Development Level

Tbio 1 | 11,445

IMPC Phenotype

enlarged spleen 1 | 41
preweaning lethality, complete... 1 | 979

Disease

Abnormal behavior 1 | 52
Abnormal skeletal development 1 | 60
Abnormality of metabolism/homeostasis 1 | 134
Abnormality of retinal pigmentation 1 | 111
Abnormality of the liver 1 | 21
Abnormality of the palate 1 | 17
Addison Disease 1 | 18
Adrenal cortical hypofunction 1 | 23
Adrenoleukodystrophy 1 | 29
Adrenoleukodystrophy, Neonatal 1 | 13
Big calvaria 1 | 147
Blepharoptosis 1 | 231
Chromosome 17q12 deletion syndrome 1 | 16
Clouding of corneal stroma 1 | 50
Corneal Opacity 1 | 53
Death in early childhood 1 | 82
Death in infancy 1 | 82
Decreased liver function 1 | 24
Decreased to absent deep tendon reflexes 1 | 42
Developmental regression 1 | 95
Difficulties with night vision 1 | 87
Electroencephalogram abnormal 1 | 101
Elevated levels of phytanic acid 1 | 15
Embryotoxon 1 | 28
Flat back of the head 1 | 26
Flat face 1 | 52
Flat occiput 1 | 26
Global developmental delay, severe 1 | 47
High forehead 1 | 102
Hydronephrosis 1 | 89
Hyperreflexia 1 | 209
Hypotonia, neonatal, generalized 1 | 7
Hypotonia, severe 1 | 33
Icterus 1 | 82
Impaired cognition 1 | 96
Increased head circumference 1 | 147
Increased size of cranium 1 | 147
Increased size of skull 1 | 147
Infantile Refsum Disease (disorder) 1 | 13
Infantile Refsum disease 1 | 23
Liver Dysfunction 1 | 99
Liver Failure 1 | 73
Liver diseases 1 | 87
Liver dysfunction, mild 1 | 24
Long narrow head 1 | 75
Loss of developmental milestones 1 | 95
Low Vision 1 | 174
Malabsorption 1 | 82
Malformations of Cortical Development, Group II 1 | 31
Malformed pinnae 1 | 37
Mental deterioration in childhood 1 | 95
Mental impairment 1 | 95
Movement Disorders 1 | 55
Muscle Spasticity 1 | 195
Muscle weakness, progressive 1 | 22
Narrow cranium shape 1 | 75
Narrow head shape 1 | 75
Narrow skull shape 1 | 75
Neonatal Hypotonia 1 | 64
Neonatal adrenoleucodystrophy 1 | 5
Neonatal adrenoleukodystrophy 1 | 14
Neurodevelopmental regression 1 | 95
Night Blindness 1 | 101
Osteochondrodysplasias 1 | 72
PEROXISOME BIOGENESIS DISORDER 2B 1 | 5
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER) 1 | 1
PEROXISOME BIOGENESIS DISORDER 7B 1 | 1
Penile hypospadias 1 | 106
Peroxisomal disease 1 | 22
Peroxisome Biogenesis Disorder 1A (Zellweger) 1 | 12
Peroxisome Biogenesis Disorder 3B 1 | 11
Peroxisome biogenesis disorders 1 | 11
Polymicrogyria 1 | 48
Posterior embryotoxon 1 | 28
Premature Birth 1 | 77
Premature birth of newborn 1 | 67
Profound global developmental delay 1 | 17
Psychomotor regression 1 | 95
Psychomotor regression beginning in infancy 1 | 95
Psychomotor regression in infants 1 | 95
Psychomotor regression, progressive 1 | 95
Psychomotor retardation, profound 1 | 17
Pyloric Stenosis 1 | 47
Refsum Disease, Infantile 1 | 3
Respiratory Insufficiency 1 | 132
Respiratory function loss 1 | 121
Retinal pigment epithelial abnormality 1 | 111
Sensorineural Hearing Loss (disorder) 1 | 284
Severe psychomotor retardation 1 | 47
Stippled epiphyses 1 | 28
Tall forehead 1 | 102
Turridolichocephaly 1 | 75
Underdeveloped brows 1 | 38
Underdeveloped supraorbital ridges 1 | 38
Very long chain fatty acid accumulation 1 | 13
Visual Impairment 1 | 174
Visual field constriction 1 | 36
Wide anterior fontanel 1 | 44
Williams-Beuren syndrome 1 | 50
Zellweger syndrome 1 | 37

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: Peroxisome biogenes... 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 
Peroxisome assembly protein 26 PEX26 Tbio Non-IDG -1.04829 11.8 85