Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
1231 to 1240 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1231
Secreted phosphoprotein 1
BNSP, BSPI, ETA-1, OPN
Alzheimer disease, Asbestosis, Biliary atresia, Brain neoplasms, Breast neoplasms, Calcinosis, Carotid artery stenosis, Cerebral hemorrhage, Persistent hepatitis, Coronary restenosis, Dementia, Allergic contact dermatitis, Diabetic cardiomyopathy, Focal glomerulosclerosis, Glioma
View all (26 more)

1232
Secreted phosphoprotein 2
SPP-24, SPP24
Alzheimer disease, Osteoporosis, Post-traumatic stress disorder, Retinitis pigmentosa, Scoliosis, Amyotrophic lateral sclerosis, Diabetes mellitus type 2

1233
Signal peptide peptidase like 2A
IMD86, IMP3, PSL2
Alzheimer disease, Obstructive pulmonary disease, Coronary artery disease, Eosinophilia, Gout, Immunodeficiency, Venous thromboembolism

1234
Signal peptide peptidase like 2B
IMP-4, IMP4, PSH4, PSL1
Parkinson disease

1235
Signal peptide peptidase like 2C
IMP5
Alzheimer disease, Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Corticobasal degeneration, Parkinson disease

1236
Signal peptide peptidase like 3
IMP2, MDHV1887, PRO4332, PSH1, PSL4
Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cannabis abuse, Colorectal cancer, Coronary artery disease, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Seasonal allergic rhinitis, Systemic lupus erythematosus, Tourette syndrome, Diabetes mellitus type 2

1237
Sepiapterin reductase
SDR38C1
Hyperphenylalaninemia, Bipolar disorder, Desbuquois syndrome, Dopa-responsive dystonia, Dystonia, Dystonia, dopa-responsive, with or without hyperphenylalaninemia, Intellectual developmental disorder, Mood disorder

1238
Sprouty related EVH1 domain containing 1
LGSS, NFLS, PPP1R147, hSpred1, spred-1
Cafe-au-lait spots, Congenital neurologic anomalies, Costello syndrome, Desbuquois syndrome, Male infertility spermatogenesis disorder, Neurofibromatosis, Neurofibromatosis-noonan syndrome, Noonan syndrome, Psychotic disorders, Scoliosis

1239
Sprouty related EVH1 domain containing 2
NS14, Spred-2
Alzheimer disease, Anorexia nervosa, Aortic stenosis, Aortic valve disease, Rheumatoid arthritis, Attention deficit hyperactivity disorder, Coronary artery disease, Crohn disease, Desbuquois syndrome, Gout, Immune system disease, Inflammatory bowel disease, Lung cancer, Metabolic syndrome, Multiple sclerosis
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1240
SREBF pathway regulator in golgi 1
C12orf49, LUR1, POST1, SPRING
Asthma, Neurotic disorder