Development Level

Tbio 1 | 11,651

Disease

Abnormal vision 1 | 52
Abnormality of retinal pigmentation 1 | 111
Abnormality of vision 1 | 40
Amblyopia 1 | 38
Aniridia 1 | 25
Aniridia 1 1 | 5
Aniridia cerebellar ataxia mental deficiency 1 | 2
Aniridia type 2 1 | 1
Anterior Segment Dysgenesis 5 1 | 4
Aplasia/Hypoplasia of the macula 1 | 8
Autistic Disorder 1 | 364
Axenfeld-Rieger Syndrome, Type 1 1 | 3
Axenfeld-Rieger syndrome 1 | 14
Blepharoptosis 1 | 231
Blindness 1 | 88
CATARACT, AUTOSOMAL DOMINANT 1 | 4
Clouding of corneal stroma 1 | 50
Cloudy cornea 1 | 33
Coloboma 1 | 51
Coloboma of Optic Nerve 1 | 2
Coloboma of eyelid 1 | 15
Coloboma of lens 1 | 4
Coloboma of macula 1 | 4
Coloboma of optic disc 1 | 9
Coloboma, Ocular, Autosomal Dominant 1 | 6
Congenital aphakia 1 | 6
Congenital coloboma of iris 1 | 4
Congenital ectopic pupil 1 | 7
Congenital neurologic anomalies 1 | 20
Congenital nystagmus 1 | 26
Congenital ocular coloboma (disorder) 1 | 40
Contiguous gene syndrome 1 | 2
Corneal Opacity 1 | 53
Corneal disease 1 | 31
Corneal stromal opacities 1 | 33
Craniofacial Abnormalities 1 | 151
Deletion 11p13 1 | 3
Diabetes Mellitus, Experimental 1 | 108
Diabetes Mellitus, Non-Insulin-Dependent 1 | 145
Diabetes Mellitus, Type 2 1 | 142
Disorder of the optic nerve 1 | 1
Displacement of the external urethral meatus 1 | 3
Dull foveal reflex 1 | 9
Ectropion 1 | 38
Everted lower lip vermilion 1 | 54
Explosive speech 1 | 9
FOVEAL HYPOPLASIA 1 1 | 1
Foveal hypoplasia (finding) 1 | 9
Foveal hypoplasia and presenile cataract syndrome 1 | 1
Foveal hypoplasia-presenile cataract syndrome 1 | 1
Generalized hyperpigmentation 1 | 22
Gillespie syndrome 1 | 2
Hearing abnormality 1 | 12
Hereditary macular coloboma 1 | 5
Hydrophthalmos 1 | 19
Hypoplasia of the optic nerve 1 | 17
Irido-corneo-trabecular dysgenesis (disorder) 1 | 10
Keratitis 1 | 62
Keratitis, hereditary 1 | 1
Keratopathy 1 | 12
Lens subluxation 1 | 12
Low Vision 1 | 174
Mask-like facies 1 | 25
Melanoma 1 | 711
Microcephaly 1 | 166
Microphthalmia 1 | 76
Morning glory syndrome 1 | 1
Movement Disorders 1 | 55
Myopia 1 | 176
Neoplasm Invasiveness 1 | 161
Nephroblastoma 1 | 51
Nervous System Malformations 1 | 10
O'Donnell Pappas syndrome 1 | 1
Optic Nerve Diseases 1 | 1
Optic Nerve Hypoplasia, Bilateral 1 | 1
Optic disc abnormalities 1 | 12
Optic nerve aplasia 1 | 3
Penile hypospadias 1 | 106
Persistent hyperplastic primary vitreous 1 | 20
Peters anomaly 1 | 16
Presenile cataract 1 | 1
Protruding lower lip 1 | 54
Ptosis 1 | 48
Reduced visual acuity 1 | 63
Renal coloboma syndrome 1 | 4
Retinal Degeneration 1 | 106
Retinal Detachment 1 | 51
Retinal pigment epithelial abnormality 1 | 111
Scanning speech 1 | 9
Scleral staphyloma 1 | 1
Somatic mutation 1 | 61
Stomach Neoplasms 1 | 300
Strabismus 1 | 270
Streak ovary 1 | 15
Tooth Abnormalities 1 | 69
Vaginal malformation 1 | 7
Visual Impairment 1 | 174
WAGR syndrome 1 | 10
Waardenburg's syndrome 1 | 17
atypical teratoid/rhabdoid tumor 1 | 357

Tissue

Blood and immune system 1 | 16,909
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

Foveal hypoplasia 1 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 
Paired box protein Pax-6 PAX6 Tbio Transcription Factor -3.16650 1458.6 570