Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1291 to 1300 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1291
Sterol regulatory element binding transcription factor 2
SREBP-2, SREBP2, bHLHd2
Alzheimer disease, Breast neoplasm, Hepatocellular carcinoma, Carotid artery disease, Vascular dementia, Diabetes mellitus type 1, Diabetes mellitus type 2, Hypercholesterolemia, Hypothyroidism, Diabetes mellitus, type 2, Kidney failure, Schizophrenia, Hereditary spastic paraplegia, Stomach neoplasms

1292
SREK1 interacting protein 1
P18SRP, SFRS12IP1
Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Glioblastoma, Glioma

1293
SRF
Serum response factor
MCM1
Cardiomyopathy, Congenital heart disease, Tetralogy of fallot

1294
Serum response factor binding protein 1
BUD22, P49, Rlb1, STRAP, p49/STRAP
Aortic aneurysm, Obstructive pulmonary disease, Congenital aneurysm of ascending aorta, Connective tissue disease, Coronary artery disease, Cutis laxa, Dissection of aorta, Thoracic aortic aneurysm and aortic dissection, Myocardial infarction, Venous thromboembolism

1295
SLIT-ROBO Rho GTPase activating protein 1
ARHGAP13, NMTC2
Congenital anomalies of the kidney and urinary tract, Basal cell carcinoma, Color vision deficiency, Colorectal cancer, Congenital anomalies of kidney and urinary tract, Ovarian epithelial cancer, Nephronophthisis, Ovarian cancer, Pancreatic cancer, Scoliosis, Follicular thyroid cancer, Nonmedullary thyroid cancer, Hypertension

1296
SLIT-ROBO Rho GTPase activating protein 2
ARHGAP34, FNBP2, SRGAP2A, SRGAP3
Asthma, Obstructive pulmonary disease, Dupuytren contracture, Intellectual developmental disorder, Developmental and epileptic encephalopathy, Respiratory system disease, Systemic lupus erythematosus, Diabetes mellitus, type 2

1297
SLIT-ROBO Rho GTPase activating protein 3
ARHGAP14, MEGAP, SRGAP2, WRP
Alzheimer disease, Breast cancer, Chromosome 3p25 monosomy, Color vision deficiency, Intellectual developmental disorder, Metabolic syndrome, Moyamoya angiopathy, Neurodevelopmental disorder, Schizophrenia, Diabetes mellitus, type 2

1298
Serglycin
PPG, PRG, PRG1
Color vision deficiency, Liver cirrhosis

1299
SRI
Sorcin
CP-22, CP22, SCN, V19
Hypertrophic cardiomyopathy, Liver cirrhosis

1300
SRL
Sarcalumenin
SAR
Diverticular disease, Hypertrophic cardiomyopathy, Obesity