3661
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|
|
SUFU negative regulator of hedgehog signaling |
BCNS2, JBTS32, PRO1280, SUFUH, SUFUXL |
Curated: Apraxia, Atrial fibrillation, Basal cell nevus syndrome, Bipolar disorder, Basal cell carcinoma, Ciliopathy, Crohn disease, Medulloblastoma, Aplasia of the vermis, Meningioma, Gastrointestinal stromal tumor, Gorlin syndrome, Heart failure, Inflammatory bowel disease, Joubert syndrome, Major depressive disorder, Microform holoprosencephaly, Neurodevelopmental disorder, Obesity, Schizophrenia, Ulcerative colitis, Uterine fibroid, Vitiligo
Unreviewed: Accessory Rib, Acquired Kyphoscoliosis, Acrocallosal Syndrome, Agenesis Of Corpus Callosum, Ambiguous Genitalia, Ameloblastoma, Amnesia, Arachnodactyly, Asthma, Basal Cell Neoplasm, Brachycephaly, Brachydactyly, Brain disease, Brain Neoplasms, Brain stem compression, Calcification of falx cerebri, Carcinogenesis, Carcinoma, Cardiac fibroma, Cardiac rhabdomyoma, Cataract, Cerebellar diseases, Cerebellar vermis agenesis, Choanal Atresia, Ciliopathies, Colon Carcinoma, Colonic Neoplasms, Congenital Anomaly Of Neck, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital Hypoplasia Of Penis, Congenital kyphoscoliosis, Cryptorchidism, Cyclocephaly, Dandy-Walker Syndrome, Desmoplastic/Nodular Medulloblastoma, Developmental Delay, Developmental disability, Duodenal Atresia, Dwarfism, Dysarthria, Eczema, Embryonal Rhabdomyosarcoma, Encephalocele, Endometrial Cancer, Endometrial carcinoma, Erectile Dysfunction, Esophageal squamous cell carcinoma, Facial paralysis, Fibroma, Frontal bossing, Fused incisors, Glaucoma, Gorlin Syndrome, Graft-versus-host disease, Graft-Vs-Host Disease, Growth Hormone Deficiency, Hamartoma, Hearing Loss, Hemangioma, Hereditary Hemochromatosis, Hirschsprung Disease, Holoprosencephaly, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadotropic Hypogonadism, Hypospadias, Hypothalamic hypothyroidism, Hypothyroidism, Inflammatory Bowel Disease, Intellectual developmental disorder, Intracranial Meningioma, Keratocystic Odontogenic Tumor, Liver Fibrosis, Lung neoplasms, Macrocephaly, Malignant Mesothelioma, Malignant Neoplasm, Malocclusion, Medulloblastoma With Extensive Nodularity, Medullomyoblastoma, Melanocytic nevus, Melanoma, Mental retardation, Microcephaly, Microform Holoprosencephaly, Microphthalmos, Mood swings, Motor delay, Mucoepidermoid carcinoma, Multiple Meningioma, Neoplasms, Neural Tube Defect, Neuroblastoma, Neurofibroma, Oculodentodigital dysplasia, Oculomotor apraxia, Oculomotor nerve palsy, Oculovestibuloauditory Syndrome, Orbital cyst, Osteoporosis, Ovarian cancer, Ovarian Carcinoma, Ovarian diseases, Ovarian Epithelial carcinoma, Ovarian fibromata, Pancreatic ductal carcinoma, Pancreatic neoplasm, Panhypopituitarism, Papilledema, Patent ductus arteriosus, Periodontitis, Pituitary dwarfism, Polydactyly, Postaxial hand polydactyly, Primitive Neuroectodermal Tumor, Proptosis, Prostatic neoplasm, Renal agenesis, Rhabdomyoma, Rhabdomyosarcoma, Rib fusion, Scoliosis, Sepsis, Septicemia, Skin Lesion, Speech Disorders, Spina Bifida, Spinal Meningioma, Split-Hand-Foot Malformation, Sprengel Deformity, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Syndromic microphthalmia, Tetralogy of Fallot, Tongue Neoplasms, Trigeminal neuralgia
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3662
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|
|
Succinyl-CoA:glutarate-CoA transferase |
C7orf10, DERP13, GA3, ORF19 |
Curated: Asthma, Color vision deficiency, Hemorrhoid, Language development disorders, Melanoma, Migraine, Moyamoya disease, Pancreatic cancer, Pancreatic neoplasms, Peripheral neuropathy, Post-operative myocardial infarction, Prostate cancer, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2, glutaric acidemia type 3
Unreviewed: Abdominal Migraine, Acne, Common Migraine, Confusional Migraine, Glutaric acidemia, Hemicrania Migraine, Hypertension, Malignant Neoplasm, Neuroblastoma, Pancreatic carcinoma, Pancreatic Neoplasm, Prostate Cancer, Hereditary, Prostatic neoplasm, Status Migrainosus, Thrombosis, Venous thromboembolism
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3663
|
|
|
SUGCT antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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3664
|
|
|
SURP and G-patch domain containing 1 |
F23858, RBP, SF4 |
Curated: Atrial fibrillation, Cancer, Liver cirrhosis, Coronary artery disease, Diabetes mellitus, Diabetic eye disease, Heart failure, Liver neoplasms, Migraine, Nonalcoholic fatty liver disease, Stroke, Diabetes mellitus type 2
Unreviewed: Alcoholic Liver Cirrhosis, Alzheimer disease, Amyotrophic Lateral Sclerosis, Atrial Fibrillation, Autoimmune Diseases, Brain Neoplasms, Breast neoplasm, Burkitt lymphoma, Cadasil, Carcinogenesis, Cardiomyopathy, Cardiovascular disease, Choriocarcinoma, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Coronary Heart Disease, Diabetes, Diabetes Mellitus, Discoid lupus erythematosus, Esophageal Carcinoma, Esophagus Neoplasm, Fatty Liver, Frontotemporal dementia, Glioblastoma, Glioma, Heart Failure, Hepatocellular carcinoma, Hyperlipidemia, Ischemic myocardial dysfunction, Kaposi Sarcoma, Kidney Failure, Lateral Sclerosis, Liver carcinoma, Liver disease, Liver Fibrosis, Lung Cancer, Lung carcinoma, Lymphocytic Leukemia, Malignant Neoplasm, Multiple Sclerosis, Neoplasms, Neurodegenerative disorder, Neurodegenerative Disorders, Neuromuscular disease, Obesity, Osteoarthritis, Parkinson disease, Periodontitis, Prostate cancer, Prostatic neoplasm, Psoriasis, Rheumatoid arthritis, Sarcoma, Schizophrenia, Squamous cell carcinoma, Stomach neoplasms, Systemic lupus erythematosus, T-Cell Lymphoma/Leukemia, Triple negative breast cancer, Urinary bladder neoplasms, Visual disorder
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3665
|
|
|
SURP and G-patch domain containing 2 |
SFRS14, SRFS14 |
Curated: Hyperlipidemia
Unreviewed: Diabetes mellitus, Hemochromatosis, Iron overload
|
3666
|
|
|
SGT1 assembly cochaperone of MIS12 kinetochore complex |
SGT1 |
Curated: Alzheimer disease
Unreviewed: Congestive Heart Failure, Heart Failure, Inflammatory bowel disease, Lewy Body Disease, Malignant Neoplasm, Parkinson disease, Stomach Carcinoma, Stomach Neoplasms
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3667
|
|
|
SUGT1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
3668
|
|
|
SUGT1 pseudogene 1 |
SGT1P, SUGT1P, bA255A11.1 |
Curated: N/A
Unreviewed: N/A
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3669
|
|
|
SUGT1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
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3670
|
|
|
SUGT1 pseudogene 3 |
SUGT1L1 |
Curated: N/A
Unreviewed: N/A
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