Development Level

Tbio 1 | 11,445

Disease

Acquired scoliosis 1 | 281
Advanced bone age 1 | 35
Anteverted nostril 1 | 191
Anxiety 1 | 136
Anxiety disease 1 | 113
Atrial Septal Defects 1 | 85
Bipolar Disorder 1 | 666
Blue sclera 1 | 32
Breast cancer 1 | 3,578
Bulging forehead 1 | 66
Bullet-shaped middle phalanges of the hand 1 | 1
Bushy eyebrows 1 | 49
Cerebral atrophy 1 | 178
Choanal Atresia 1 | 42
Choanal stenosis 1 | 11
Chromosome 19p13.13 deletion syndrome 1 | 5
Concave bridge of nose 1 | 195
Congenital deafness 1 | 185
Curvature of spine 1 | 282
Deafness 1 | 198
Death in childhood 1 | 14
Decreased projection of midface 1 | 105
Decreased size of mandibular ramus 1 | 2
Degenerative brain disorder 1 | 100
Depressed nasal bridge 1 | 195
Depressed nasal root/bridge 1 | 195
Distal widening of metacarpals 1 | 1
Dull intelligence 1 | 645
Episodic ataxia 1 | 22
Failure to gain weight 1 | 365
Fetal overgrowth 1 | 16
Frontal bossing 1 | 157
Generalized overgrowth 1 | 16
Gingival Hyperplasia 1 | 34
Gingival Hypertrophy 1 | 34
Gingival Overgrowth 1 | 36
Glossoptosis 1 | 10
Hearing Loss, Partial 1 | 185
Hypoplastic sternum 1 | 5
Hypotrophic malar bone 1 | 129
Hypotrophic midface 1 | 105
Idiopathic pulmonary arterial hypertension 1 | 40
Irregular dentition 1 | 3
Isolated cases 1 | 72
Large sternal ossification centers 1 | 1
Laryngomalacia 1 | 14
Malan overgrowth syndrome 1 | 1
Malar flattening 1 | 129
Marshall-Smith syndrome 1 | 5
Midface retrusion 1 | 105
Motor delay 1 | 147
Narrow face 1 | 54
No development of motor milestones 1 | 147
ODONTOID HYPOPLASIA 1 | 16
Overfolded helix 1 | 24
Overgrowth 1 | 16
Pachygyria 1 | 41
Pectus excavatum 1 | 100
Pediatric failure to thrive 1 | 365
Posterior displacement of the tongue 1 | 10
Prominent forehead 1 | 66
Prominent premaxilla 1 | 3
Pulmonary hypertension 1 | 85
Recurrent aspiration pneumonia 1 | 4
Retrognathia 1 | 54
SOTOS SYNDROME 2 1 | 1
Scoliosis 1 | 44
Shallow orbits 1 | 13
Short distal phalanges 1 | 50
Short mandibular rami 1 | 2
Short nose 1 | 132
Short philtrum 1 | 53
Short sternum 1 | 5
Sleep Apnea, Obstructive 1 | 10
Slender, gracile long tubular bones 1 | 21
Small midface 1 | 105
Small nose 1 | 132
Sotos syndrome 1 | 13
Supratentorial atrophy 1 | 94
Synophrys 1 | 40
Tall stature 1 | 34
Thin face 1 | 54
Umbilical hernia 1 | 93
Underweight 1 | 17
Weight decreased 1 | 103
Weight less than 3rd percentile 1 | 17
acute myeloid leukemia 1 | 783
astrocytic glioma 1 | 2,597
breast carcinoma 1 | 1,638
ductal carcinoma in situ 1 | 1,745
hearing impairment 1 | 199
invasive ductal carcinoma 1 | 2,951
lung adenocarcinoma 1 | 2,716
lung carcinoma 1 | 2,843
oligodendroglioma 1 | 2,850
osteosarcoma 1 | 7,950
pituitary cancer 1 | 1,972
primary pancreatic ductal adenocarcinoma 1 | 1,109
psoriasis 1 | 6,694
pulmonary arterial hypertension 1 | 75

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

Transcription Factor 1 | 1,400

OMIM Phenotype

Marshall-Smith syndrome 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 
Nuclear factor 1 X-type NFIX Tbio Transcription Factor -1.70265 49.7 74