41
|
|
|
Sphingosine-1-phosphate receptor 5 |
EDG8, Edg-8, S1P5, SPPR-1, SPPR-2 |
Curated: Inflammatory bowel disease, Scleroderma, Systemic sclerosis, Venous thromboembolism
Unreviewed: Chronic Obstructive Pulmonary Disease, Endometriosis, Glioblastoma, Graft-Vs-Host Disease, Huntington Disease, Leukemia, Lymphopenia, Malignant Neoplasm, Mouth disease, Mouth neoplasm, Multiple sclerosis, Neoplasms, Obesity, Parkinson disease, Prostate cancer, Ulcerative colitis
|
42
|
|
|
Serum amyloid A1 |
PIG4, SAA, SAA2, TP53I4 |
Curated: Contact dermatitis, Lewy body disease
Unreviewed: N/A
|
43
|
|
|
Serum amyloid A2 |
SAA, SAA1 |
Curated: Bipolar disorder, Major depressive disorder, Schizophrenia
Unreviewed: AA amyloidosis, Adenocarcinoma, Alzheimer disease, AMYLOID CARDIOMYOPATHY, Amyloid Nephropathy, Amyloidosis, Anemia, Ankylosing Spondylitis, Appendicitis, Arteriosclerosis, Arthritis, Asthma, Astrocytoma, Atherosclerosis, Atrial Septal Defect, Autism Spectrum Disorder, Autoimmune Diseases, Autoinflammatory Disease, Behcet Syndrome, Blood coagulation disorder, Breast neoplasm, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Cardiovascular disease, Cardiovascular Diseases, Carotid artery disease, Cerebral Infarction, Childhood obesity, Cholestasis, Chronic Obstructive Pulmonary Disease, Cirrhosis, Colitis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Congenital heart defects, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Crohn Disease, Cryopyrin-Associated Periodic Syndromes, Cystic Fibrosis, Deficiency Of Mevalonate Kinase, Dermatitis, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Dilated cardiomyopathy, Eczema, Familial mediterranean fever, Fuchs Endothelial Dystrophy, Glaucoma, Glioblastoma, Glioma, Granulomatosis with polyangiitis, Granulomatous Disease, Heart failure, Hematuria, Hemolytic Uremic Syndrome, Hepatocellular adenoma, Hepatocellular carcinoma, Hermansky-Pudlak Syndrome, Hidradenitis suppurativa, Homocystinuria, Hyperimmunoglobulinemia, Hyperlipidemia, Hypertension, Hyperuricemia, Hypoglycemia, Hypothyroidism, Idiopathic pulmonary fibrosis, Inflammatory Bowel Disease, Ischemic Stroke, Kidney Disease, Kidney Failure, Leukemia, Liver carcinoma, Liver Cirrhosis, Liver neoplasms, Lung Cancer, Lung carcinoma, Lung disease, Malabsorption Syndrome, Malignant Neoplasm, Malnutrition, Mental Depression, Mental Disorders, Metabolic Syndrome, Methylenetetrahydrofolate Reductase Deficiency, Multiple myeloma, Myelodysplastic Syndrome, Myocardial Infarction, Myocardial Ischemia, Nasopharyngeal Cancer, Nasopharyngeal carcinoma, Neoplasms, Nephrotic Syndrome, Neuroblastoma, Obesity, Osteoarthritis, Osteoporosis, Ovarian cancer, Ovarian neoplasm, Pancytopenia, Periodontitis, Peripheral arterial disease, Phenylketonuria, Platelet disorder, Polycystic ovary syndrome, Prostate cancer, Psoriasis, Psychosis, Pulmonary arterial hypertension, Pulmonary hypertension, Reactive Systemic Amyloidosis, Renal cell carcinoma, Respiratory system infectious disease, Retinopathy, Retinopathy of prematurity, Rheumatoid arthritis, Rosacea, Sarcoidosis, Sarcopenia, Sepsis, Septicemia, Squamous cell carcinoma, Stomach neoplasms, Syndromic microphthalmia, T-Cell Lymphoma, Triple negative breast cancer, Triple Negative Breast Neoplasms, Ulcerative colitis, Uterine neoplasm, Vascular Diseases, Visceral amyloidosis
|
44
|
|
|
SAA2-SAA4 readthrough |
- |
Curated: Bipolar disorder, Color vision deficiency, Major depressive disorder, Schizophrenia
Unreviewed: Mental Disorders, Psychosis
|
45
|
|
|
Serum amyloid A3, pseudogene |
SAA3 |
Curated: N/A
Unreviewed: Arteriosclerosis, Arthritis, Atherosclerosis, Hyperhomocysteinemia, Hyperlipidemia, Inflammatory Bowel Disease, Kidney Disease, Lung Diseases, Malignant Neoplasm, Obesity, Osteoporosis, Pancreatic Neoplasm, Rheumatoid arthritis, Synovitis
|
46
|
|
|
Serum amyloid A4, constitutive |
C-SAA, CSAA |
Curated: Color vision deficiency
Unreviewed: AA amyloidosis, Amyloidosis, Carcinoma, Glioma, Hemophagocytic lymphohistiocytosis, Hepatocellular carcinoma, Osteosarcoma, Ovarian cancer, Ovarian neoplasm, Periodontitis, Reactive Systemic Amyloidosis, Rheumatoid arthritis, Urinary bladder neoplasms, Uterine neoplasm
|
47
|
|
|
Serum amyloid A like 1 |
SPACIA1 |
Curated: Insomnia
Unreviewed: Arthritis, Carcinogenesis, Hepatocellular carcinoma, Rheumatoid arthritis, Synovitis, Urinary bladder neoplasms
|
48
|
|
|
SAC3 domain containing 1 |
HSU79266, SHD1 |
Curated: Melanoma
Unreviewed: Colon Carcinoma, Colonic Neoplasms, Hepatocellular carcinoma, Liver carcinoma, Osteosarcoma, Stomach neoplasms
|
49
|
|
|
SAC1 like phosphatidylinositide phosphatase |
SAC1 |
Curated: N/A
Unreviewed: Brain Infarction, Breast Cancer, Breast neoplasm, Carotid artery stenosis, Coronary artery disease, Diabetes, Diabetes Mellitus, Hemophilia, Hypercholesterolemia, Hypertension, Hyperthyroxinemia, Dysalbuminemic, Hypocholesterolemia, Kidney Disease, Leukemia, Lymphoblastic Leukemia, Lymphocytic Leukemia, Mason type diabetes, Parkinson Disease, Rheumatoid arthritis, Secondary parkinson disease, Seizure, Seizures, Stroke, T-cell leukemia, T-Cell Lymphoma/Leukemia, von Willebrand disorder
|
50
|
|
|
Sacsin molecular chaperone |
ARSACS, DNAJC29, PPP1R138, SPAX6 |
Curated: Ataxia, spastic, autosomal recessive with optic atrophy and impaired intellect, Spastic ataxia of charlevoix-saguenay, Bipolar disorder, Charcot-marie-tooth disease, x-linked, Hereditary ataxia, Pelvic organ prolapse, Spastic ataxia, Spastic paraplegia, Hereditary spastic paraplegia, Diabetes mellitus type 2
Unreviewed: Action Myoclonus-Renal Failure Syndrome, Arachnoid cyst, Ataxia, Autonomic nervous system disease, beta Thalassemia, Brachydactyly, Cardiomegaly, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar diseases, Cerebral palsy, Charcot-Marie-Tooth Disease, Colorectal Cancer, Constipation, Corpus callosum agenesis neuronopathy syndrome, Cystic Fibrosis, Demyelinating diseases, Demyelinating neuropathy, Dentatorubral Pallidoluysian Atrophy, Developmental Delay, Diabetic foot, Distal amyotrophy, Drachtman Weinblatt Sitarz syndrome, Dysarthria, Dysmorphic Features, Dysphagia, Epilepsy, Erectile Dysfunction, Heart disease, Hereditary motor and sensory neuropathy, Hypercholesterolemia, Hyperlipoproteinemia, Hypertyrosinemia, Hypoplasia Of Corpus Callosum, Inclusion-Body Disease, Intracranial hypertension, May-White Syndrome, Mental retardation, Mitral Valve Prolapse, Movement Disorders, Multiple Sclerosis, Myoclonic Epilepsy, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neurodegenerative Disorders, Nystagmus, Oculopharyngeal Muscular Dystrophy, Peripheral Neuropathy, Polyneuropathy, Sensorimotor neuropathy, Sleep Apnea, Spastic Ataxia, Spastic Ataxia Of Charlevoix-Saguenay, Spastic Paraplegia, Spinocerebellar Ataxia, Tyrosinemia, Urinary bladder diseases, Urinary bladder neoplasms, Vitamin D Deficiency
|