Development Level

Tbio 1 | 11,445

Disease

Acquired flat foot 1 | 72
Action Tremor 1 | 22
Amenorrhea 1 | 58
Anxiety 1 | 136
Anxiety Disorders 1 | 38
Anxiety disease 1 | 113
Atypical autism 1 | 26
Autonomic nervous system disorders 1 | 19
Brain disease 1 | 96
CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME 1 | 1
Cerebellar Dysmetria 1 | 56
Class III malocclusion 1 | 78
Congenital Abnormalities 1 | 11
Congenital Abnormality 1 | 11
Congenital macroorchidism 1 | 1
Craniofacial Abnormalities 1 | 151
Decreased distal vibration sense 1 | 4
Depressive Symptoms 1 | 28
Diffuse cerebellar atrophy 1 | 2
Diffuse cerebral atrophy 1 | 8
Dysautonomia 1 | 20
Dysdiadochokinesis 1 | 25
Dysesthesia 1 | 6
Elevated gonadotropins 1 | 15
Enophthalmos 1 | 75
Erectile dysfunction 1 | 32
FRAGILE X TREMOR/ATAXIA SYNDROME 1 | 1
FRAXA Syndrome 1 | 1
Facies 1 | 8
Fecal Incontinence 1 | 7
Flatfoot 1 | 73
Folate-dependent fragile site at Xq28 1 | 1
Forgetful 1 | 40
Fragile 10 Mental Retardation Syndrome 1 | 2
Fragile 10 Tremor/Ataxia Syndrome 1 | 1
Fragile X Tremor Ataxia Syndrome 1 | 1
Fragile X-associated tremor/ataxia syndrome 1 | 6
Gonadal Dysgenesis 1 | 28
Gynecomastia 1 | 64
Head movements abnormal 1 | 1
High pitched voice 1 | 23
Hyperactive behavior 1 | 91
Hyperplasia of forehead 1 | 3
Hypertrophy of forehead 1 | 3
Hypertrophy of lower jaw 1 | 78
Hypoplastic feet 1 | 66
Increased frequency of micturition 1 | 2
Increased size of mandible 1 | 78
Inertia 1 | 1
Irregular periods 1 | 6
Joint laxity 1 | 54
Large forehead 1 | 3
Learning disability 1 | 17
Macroorchidism 1 | 7
Macroorchidism, postpubertal 1 | 2
Mandibular hyperplasia 1 | 78
Mask-like facies 1 | 25
Memory Loss 1 | 40
Memory impairment 1 | 40
Mild Mental Retardation 1 | 70
Mitral Valve Prolapse Syndrome 1 | 39
Mixed anxiety and depressive disorder 1 | 12
Mood instability 1 | 2
Mucopolysaccharidosis II 1 | 5
Muscle Rigidity 1 | 49
Muscle Weakness 1 | 170
Myalgia 1 | 54
Narrow face 1 | 54
Obesity, Abdominal 1 | 24
Obsessive compulsive behavior 1 | 25
Obsessive-compulsive trait 1 | 4
Ovarian Failure, Premature 1 | 9
Ovarian dysfunction 1 | 18
Paranasal Sinus Diseases 1 | 34
Parkinsonian Disorders 1 | 56
Periventricular neuronal heterotopia 1 | 6
Poor eye contact 1 | 12
Poor fine motor coordination 1 | 4
Premature Menopause 1 | 31
Premature ovarian failure 1 | 65
Premature ovarian failure 1 1 | 2
Primary Ovarian Insufficiency 1 | 6
Primary Ovarian Insufficiency, Fragile X-Associated 1 | 1
Resting Tremor 1 | 9
Saccadic smooth pursuit 1 | 3
Sinusitis 1 | 65
Small hand 1 | 36
Small testicle 1 | 75
Social disinhibition 1 | 14
Sparse body hair 1 | 32
Sphincter disturbances 1 | 16
Static Tremor 1 | 21
Sunken eyes 1 | 63
Terminal tremor 1 | 20
Thin face 1 | 54
X-linked dominant 1 | 57
Xq27.3q28 duplication syndrome 1 | 1
mandibular excess (physical finding) 1 | 78
obsessive-compulsive disorder 1 | 61
sarcoidosis 1 | 370

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

Epigenetic 1 | 242

OMIM Phenotype

Premature ovarian failure 1 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 
Synaptic functional regulator FMR1 FMR1 Tbio Epigenetic -3.38241 2443.7 484