Development Level

Tclin 1 | 613

Disease

Abnormal behavior 1 | 52
Abnormality of vision 1 | 40
Administration of Corneal Anesthesia 1 | 6
Administration of Local Anesthetic Nerve Block 1 | 14
Administration of Regional Anesthesia 1 | 7
Anesthesia for cesarean section 1 | 8
Autistic Disorder 1 | 364
Autosomal dominant nonsyndromic deafness 16 1 | 2
Benign familial infantile epilepsy 1 | 6
Benign familial neonatal-infantile seizures 1 | 1
Bipolar disorder in remission 1 | 19
Cardioversion of Atrial Fibrillation 1 | 9
Choreoathetoid movements 1 | 32
Choreoathetosis 1 | 32
Cough 1 | 23
Cyanosis 1 | 17
Dialeptic seizures 1 | 1
Disturbance of consciousness 1 | 12
Dysesthesia 1 | 6
Dyskinetic syndrome 1 | 16
Dysuria 1 | 26
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 1 | 1
Early infantile epileptic encephalopathy with suppression bursts 1 | 10
Enophthalmos 1 | 75
Epilepsies, Myoclonic 1 | 32
Epilepsy characterized by intractable complex partial seizures 1 | 28
Epilepsy, Benign Neonatal, 3 1 | 1
Epileptic Encephalopathy, Early Infantile, 6 1 | 8
Epileptic encephalopathy 1 | 26
Familial benign neonatal epilepsy 1 | 5
Febrile Convulsions 1 | 14
Focal Clonic Seizures 1 | 9
Focal seizures, afebril 1 | 1
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 1 | 7
Generalized epilepsy with febrile seizures plus 1 | 7
Generalized myoclonic seizures 1 | 30
Hemorrhoids 1 | 13
Highly variable severity 1 | 157
Infantile Severe Myoclonic Epilepsy 1 | 8
Infantile onset 1 | 238
Infestation by Phthirus pubis 1 | 7
Infestation by Sarcoptes scabiei var hominis 1 | 7
Itching of skin 1 | 18
Lennox-Gastaut syndrome 1 | 34
Life-Threatening Ventricular Tachycardia 1 | 15
Local Anesthesia for Endotracheal Intubation 1 | 6
Local Anesthesia for Ophthalmologic Procedure 1 | 7
Local Anesthesia for Urethral Pain 1 | 6
Local anesthesia 1 | 40
Local anesthesia, by infiltration 1 | 14
Local anesthetic intrathecal block 1 | 7
Localization-related epilepsy 1 | 13
Major Nerve Block for Surgery 1 | 8
Minor Skin Wound Pain 1 | 12
Motor cortex epilepsy 1 | 10
Mouth Irritation 1 | 12
Muscle Hypertonia 1 | 88
Myoclonic Epilepsies, Progressive 1 | 44
Myoclonus 1 | 74
Neuralgia 1 | 20
Normal interictal EEG 1 | 2
Obtundation status 1 | 7
Partial seizure 1 | 15
Partial seizures with secondary generalisation 1 | 4
Pediculosis capitis 1 | 7
Photosensitivity of skin 1 | 51
Postherpetic neuralgia 1 | 11
Premature ejaculation 1 | 16
Prevent Minor Bacterial Skin Infection 1 | 10
Prevention of Seizures following Cranial Trauma or Surgery 1 | 7
Pruritus ani 1 | 14
Pseudobulbar affect 1 | 5
Regional Anesthesia for Labor Pain 1 | 9
Regional Anesthesia for Ophthalmologic Surgery 1 | 6
Regional Anesthesia for Postoperative Pain 1 | 9
Regional Anesthesia for Surgery 1 | 9
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 1 | 1
Scrapie 1 | 17
Seizures in Neurosurgery 1 | 7
Seizures, Febrile 1 | 7
Seizures, Focal 1 | 14
Sickle Cell Anemia 1 | 53
Simple partial seizure 1 | 26
Skin irritation 1 | 12
Sore throat symptom 1 | 12
Spastic Quadriplegia 1 | 42
Sunken eyes 1 | 63
Suppression of the Gag Reflex 1 | 12
Thalassemia 1 | 53
Tinea Infections 1 | 10
Tinea corporis 1 | 25
Tonic - clonic seizures 1 | 44
Tonic-clonic epilepsy 1 | 47
Tonic-clonic seizure 1 | 11
Tremor 1 | 113
Urethritis 1 | 10
Urinary Tract Irritation 1 | 24
Variable expressivity 1 | 157
Ventricular arrhythmia 1 | 27
West Syndrome 1 | 28

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

Ion Channel 1 | 344

OMIM Phenotype

Phenotype: Seizures, benign fa... 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 
Sodium channel protein type 2 subunit alpha SCN2A Tclin Ion Channel -3.11580 1268.8 107