Development Level

Tbio 1 | 11,445

Disease

Abnormal collecting system 1 | 2
Abnormality of the cerebrum 1 | 3
Absent auditory canals 1 | 23
Absent external auditory canals 1 | 23
Astrocytoma, Pilocytic 1 | 3,081
Atresia of the external auditory canal 1 | 23
Atretic auditory canal 1 | 23
Autosomal dominant nonsyndromic deafness 10 1 | 4
Autosomal dominant nonsyndromic deafness 23 1 | 3
BRANCHIOOTIC SYNDROME 1 1 | 2
BRANCHIOOTIC SYNDROME 3 (disorder) 1 | 1
Branchio-Oto-Renal Syndrome 1 | 4
Branchioma 1 | 3
Branchiootic syndrome 1 | 12
Branchiootic syndrome 3 1 | 1
Branchiootorenal syndrome 1 | 8
Breast cancer 1 | 3,578
Bulbous internal auditory canal 1 | 5
Byzanthine arch palate 1 | 194
Cancer 1 | 2,499
Cholesteatoma 1 | 16
Cleft Palate 1 | 271
Cleft uvula 1 | 27
Commissural lip pit 1 | 1
Conductive hearing loss 1 | 123
Congenital Abnormalities 1 | 11
Congenital Abnormality 1 | 11
Congenital absence of kidney 1 | 31
Congenital deafness 1 | 185
Congenital malrotation of intestine 1 | 16
Craniofacial Abnormalities 1 | 151
DEAFNESS, AUTOSOMAL DOMINANT 23 1 | 1
Deafness 1 | 198
Decreased size of teeth 1 | 62
Decreased width of tooth 1 | 59
Deep overbite 1 | 4
Endometrial Neoplasms 1 | 55
Enlarged cochlear aqueduct 1 | 2
Euthyroid Goiter 1 | 3
Eye and adnexa disease 1 | 18
Fistula of branchial cleft 1 | 2
Glaucoma 1 | 239
Gustatory lacrimation 1 | 2
Hearing Loss, Mixed Conductive-Sensorineural 1 | 12
Hearing Loss, Partial 1 | 185
Highly variable severity 1 | 157
Hip Dislocation, Congenital 1 | 48
Hypoplastic cochlea 1 | 6
Incomplete partition of the cochlea type II 1 | 3
Long face 1 | 71
Malformed ossicles 1 | 3
Malformed pinnae 1 | 37
Malrotation of kidney 1 | 2
Melnick-Fraser syndrome 1 | 2
Microdontia (disorder) 1 | 59
Middle ear malformations 1 | 5
Mondini malformation 1 | 3
Narrow face 1 | 54
Narrowing of ear canal 1 | 13
Nonsyndromic deafness 1 | 142
Overbite 1 | 4
Polycystic Kidney - body part 1 | 18
Polycystic Kidney Diseases 1 | 20
Posterior lingual occlusion of mandibular teeth 1 | 4
Preauricular Fistulae, Congenital 1 | 27
Preauricular dimple 1 | 27
Preauricular sinus 1 | 27
Preauricular skin tag 1 | 19
RENAL ADYSPLASIA 1 | 25
Renal agenesis 1 | 29
Renal dysplasia 1 | 28
Renal hypoplasia/aplasia 1 | 7
Renal steatosis 1 | 4
Sensorineural Hearing Loss (disorder) 1 | 284
Skin tag on the posterior cheek 1 | 19
Stenosis of external auditory canal 1 | 13
Stenosis of nasolacrimal duct 1 | 4
Thin face 1 | 54
Townes-Brocks syndrome 1 | 15
Uranostaphyloschisis 1 | 167
Variable expressivity 1 | 157
Vesico-Ureteral Reflux 1 | 33
Wilms Tumor 1 | 28
adult high grade glioma 1 | 3,801
atypical teratoid / rhabdoid tumor 1 | 5,112
breast carcinoma 1 | 1,638
glioblastoma 1 | 5,792
group 4 medulloblastoma 1 | 1,855
hearing impairment 1 | 199
intraductal papillary-mucinous neoplasm (IPMN) 1 | 3,291
invasive ductal carcinoma 1 | 2,951
lung adenocarcinoma 1 | 2,716
lung cancer 1 | 4,740
lung carcinoma 1 | 2,843
malignant mesothelioma 1 | 3,232
medulloblastoma, large-cell 1 | 6,241
nasopharyngeal carcinoma 1 | 1,058
non primary Sjogren syndrome sicca 1 | 891
non-small cell lung cancer 1 | 2,890
ovarian cancer 1 | 8,520

Tissue

Blood and immune system 1 | 16,909
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

Transcription Factor 1 | 1,400

OMIM Phenotype

Phenotype: Branchiootic syndro... 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 
Homeobox protein SIX1 SIX1 Tbio Transcription Factor -2.64041 433.7 111