Development Level

Tbio 1 | 11,445

IMPC Phenotype

abnormal behavior 1 | 298
decreased circulating choleste... 1 | 93
decreased heart rate 1 | 18
premature death 1 | 5
preweaning lethality, incomple... 1 | 499

Disease

Abnormalities, Multiple 1 | 13
Abnormality of the nasopharynx 1 | 9
Absent speech 1 | 43
Atrial Septal Defects 1 | 85
Bicornuate uterus 1 | 11
Blepharoptosis 1 | 231
Brachycephaly 1 | 88
Breast Neoplasms 1 | 445
Broad cranium shape 1 | 88
Broad ribs 1 | 12
Bulging forehead 1 | 66
Choanal stenosis 1 | 11
Chromosome 15q24 deletion syndrome 1 | 12
Coarse facial features 1 | 108
Congenital clubfoot 1 | 109
Craniofacial Abnormalities 1 | 151
Decreased projection of midface 1 | 105
Degenerative brain disorder 1 | 100
Dilatation of ureter 1 | 15
Dilated ventricles (finding) 1 | 121
Downward slant of palpebral fissure 1 | 158
Facial hemangioma 1 | 2
Hematologic cancer 1 | 12
Hepatoblastoma 1 | 19
High forehead 1 | 102
Hydronephrosis 1 | 89
HyperCalcification of skull base 1 | 5
HyperMineralization of skull base 1 | 5
Hypertrichosis 1 | 46
Hypomyelinating leukodystrophy 1 | 9
Hypoplasia of corpus callosum 1 | 90
Hypoplasia of first ribs 1 | 3
Hypoplasia of nipple 1 | 16
Hypoplasia of scrotum 1 | 24
Hypoplastic labia minora 1 | 10
Hypoplastic sternum 1 | 5
Hypoplastic/aplastic pubic bones 1 | 2
Hypotrophic malar bone 1 | 129
Hypotrophic midface 1 | 105
Hypsarrhythmia 1 | 25
Inadequate arch length for tooth size 1 | 45
Increased density of long bones 1 | 1
Intermediate coronary syndrome 1 | 11
Intestinal disease 1 | 14
Juvenile Myelomonocytic Leukemia 1 | 21
Language Development Disorders 1 | 11
Leukemia, Myelocytic, Acute 1 | 120
Leukemia, Myeloid 1 | 18
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative 1 | 2
Leukemia, Myelomonocytic, Juvenile 1 | 20
Long clavicle 1 | 7
MYELODYSPLASTIC SYNDROME 1 | 53
Macroglossia 1 | 65
Malar flattening 1 | 129
Mammary Neoplasms 1 | 425
Mastitis 1 | 48
Mental Retardation, Autosomal Dominant 29 1 | 1
Metopic suture patent to nasal root 1 | 1
Midface retrusion 1 | 105
Motor delay 1 | 147
Myeloid Leukemia 1 | 19
Myeloid Leukemia, Chronic 1 | 23
Narrow palate 1 | 20
No development of motor milestones 1 | 147
Opisthotonus 1 | 14
Overcurvature of nail 1 | 6
Penile hypospadias 1 | 106
Pointed chin 1 | 33
Postnatal growth retardation 1 | 57
Prominent forehead 1 | 66
Schinzel-Giedion syndrome 1 | 1
Sclerosis of skull base 1 | 5
Shallow orbits 1 | 13
Short distal phalanges 1 | 50
Short first metacarpals 1 | 11
Short sternum 1 | 5
Single transverse palmar crease 1 | 29
Small labia majora 1 | 16
Small midface 1 | 105
Staphyloenterotoxemia 1 | 18
Stenosis of ureter 1 | 2
Structure of wormian bone 1 | 24
Supratentorial atrophy 1 | 94
Synophrys 1 | 40
Tall forehead 1 | 102
Teratoma 1 | 8
Thickened cortex of long bones 1 | 4
Thickened facial skin with coarse facial features 1 | 108
Thin upper lip vermilion 1 | 67
Tibial bowing 1 | 19
Tooth Crowding 1 | 45
Tooth mass arch size discrepancy 1 | 45
Tooth size discrepancy 1 | 45
Toxic shock syndrome 1 | 28
Uroureter 1 | 15
Weight Gain 1 | 100
Wide distal metaphysis of femur 1 | 1
Wide skull shape 1 | 88
Widely patent fontanels and sutures 1 | 12
nonverbal 1 | 43

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: Schinzel-Giedion mi... 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 
SET-binding protein SETBP1 Tbio Non-IDG -2.46805 281.6 98