Development Level

Tbio 1 | 11,445

Disease

Animal Mammary Neoplasms 1 | 136
Arrhythmogenic right ventricular cardiomyopathy 1 | 30
Atrial Fibrillation 1 | 124
Autosomal recessive predisposition 1 | 1,442
Avian influenza 1 | 7
Bell Palsy 1 | 58
Breast Neoplasms 1 | 445
Bulbar palsy 1 | 19
Bulbar weakness 1 | 19
CARDIOMYOPATHY, DILATED, 1I 1 | 1
Carcinoma 1 | 11,493
Cardiac Arrhythmia 1 | 103
Cardiac conduction abnormalities 1 | 78
Cardiomyopathy 1 | 116
Cardiomyopathy, Dilated 1 | 83
Conduction disorder of the heart 1 | 79
Congenital clubfoot 1 | 109
Constipation 1 | 181
Diarrhea 1 | 253
Dilated cardiomyopathy 1 | 56
Distal limb muscle weakness due to peripheral neuropathy 1 | 62
Distal muscle weakness 1 | 62
Dyschezia 1 | 135
EKG abnormalities 1 | 78
EMG: myopathic abnormalities 1 | 22
Electrocardiogram abnormal 1 | 81
Electrocardiogram change 1 | 78
Facial Paresis 1 | 59
Facial muscle weakness of muscles innervated by CN VII 1 | 58
Familial isolated dilated cardiomyopathy 1 | 41
Fetal Growth Retardation 1 | 189
Flexion contracture - elbow 1 | 32
Foot dorsiflexor weakness 1 | 27
Foot-drop 1 | 27
Glomerulonephritis 1 | 46
Hernias, Diaphragmatic, Congenital 1 | 17
Highly variable clinical phenotype 1 | 150
Highly variable phenotype and severity 1 | 150
Highly variable phenotype, even within families 1 | 150
Hyperhomocysteinemia 1 | 37
Hypertrophic Cardiomyopathy 1 | 117
Hyporeflexia of lower limbs 1 | 10
LEFT VENTRICULAR NONCOMPACTION 10 1 | 40
LEFT VENTRICULAR NONCOMPACTION 8 1 | 40
Late-onset proximal muscle weakness 1 | 2
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R 1 | 1
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED 1 | 1
Mammary Neoplasms 1 | 425
Mammary Neoplasms, Animal 1 | 136
Mammary Neoplasms, Experimental 1 | 154
Muscle biopsy shows dystrophic changes 1 | 39
Muscular Dystrophy, Limb-Girdle, Type 1E 1 | 2
Muscular dystrophy 1 | 75
Myofibrillar Myopathy 1 | 9
Myofibrillar myopathy 1 1 | 6
Myopathy 1 | 185
Neck muscle weakness 1 | 17
Nephrosis 1 | 21
Peroneal muscle atrophy 1 | 2
Phenotypic variability 1 | 150
Progressive disorder 1 | 142
Reduced systolic function 1 | 5
Respiratory insufficiency due to muscle weakness 1 | 37
Restrictive heart failure 1 | 1
Scapular weakness 1 | 23
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type 1 | 1
Scapuloperoneal weakness 1 | 3
Shoulder girdle muscle atrophy 1 | 6
Stomach Neoplasms 1 | 300
Winged scapula 1 | 23
colon cancer 1 | 1,478
limb-girdle muscular dystrophy 1 | 37
lung adenocarcinoma 1 | 2,716
lung carcinoma 1 | 2,843
non-small cell lung cancer 1 | 2,890
pancreatic cancer 1 | 2,398
primary pancreatic ductal adenocarcinoma 1 | 1,109
psoriasis 1 | 6,694

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

Non-IDG 1 | 12,091

OMIM Phenotype

Phenotype: Myopathy, myofibril... 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 
Desmin DES Tbio Non-IDG -1.56068 36.6 991