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	Appendicitis, Attention deficit hyperactivity disorder, Autism, Breast cancer, Cholecystitis, Cholecystolithiasis, Color vision deficiency, Coronary artery disease, Dementia, Major depressive disorder, Gout, Keppen-lubinsky syndrome, Depression, Metabolic syndrome, Parkinson disease View all (5 more)
132	3764	KCNJ8	Potassium inwardly rectifying channel subfamily J member 8	KIR6.1, uKATP-1	Brugada syndrome, Cantu syndrome, Cardiac arrest, Cardiac arrhythmia, Genetic predisposition to disease, Hypertrichosis, Liver cirrhosis, Long qt syndrome, Myocardial ischemia, Ventricular fibrillation
133	3766	KCNJ10	Potassium inwardly rectifying channel subfamily J member 10	BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME	Nonsyndromic hearing loss, Cerebellar ataxia, Congenital neurologic anomalies�, Deafness, East syndrome, Intellectual developmental disorder, Littles disease, Multiple sclerosis, Paroxysmal dystonic choreoathetosis, Paroxysmal dyskinesia, Pendred syndrome, Peripheral neuropathy, Seizures, tonic-clonic, photosensitive
134	3767	KCNJ11	Potassium inwardly rectifying channel subfamily J member 11	BIR, HHF2, IKATP, KIR6.2, MODY13, PHHI, PNDM2, TNDM3	Hyperinsulinism, Congenital microcephaly, Coronary artery disease, Dend syndrome, Atopic dermatitis, Diabetes mellitus, Experimental diabetes, Diabetes mellitus type 1, Diabetes mellitus type 2, Diabetes mellitus permanent neonatal, Diabetes mellitus transient neonatal, Hyperinsulinemic hypoglycemia, Hypertrichosis, Hypoglycemia, Diabetes mellitus, type 2 View all (5 more)
135	3769	KCNJ13	Potassium inwardly rectifying channel subfamily J member 13	KIR1.4, KIR7.1, LCA16, SVD	Coronary artery disease, Leber congenital amaurosis, Major depressive disorder, Marshall syndrome, Retinitis pigmentosa, Vitreoretinal degeneration
136	3772	KCNJ15	Potassium inwardly rectifying channel subfamily J member 15	IRKK, KIR1.3, KIR4.2	Juvenile arthritis, Color vision deficiency, Juvenile idiopathic arthritis, Lung neoplasms, Oligoarticular juvenile idiopathic arthritis
137	3775	KCNK1	Potassium two pore domain channel subfamily K member 1	DPK, HOHO, K2P1, K2p1.1, KCNO1, TWIK-1, TWIK1	Alzheimer disease, Colorectal cancer, Dementia, Diabetic retinopathy, Hyperplasia, Obstructive sleep apnea syndrome, Periodontitis, Sinusitis, Hypertension
138	3776	KCNK2	Potassium two pore domain channel subfamily K member 2	K2p2.1, TPKC1, TREK, TREK-1, TREK1, hTREK-1c, hTREK-1e	Anhedonia, Breast cancer, Color vision deficiency, Major depressive disorder, Estrogen-receptor negative breast cancer, Depression
139	3777	KCNK3	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 View all (1 more)
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	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 View all (18 more)

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