Development Level

Tclin 1 | 613

Disease

ANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME 1 | 1
Abnormalities, Multiple 1 | 13
Acquired scoliosis 1 | 281
Acute lymphoid leukemia 1 | 25
Acute myeloid leukemia, disease 1 | 30
Acute promyelocytic leukemia, FAB M3 1 | 11
Adenocarcinoma of pancreas 1 | 14
Atrophic condition of skin 1 | 25
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 1 | 1
Cancer 1 | 2,499
Carcinoma 1 | 11,493
Colorectal Neoplasms 1 | 243
Congenital hereditary endothelial dystrophy of cornea 1 | 8
Contracture 1 | 96
Contracture of joint 1 | 93
Convex nasal ridge 1 | 37
Cryptorchidism 1 | 296
Curvature of spine 1 | 282
Deafness 1 | 198
Elevated hepatic transaminases 1 | 81
Endometrial Neoplasms 1 | 55
Exophthalmos 1 | 112
Familial adenomatous polyposis 1 | 32
Flexion contracture 1 | 93
Flexion contractures of joints 1 | 93
Hepatic enzyme increased 1 | 81
Hepatomegaly 1 | 285
High pitched voice 1 | 23
Hyperkyphosis 1 | 111
Hypertriglyceridemia result 1 | 37
Hypogonadism 1 | 173
Hypoplastic mandible condyle 1 | 275
Inadequate arch length for tooth size 1 | 45
Insulin Resistance 1 | 72
Jaw Abnormalities 1 | 5
Kidney cancer 1 | 2,613
Kyphosis deformity of spine 1 | 114
Lack of skin elasticity 1 | 10
Leukodystrophy 1 | 55
Lipodystrophy 1 | 40
Liver Dysfunction 1 | 99
Liver enzymes abnormal 1 | 81
Liver function test increased 1 | 81
Liver function tests abnormal finding 1 | 81
Lymphomatous meningitis 1 | 3
Lynch syndrome 1 | 35
MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME 1 | 1
Malignant tumor of ovary 1 | 25
Mandibular hypoplasia 1 | 275
Mandibular hypoplasia-deafness-progeroid syndrome 1 | 1
Meningeal Leukemia 1 | 7
Metastatic Breast Carcinoma 1 | 21
Micrognathism 1 | 275
Microstomia 1 | 78
Osteoporosis 1 | 363
Prominent eyes 1 | 96
Prominent globes 1 | 96
Protruding eyes 1 | 96
Sensorineural Hearing Loss (disorder) 1 | 284
Spider Veins 1 | 17
Steatohepatitis 1 | 44
Stretched skin 1 | 10
Subclinical abnormal liver function tests 1 | 81
Telangiectasis 1 | 36
Tooth Crowding 1 | 45
Tooth mass arch size discrepancy 1 | 45
Tooth size discrepancy 1 | 45
Transaminases increased 1 | 81
atypical teratoid / rhabdoid tumor 1 | 5,112
diabetes mellitus 1 | 1,728
group 3 medulloblastoma 1 | 4,104
lung adenocarcinoma 1 | 2,716
malignant mesothelioma 1 | 3,232
medulloblastoma, large-cell 1 | 6,241
non-small cell lung cancer 1 | 2,890
primitive neuroectodermal tumor 1 | 3,035
psoriasis 1 | 6,694

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

Mandibular hypoplasia, deafnes... 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 
DNA polymerase delta catalytic subunit POLD1 Tclin Enzyme -2.06760 110.4 225