Development Level

Tbio 1 | 11,445

IMPC Phenotype

abnormal embryo size 1 | 220
abnormal tail morphology 1 | 25
enlarged lymph nodes 1 | 37
hemorrhage 1 | 23
no spontaneous movement 1 | 1
preweaning lethality, complete... 1 | 979

Disease

Abnormality of the cranial nerves 1 | 7
Achondroplasia 1 | 21
Anteverted ears 1 | 2
Autosomal recessive nonsyndromic deafness 63 1 | 10
Autosomal recessive predisposition 1 | 1,442
Breast Neoplasms 1 | 445
Broad flat nasal bridge 1 | 236
Cancer 1 | 2,499
Carcinoma, Hepatocellular 1 | 228
Cleft Lip 1 | 141
Cleft Palate 1 | 271
Congenital aplasia of inner ear 1 | 1
Congenital small ears 1 | 48
Cranial nerve abnormality 1 | 7
Craniofacial Abnormalities 1 | 151
Deafness with labyrinthine aplasia, microtia, and microdontia 1 | 1
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia 1 | 1
Decreased size of teeth 1 | 62
Decreased width of tooth 1 | 59
Downward slant of palpebral fissure 1 | 158
Gross motor development delay 1 | 21
Hearing Loss, Sensorineural 1 | 11
Hypochondroplasia 1 | 10
Hypoplastic mandible condyle 1 | 275
LADD syndrome 1 | 9
Liver carcinoma 1 | 240
Long face 1 | 71
Mammary Neoplasms 1 | 425
Mandibular hypoplasia 1 | 275
Microdontia (disorder) 1 | 59
Micrognathism 1 | 275
Microtia, first degree 1 | 3
Nasal bridge wide 1 | 236
Oculootodental Syndrome 1 | 2
Otodental Dysplasia 1 | 2
Otodental syndrome 1 | 1
Peg-shaped teeth 1 | 8
Pointed chin 1 | 33
Pointed teeth 1 | 8
Profound sensorineural hearing impairment 1 | 4
Sensorineural Hearing Loss (disorder) 1 | 284
Sensorineural hearing loss 1 | 106
Skin tag 1 | 14
Stomatognathic Diseases 1 | 2
Thin hypoplastic alae nasi 1 | 51
Tooth agenesis 1 | 44
Type 1 diabetes mellitus 12 1 | 2
Type 1 diabetes mellitus 4 1 | 7
Type 1 diabetes mellitus 5 1 | 4
Type 1 diabetes mellitus 8 1 | 6
Widely spaced teeth 1 | 31
lung cancer 1 | 4,740
type 1 diabetes mellitus 2 1 | 3

Target Family

Non-IDG 1 | 12,091

OMIM Phenotype

Phenotype: Deafness, congenita... 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 
Fibroblast growth factor 3 FGF3 Tbio Non-IDG -2.29270 192.7 118