Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13051 to 13060 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13051
Synaptoporin
SPO
Alzheimer disease, Anaphylaxis, Autism, Autoimmune hepatitis, Central nervous system cancer, Color vision deficiency, Congenital heart disease, Congenital left-sided heart lesions, Diverticulitis, Gestational diabetes, Glioblastoma, Glioma, Intellectual developmental disorder, Major depressive disorder, Psychiatric disorders
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13052
Synaptophysin
MRX96, MRXSYP, XLID96
Non-small-cell lung carcinoma, Neuronal ceroid lipofuscinosis, Intellectual developmental disorder, x-linked, Learning disorders, Memory disorders, X-linked intellectual disability, Schizophrenia

13053
Synaptophysin like 1
H-SP1, SYPL
Alzheimer disease, Crohn disease, Intellectual developmental disorder, Multiple sclerosis

13054
Synaptophysin like 2
MG29
Kidney disease

13055
SYS1 golgi trafficking protein
C20orf169, dJ453C12.4, dJ453C12.4.1
Multiple sclerosis, Psoriasis

13056
Synaptotagmin 1
BAGOS, P65, SVP65, SYT
Attention deficit hyperactivity disorder, Autism, Bladder exstrophy, Color vision deficiency, Dental enamel hypoplasia, Gout, Insomnia, Neurodevelopmental disorder, Obesity, Systemic lupus erythematosus

13057
Synaptotagmin 10
-
Anxiety disorder, Atrial fibrillation, Diverticular disease, Metabolic syndrome, Parkinson disease, Scoliosis, Diabetes mellitus type 2

13058
Synaptotagmin 11
SYT12, sytXI
Alzheimer disease, Gout, Schizophrenia

13059
Synaptotagmin 12
SYT11, sytXII
Lung cancer, Schizophrenia

13060
Synaptotagmin 13
-
Major depressive disorder, Schizophrenia