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Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins. It may associate with two other G-protein-activated potassium channels to form a heteromultimeric pore-forming complex. [provided by RefSeq, Jul 2008]
[中文简述(自动翻译):]  钾通道存在于大多数哺乳动物细胞,在那里他们参与广泛的生理反应。由该基因编码的蛋白质是一种完整的膜蛋白和向内整流型钾通道。所编码的蛋白质,其具有更大的趋势,以允许钾流入细胞而不是出于细胞的,是由G蛋白控制。它可以与其它两种G蛋白活化的钾通道相关联,以形成异源多孔隙形成复合物。 [由RefSeq的,2008年7月提供]
KCNJ5基因(以及对应的蛋白质)的细胞分布位置:
KCNJ5基因的本体(GO)信息:
| 疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
| LONG QT SYNDROME 13 | 0.36 | 1 | 1 | CLINVAR_CTD_human_UNIPROT |
| HYPERALDOSTERONISM, FAMILIAL, TYPE III | 0.36 | 2 | 5 | CLINVAR_ORPHANET_UNIPROT |
| Andersen Syndrome | 0.240271442 | 1 | 2 | BeFree_CLINVAR_ORPHANET |
| Adenoma | 0.127871814 | 31 | 0 | BeFree_CTD_human |
| Romano-Ward Syndrome | 0.12 | 0 | 0 | ORPHANET |
| Conn Syndrome | 0.005157396 | 19 | 1 | BeFree |
| Cardiovascular Diseases | 0.00272435 | 1 | 0 | LHGDN |
| Lung Neoplasms | 0.00272435 | 1 | 0 | LHGDN |
| Atrial Fibrillation | 0.002367032 | 1 | 0 | GAD |
| Hyperaldosteronism | 0.001628651 | 6 | 0 | BeFree |
| Familial Hyperaldosteronism | 0.001628651 | 6 | 0 | BeFree |
| Congenital adrenal hyperplasia | 0.000814326 | 3 | 0 | BeFree |
| Hypertensive disease | 0.000814326 | 3 | 0 | BeFree |
| Fibrillation | 0.000814326 | 3 | 0 | BeFree |
| Adrenal hypertrophy or hyperplasia | 0.000814326 | 3 | 0 | BeFree |
| Adrenal hyperplasia | 0.000814326 | 3 | 0 | BeFree |
| Adrenal Gland Neoplasms | 0.000542884 | 2 | 0 | BeFree |
| Diabetes | 0.000542884 | 2 | 0 | BeFree |
| Diabetes Mellitus | 0.000542884 | 2 | 0 | BeFree |
| Long QT Syndrome | 0.000542884 | 2 | 1 | BeFree |
| Obesity | 0.000542884 | 2 | 0 | BeFree |
| Left Ventricular Hypertrophy | 0.000542884 | 2 | 0 | BeFree |
| Adrenocortical carcinoma | 0.000542884 | 2 | 1 | BeFree |
| Metabolic Syndrome X | 0.000542884 | 2 | 0 | BeFree |
| Hyperaldosteronism, Familial, Type II | 0.000542884 | 2 | 0 | BeFree |
| Diabetes Insipidus | 0.000271442 | 1 | 0 | BeFree |
| insulinoma | 0.000271442 | 1 | 0 | BeFree |
| Acute lymphocytic leukemia | 0.000271442 | 1 | 0 | BeFree |
| nervous system disorder | 0.000271442 | 1 | 0 | BeFree |
| Neuroblastoma | 0.000271442 | 1 | 0 | BeFree |
| Nodule | 0.000271442 | 1 | 0 | BeFree |
| Pheochromocytoma | 0.000271442 | 1 | 0 | BeFree |
| Gilles de la Tourette syndrome | 0.000271442 | 1 | 0 | BeFree |
| Li-Fraumeni Syndrome | 0.000271442 | 1 | 0 | BeFree |
| Essential Hypertension | 0.000271442 | 1 | 5 | BeFree |
| Adrenal Cortical Adenoma | 0.000271442 | 1 | 0 | BeFree |
| Carney Complex | 0.000271442 | 1 | 0 | BeFree |
| Central Diabetes Insipidus | 0.000271442 | 1 | 0 | BeFree |
| Chronic atrial fibrillation | 0.000271442 | 1 | 0 | BeFree |
| Central neuroblastoma | 0.000271442 | 1 | 0 | BeFree |
| Congenital long QT syndrome | 0.000271442 | 1 | 0 | BeFree |
| Brugada Syndrome (disorder) | 0.000271442 | 1 | 0 | BeFree |
| Attention deficit hyperactivity disorder | 0.000271442 | 1 | 0 | BeFree |
| Cortisone reductase deficiency | 0.000271442 | 1 | 0 | BeFree |
| Channelopathies | 0.000271442 | 1 | 0 | BeFree |
| Familial hyperaldosteronism type 3 | 0.000271442 | 1 | 0 | BeFree |
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