Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "K"

131 to 140 of 320 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
131	3763	KCNJ6	Potassium inwardly rectifying channel subfamily J member 6	BIR1, GIRK-2, GIRK2, KATP-2, KATP2, KCNJ7, KIR3.2, KPLBS, hiGIRK2	High palate, Mental retardation, Keppen-lubinsky syndrome, Lipodystrophy, Mental depression, Microcephaly, Micrognathism, Proptosis, Scoliosis, Spastic tetraparesis
132	3764	KCNJ8	Potassium inwardly rectifying channel subfamily J member 8	KIR6.1, uKATP-1	Atrial fibrillation, Atrioventricular block, Brugada syndrome, Bundle branch block, Cardiac conduction disease, Congenital epicanthus, Congenital exomphalos, Hypertrichotic osteochondrodysplasia, Hypertrophic cardiomyopathy, Macrocephaly, Macrostomia, Mental retardation, Myocardial ischemia, Osteochondrodysplasia, Osteoporosis View all (10 more)
133	3766	KCNJ10	Potassium inwardly rectifying channel subfamily J member 10	BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME	Cerebellar atrophy, Compensated hypothyroidism, Congenital sensorineural hearing loss, Deafness, Developmental delay, East syndrome, Glycosylphosphatidylinositol deficiency, Hearing loss, Hyperaldosteronism, Hyperparathyroidism, Hypokalemia, Hypothyroidism, Kidney disease, Spastic diplegia, Mental retardation View all (8 more)
134	3767	KCNJ11	Potassium inwardly rectifying channel subfamily J member 11	BIR, HHF2, IKATP, KIR6.2, MODY13, PHHI, PNDM2, TNDM3	Apraxia, Arthrogryposis multiplex congenita, Autoimmune diabetes, Camptodactyly of fingers, Clinodactyly, Clonic seizures, Congenital heart defects, Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Coronary heart disease, Dend syndrome, Dermatitis, Developmental delay, Diabetes mellitus, Diabetes mellitus, with neurologic features View all (28 more)
135	3769	KCNJ13	Potassium inwardly rectifying channel subfamily J member 13	KIR1.4, KIR7.1, LCA16, SVD	Cataract, Ciliopathies, Congenital cerebral hernia, Coronary artery disease, Developmental delay, Disorder of eye, Hemiplegia/hemiparesis, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Nyctalopia, Nystagmus, Snowflake vitreoretinal degeneration, Vitreoretinal degeneration
136	3772	KCNJ15	Potassium inwardly rectifying channel subfamily J member 15	IRKK, KIR1.3, KIR4.2	Arthritis, Breast cancer, Juvenile arthritis, Leukemia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease
137	3775	KCNK1	Potassium two pore domain channel subfamily K member 1	DPK, HOHO, K2P1, K2p1.1, KCNO1, TWIK-1, TWIK1	Chronic obstructive pulmonary disease, Ischemic stroke
138	3776	KCNK2	Potassium two pore domain channel subfamily K member 2	K2p2.1, TPKC1, TREK, TREK-1, TREK1, hTREK-1c, hTREK-1e	Anhedonia, Melancholia, Mental depression
139	3777	KCNK3	Potassium two pore domain channel subfamily K member 3	K2p3.1, OAT1, PPH4, TASK, TASK-1, TASK1, TBAK1	Diverticular diseases, Heritable pulmonary arterial hypertension, Hypertension, Ischemic stroke, Pulmonary arterial hypertension, Pulmonary hypertension, Pulmonary hypertension with hereditary hemorrhagic telangiectasia, Stroke
140	3778	KCNMA1	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	Abducens palsy, Asymmetric crying face association, Autism, Bilateral convulsive seizures, Cataplexy, Cerebellar atrophy, Cerebellar atrophy, developmental delay, and seizures, Chromophobe carcinoma, Chronic obstructive pulmonary disease, Congenital epicanthus, Developmental delay, Dyskinesia, Dyskinetic syndrome, Epilepsy-paroxysmal dyskinesia syndrome, Esotropia View all (22 more)

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