Development Level

Tbio 1 | 11,445

Disease

Abnormality of the nasopharynx 1 | 9
Abnormality of the rib cage 1 | 12
Abnormally folded helix 1 | 2
Aneurysm of ascending aorta 1 | 5
Anteriorly placed anus 1 | 7
Asymmetry of the posterior cranium 1 | 20
Birthmark 1 | 35
Blepharophimosis syndrome Ohdo type 1 | 1
Breast fibroadenoma 1 | 8
Broad hallux 1 | 29
Broad thumbs 1 | 28
Cafe-au-Lait Spots 1 | 37
Choanal Atresia 1 | 42
Claw hand 1 | 26
Congenital Camptodactyly 1 | 40
Connective tissue cancer 1 | 10
Contracture of joint of hand 1 | 30
Convex nasal bridge 1 | 57
DOID:9917 1 | 31
Decreased projection of maxilla 1 | 66
Deep philtrum 1 | 21
Deficiency of upper jaw bones 1 | 66
Delayed closure of the soft spot on the skull 1 | 11
Depressed philtrum 1 | 21
Disorder of the genitourinary system 1 | 6
Ectopic Tissue 1 | 14
Fine hair 1 | 42
Flattening of cranial vault 1 | 20
Flattening of head 1 | 20
Full lower lip 1 | 64
Generalized hypotonia 1 | 37
Genitourinary dysplasia 1 | 6
Hair whorls 1 | 3
High pitched voice 1 | 23
Hyperactive behavior 1 | 91
Hypernasal voice 1 | 39
Hypoplasia of scrotum 1 | 24
Hypoplasia of the maxilla 1 | 66
Hypotrophic maxilla 1 | 66
Inadequate arch length for tooth size 1 | 45
Joint laxity 1 | 54
Joint swelling onset late infancy 1 | 1
Kaposi's sarcoma 1 | 22
Late closure of anterior fontanel 1 | 11
Leiomyoma 1 | 32
Leiomyosarcoma 1 | 24
Long nose 1 | 15
Low frustration tolerance 1 | 2
Lujan Fryns syndrome 1 | 3
Macrocephaly, postnatal 1 | 2
Macroorchidism 1 | 7
Marfanoid body habitus 1 | 11
Maxillary retrognathia 1 | 66
Microtia, first degree 1 | 3
Narrow face 1 | 54
Narrow nose 1 | 20
Narrow palate 1 | 20
Nasal voice 1 | 39
Nonorganic psychosis 1 | 84
Obsessive compulsive behavior 1 | 25
Ohdo Syndrome, X-Linked 1 | 1
Ohdo syndrome 1 | 5
Ohdo syndrome, Maat-Kievit-Brunner type 1 | 1
Open mouth 1 | 45
Opitz-GBBB syndrome 1 | 18
Opitz-Kaveggia Syndrome 1 | 3
Partial agenesis of corpus callosum 1 | 9
Partial or complete agenesis of corpus callosum 1 | 9
Phyllodes Tumor 1 | 5
Pinched bridge of nose 1 | 14
Pinched nasal bridge 1 | 14
Plagiocephaly 1 | 20
Plagiocephaly, Nonsynostotic 1 | 20
Prominent fingertip pads 1 | 6
Prominent lower lip 1 | 64
Prominent nasal bridge 1 | 57
Retrusion of upper jaw bones 1 | 66
Rhomboid shaped head 1 | 20
Single transverse palmar crease 1 | 29
Skin tag 1 | 14
Smooth muscle tumor 1 | 13
Social Communication Disorder 1 | 4
Spontaneous ocular nystagmus 1 | 4
Sternal anomalies 1 | 19
Stricture of anus 1 | 13
Thin face 1 | 54
Tooth Crowding 1 | 45
Tooth mass arch size discrepancy 1 | 45
Tooth size discrepancy 1 | 45
Underweight 1 | 17
Upswept frontal hair pattern 1 | 3
Upswept frontal hairline 1 | 3
Urogenital Abnormalities 1 | 9
Uterine fibroid 1 | 28
Vestibular nystagmus 1 | 6
Weight less than 3rd percentile 1 | 17
Wrinkled face 1 | 2
X- linked recessive 1 | 110
X-linked intellectual disability with marfanoid habitus 1 | 3
obsessive-compulsive disorder 1 | 61

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

Enzyme 1 | 4,145

OMIM Phenotype

Ohdo syndrome, X-linked 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 
Mediator of RNA polymerase II transcription subunit 12 MED12 Tbio Enzyme -2.60835 402.9 124