Development Level

Tbio 1 | 11,445

Disease

Abnormal vision 1 | 52
Abnormality of retinal pigmentation 1 | 111
Abnormality of the retinal vasculature 1 | 59
Anteverted nostril 1 | 191
Attenuation of retinal blood vessels 1 | 16
Atypical scarring of skin 1 | 62
Autosomal recessive predisposition 1 | 1,442
Blind Vision 1 | 111
Blindness 1 | 88
Blindness, Legal 1 | 110
Breast cancer 1 | 3,578
Broad flat nasal bridge 1 | 236
Carcinoma 1 | 11,493
Cataract 1 | 297
Conductive hearing loss 1 | 123
Congenital anomaly of testis 1 | 52
Congenital hypoplasia of penis 1 | 176
Congenital sensorineural hearing loss 1 | 12
DOID:2627 1 | 94
DOID:9917 1 | 31
Difficulties with night vision 1 | 87
Dull intelligence 1 | 645
Electroretinogram abnormal 1 | 95
Endometrial cancer 1 | 311
Fundus dystrophy 1 | 83
Fundus with peripheral 'bony spicules' 1 | 12
Glaucoma 1 | 239
Hemianopsia 1 | 15
Hyperinsulinism 1 | 133
Hypogonadism 1 | 173
Immune system cancer 1 | 140
Intellectual disability 1 | 1,016
Keratoconus 1 | 113
Kidney cancer 1 | 2,613
Large intestine cancer 1 | 126
Lens Opacities 1 | 231
Liver cancer 1 | 604
Low Vision 1 | 174
Low intelligence 1 | 645
Lymphoid leukemia 1 | 160
Melanoma 1 | 711
Mental Retardation 1 | 645
Mental deficiency 1 | 645
Myopia 1 | 176
Nasal bridge wide 1 | 236
Night Blindness 1 | 101
Night blindness, progressive 1 | 51
Nonsyndromic deafness 1 | 142
Nystagmus 1 | 317
Obesity 1 | 678
Ophthalmoplegia 1 | 106
Optic Atrophy 1 | 242
Ovarian lymphoma 1 | 2
Photodysphoria 1 | 121
Photophobia 1 | 121
Pigmentary iris degeneration 1 | 20
Poor school performance 1 | 645
RETINITIS PIGMENTOSA 39 (disorder) 1 | 1
Retinal blind spot 1 | 11
Retinal pigment epithelial abnormality 1 | 111
Retinitis Pigmentosa 1 | 226
Scotoma 1 | 22
Sensorineural Hearing Loss (disorder) 1 | 284
Sensorineural hearing loss 1 | 106
Skin cancer 1 | 469
USHER SYNDROME, TYPE IIA 1 | 1
Usher Syndrome, Type 1 1 | 7
Usher Syndrome, Type II 1 | 5
Usher syndrome 1 | 32
Usher syndrome type 2 1 | 5
Usher syndrome, type 2A 1 | 2
Visual Impairment 1 | 174
Visual field defects 1 | 19
cone-rod dystrophy 1 | 59
group 3 medulloblastoma 1 | 4,104
lung cancer 1 | 4,740
medulloblastoma, large-cell 1 | 6,241
ovarian cancer 1 | 8,520
pancreatic cancer 1 | 2,398
retinitis pigmentosa 39 1 | 1

Tissue

Cardiovascular System 1 | 15,192
Endocrine System 1 | 18,159
Liver and Pancreas 1 | 16,750
Male tissues 1 | 17,142
Urinary Tract 1 | 16,678

Target Family

Non-IDG 1 | 12,091

OMIM Phenotype

Phenotype: Usher syndrome, typ... 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 
Usherin USH2A Tbio Non-IDG -2.45871 284.8 38