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"
991 to 1000 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

991
Small nuclear RNA activating complex polypeptide 2
PTFDELTA, SNAP45
Alzheimer disease, Diabetes mellitus type 2

992
Small nuclear RNA activating complex polypeptide 3
PTFbeta, SNAP50
Schizophrenia

993
Small nuclear RNA activating complex polypeptide 4
NEDRSO, PTFalpha, SNAP190
Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Neurodevelopmental disorder, Rheumatoid arthritis, Ulcerative colitis

994
Small nuclear RNA activating complex polypeptide 5
SNAP19
Cardiofaciocutaneous syndrome, Noonan syndrome, Prostate cancer

995
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)

996
Synuclein alpha interacting protein
SYPH1, Sph1
Diabetic neuropathy, Parkinson disease, Hereditary parkinson disease

997
Synuclein beta
-
Dementia, Lewy body disease, Parkinson disease, Schizophrenia

998
Synuclein gamma
BCSG1, SR
Breast neoplasms, Carcinoma, Hyperkinesia, Lewy body disease

999
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

1000
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