3691
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|
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Sulfotransferase family 4A member 1 |
BR-STL-1, BRSTL1, DJ388M5.3, NST, SULTX3, hBR-STL-1 |
Curated: Schizoaffective disorder, Schizophrenia, Diabetes mellitus type 2
Unreviewed: 22q13 monosomy syndrome, Adenocarcinoma, Breast Cancer, Breast Carcinoma, Carcinoma, Coronary Syndrome, Ductal Carcinoma, Glioblastoma, Leukemia, Macrocephaly, Malignant Peripheral Nerve Sheath Tumor, Melanoma, Mental Disorders, Mucinous Adenocarcinoma, Myeloid Leukemia, Neoplasms, Parkinson disease, Schizoaffective Disorder
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3692
|
|
|
Sulfotransferase family 6B member 1 |
ST6B1 |
Curated: Schizophrenia
Unreviewed: N/A
|
3693
|
|
|
Sulfotransferase family 6B member 2, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
|
3694
|
|
|
Sulfatase modifying factor 1 |
AAPA3037, FGE, UNQ3037 |
Curated: Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Bipolar disorder, Bone fracture, Cholecystitis, Cholecystolithiasis, Obstructive pulmonary disease, Colorectal cancer, Congenital left-sided heart lesions, Desbuquois syndrome, Eating disorder, Mucosulfatidosis, Multiple sclerosis, Neurodevelopmental disorder, Oligodendroglioma, Osteoarthritis, Pancreatic cancer, Periodontitis, Willis-ekbom disease, Scoliosis, Spinocerebellar ataxia, Spondylosis, Amyotrophic lateral sclerosis, Substance abuse, Diabetes mellitus type 2
Unreviewed: Apnea, Ataxia, Autism, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cataract, Central Nervous System Demyelination, Cerebellar atrophy, Cerebral Atrophy, Chondrodysplasia, Chondrodysplasia Punctata, Chronic Obstructive Pulmonary Disease, Cystic Fibrosis, Deafness, Developmental Delay, Developmental regression, Dwarfism, Emphysema, Glioblastoma, Hearing Loss, Hematologic disease, Hydrocephalus, Hypotonia, Ichthyosis, Inborn Errors Of Metabolism, Macrocephaly, Malignant Neoplasm, Mental retardation, Metachromatic Leukodystrophy, Microcephaly, Mucopolysaccharidosis, Multiple Sclerosis, Multiple Sulfatase Deficiency, Narcolepsy, Neurodegenerative disorder, Optic Atrophy, Pfaundler-Hurler Syndrome, Placental Steroid Sulfatase Deficiency, Pulmonary hypertension, Schizophrenia, Spinocerebellar Ataxia, Splenomegaly, Sulfatidosis, Tremor, Ulcerative colitis
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3695
|
|
|
Sulfatase modifying factor 2 |
pFGE |
Curated: N/A
Unreviewed: Aortic dissection, Arthritis, Ataxia Telangiectasia, Colorectal Cancer, Colorectal neoplasm, Crohn disease, Cystic Fibrosis, Cystitis, Diabetes Insipidus, Facioscapulohumeral Muscular Dystrophy, Guillain-Barre Syndrome, Hemolytic Uremic Syndrome, Huntington disease, Inflammatory Bowel Disease, IRAK4 Deficiency, Irritable Bowel Syndrome, Keratitis, Marfan Syndrome, Osteomyelitis, Pharyngitis, Septicemia, Toxic Shock Syndrome
|
3696
|
|
|
Small ubiquitin like modifier 1 |
DAP1, GMP1, OFC10, PIC1, SENP2, SMT3, SMT3C, SMT3H3, UBL1 |
Curated: Cleft lip, Cleft palate, Complete unilateral cleft lip, Coronary artery disease, Myocardial infarction, Orofacial cleft
Unreviewed: Alzheimer disease, Amyotrophic Lateral Sclerosis, Anaplasia, Arteriosclerosis, Atherosclerosis, Atrial Septal Defect, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchopulmonary Dysplasia, Carcinoma, Cholestasis, Cleft Lip With Or Without Cleft Palate, Cognitive disorder, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Congenital Heart Disease, Congestive Heart Failure, Coronary Heart Disease, Dentatorubral Pallidoluysian Atrophy, Dermatomyositis, Diabetes Mellitus, Diabetic Retinopathy, Dysmorphism, Embryonal carcinoma, Endometrial Cancer, Endometrial carcinoma, Endometrial neoplasm, Frontotemporal dementia, Glioblastoma, Glioma, Heart Failure, Hepatocellular carcinoma, Huntington Disease, Hyperoxaluria, Hypodontia, Hypoplasia of the maxilla, Impaired Cognition, Inflammatory Myopathy, Intraepithelial Neoplasia, Kaposi Sarcoma, Leukemia, Liver Cancer, Liver carcinoma, Liver neoplasms, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lymphoma, Malignant Neoplasm, Melanoma, Mesothelioma, Microdontia, Micrognathism, Multiple myeloma, Myeloproliferative disorder, Myocardial Infarction, Myopathy, Neoplasms, Neuroblastoma, Neurodegenerative Disorders, Neuronal Intranuclear Inclusion Disease, Oligodontia, Oral cavity carcinoma, Orofacial Cleft, Osteosarcoma, Papillary thyroid carcinoma, Partial Lipodystrophy, Promyelocytic Leukemia, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Pulmonary arterial hypertension, Renal Carcinoma, Renal cell carcinoma, Rheumatoid arthritis, Sarcoma, Schizophrenia, Scleroderma, Sleep Apnea, Spinocerebellar Ataxia, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Syndromic microphthalmia, Urinary bladder neoplasms, Ventricular septal defect, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS, Waldenstrom macroglobulinemia, Werner Syndrome
|
3697
|
|
|
SUMO1 pseudogene 1 |
PIC1L, UBL2, UBL6 |
Curated: N/A
Unreviewed: Hemolysis, Polycystic Ovary Syndrome
|
3698
|
|
|
SUMO1 pseudogene 2 |
bA375F2.1 |
Curated: N/A
Unreviewed: N/A
|
3699
|
|
|
SUMO1 pseudogene 3 |
- |
Curated: N/A
Unreviewed: Breast Cancer, Breast Carcinoma, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Head and neck neoplasm, Hepatocellular carcinoma, Liver carcinoma, Lung adenocarcinoma, Lung carcinoma, Lymphatic metastasis, Malignant Neoplasm, Neoplasms, Pancreatic cancer, Pancreatic carcinoma, Stomach Carcinoma, Stomach Neoplasms, Urinary bladder neoplasms
|
3700
|
|
|
SUMO1 pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|