Development Level

Tbio 1 | 11,651
Tchem 1 | 1,388

Disease

Carcinoma 2 | 11,493
Defective or absent horizontal voluntary eye movements 2 | 25
Deglutition Disorders 2 | 132
Dementia 2 | 175
Depressive disorder 2 | 409
Dyspnea 2 | 76
Fatigue 2 | 182
Muscle Rigidity 2 | 49
Muscle Spasticity 2 | 195
Muscle hypotonia 2 | 571
Myoclonus 2 | 74
Neurodegenerative disease 2 | 414
Oculomotor apraxia 2 | 25
Ophthalmoplegia 2 | 106
PARKINSON DISEASE, LATE-ONSET 2 | 20
Parkinson's disease 2 | 392
Abnormal respiratory patterns 1 | 20
Abnormality of aortic arch 1 | 9
Aortic calcification 1 | 2
Apathy 1 | 16
Aseptic Necrosis of Bone 1 | 8
Aseptic necrosis 1 | 8
Ataxia, Appendicular 1 | 25
Atrophoderma maculatum 1 | 4
Autosomal dominant late onset Parkinson disease 1 | 7
Bone disease 1 | 10
Bone infarction 1 | 8
Bone necrosis 1 | 9
Bulbar signs 1 | 4
Cerebellar Dysmetria 1 | 56
Collapse of vertebra 1 | 14
Compression fracture of vertebral column 1 | 14
Congenital Nonbullous Ichthyosiform Erythroderma 1 | 16
Coughing 1 | 25
Decrease in jaw opening 1 | 5
Delayed Puberty 1 | 97
Dementia, Lewy Body 1 | 3
Desquamation of skin soon after birth 1 | 10
Dilated fourth ventricle 1 | 4
Drooping upper lip 1 | 4
Dysdiadochokinesis 1 | 25
Dysmetric saccades 1 | 9
Ectropion 1 | 38
Erlenmeyer flask femora 1 | 4
Everted lower lip vermilion 1 | 54
Everted upper lip vermilion 1 | 4
Familial dysautonomia 1 | 3
Fatigable weakness of respiratory muscles 1 | 28
Fatigable weakness of swallowing muscles 1 | 28
Gaucher Disease 1 | 4
Gaucher Disease, Type 1 1 | 2
Glaucoma, Primary Open Angle 1 | 8
Globulin gamma serum plasma increased result 1 | 9
Hereditary spastic paraplegia 36 1 | 3
Horizontal Nystagmus 1 | 10
Hydrops Fetalis 1 | 21
Hydrops Fetalis, Non-Immune 1 | 8
Hypergammaglobulinemia 1 | 10
Hyperglobulinemia 1 | 9
Hyperkyphosis 1 | 111
Hypertension, Pulmonary 1 | 37
Idiopathic pulmonary arterial hypertension 1 | 40
Impaired horizontal smooth pursuit 1 | 6
Kyphosis deformity of spine 1 | 114
Lewy body dementia 1 | 4
Limited jaw mobility 1 | 5
Limited jaw opening 1 | 5
Lung Diseases, Interstitial 1 | 5
Movement disease 1 | 11
Mucolipidosis Type IV 1 | 2
Muscle Cramp 1 | 55
Neonatal Death 1 | 14
Nystagmus, End-Position 1 | 12
Olivopontocerebellar Atrophies 1 | 6
Olivopontocerebellar atrophy 1 | 9
Opisthotonus 1 | 14
Osteosclerosis 1 | 31
Pain 1 | 103
Paraparesis, Spastic 1 | 16
Petechiae 1 | 13
Plasmacytoma 1 | 7
Progressive cerebellar ataxia 1 | 13
Protruding lower lip 1 | 54
Protruding upper lip 1 | 4
Protuberant abdomen 1 | 16
Raised level of immunoglobulins NOS 1 | 9
Recurrent aspiration pneumonia 1 | 4
Reticulate hyperpigmentation 1 | 5
Slowed saccades 1 | 12
Spinocerebellar ataxia 2 1 | 1
Spinocerebellar ataxia type 2 1 | 23
Spinocerebellar ataxia type 36 1 | 2
Spinocerebellar tract degeneration 1 | 4
Static Tremor 1 | 21
Stillbirth 1 | 17
Supranuclear ophthalmoplegia 1 | 4
Trismus 1 | 6
Vascular Calcification 1 | 3
Xerostomia 1 | 42
gamma globulins increased 1 | 9

Tissue

Blood and immune system 2 | 16,909
Cardiovascular System 2 | 15,192
Digestive Tract 2 | 17,369
Endocrine System 2 | 18,159
Female tissues 2 | 17,400
Liver and Pancreas 2 | 16,750
Male tissues 2 | 17,142
Nervous System 2 | 16,725
Respiratory system 2 | 16,393
Skin and soft tissues 2 | 17,230
Urinary Tract 2 | 16,678

Target Family

Enzyme 1 | 4,145
Non-IDG 1 | 12,091

OMIM Phenotype

Parkinson disease, late-onset,... 2 | 2
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

This is where graphics are reside..
Name Gene Development Level Target Family Log Novelty  Pubmed Score  Antibody Count  Knowledge Availability 
Ataxin-2 ATXN2 Tbio Non-IDG -2.32523 224.6 194
Glucosylceramidase GBA Tchem Enzyme -3.22080 1617.1 299