNA8, KCNA9, KVLQT1, Kv1.9, Kv7.1, LQT, LQT1, RWS, SQT2, WRS |
Adenocarcinoma, Adrenocortical carcinoma, Atrial fibrillation, Atrioventricular block, Beckwith-wiedemann syndrome, Carcinoma, Cardiomyopathy, Clinodactyly, Congenital epicanthus, Congenital hemihypertrophy, Congenital long qt syndrome, Congenital microcephaly, Congenital omphalocele, Congenital sensorineural hearing loss, Coronary heart disease, Cryptorchidism, Developmental delay, Diabetes mellitus, Dysautonomia, Gonadoblastoma, Gout, Gouty arthritis, Hepatoblastoma, High palate, Hypertrophic cardiomyopathy, Hyperuricemia, Intestinal neoplasms, Intestinal cancer, Iron deficiency anemia, Jervell-lange nielsen syndrome, Kidney failure, Leukemia, Long qt syndrome, Long qt syndrome digenic, Macroglossia, Marfan syndrome, Hypoglycemia, Hypotonia, Nephroblastoma, Nephrocalcinosis, Nephrolithiasis, Paroxysmal ventricular fibrillation, Phakomatosis pigmentovascularis, Proptosis, Romano-ward syndrome, Microcephaly, Sensorineural hearing loss, Short qt syndrome, Stroke, Thromboembolic stroke, Torsades de pointes, Ventricular arrhythmia, Ventricular fibrillation, Vesicoureteral reflux, Wolff-parkinson-white syndromeView all (40 more) |
147
|
|
|
Potassium voltage-gated channel subfamily Q member 2 |
BFNC, DEE7, EBN, EBN1, ENB1, HNSPC, KCNA11, KV7.2 |
Apraxia, Benign epilepsy, Benign rolandic epilepsy, Benign seizures and/or myokomia, Bipolar disorder, Cerebral atrophy, Choreoathetosis, Clonic seizures, Convulsions, Development disorder, Developmental delay, Dysgraphia, Dyskinetic syndrome, Dysmorphic features, Dysphasia, Epilepsy, Epilepsy, benign and/or myokymia, Epileptic encephalopathy, Esophagus neoplasm, Focal clonic seizures, Hallucinations, Hypoplasia of corpus callosum, Hypotonic seizures, Impaired cognition, Jacksonian seizure, Major affective disorder, Mental retardation, Migraine, Movement disorders, Nervous system disorder, Neurodevelopmental disorders, Salaam seizures, Schizophrenia, Seizure, Spasms x-linked, Spastic tetraparesisView all (21 more) |
148
|
|
|
Potassium voltage-gated channel subfamily Q member 3 |
BFNC2, EBN2, KV7.3 |
Angelman syndrome, Benign epilepsy, Bipolar disorder, Choreoathetosis, Developmental delay, Diabetes mellitus, Dyskinetic syndrome, Dysphasia, Epilepsy, Febrile seizures, Focal clonic seizures, Hallucinations, Impaired cognition, Mental retardation, Migraine, Mouth abnormalities, Myoclonic epilepsy, Photosensitive tonic-clonic seizures, Schizophrenia, Seizure, Status epilepticusView all (6 more) |
149
|
|
|
Potassium voltage-gated channel modifier subfamily S member 3 |
KV9.3 |
|
150
|
|
|
Kinase insert domain receptor |
CD309, FLK1, VEGFR, VEGFR2 |
Adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Capillary hemangioma, Carcinoma, Chondrodystrophic myotonia, Colorectal cancer, Colorectal neoplasms, Diabetic nephropathy, Dyschondroplasias, Epilepsy, Esophagus neoplasm, Glomerulosclerosis, Hemangioma, Hemangiosarcoma, Lung carcinoma, Lung adenocarcinoma, Malignant neoplasm, Marfan syndrome, Melnick-needles syndrome, Mental depression, Multiple epiphyseal dysplasia, Myocardial ischemia, Osteochondrodysplasia, Pancreatic neoplasm, Pancreatic cancer, Renal carcinoma, Schizophrenia, Schwartz-jampel syndrome, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia, Strawberry nevus of skin, Thrombosis, Uremia, Van buchem diseaseView all (21 more) |