Development Level

Tbio 1 | 11,445

Disease

11 pairs of ribs 1 | 7
Abnormality of the urinary system 1 | 21
Anemia 1 | 365
Anemia, Diamond-Blackfan 1 | 16
Anemia, Macrocytic 1 | 18
Aortic coarctation 1 | 30
Arthritis 1 | 290
Atrial Septal Defects 1 | 85
Bifid thoracic vertebrae 1 | 1
Bowen-Conradi syndrome 1 | 16
Byzanthine arch palate 1 | 194
Cardiac Arrhythmia 1 | 103
Cardiac conduction abnormalities 1 | 78
Cleft Lip 1 | 141
Cleft Palate 1 | 271
Conduction disorder of the heart 1 | 79
Congenital dyserythropoietic anemia 1 | 18
Congenital hypoplasia of radius 1 | 23
Congestive heart failure 1 | 113
Decreased platelet count 1 | 111
Delayed Puberty 1 | 97
Depressed nasal ridge 1 | 51
Diamond-Blackfan Anemia 1 1 | 1
Diamond-Blackfan anemia 1 | 31
Disease Progression 1 | 136
Downward slant of palpebral fissure 1 | 158
EKG abnormalities 1 | 78
Electrocardiogram abnormal 1 | 81
Electrocardiogram change 1 | 78
Elevated red cell adenosine deaminase activity 1 | 3
Endemic typhus 1 | 2
Failure to gain weight 1 | 365
Fatigue 1 | 182
Fetal Growth Retardation 1 | 189
Hand deformities 1 | 32
Heart failure 1 | 162
Hypertension 1 | 396
Hypoplasia of thumb 1 | 26
Hypoplastic coccygeal vertebrae 1 | 1
Hypoplastic ilia 1 | 12
Hypoplastic mandible condyle 1 | 275
Hypoplastic myelodysplasia 1 | 18
Hypoplastic sacral vertebrae 1 | 1
Increased number of platelets 1 | 14
Infant, Small for Gestational Age 1 | 176
Infantile onset 1 | 238
Intermittent migraine headaches 1 | 68
Intrauterine retardation 1 | 176
Late fontanel closure 1 | 28
MYELODYSPLASTIC SYNDROME 1 | 53
Malignant tumor of colon 1 | 19
Mandibular hypoplasia 1 | 275
Micrognathism 1 | 275
Migraine Disorders 1 | 76
Multiple myeloma 1 | 1,332
Narrow thorax 1 | 53
Neck webbing 1 | 35
Neutrophil count decreased 1 | 47
Orbital separation excessive 1 | 244
Pallor 1 | 40
Partial duplication of thumb phalanx 1 | 6
Pediatric failure to thrive 1 | 365
Premature Birth 1 | 77
Premature birth of newborn 1 | 67
Prostatic Neoplasms 1 | 495
Radial ray hypoplasia 1 | 23
Reticulocytopenia 1 | 10
Retinitis pigmentosa 12 1 | 9
Retrognathia 1 | 54
Sensorineural hearing loss 1 | 106
Short neck 1 | 140
Short stature 1 | 531
Small head 1 | 374
Small wings of the pelvic girdle 1 | 12
Stomach Neoplasms 1 | 300
Strabismus 1 | 270
Thrombocytopenia 1 | 197
Thrombocytosis 1 | 38
Thumb aplasia 1 | 16
Triphalangeal thumb 1 | 9
Uranostaphyloschisis 1 | 167
Ventricular Septal Defects 1 | 119
astrocytoma 1 | 1,146
atypical teratoid / rhabdoid tumor 1 | 5,112
diabetes mellitus 1 | 1,728
fibroadenoma 1 | 559
genital abnormal 1 | 17
glioblastoma multiforme 1 | 142
group 3 medulloblastoma 1 | 4,104
lung cancer 1 | 4,740
medulloblastoma, large-cell 1 | 6,241
osteosarcoma 1 | 7,950
primitive neuroectodermal tumor 1 | 3,035
reproductive system abnormality 1 | 17

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

Non-IDG 1 | 12,091

OMIM Phenotype

Phenotype: Diamond-Blackfan an... 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 
40S ribosomal protein S19 RPS19 Tbio Non-IDG -3.14746 1380.8 267