Development Level

Tbio 1 | 11,445

Disease

Abnormal hair whorls 1 | 5
Abnormality of retinal pigmentation 1 | 111
Abnormality of the thorax 1 | 19
Abnormality of the voice 1 | 46
Aging, Premature 1 | 4
Aplasia/Hypoplasia of the skin 1 | 16
Aplasia/Hypoplasia of the testes 1 | 1
Autosomal recessive predisposition 1 | 1,442
Baller-Gerold syndrome 1 | 12
Bloom syndrome 1 | 29
Calcium pyrophosphate deposition disease 1 | 13
Cancer 1 | 2,499
Carcinoma 1 | 11,493
Cataract 1 | 297
Cockayne syndrome 1 | 60
Congestive heart failure 1 | 113
Convex nasal ridge 1 | 37
Decreased fertility 1 | 33
Diabetes Mellitus, Non-Insulin-Dependent 1 | 145
Fanconi anemia 1 | 56
Hair shaft abnormalities 1 | 30
Heart disease 1 | 306
Heart failure 1 | 162
Hyperkeratosis 1 | 50
Hypogonadism 1 | 173
Insulin Resistance 1 | 72
Kidney cancer 1 | 2,613
Lack of skin elasticity 1 | 10
Lens Opacities 1 | 231
Lipoatrophy 1 | 19
Meningioma 1 | 41
Myocardial Infarction 1 | 151
Narrow face 1 | 54
Neurogenic Muscular Atrophy 1 | 139
Neurogenic muscle atrophy, especially in the lower limbs 1 | 139
Nijmegen breakage syndrome 1 | 24
Osteoporosis 1 | 363
Osteosclerosis 1 | 31
Photosensitive trichothiodystrophy 1 | 30
Pili Torti 1 | 6
Premature aging syndrome 1 | 4
Premature arteriosclerosis 1 | 5
Premature canities 1 | 24
Premature hardening of arteries 1 | 5
Progeria 1 | 25
Prostate cancer 1 | 175
Pulmonary artery stenosis 1 | 22
Rapadilino syndrome 1 | 7
Retinal Degeneration 1 | 106
Retinal pigment epithelial abnormality 1 | 111
Rothmund-Thomson syndrome 1 | 19
Short stature 1 | 531
Skeletal muscle atrophy 1 | 139
Skin Ulcer 1 | 48
Slender build 1 | 14
Small hand 1 | 36
Sparse scalp hair 1 | 42
Stretched skin 1 | 10
Subcutaneous calcification 1 | 2
Telangiectasia of the skin 1 | 39
Thin face 1 | 54
Vertical Talus 1 | 25
Warsaw breakage syndrome 1 | 11
Werner syndrome 1 | 29
White forelock 1 | 12
Wizened face 1 | 9
XFE progeroid syndrome 1 | 3
Xeroderma pigmentosum 1 | 43
diabetes mellitus 1 | 1,728
hair abnormalities (non-specific) 1 | 30
lung cancer 1 | 4,740
medulloblastoma, large-cell 1 | 6,241
muscle degeneration 1 | 139
osteosarcoma 1 | 7,950
psoriasis 1 | 6,694
sonic hedgehog group medulloblastoma 1 | 467

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

Enzyme 1 | 4,145

OMIM Phenotype

Phenotype: Werner 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 
Werner syndrome ATP-dependent helicase WRN Tbio Enzyme -2.73759 569.7 210