Development Level

Tbio 4 | 11,445

Disease

Bilateral fifth finger clinodactyly 4 | 110
Broad forehead 4 | 59
Congenital heart disease 4 | 93
Curvature of little finger 4 | 110
Exophthalmos 4 | 112
Preauricular Fistulae, Congenital 4 | 27
Preauricular dimple 4 | 27
Preauricular sinus 4 | 27
Prominent eyes 4 | 96
Prominent globes 4 | 96
Protruding eyes 4 | 96
Tetralogy of Fallot 4 | 63
Ventricular Septal Defects 4 | 119
Abnormal nasal morphology 3 | 16
Aortic coarctation 3 | 30
Atrial Septal Defects 3 | 85
Atrioventricular Septal Defect 3 | 22
Brachydactyly 3 | 156
Cognitive delay 3 | 608
Cryptorchidism 3 | 296
Fetal Growth Retardation 3 | 189
Global developmental delay 3 | 608
Holt-Oram syndrome 3 | 12
Infant, Small for Gestational Age 3 | 176
Intrauterine retardation 3 | 176
Long narrow head 3 | 75
Mental and motor retardation 3 | 608
Narrow cranium shape 3 | 75
Narrow head shape 3 | 75
Narrow skull shape 3 | 75
Short stature 3 | 531
Thin lips 3 | 49
Turridolichocephaly 3 | 75
Underdeveloped brows 3 | 38
Underdeveloped supraorbital ridges 3 | 38
psoriasis 3 | 6,694
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 2 | 21
Abnormality of metabolism/homeostasis 2 | 134
Atrial heart septal defect 2 | 18
Attention deficit hyperactivity disorder 2 | 278
Autosomal recessive predisposition 2 | 1,442
Broad flat nasal bridge 2 | 236
Broad hallux 2 | 29
Cancer 2 | 2,499
Cardiomegaly 2 | 116
Cardiomyopathy 2 | 116
Congenital Epicanthus 2 | 177
Congenital Heart Defects 2 | 58
Congenital hypoplasia of kidney 2 | 32
Conotruncal Heart Malformations 2 | 10
Constipation 2 | 181
Discordant ventriculoarterial connection 2 | 17
Double Outlet Right Ventricle 2 | 11
Dyschezia 2 | 135
Ebstein anomaly 2 | 16
Embryotoxon 2 | 28
Epilepsy 2 | 792
Heart Defects, Congenital 2 | 37
Heart Septal Defects, Ventricular 2 | 6
High forehead 2 | 102
Hypoplastic mandible condyle 2 | 275
Hypothyroidism 2 | 122
Low set ears 2 | 181
Mandibular hypoplasia 2 | 275
Micrognathism 2 | 275
Mild Mental Retardation 2 | 70
Muscle hypotonia 2 | 571
Myocardial Infarction 2 | 151
Nasal bridge wide 2 | 236
Orbital separation excessive 2 | 244
Osteoporosis 2 | 363
Ostium secundum atrial septal defect 2 | 9
POLYDACTYLY, POSTAXIAL 2 | 13
Persistant truncus arteriosus 2 | 17
Polycystic ovary syndrome 2 | 360
Posterior embryotoxon 2 | 28
RENAL ADYSPLASIA 2 | 25
Renal dysplasia 2 | 28
Right atrial isomerism 2 | 29
Schizophrenia 2 | 1,160
Seizures 2 | 596
Short neck 2 | 140
Small head 2 | 374
Specific learning disability 2 | 47
Tall forehead 2 | 102
Umbilical hernia 2 | 93
Upward slant of palpebral fissure 2 | 75
atypical teratoid / rhabdoid tumor 2 | 5,112
gastric carcinoma 2 | 807
group 3 medulloblastoma 2 | 4,104
malignant mesothelioma 2 | 3,232
medulloblastoma, large-cell 2 | 6,241
osteosarcoma 2 | 7,950
pancreatic cancer 2 | 2,398
primary pancreatic ductal adenocarcinoma 2 | 1,109
ventricular septal defect 2 | 20
Diaphragmatic Hernia 1 | 40
Hand deformities 1 | 32
Hernia, Diaphragmatic 1 | 40
Nasal voice 1 | 39

Tissue

Blood and immune system 4 | 16,909
Cardiovascular System 4 | 15,192
Female tissues 4 | 17,400
Digestive Tract 3 | 17,369
Endocrine System 3 | 18,159
Liver and Pancreas 3 | 16,750
Male tissues 3 | 17,142
Respiratory system 3 | 16,393
Urinary Tract 3 | 16,678
Nervous System 2 | 16,725
Skin and soft tissues 2 | 17,230

Target Family

Transcription Factor 3 | 1,400
Non-IDG 1 | 12,091

OMIM Phenotype

Tetralogy of Fallot 4 | 4
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
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 
T-box transcription factor TBX1 TBX1 Tbio Transcription Factor -1.99519 95.5 207
Transcription factor GATA-4 GATA4 Tbio Transcription Factor -2.90202 763.9 496
Protein jagged-1 JAG1 Tbio Non-IDG -3.09216 1190.8 473
Homeobox protein Nkx-2.5 NKX2-5 Tbio Transcription Factor -2.79738 600.1 385