Development Level

Tbio 1 | 11,445

Disease

Abnormality of epiphysis morphology 1 | 39
Abnormality of female external genitalia 1 | 8
Abnormality of the metaphyses 1 | 48
Absence of eyebrows 1 | 31
Absent earlobe 1 | 9
Accessory proximal metacarpal ossification centers 1 | 7
Acquired scoliosis 1 | 281
Agenesis of teeth 1 | 21
Aplasia/Hypoplasia of the earlobes 1 | 10
Aplasia/Hypoplasia of the eyebrow 1 | 31
Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines 1 | 1
Bilateral fifth finger clinodactyly 1 | 110
Birthmark 1 | 35
Brachydactyly 1 | 156
Brain Aneurysm 1 | 8
Broad flat nasal bridge 1 | 236
Cachexia 1 | 50
Cafe au lait spots, multiple 1 | 17
Cafe-au-Lait Spots 1 | 37
Cerebral arterial aneurysm 1 | 8
Cone-shaped epiphyses 1 | 24
Congenital small ears 1 | 48
Convex nasal bridge 1 | 57
Convex nasal ridge 1 | 37
Curvature of little finger 1 | 110
Decreased size of teeth 1 | 62
Decreased width of tooth 1 | 59
Defective enamel matrix 1 | 35
Defective tooth enamel 1 | 31
Dental Enamel Hypoplasia 1 | 43
Downward slant of palpebral fissure 1 | 158
Dry skin 1 | 75
Dubowitz syndrome 1 | 13
Dysplasia of tooth enamel 1 | 35
Dystrophic tooth enamel 1 | 31
Enamel abnormalities 1 | 31
Endometrial cancer 1 | 311
Fine hair 1 | 42
High pitched voice 1 | 23
Hip Dislocation, Congenital 1 | 48
Hip joint varus deformity - observation 1 | 24
Hypernasal voice 1 | 39
Hyperopia 1 | 70
Hyperplasia of nose 1 | 23
Hypertrophy of nose 1 | 23
Hypoplastic iliac wing 1 | 19
Impaired cognition 1 | 96
Isolated growth hormone deficiency 1 | 30
Joint hyperflexibility 1 | 78
Large nose 1 | 23
Major Depressive Disorder 1 | 301
Mental impairment 1 | 95
Microcephalic Osteodysplastic Primordial Dwarfism, Type II 1 | 1
Microcephalic osteodysplastic primordial dwarfism type 2 1 | 1
Microcephalic osteodysplastic primordial dwarfism type II 1 | 13
Microcephaly 1 | 166
Microdontia (disorder) 1 | 59
Mild global developmental delay 1 | 14
Moyamoya phenomenon 1 | 3
Narrow face 1 | 54
Narrow pelvis 1 | 6
Nasal bridge wide 1 | 236
Nasal voice 1 | 39
Nonorganic psychosis 1 | 84
Obesity, Abdominal 1 | 24
Penile hypospadias 1 | 106
Postnatal growth retardation 1 | 57
Precocious Puberty 1 | 28
Precociously senile appearance 1 | 18
Prominent nasal bridge 1 | 57
Psychomotor retardation, mild 1 | 14
Psychotic Disorders 1 | 151
Radial bowing 1 | 13
Reduced number of teeth 1 | 21
Retrognathia 1 | 54
SECKEL SYNDROME 2 1 | 2
Sandal gap 1 | 24
Seckel syndrome 1 | 34
Seckel syndrome 1 1 | 3
Sensorineural Hearing Loss (disorder) 1 | 284
Short distal phalanges 1 | 50
Short first metacarpals 1 | 11
Short stature, disproportionate 1 | 9
Short stature, severe disproportionate 1 | 9
Skull malformation 1 | 38
Slender, gracile long tubular bones 1 | 21
Slipped Capital Femoral Epiphyses 1 | 3
Sparse or absent eyebrows 1 | 31
Sparse scalp hair 1 | 42
Sparse/absent eyebrows 1 | 31
Splayed metaphyses 1 | 19
Thin dental enamel 1 | 35
Thin face 1 | 54
Thin hypoplastic alae nasi 1 | 51
Tibial bowing 1 | 19
Ulnar bowing 1 | 10
Unipolar Depression 1 | 250
Xerosis 1 | 75
hypopigmented skin patch 1 | 59
tick-borne encephalitis 1 | 14

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: Microcephalic osteo... 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 
Pericentrin PCNT Tbio Non-IDG -2.48224 282.2 129