Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
12791 to 12800 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12791
Steroid 5 alpha-reductase 2
-
46, xy disorder of sex development, Androgenetic alopecia, Autism, Endometrial neoplasms, Endometriosis, Prostate cancer, Gout, Hypogonadism, Hypospadias, Idiopathic pulmonary fibrosis, Micropenis, Prostatic hyperplasia, Prostatic neoplasms, Schizophrenia, Hypertension
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12792
Steroid 5 alpha-reductase 3
CDG1P, CDG1Q, KRIZI, S5AR, S5AR 3, SRD5A2L, SRD5A2L1
Autism, Cone dystrophy, Congenital disorder of glycosylation, Congenital neurologic anomalies, Creutzfeldt-jakob disease, Global developmental delay, Intellectual developmental disorder, Osteoarthritis, Retinitis pigmentosa

12793
Sterol regulatory element binding transcription factor 1
HMD, IFAP2, SREBP1, bHLHd1
Alzheimer disease, Attention deficit hyperactivity disorder, Breast cancer, Hepatocellular carcinoma, Ischemic heart disease, Coronary artery disease, Dementia, Experimental diabetes, Diabetes mellitus type 2, Fatty liver, Fatty liver, alcoholic, Gallstones, Gastroesophageal reflux disease, Hirschsprung disease, Iga nephropathy
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12794
Sterol regulatory element binding transcription factor 2
SREBP-2, SREBP2, bHLHd2
Alzheimer disease, Breast neoplasms, Hepatocellular carcinoma, Carotid artery disease, Vascular dementia, Diabetes mellitus type 1, Diabetes mellitus type 2, Hypercholesterolemia, Hypothyroidism, Kidney failure, Schizophrenia, Hereditary spastic paraplegia, Stomach neoplasms

12795
SREK1 interacting protein 1
P18SRP, SFRS12IP1
Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Glioblastoma, Glioma

12796
Serum response factor
MCM1
Cardiomyopathy, Congenital heart disease, Tetralogy of fallot

12797
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

12798
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

12799
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

12800
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