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"
1221 to 1230 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1221
SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)
SLC62A3, SLC63A3
Clonal hematopoiesis, Coronary artery disease, Psychiatric disorders, Schizophrenia, Small cell lung carcinoma

1222
SPO11 initiator of meiotic double strand breaks
CT35, SPATA43, TOPOVIA, TOPVIA
Testicular azoospermia

1223
SPOC domain containing 1
PPP1R146
Male infertility single gene azoospermia

1224
SPARC (osteonectin), cwcv and kazal like domains proteoglycan 1
SPOCK, TESTICAN, TIC1
Atrial fibrillation, Attention deficit hyperactivity disorder, Bronchopulmonary dysplasia, Carotid artery disease, Colorectal cancer, Generalized epilepsy, Insomnia, Metabolic syndrome, Prostatic neoplasms, Substance abuse, Diabetes mellitus type 2

1225
SPARC (osteonectin), cwcv and kazal like domains proteoglycan 2
testican-2
Colorectal cancer, Intervertebral disc displacement, Osteoarthritis, Thyroid cancer, Diabetes mellitus type 2

1226
SPARC (osteonectin), cwcv and kazal like domains proteoglycan 3
HSAJ1454, TES-3, TICN3
Alzheimer disease, Carotid artery disease, Conotruncal cardiac defect, Dementia, Hypertension, Ovarian epithelial cancer, Metabolic syndrome, Multinodular goiter, Obesity, Ovarian cancer, Schizophrenia, Scoliosis, Diabetes mellitus type 2

1227
Spondin 1
VSGP/F-spondin, f-spondin
Alzheimer disease, Atrial fibrillation, Breast cancer, Scoliosis

1228
Spondin 2
DIL-1, DIL1, M-SPONDIN, MINDIN
Basal cell carcinoma, Prostatic neoplasms

1229
Speckle type BTB/POZ protein
BTBD32, NEDMACE, NEDMIDF, NSDVS1, NSDVS2, TEF2
Ductal carcinoma, Connective tissue disease, Endometrial neoplasms, Microcephaly, Mixed connective tissue disease, Neurodevelopmental disorder, Oligodendroglioma, Prostatic neoplasms

1230
SPOUT domain containing methyltransferase 1
C9orf114, CENP-32, CENP32, HSPC109, NEDGSB
Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Non-specific syndromic intellectual disability