Development Level

Tclin 1 | 613

Disease

ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 1 | 21
Adenocarcinoma 1 | 122
Adrenocortical cytomegaly 1 | 3
Advanced bone age 1 | 35
Atrial Fibrillation 1 | 124
Atrial Fibrillation, Familial, 3 1 | 2
Atrioventricular block 1 | 35
Autosomal recessive predisposition 1 | 1,442
Beckwith-Wiedemann syndrome 1 | 44
Brugada syndrome 1 | 29
Carcinoma 1 | 11,493
Cardiac Arrhythmia 1 | 103
Cardiac arrest 1 | 36
Cardiomegaly 1 | 116
Cardiomyopathies 1 | 110
Cardiomyopathy 1 | 116
Catecholaminergic polymorphic ventricular tachycardia 1 | 12
Coarse facial features 1 | 108
Congenital ear anomaly NOS (disorder) 1 | 29
Congenital hemihypertrophy 1 | 6
Congenital omphalocele 1 | 20
Congenital sensorineural hearing loss 1 | 12
Cryptorchidism 1 | 296
Diabetes Mellitus, Non-Insulin-Dependent 1 | 145
Diabetes Mellitus, Type 2 1 | 142
Diastasis recti 1 | 9
Eaton-Lambert syndrome 1 | 40
Elevated heart rate 1 | 25
Enlarged kidney 1 | 14
Epilepsy 1 | 792
Exophthalmos 1 | 112
Familial atrial fibrillation 1 | 23
Fetal overgrowth 1 | 16
Generalized overgrowth 1 | 16
Gestational diabetes 1 | 26
Gonadoblastoma 1 | 34
Hearing Loss, Noise-Induced 1 | 5
Heart conduction disease 1 | 83
Hepatoblastoma 1 | 19
Hepatomegaly 1 | 285
Intestinal Neoplasms 1 | 12
Jervell and Lange-Nielsen syndrome 1 1 | 2
Jervell-Lange Nielsen syndrome 1 | 4
Large bregma sutures 1 | 46
Large fontanelle 1 | 46
Large, late-closing fontanelle 1 | 46
Long QT syndrome 1 | 39
Long QT syndrome 1 1 | 20
Macroglossia 1 | 65
Multiple Sclerosis 1 | 540
Neonatal hypoglycemia 1 | 17
Nephroblastoma 1 | 51
Noise-induced hearing loss 1 | 5
Overgrowth 1 | 16
Overgrowth of external genitalia 1 | 3
Pancreatic hyperplasia 1 | 3
Prolonged QT interval 1 | 15
Prominent back of the head 1 | 21
Prominent eyes 1 | 96
Prominent globes 1 | 96
Prominent occiput 1 | 21
Protruding eyes 1 | 96
Romano-Ward Syndrome 1 | 12
SHORT QT SYNDROME 2 (disorder) 1 | 1
Sensorineural hearing loss 1 | 106
Short QT Syndrome 1 1 | 4
Short QT syndrome 1 | 12
Short Qt Syndrome 2 1 | 1
Shortened QT interval 1 | 5
Sudden Cardiac Death 1 | 29
Sudden infant death syndrome 1 | 32
Syncope 1 | 22
Tachycardia 1 | 43
Thickened facial skin with coarse facial features 1 | 108
Thromboembolic stroke 1 | 2
Timothy syndrome 1 | 11
Torsades de Pointes 1 | 8
Type 2 diabetes mellitus 1 | 272
Ventricular Fibrillation 1 | 17
Wide bregma sutures 1 | 46
adrenocortical carcinoma 1 | 1,428
diabetes mellitus 1 | 1,728
esophageal adenocarcinoma 1 | 737
gastric carcinoma 1 | 807
lung adenocarcinoma 1 | 2,716
primary pancreatic ductal adenocarcinoma 1 | 1,109
tuberculosis 1 | 2,010

Tissue

Blood and immune system 1 | 16,909
Cardiovascular System 1 | 15,192
Digestive Tract 1 | 17,369
Endocrine System 1 | 18,159
Female tissues 1 | 17,400
Liver and Pancreas 1 | 16,750
Male tissues 1 | 17,142
Nervous System 1 | 16,725
Respiratory system 1 | 16,393
Skin and soft tissues 1 | 17,230
Urinary Tract 1 | 16,678

Target Family

Ion Channel 1 | 344

OMIM Phenotype

Atrial fibrillation, familial,... 1 | 1
Abacavir hypersensitivity, sus... 35 | 35
Phenotype: {Spondyloarthropath... 35 | 35
Stevens-Johnson syndrome, susc... 35 | 35
Synovitis, chronic, susceptibi... 35 | 35
Toxic epidermal necrolysis, su... 35 | 35
Phenotype: {Hypersensitivity s... 21 | 21
HIV-1 viremia, susceptibility ... 14 | 14
Phenotype: {Psoriasis suscepti... 14 | 14
Multiple sclerosis, susceptibi... 13 | 13
Phenotype: {Sarcoidosis, susce... 13 | 13
Colorectal cancer, somatic 8 | 8
Gastric cancer, somatic 6 | 6
Diabetes mellitus, noninsulin-... 5 | 5
Pheochromocytoma 5 | 5
ACTH-independent macronodular ... 4 | 4
Alzheimer disease, susceptibil... 4 | 4
Malaria, resistance to 4 | 4
McCune-Albright syndrome, soma... 4 | 4
Mycobacterium tuberculosis, su... 4 | 4
Osseous heteroplasia, progress... 4 | 4
Phenotype: Colorectal cancer, ... 4 | 4
Phenotype: Pseudohypoparathyro... 4 | 4
Phenotype: [Blood group 4 | 4
Phenotype: {Myocardial infarct... 4 | 4
Phenotype: {Schizophrenia, sus... 4 | 4
Pituitary adenoma 3, multiple ... 4 | 4
Pseudohypoparathyroidism Ib 4 | 4
Pseudohypoparathyroidism Ic 4 | 4
Pseudopseudohypoparathyroidism 4 | 4
Renal tubular dysgenesis 4 | 4
Tetralogy of Fallot 4 | 4
Afibrinogenemia, congenital 3 | 3
Aplastic anemia 3 | 3
Bladder cancer, somatic 3 | 3
COACH syndrome 3 | 3
Central hypoventilation syndro... 3 | 3
Dejerine-Sottas disease 3 | 3
Diabetes mellitus, permanent n... 3 | 3
LADD syndrome 3 | 3
Leukemia, acute myeloid 3 | 3
Lung cancer, susceptibility to 3 | 3
Mismatch repair cancer syndrom... 3 | 3
Multiple pterygium syndrome, l... 3 | 3
Myocardial infarction, suscept... 3 | 3
Neuropathy, distal hereditary ... 3 | 3
Omenn syndrome 3 | 3
Paraganglioma and gastric stro... 3 | 3
Parkinson disease, susceptibil... 3 | 3
Phenotype: Anterior segment dy... 3 | 3
Phenotype: Bethlem myopathy 1 3 | 3
Phenotype: Dysfibrinogenemia, ... 3 | 3
Phenotype: Epilepsy, progressi... 3 | 3
Phenotype: Leigh syndrome due ... 3 | 3
Phenotype: Orthostatic intoler... 3 | 3
Phenotype: {Breast cancer, sus... 3 | 3
Prostate cancer, susceptibilit... 3 | 3
Retinitis punctata albescens 3 | 3
Roussy-Levy syndrome 3 | 3
Schimmelpenning-Feuerstein-Mim... 3 | 3
Schizencephaly 3 | 3
Ullrich congenital muscular dy... 3 | 3
Arthrogryposis, distal, type 2... 2 | 2
Asthma, susceptibility to 2 | 2
Brachydactyly, type A2 2 | 2
Cerebrooculofacioskeletal synd... 2 | 2
De Sanctis-Cacchione syndrome 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Hypercholesterolemia, familial... 2 | 2
Hypofibrinogenemia, congenital 2 | 2
Ichthyosis, cyclic, with epide... 2 | 2
Jackson-Weiss syndrome 2 | 2
Leukemia, acute lymphoblastic,... 2 | 2
Leukemia, acute myeloid, somat... 2 | 2
Macular degeneration, age-rela... 2 | 2
Melanoma, cutaneous malignant,... 2 | 2
Microvascular complications of... 2 | 2
Ovarian cancer, somatic 2 | 2
Phenotype: Cockayne syndrome, ... 2 | 2
Phenotype: Epidermodysplasia v... 2 | 2
Phenotype: Epidermolysis bullo... 2 | 2
Phenotype: Epidermolytic hyper... 2 | 2
Phenotype: Hemochromatosis 2 | 2
Phenotype: Lacticacidemia due ... 2 | 2
Phenotype: Meesmann corneal dy... 2 | 2
Phenotype: Obesity, severe 2 | 2
Phenotype: Paroxysmal nonkines... 2 | 2
Phenotype: T-cell immunodefici... 2 | 2
Phenotype: Vitreoretinopathy, ... 2 | 2
Phenotype: {Alcohol dependence... 2 | 2
Phenotype: {Diabetes mellitus,... 2 | 2
Phenotype: {Nephrolithiasis, u... 2 | 2
Pick disease 2 | 2
Porphyria cutanea tarda, susce... 2 | 2
Porphyria variegata, susceptib... 2 | 2
Premature ovarian failure 11 2 | 2
Restrictive dermopathy, lethal 2 | 2
UV-sensitive syndrome 1 2 | 2
[Transferrin serum level QTL2] 2 | 2

This is where graphics are reside..
Name Gene Development Level Target Family Log Novelty  Pubmed Score  Antibody Count  Knowledge Availability 
Potassium voltage-gated channel subfamily KQT member 1 KCNQ1 Tclin Ion Channel -2.90675 800.2 365