Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6631 to 6640 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6631
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

6632
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

6633
Potassium inwardly rectifying channel subfamily J member 16
BIR9, HKTD, KIR5.1
Brugada syndrome, Periodontitis

6634
Potassium inwardly rectifying channel subfamily J member 18
KIR2.6, TTPP2
Asthma, Obstructive pulmonary disease, Thyrotoxic periodic paralysis

6635
Potassium inwardly rectifying channel subfamily J member 2
ATFB9, HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7, SQT3
Andersen-tawil syndrome, Cardiac arrhythmias, Atrial fibrillation, Brugada syndrome, Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Congenital heart disease, Congenital short qt syndrome, Dermatologic disorder, Desbuquois syndrome, Long qt syndrome, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Polymorphic catecholaminergic ventricular tachycardia, Short qt syndrome
View all (3 more)

6636
Potassium inwardly rectifying channel subfamily J member 3
GIRK1, KGA, KIR3.1
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Dental caries, Emphysema, Hereditary atrial fibrillation, Malunion fracture, Peripheral arterial disease, Schizophrenia, Substance abuse, Uveal melanoma

6637
Potassium inwardly rectifying channel subfamily J member 4
HIR, HIRK2, HRK1, IRK-3, IRK3, Kir2.3
Conotruncal cardiac defect, Parkinson disease

6638
Potassium inwardly rectifying channel subfamily J member 5
CIR, GIRK4, KATP1, KIR3.4, LQT13
Andersen-tawil syndrome, Atrial fibrillation, Atrial flutter, Cardioembolic stroke, Cushing syndrome, Hyperaldosteronism, Long qt syndrome, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Sick sinus syndrome

6639
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, Metabolic syndrome, Parkinson disease, Retinal degeneration
View all (4 more)

6640
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, Long qt syndrome, Myocardial ischemia, Ventricular fibrillation