Development Level

Tclin 1 | 613

Disease

Abnormal cortical bone morphology 1 | 22
Abnormality of epiphysis morphology 1 | 39
Abnormality of metabolism/homeostasis 1 | 134
Abnormality of the ankles 1 | 5
Abnormality of the hip bone 1 | 16
Abnormality of the knee 1 | 6
Abnormality of the musculature 1 | 16
Absence Epilepsy 1 | 22
Acral ulceration leading to autoamputation of digits 1 | 3
Acro-Osteolysis 1 | 12
Administration of Local Anesthetic Nerve Block 1 | 14
Administration of Regional Anesthesia 1 | 7
Anhidrosis 1 | 23
Anosmia 1 | 22
Autonomic nervous system disorders 1 | 19
Bipolar disorder in remission 1 | 19
Blurred vision 1 | 19
Bradycardia 1 | 36
Burning mouth syndrome 1 | 7
Chronic pain 1 | 9
DOID:2627 1 | 94
Decreased bone mineral density Z score 1 | 31
Decreased nerve conduction velocity 1 | 35
Decreased pain sensation 1 | 17
Decreased sensory nerve conduction velocities (NCV) 1 | 8
Dental caries 1 | 164
Dysautonomia 1 | 20
Dystrophic fingernails 1 | 18
Dystrophic toenail changes 1 | 12
Elevated heart rate 1 | 25
Epilepsies, Myoclonic 1 | 32
Epileptic Encephalopathy, Early Infantile, 6 1 | 8
Epileptic drop attack 1 | 11
Erythema 1 | 58
Erythermalgia, Primary 1 | 1
Eye pain 1 | 2
Febrile Convulsions 1 | 14
Flushing 1 | 60
Focal Clonic Seizures 1 | 9
Foot acroosteolysis 1 | 5
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 1 | 7
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 1 | 2
Generalized Epilepsy With Febrile Seizures Plus, 7 1 | 1
Generalized epilepsy with febrile seizures plus 1 | 7
Generalized epilepsy with febrile seizures plus, type 7 1 | 1
Generalized myoclonic seizures 1 | 30
Glossopharyngeal neuralgia 1 | 5
Hemorrhoids 1 | 13
Hereditary Motor and Sensory-Neuropathy Type II 1 | 4
Hereditary sensory and autonomic neuropathy type 2 1 | 4
Hereditary sensory neuropathy 1 | 11
Herpesviridae Infections 1 | 3
Hyperekplexia 1 | 16
Hyperhidrosis disorder 1 | 81
Hyperhidrosis, episodic 1 | 4
Hypogeusia 1 | 5
Hypohidrosis 1 | 34
Hypotonic seizures 1 | 11
Increased sweating 1 | 81
Indifference to Pain, Congenital, Autosomal Recessive 1 | 1
Infantile Severe Myoclonic Epilepsy 1 | 8
Jaw pain 1 | 2
Lacrimation abnormality 1 | 4
Local Anesthesia for Endotracheal Intubation 1 | 6
Local anesthesia, by infiltration 1 | 14
Lordosis 1 | 54
Mixed Epilepsy 1 | 3
Mouth Irritation 1 | 12
Myalgia 1 | 54
Myoclonic Epilepsies, Progressive 1 | 44
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA 1 | 4
Neonatal onset 1 | 21
Neuralgia, Postherpetic 1 | 3
Neuropathy, Hereditary Sensory and Autonomic, Type 2A 1 | 4
Obtundation status 1 | 7
Pain 1 | 103
Palpitations 1 | 18
Paronychia Inflammation 1 | 9
Partial Epilepsy Treatment Adjunct 1 | 16
Pediculosis capitis 1 | 7
Peripheral Neuropathy 1 | 134
Photosensitivity of skin 1 | 51
Prevention of Seizures following Cranial Trauma or Surgery 1 | 7
Pruritus 1 | 58
Regional Anesthesia for Ophthalmologic Surgery 1 | 6
Seizures in Neurosurgery 1 | 7
Seizures, Focal 1 | 14
Sense of smell impaired 1 | 21
Sweating 1 | 81
Tapering fingers (finding) 1 | 25
Tinea Infections 1 | 10
Tinea corporis 1 | 25
Tonic - clonic seizures 1 | 44
Tremor 1 | 113
Trigeminal Neuralgia 1 | 24
Urethritis 1 | 10
Urinary Incontinence 1 | 50
Urinary Tract Irritation 1 | 24
Xerostomia 1 | 42
multidrug-resistant tuberculosis 1 | 7

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

Ion Channel 1 | 344

OMIM Phenotype

Insensitivity to pain, congeni... 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 9 subunit alpha SCN9A Tclin Ion Channel -2.57994 379.2 327