Development Level

Tbio 1 | 10,625

Disease

Amblyopia 1 | 24
Aniridia 1 | 26
Aniridia 1 1 | 5
Aniridia type 2 1 | 1
Anterior Segment Dysgenesis 5 1 | 4
Autistic Disorder 1 | 320
Axenfeld-Rieger Syndrome, Type 1 1 | 3
Bilateral optic nerve hypoplasia 1 | 1
Blindness 1 | 84
Breast cancer 1 | 3,098
CATARACT, AUTOSOMAL DOMINANT 1 | 4
Cancer 1 | 2,346
Cataract 1 | 104
Coloboma 1 | 52
Coloboma of macula 1 | 4
Coloboma of optic disc 1 | 1
Coloboma of optic nerve 1 | 2
Coloboma, ocular, autosomal dominant 1 | 6
Congenital aphakia 1 | 6
Congenital ectopic pupil 1 | 1
Congenital neurologic anomalies 1 | 9
Congenital nystagmus 1 | 26
Congenital ocular coloboma (disorder) 1 | 12
Corneal disease 1 | 32
Craniofacial Abnormalities 1 | 147
Deletion 11p13 1 | 3
Diabetes Mellitus, Experimental 1 | 106
Diabetes Mellitus, Non-Insulin-Dependent 1 | 161
Disorder of the optic nerve 1 | 1
Ectropion 1 | 18
Foveal hypoplasia 1 1 | 1
Foveal hypoplasia and presenile cataract syndrome 1 | 1
Foveal hypoplasia-presenile cataract syndrome 1 | 1
Gillespie syndrome 1 | 2
Glaucoma 1 | 135
Intellectual disability 1 | 573
Irido-corneo-trabecular dysgenesis (disorder) 1 | 6
Keratitis hereditary 1 | 1
Keratitis, hereditary 1 | 1
Keratopathy 1 | 12
Melanoma 1 | 261
Microphthalmia 1 | 79
Morning glory syndrome 1 | 1
Myopia 1 | 99
Neoplasm Invasiveness 1 | 127
O'Donnell Pappas syndrome 1 | 1
Optic Nerve Aplasia, Bilateral 1 | 1
Optic Nerve Hypoplasia, Bilateral 1 | 1
Persistent hyperplastic primary vitreous 1 | 20
Peters anomaly 1 | 4
Ptosis 1 | 42
Retinal detachment 1 | 33
Scleral staphyloma 1 | 2
Sclerocornea 1 | 16
Stomach Neoplasms 1 | 282
Tooth Abnormalities 1 | 10
WAGR syndrome 1 | 12
Waardenburg's syndrome 1 | 16
atypical teratoid/rhabdoid tumor 1 | 1,095
diabetes mellitus 1 | 1,663
glioblastoma 1 | 5,572
malignant mesothelioma 1 | 3,163
medulloblastoma, large-cell 1 | 6,234
pilocytic astrocytoma 1 | 3,086
pituitary cancer 1 | 1,972
posterior fossa group A ependymoma 1 | 1,511
sonic hedgehog group medulloblastoma 1 | 1,482

Tissue

Blood and immune system 1 | 17,994
Cardiovascular System 1 | 17,957
Digestive Tract 1 | 18,472
Endocrine System 1 | 18,511
Female tissues 1 | 18,646
Liver and Pancreas 1 | 18,135
Male tissues 1 | 17,968
Nervous System 1 | 18,560
Respiratory system 1 | 17,483
Skin and soft tissues 1 | 18,114
Urinary Tract 1 | 18,443

Target Family

Transcription Factor 1 | 1,400

OMIM Phenotype

Coloboma, ocular 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
Rheumatoid arthritis, suscepti... 13 | 13
Sarcoidosis, susceptibility to... 13 | 13
Colorectal cancer, somatic 8 | 8
Gastric cancer, somatic 6 | 6
Diabetes mellitus, noninsulin-... 5 | 5
Phenotype: {Schizophrenia, sus... 5 | 5
Pheochromocytoma 5 | 5
ACTH-independent macronodular ... 4 | 4
Acromegaly, somatic 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
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
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
Peters anomaly 3 | 3
Phenotype: Bethlem myopathy 1 3 | 3
Phenotype: Corneal opacificati... 3 | 3
Phenotype: Dysfibrinogenemia, ... 3 | 3
Phenotype: Epilepsy, progressi... 3 | 3
Phenotype: Leigh syndrome due ... 3 | 3
Phenotype: Orthostatic intoler... 3 | 3
Phenotype: Paroxysmal nonkines... 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
Ullrich congenital muscular dy... 3 | 3
?Bardet-Biedl syndrome 14 2 | 2
Arthrogryposis, distal, type 2... 2 | 2
Asthma, susceptibility to 2 | 2
Brachydactyly, type A2 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
Lung cancer, susceptibility to 2 | 2
Melanoma, cutaneous malignant,... 2 | 2
Microvascular complications of... 2 | 2
Ovarian cancer, somatic 2 | 2
Phenotype: Carnitine deficienc... 2 | 2
Phenotype: Epidermodysplasia v... 2 | 2
Phenotype: Epidermolysis bullo... 2 | 2
Phenotype: Epidermolytic hyper... 2 | 2
Phenotype: Hemochromatosis 2 | 2
Phenotype: Homocystinuria, B6-... 2 | 2
Phenotype: Meesmann corneal dy... 2 | 2
Phenotype: Obesity, severe 2 | 2
Phenotype: T-cell immunodefici... 2 | 2
Phenotype: Vitreoretinopathy, ... 2 | 2
Phenotype: {Alcohol dependence... 2 | 2
Phenotype: {Diabetes mellitus,... 2 | 2
Phenotype: {Gastric cancer ris... 2 | 2
Phenotype: {Nephrolithiasis, u... 2 | 2
Pick disease 2 | 2
Porphyria cutanea tarda, susce... 2 | 2
Porphyria variegata, susceptib... 2 | 2
Restrictive dermopathy, lethal 2 | 2
Stroke, ischemic, susceptibili... 2 | 2
Thrombosis, hyperhomocysteinem... 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 
Paired box protein Pax-6 PAX6 Tbio Transcription Factor -3.14190 1375.5 488