Development Level

Tbio 1 | 11,445

Disease

Absence of septum pellucidum 1 | 13
Adducted thumb 1 | 22
Agenesis of corpus callosum 1 | 83
Aphasia 1 | 26
Aqueductal Stenosis 1 | 5
Astrocytoma, Pilocytic 1 | 3,081
Big calvaria 1 | 147
Bilateral fifth finger clinodactyly 1 | 110
CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED 1 | 1
Cancer 1 | 2,499
Carcinoma 1 | 11,493
Carcinoma, Renal Cell 1 | 124
Cerebellar Hypoplasia 1 | 61
Clenched hands 1 | 6
Congenital Hand Deformities 1 | 8
Congenital anomaly of face 1 | 56
Congenital clubfoot 1 | 109
Congenital pes cavus 1 | 88
Contracture of joint of thumb 1 | 1
Corticospinal tract hypoplasia 1 | 3
Curvature of little finger 1 | 110
Delayed speech and language development 1 | 112
Dilated ventricles (finding) 1 | 121
Distortion of face 1 | 46
Dull intelligence 1 | 645
Dysmorphic facies 1 | 46
Epilepsy 1 | 792
Flexion contracture of proximal interphalangeal joint 1 | 75
Funny looking face 1 | 46
Gait Disorders, Neurologic 1 | 3
Gait abnormality 1 | 135
Gait, Shuffling 1 | 8
Hand Deformities, Congenital 1 | 8
Hemiplegia and hemiparesis 1 | 38
Hirschsprung Disease 1 | 31
Hirschsprung's disease 1 | 46
Hydrocephalus 1 | 152
Hydrocephalus, X-linked 1 | 1
Hyperkyphosis 1 | 111
Hyperreflexia 1 | 209
Increased head circumference 1 | 147
Increased size of cranium 1 | 147
Increased size of skull 1 | 147
Inferior vermis hypoplasia 1 | 2
Intellectual disability 1 | 1,016
Intracranial hypertension 1 | 32
Kidney cancer 1 | 2,613
Kyphosis deformity of spine 1 | 114
Language Delay 1 | 112
Lordosis 1 | 54
Low intelligence 1 | 645
MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome 1 | 1
MASA SYNDROME (disorder) 1 | 1
MASA syndrome 1 | 8
Megacolon 1 | 29
Mental Retardation 1 | 645
Mental deficiency 1 | 645
Muscle Spasticity 1 | 195
Muscle Weakness 1 | 170
Neurodegenerative disease 1 | 414
Paraplegia 1 | 74
Partial agenesis of corpus callosum 1 | 9
Partial or complete agenesis of corpus callosum 1 | 9
Poor school performance 1 | 645
Renal Cell Carcinoma 1 | 214
Seizures 1 | 596
Severe mental retardation (I.Q. 20-34) 1 | 99
Short stature 1 | 531
Small head 1 | 374
Spastic Paraplegia 1 | 42
Speech Delay 1 | 112
Speech impairment 1 | 112
Strabismus 1 | 270
X- linked recessive 1 | 110
X-linked complicated corpus callosum dysgenesis 1 | 1
X-linked hydrocephalus syndrome 1 | 1
adult high grade glioma 1 | 3,801
aldosterone-producing adenoma 1 | 665
astrocytic glioma 1 | 2,597
atypical teratoid / rhabdoid tumor 1 | 5,112
colon cancer 1 | 1,478
ependymoma 1 | 4,679
facial deformity 1 | 46
glioblastoma 1 | 5,792
hereditary spastic paraplegia 1 | 318
interstitial cystitis 1 | 2,312
malignant mesothelioma 1 | 3,232
oligodendroglioma 1 | 2,850
osteosarcoma 1 | 7,950
ovarian cancer 1 | 8,520
sonic hedgehog group medulloblastoma 1 | 467
subependymal giant cell astrocytoma 1 | 2,287

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

Non-IDG 1 | 12,091

OMIM Phenotype

Corpus callosum, partial agene... 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 
Neural cell adhesion molecule L1 L1CAM Tbio Non-IDG -2.67946 463.0 613