1031
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SKI proto-oncogene |
SGS, SKV |
Curated: 1p36 deletion syndrome, Aortic aneurysm, Congenital contractural arachnodactyly, Congenital musculoskeletal anomalies, Coronary artery disease, Craniofacial abnormalities, Desbuquois syndrome, Thoracic aortic aneurysm and aortic dissection, Gastroesophageal reflux disease, Gout, Intellectual developmental disorder, Larsen syndrome, Metabolic syndrome, Migraine, Myocardial infarction, Neural tube defect, Neural tube defects, x-linked, Neurodevelopmental disorder, Ruptured abdominal aortic aneurysm, Ruptured aortic aneurysm, Ruptured thoracic aortic aneurysm, Shprintzen-goldberg syndrome, Thoracoabdominal aortic aneurysm, Diabetes mellitus type 2
Unreviewed: 1p36 Deletion Syndrome, Acrania, Adenoma, Age-related macular degeneration, Agenesis Of Corpus Callosum, Anencephaly, Aneurysm Of Aortic Arch, Annular pancreas, Anophthalmia, Aortic Aneurysm, Arachnodactyly, Arnold-Chiari malformation, Attention Deficit Hyperactivity Disorder, Autism, Autoimmune Diseases, Barrett esophagus, Brachycephaly, Brachydactyly, Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Camptodactyly of fingers, Carcinogenesis, Carcinoma, Cardiomyopathy, Cardiovascular abnormalities, Cataract, Cerebral cortical atrophy, Chromosome 1p36 deletion syndrome, Cleft lip, Cleft palate, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Communicating Hydrocephalus, Congenital Anomaly Of Neck, Congenital Camptodactyly, Congenital Epicanthus, Congenital Exomphalos, Congenital genu recurvatum, Congenital heart defect, Congenital Hypoplasia Of Penis, Congenital Musculoskeletal Anomalies, Congenital Pectus Carinatum, Congenital Pectus Excavatum, Cranial Nerve Paralysis, Craniofacial dysostosis, Craniorachischisis, Craniosynostosis, Cryptorchidism, Developmental Delay, Diastematomyelia, Dolichocephaly, Down syndrome, Dwarfism, Dysmorphic Features, Dysphagia, Esophageal Cancer, Fatty Liver, Fragile X Syndrome, Frontal bossing, Gastroesophageal Reflux Disease, Glioblastoma, Glioma, Growth disorder, Hearing Loss, Heart disease, Heart Septal Defects, Hemiplegia/hemiparesis, High palate, Hodgkin Disease, Hydronephrosis, Hypogonadism, Hypoplasia of the maxilla, Hypospadias, Hypothyroidism, Infantile Spasms, Intermittent Porphyria, Left ventricular noncompaction, Leiomyosarcoma, Leukemia, Lung adenocarcinoma, Lymphoma, Macrocytic anemia, Macular degeneration, Malignant Neoplasm, Melanoma, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Microtia, Mitral Valve Prolapse, Multiple Congenital Anomalies, Multiple myeloma, Myelodysplastic Syndrome, Myeloid Leukemia, Myeloproliferative disorder, Myopathy, Myopia, Neoplasms, Neural Tube Defect, Neurenteric Cyst, Neuroblastoma, Neurofibromatosis, Nystagmus, Obesity, Ocular albinism, Optic Atrophy, Osteopenia, Osteosarcoma, Pachyonychia Congenita, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Patent ductus arteriosus, Polycystic kidney disease, Polydactyly Of Toes, Posteriorly Rotated Ear, Primary Tethered cord syndrome, Proptosis, Prostate cancer, Prostatic neoplasm, Ptosis, Pulmonary Fibrosis, Renal cyst, Rib fusion, Sarcoma, Schinzel-Giedion Syndrome, Scoliosis, Shprintzen-Goldberg Syndrome, Spina Bifida, Spinal Cord Myelodysplasia, Stereotyped Behavior, Stomach neoplasms, Strabismus, Succinic Semialdehyde Dehydrogenase Deficiency, Syndromic microphthalmia, Tetralogy of Fallot, Thoracic Aortic Aneurysm And Aortic Dissection, Trichohepatoenteric Syndrome, Triple Negative Breast Neoplasms, Uterine neoplasm, West Syndrome
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1032
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SKI2 subunit of superkiller complex |
170A, DDX13, HLP, SKI2, SKI2W, SKIV2, SKIV2L, SKIV2L1, THES2 |
Curated: Atrophic macular degeneration, Coronary artery disease, Macular and posterior pole degeneration, Glaucoma, Immunodeficiency, Macular degeneration, Migraine, Mouth neoplasms, Nonalcoholic fatty liver disease, Psoriatic arthritis, Trichohepatoenteric syndrome, Diabetes mellitus type 2, Age-related macular degeneration
Unreviewed: Aortic Valve Insufficiency, Asthma, Atrial Septal Defect, Autoimmune disease, Bicuspid aortic valve, Biliary Cirrhosis, Breast Cancer, Cirrhosis, Clastothrix, Colitis, Colorectal Cancer, Congenital Hypoplasia Of Thymus, Coronary Heart Disease, Craniocerebral trauma, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 2, Diarrhea, Dubowitz syndrome, Dwarfism, Exudative Macular Degeneration, Facial dysmorphism syndrome, Gastritis, Geographic Atrophy, Glycogen Storage Disease, Hepatoblastoma, Hypothyroidism, Immune System Diseases, Immunologic Deficiency Syndromes, Intellectual developmental disorder, Liver carcinoma, Liver cirrhosis, Liver disease, Liver Fibrosis, Liver neoplasms, Lupus Erythematosus, Lymphopenia, Malignant Neoplasm, Mental retardation, Mouth neoplasm, Multiple myeloma, Multiple Sclerosis, Neoplasms, Patent ductus arteriosus, Peripheral pulmonary artery stenosis, Polycystic kidney disease, Psoriatic Arthritis, Renal hypoplasia, Rheumatoid arthritis, Systemic lupus erythematosus, Tetralogy of Fallot, Thrombocytosis, Trichohepatoenteric Syndrome, Ventricular septal defect
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1033
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SKI3 subunit of superkiller complex |
KIAA0372, Ski3, THES, TTC37 |
Curated: Urinary system neoplasms, Trichohepatoenteric syndrome
Unreviewed: Aortic Valve Insufficiency, Atrial Septal Defect, Bicuspid aortic valve, Cirrhosis, Clastothrix, Colitis, Common variable immunodeficiency, Congenital heart defect, Congenital Hypoplasia Of Thymus, Developmental Delay, Diarrhea, Dwarfism, Facial dysmorphism, Facial dysmorphism syndrome, Frontal bossing, Gastritis, Glaucoma, Hepatoblastoma, Hypoalbuminemia, Hypogammaglobulinemia, Hypothyroidism, Immune System Diseases, Immunologic Deficiency Syndromes, Impaired Cognition, Inflammatory bowel disease, Liver Cirrhosis, Liver failure, Liver Fibrosis, Lymphopenia, Macrostomia, Mental retardation, Microstomia, Microtia, Microvillus inclusion disease, Patent ductus arteriosus, Peripheral pulmonary artery stenosis, Polycystic kidney disease, Proptosis, Renal hypoplasia, Sepsis, Tetralogy of Fallot, Thrombocytosis, Trichohepatoenteric Syndrome, Trichorrhexis nodosa syndrome, Varicose veins, Ventricular septal defect
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1034
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SKI8 subunit of superkiller complex |
REC14, SKI8, WDR61 |
Curated: Brain aneurysm
Unreviewed: Squamous cell carcinoma
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1035
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SKI/DACH domain containing 1 |
C10orf140, DLN-1 |
Curated: Asthma, Breast cancer, Cholecystolithiasis, Coronary artery disease, Gallstones, Gastroesophageal reflux disease, Heart failure, Obesity, Osteoarthritis, Uterine fibroid
Unreviewed: N/A
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1036
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SKI like proto-oncogene |
SNO, SnoA, SnoI, SnoN |
Curated: Dermatologic disorder, Insomnia, Paraquat lung disease, Prostate cancer, Pulmonary fibrosis, Skin disease
Unreviewed: Adenoma, Alveolitis, Anodontia, Arsenic Encephalopathy, Atherosclerosis, Autism Spectrum Disorder, Barrett esophagus, Brain Neoplasms, Breast neoplasm, Carcinogenesis, Carcinoma, Castleman disease, Colorectal neoplasm, Colorectal Neoplasms, Congenital hyperinsulinism, Coronary artery disease, Dermatologic Disorders, Diabetes Mellitus, Diabetic Nephropathy, Diabetic neuropathy, Dyskinetic Syndrome, Epithelial ovarian carcinoma, Esophageal Carcinoma, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Hepatocellular carcinoma, Huntington Disease, Hyperaldosteronism, Hyperinsulinemic hypoglycemia, Long qt syndrome, Lung carcinoma, Malignant Neoplasm, Melanoma, Mouth neoplasm, Neoplasms, Neuroblastoma, Neurodegenerative Disorders, Ovarian diseases, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Parkinson disease, Pulmonary arterial hypertension, Pulmonary Fibrosis, Renal fibrosis, Rhabdomyosarcoma, Rheumatoid arthritis, Schizophrenia, Stomach neoplasms
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1037
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Skint1 like (pseudogene) |
BTN12, SKINT1, SKINTL, SKINTP |
Curated: N/A
Unreviewed: Leukemia
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1038
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SKI family transcriptional corepressor 1 |
CORL1, FUSSEL15, LBXCOR1 |
Curated: Colorectal cancer, Willis-ekbom disease, Diabetes mellitus type 2
Unreviewed: Kidney Disease, Kidney Failure, Narcolepsy, Obesity, Restless Legs Syndrome, Scleroderma, Tourette Syndrome, Tremor
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1039
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SKOR1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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1040
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SKI family transcriptional corepressor 2 |
CH18515, CORL2, FUSSEL18 |
Curated: Alzheimer disease, Dysarthria, Metabolic syndrome, Intellectual disability, Nervous system disease, Diabetes mellitus type 2
Unreviewed: Ataxia, Carcinoma Of The Head And Neck
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