Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12441 to 12450 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12441
Small nuclear RNA activating complex polypeptide 2
PTFDELTA, SNAP45
Alzheimer disease, Diabetes mellitus type 2

12442
Small nuclear RNA activating complex polypeptide 3
PTFbeta, SNAP50
Schizophrenia

12443
Small nuclear RNA activating complex polypeptide 4
NEDRSO, PTFalpha, SNAP190
Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Neurodevelopmental disorder, Rheumatoid arthritis, Ulcerative colitis

12444
Small nuclear RNA activating complex polypeptide 5
SNAP19
Cardiofaciocutaneous syndrome, Noonan syndrome, Prostate cancer

12445
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)

12446
Synuclein alpha interacting protein
SYPH1, Sph1
Diabetic neuropathy, Parkinson disease, Hereditary parkinson disease

12447
Synuclein beta
-
Dementia, Lewy body disease, Parkinson disease, Schizophrenia

12448
Synuclein gamma
BCSG1, SR
Breast neoplasms, Carcinoma, Hyperkinesia, Lewy body disease

12449
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

12450
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