6681
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Potassium two pore domain channel subfamily K member 18 |
K2p18.1, MGR13, TRESK, TRESK-2, TRESK2, TRIK |
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6682
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Potassium two pore domain channel subfamily K member 2 |
K2p2.1, TPKC1, TREK, TREK-1, TREK1, hTREK-1c, hTREK-1e |
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6683
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Potassium two pore domain channel subfamily K member 3 |
K2p3.1, OAT1, PPH4, TASK, TASK-1, TASK1, TBAK1 |
Cardiovascular disease, Cerebrovascular disorder, Corneal astigmatism, Coronary artery disease, Diverticular disease, Hypertension, Pulmonary hypertension, Heart failure, Pulmonary arterial hypertension, Major depressive disorder, Metabolic syndrome, Osteoarthritis, Potassium deficiency, Sarcoidosis, Stroke, Diabetes mellitus type 2, pulmonary hypertension, primary, 4, neurodevelopmental disorder, kcnk3-relatedView all (3 more) |
6684
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Potassium two pore domain channel subfamily K member 4 |
FHEIG, K2p4.1, TRAAK, TRAAK1 |
Facial dysmorphism syndrome, Intellectual developmental disorder, facial dysmorphism, hypertrichosis, epilepsy, intellectual and developmental delay, and gingival overgrowth syndrome (fheig), facial dysmorphism, hypertrichosis, epilepsy, intellectual and developmental delay, and gingival overgrowth syndrome, facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome, gingival overgrowth, neurodevelopmental delay, intellectual disability, hypertrichosis, seizures |
6685
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Potassium two pore domain channel subfamily K member 5 |
K2p5.1, KCNK5b, TASK-2, TASK2 |
Eczema, Cardiovascular disease, Coronary artery disease, Eating disorder, Gout, Hypertension, Major depressive disorder, Migraine, Myocardial infarction, Nephrolithiasis, Obesity, Open angle glaucoma, Pancreatic cancer, Status epilepticus, Diabetes mellitus type 2, Urolithiasis, Vascular dementiaView all (2 more) |
6686
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Potassium two pore domain channel subfamily K member 6 |
K2p6.1, KCNK8, TOSS, TWIK-2, TWIK2 |
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6687
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Potassium two pore domain channel subfamily K member 7 |
K2p7.1, TWIK3 |
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6688
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Potassium two pore domain channel subfamily K member 9 |
BIBARS, K2p9.1, KT3.2, TASK-3, TASK3, TASK32 |
Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Birk-barel syndrome, Color vision deficiency, Colorectal cancer, Dementia, Developmental disability, Absence epilepsy, Major depressive disorder, Mood disorder, Obesity, Psychiatric disorders, Schizophrenia, Scoliosis, Uterine fibroid, birk-barel mental retardation dysmorphism syndromeView all (3 more) |
6689
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Potassium calcium-activated channel subfamily M alpha 1 |
BKTM, CADEDS, IEG16, KCa1.1, LIWAS, MaxiK, PNKD3, SAKCA, SLO, SLO-ALPHA, SLO1, bA205K10.1, hSlo, mSLO1 |
Alzheimer disease, Androgenetic alopecia, Angioedema, Autism, Bell's palsy, Bone disease, Renal cell carcinoma, Cerebellar atrophy with seizures and variable developmental delay, Color vision deficiency, Generalized epilepsy, Idiopathic generalized epilepsy, Eye disease, Gingival diseases, Global developmental delay, Growth disorder, Pulmonary hypertension, Hypospadias, Intellectual developmental disorder, Lung cancer, Metabolic bone disorder, Metabolic syndrome, Obesity, Nonalcoholic fatty liver disease, Non-melanoma skin carcinoma, Osteoarthritis, Osteonecrosis, Paroxysmal nonkinesigenic dyskinesia, Willis-ekbom disease, Schizophrenia, Spastic ataxia, Status epilepticus, Diabetes mellitus type 2, developmental delay, seizures and cerebellar atrophy, generalized epilepsy and paroxysmal dyskinesia, paroxysmal non-kinesigenic dyskinesia 3 with or without generalized epilepsy, epilepsy, idiopathic generalized 16, liang-wang syndrome, cerebellar atrophy, developmental delay, and seizures, generalized epilepsy-paroxysmal dyskinesia syndrome, paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy, epilepsy, idiopathic generalized, susceptibility to, 16View all (26 more) |
6690
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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 |
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