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"
1001 to 1010 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1001
Synuclein alpha
NACP, PARK1, PARK4, PD1
Alzheimer disease, Amphetamine or sympathomimetic abuse, Ataxia, Parkinson disease, Congestive heart failure, Deficiency anemia, Degenerative disorder, Dementia, Vascular dementia, Diabetic ketoacidosis, Duchenne muscular dystrophy, Gaucher disease, Heart failure, Hemiparkinsonism, Hepatolenticular degeneration
View all (11 more)

1002
Synuclein alpha interacting protein
SYPH1, Sph1
Diabetic neuropathy, Parkinson disease, Hereditary parkinson disease

1003
Synuclein beta
-
Dementia, Lewy body disease, Parkinson disease, Schizophrenia

1004
Synuclein gamma
BCSG1, SR
Breast neoplasms, Carcinoma, Hyperkinesia, Lewy body disease

1005
Staphylococcal nuclease and tudor domain containing 1
TDRD11, TSN, Tudor-SN, p100
Attention deficit hyperactivity disorder, Autism, Kidney disease, Hemorrhoid, Hypospadias, Insomnia, Kidney failure, Lung neoplasms, Oligodendroglioma, Peptic ulcer disease, Schizophrenia, Substance abuse, Diabetes mellitus type 2

1006
SNF8 subunit of ESCRT-II
DEE115, Dot3, EAP30, NEDOA, VPS22
Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Hirschsprung disease, Non-specific syndromic intellectual disability, Schizophrenia, Diabetes mellitus type 2

1007
Smad nuclear interacting protein 1
NEDHCS, PML1, PMRED
Rolandic epilepsy, Neurodevelopmental disorder

1008
Stannin
-
Ankylosing spondylitis, Crohn disease, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

1009
Secondary ossification center associated regulator of chondrocyte maturation
ASCL830, C2orf82, UNQ830
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Schizophrenia, Tourette syndrome

1010
Syntaphilin
-
Autoimmune thrombocytopenic purpura, Color vision deficiency