Development Level

Tchem 1 | 1,598

Disease

Autosomal recessive predisposition 1 | 1,442
Bartter Syndrome 1 | 4
Bartter disease 1 | 13
Bartter disease type 1 1 | 3
Bartter syndrome, antenatal , type 2 1 | 1
Bartter syndrome, antenatal type 1 1 | 3
Bartter syndrome, type 2, antenatal 1 | 1
Big calvaria 1 | 147
Bulging forehead 1 | 66
Calcinosis 1 | 70
Calcium pyrophosphate deposition disease 1 | 13
Carcinoma 1 | 11,493
Cognitive delay 1 | 608
Constipation 1 | 181
Dehydration 1 | 40
Diarrhea 1 | 253
Dull intelligence 1 | 645
Dyschezia 1 | 135
Elevated plasma renin 1 | 9
Epilepsy 1 | 792
Failure to gain weight 1 | 365
Fetal polyuria 1 | 8
Fever 1 | 138
Frontal bossing 1 | 157
Generalized muscle weakness 1 | 57
Generalized osteopenia 1 | 99
Global developmental delay 1 | 608
Globe of eye large 1 | 20
Hyperactive renin-angiotensin system 1 | 8
Hyperaldosteronism 1 | 35
Hypercalciuria 1 | 27
Hyperprostaglandinuria 1 | 2
Hypertension 1 | 396
Hypertensive disease 1 | 292
Hypochloremia (disorder) 1 | 6
Hypokalemia 1 | 52
Hypokalemic metabolic alkalosis 1 | 4
Impaired platelet aggregation 1 | 8
Impairment of urinary concentration 1 | 5
Increased calcium level in kidney 1 | 21
Increased head circumference 1 | 147
Increased plasma renin activity 1 | 8
Increased serum prostaglandin E2 1 | 2
Increased size of cranium 1 | 147
Increased size of palpebral fissures 1 | 9
Increased size of skull 1 | 147
Increased urinary chloride 1 | 5
Increased urinary potassium 1 | 5
Intellectual disability 1 | 1,016
Kidney disease 1 | 430
Large auricle 1 | 87
Large dysplastic ears 1 | 87
Large eyes 1 | 9
Large pinnae 1 | 87
Large prominent ears 1 | 87
Large protruding ears 1 | 87
Large, floppy ears 1 | 87
Leber congenital amaurosis 16 1 | 5
Low Birth Weights 1 | 69
Low intelligence 1 | 645
Low-to-normal blood pressure 1 | 2
Macrotia 1 | 87
Mental Retardation 1 | 645
Mental and motor retardation 1 | 608
Mental deficiency 1 | 645
Metabolic acidosis 1 | 90
Muscle Cramp 1 | 55
Nephrocalcinosis 1 | 35
Osteopenia 1 | 99
Paresthesia 1 | 32
Pediatric failure to thrive 1 | 365
Polydipsia 1 | 15
Polyhydramnios 1 | 108
Polyuria 1 | 23
Poor school performance 1 | 645
Premature Birth 1 | 77
Premature birth of newborn 1 | 67
Prominent forehead 1 | 66
Renal juxtaglomerular cell hypertrophy/hyperplasia 1 | 2
Renal potassium wasting 1 | 5
Renal salt wasting 1 | 18
Seizures 1 | 596
Serum chloride level decreased (finding) 1 | 6
Short stature 1 | 531
Small for gestational age (disorder) 1 | 69
Tetany 1 | 18
Triangular face 1 | 58
Vomiting 1 | 116
adult high grade glioma 1 | 3,801
medulloblastoma, large-cell 1 | 6,241
nephrosclerosis 1 | 333
ovarian cancer 1 | 8,520
psoriasis 1 | 6,694

Tissue

Blood and immune system 1 | 16,909
Digestive Tract 1 | 17,369
Endocrine System 1 | 18,159
Female tissues 1 | 17,400
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

Phenotype: Bartter syndrome, t... 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 
ATP-sensitive inward rectifier potassium channel 1 KCNJ1 Tchem Ion Channel -2.50371 327.8 188