Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
91 to 100 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

91
SIX homeobox 2
-
Amyotrophic lateral sclerosis, Congenital anomalies of the kidney and urinary tract, Color vision deficiency, Congenital anomalies of kidney and urinary tract, Frontonasal dysplasia, Kidney disease, Motor neuron disease, Myocarditis, Wilms tumor

92
Serine and arginine rich splicing factor 10
FUSIP1, FUSIP2, NSSR, PPP1R149, SFRS13, SFRS13A, SRp38, SRrp40, TASR, TASR1, TASR2
Endometrial neoplasm, Obesity, Ovarian neoplasm, Polycystic ovary syndrome, Schizophrenia

93
Solute carrier family 17 member 3
GOUT4, NPT4, UAQTL4
Gouty arthritis, Breast cancer, Color vision deficiency, Estrogen-receptor negative breast cancer, Gout, Major depressive disorder, Nephrolithiasis, Osteoarthritis, Rheumatoid arthritis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus, type 1

94
Septin 9
AF17q25, MSF, MSF1, NAPB, PNUTL4, SEPT9, SINT1, SeptD1
Neuralgic amyotrophy, Monomelic amyotrophy, Asthma, Astrocytoma, Cardiovascular disease, Cataract, Charcot-marie-tooth disease, Endometriosis, Gestational diabetes, Gout, Hyperopia, Hypertension, Myeloid leukemia, Major depressive disorder, Obsessive-compulsive disorder
View all (4 more)

95
SHH signaling and ciliogenesis regulator SDCCAG8
BBS16, CCCAP, CCCAP SLSN7, HSPC085, NPHP10, NY-CO-8, SLSN7, hCCCAP
Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Bipolar disorder, Kidney disease, Ciliopathies, Cystic kidney disease, Focal glomerulosclerosis, Metabolic syndrome, Nephronophthisis, Obesity, Parkinson disease, Retinitis pigmentosa, Schizoaffective disorder, Schizophrenia, Senior-loken syndrome
View all (1 more)

96
StAR related lipid transfer domain containing 10
CGI-52, NY-CO-28, PCTP2, SDCCAG28
Prostatic neoplasm, Diabetes mellitus, type 2

97
Snf2 related CREBBP activator protein
DEHMBA, DOMO1, EAF1, FLHS, SWR1
Autism, Adenoid cystic carcinoma, Desbuquois syndrome, Developmental delay, Developmental delay with hypotonia and behavioral abnormalities, Intellectual developmental disorder, Multiple myeloma, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Systemic lupus erythematosus

98
Solute carrier family 26 member 1
CAON, CAON1, EDM4, HYSULF, SAT-1, SAT1
Alzheimer disease, Developmental and epileptic encephalopathy, Hyperoxaluria, Mucopolysaccharidosis, Nephrolithiasis, Pfaundler-hurler syndrome, Polymyositis, Urolithiasis

99
Solute carrier family 22 member 7
NLT, OAT2, hOAT11
Cardioembolic stroke, Gout, Hearing loss, Hypertension, Stroke, Diabetes mellitus, type 2

100
SUB1 regulator of transcription
P15, PC4, p14
Breast cancer, Crohn disease