Development Level

Tbio 1 | 11,445

Disease

Abnormality of the rib cage 1 | 12
Acquired scoliosis 1 | 281
Anxiety 1 | 136
Anxiety disease 1 | 113
Arachnodactyly 1 | 49
Atrial Septal Defects 1 | 85
Bilateral fifth finger clinodactyly 1 | 110
Blind Vision 1 | 111
Blindness, Legal 1 | 110
Brachycephaly 1 | 88
Brittle hair 1 | 25
Broad cranium shape 1 | 88
Broad flat nasal bridge 1 | 236
Bulbous nasal tip 1 | 48
Bulbous nose 1 | 48
Byzanthine arch palate 1 | 194
Capuchin ears 1 | 17
Cerebral atrophy 1 | 178
Class III malocclusion 1 | 78
Congenital Camptodactyly 1 | 40
Congenital Epicanthus 1 | 177
Congenital deafness 1 | 185
Congenital ocular coloboma (disorder) 1 | 40
Congenital pes cavus 1 | 88
Congenital phimosis 1 | 4
Contracture of joint of hand 1 | 30
Cupped ears (finding) 1 | 17
Curvature of little finger 1 | 110
Curvature of spine 1 | 282
Deafness 1 | 198
Death in early childhood 1 | 82
Death in infancy 1 | 82
Degenerative brain disorder 1 | 100
Dry hair 1 | 7
Dystrophia unguium 1 | 53
Fractured hair 1 | 25
Fragile hair 1 | 25
Growth Disorders 1 | 35
Hamel cerebro-palato-cardiac syndrome 1 | 1
Hearing Loss, Partial 1 | 185
Heart Septal Defects, Atrial 1 | 2
Hypernasal voice 1 | 39
Hyperopia 1 | 70
Hyperreflexia 1 | 209
Hypertrophy of lower jaw 1 | 78
Hypotrophic malar bone 1 | 129
Increased size of mandible 1 | 78
Large auricle 1 | 87
Large dysplastic ears 1 | 87
Large pinnae 1 | 87
Large prominent ears 1 | 87
Large protruding ears 1 | 87
Large, floppy ears 1 | 87
Laterally sparse eyebrows 1 | 12
Little's Disease 1 | 14
Macroglossia 1 | 65
Macrotia 1 | 87
Malar flattening 1 | 129
Mandibular hyperplasia 1 | 78
Mental Retardation, X-Linked 1 | 23
Microcephaly 1 | 166
Microstomia 1 | 78
Muscle Spasticity 1 | 195
Narrow face 1 | 54
Narrow foot 1 | 3
Nasal bridge wide 1 | 236
Nasal voice 1 | 39
Partington syndrome 1 | 9
Pectus excavatum 1 | 100
Penile hypospadias 1 | 106
Poor suck 1 | 17
Potato nose 1 | 48
Prominent ear 1 | 56
Protruding ears 1 | 56
Reduced tensile strength of hair 1 | 25
Renpenning syndrome 1 | 1
Renpenning syndrome 1 1 | 1
Seizures 1 | 596
Short philtrum 1 | 53
Situs Inversus 1 | 65
Situs ambiguus 1 | 25
Small testicle 1 | 75
Sparse hair 1 | 59
Spastic Paraplegia, Hereditary 1 | 5
Spastic diplegia 1 | 5
Spinocerebellar ataxia type 1 1 | 16
Strabismus 1 | 270
Supratentorial atrophy 1 | 94
Tetralogy of Fallot 1 | 63
Thin face 1 | 54
Thin upper lip vermilion 1 | 67
Thin, sparse hair 1 | 59
Triangular face 1 | 58
Upward slant of palpebral fissure 1 | 75
Ventricular Septal Defects 1 | 119
Wide skull shape 1 | 88
X- linked recessive 1 | 110
X-linked intellectual disability, Golabi-Ito-Hall type 1 | 1
hearing impairment 1 | 199
mandibular excess (physical finding) 1 | 78

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: Renpenning 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 
Polyglutamine-binding protein 1 PQBP1 Tbio Non-IDG -1.68270 53.0 101