Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
151 to 160 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
Sperm acrosome associated 7
C13orf28
Asthma, Cardiovascular disease, Central nervous system cancer, Glioblastoma, Glioma

152
Solute carrier family 24 member 4
AI2A5, NCKX4, SHEP6, SLC24A2
Alzheimer disease, Amelogenesis imperfecta, Autoimmune thrombocytopenic purpura, Kidney disease, Melanoma, Dementia, Dentin dysplasia, Dentinogenesis imperfecta, Hypomaturation amelogenesis imperfecta, Oligodendroglioma, Severe acute respiratory syndrome, Skin hair eye pigmentation variation, Venous thromboembolism

153
SLC51 subunit beta
OSTB, OSTBETA, PBAM2, SLC51A1BP
Bile acid malabsorption, Biliary cirrhosis, Cholelithiasis, Cognition disorder, Complications of diabetes mellitus, Delirium, dementia, and cognitive disorders, Diabetes complications, Liver cirrhosis, Biliary cholangitis

154
Spermatogenesis associated 33
C16orf55
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Melanoma, Eye disease, Gout, Major depressive disorder, Non-small cell lung carcinoma, Schizophrenia, Squamous cell carcinoma

155
Septin 12
SEPT12, SPGF10
Spermatogenic failure

156
Sorting nexin 20
SLIC1
Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Leprosy, Psoriasis, Respiratory system disease, Rheumatoid arthritis, Sclerosing cholangitis, Ulcerative colitis

157
Spermatogenesis associated 32
AEP2, C17orf46, TEX34, VAD1.2
Asthma, Eczema, Respiratory system disease

158
Seizure related 6 homolog
BSRPC
Gout, Liver cirrhosis, Schizophrenia

159
SPNS lysolipid transporter 2, sphingosine-1-phosphate
DFNB115, SLC62A2, SLC63A2
Deafness, Hearing impairment, Hearing loss

160
Synaptotagmin 2
CMS7, CMS7A, CMS7B, MYSPC, SytII
Benign thyroid gland neoplasm, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Epilepsy, Mitral valve prolapse, Myasthenic syndrome, Oligodendroglioma, Presynaptic congenital myasthenic syndrome