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
12731 to 12740 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12731
Steroid 5 alpha-reductase 1
S5AR 1
Major depressive disorder, Endometriosis, Polycystic ovary syndrome, Prostatic hyperplasia, Prostatic neoplasms

12732
Steroid 5 alpha-reductase 2
-
46,xy disorder of sex developmen, Androgenetic alopecia, Autism, Endometrial neoplasms, Endometriosis, Prostate cancer, Gout, Hypogonadism, Hypospadias, Idiopathic pulmonary fibrosis, Micropenis, Prostatic hyperplasia, Prostatic neoplasms, Schizophrenia, Hypertension
View all (3 more)

12733
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

12734
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, Diabetes mellitus type 2, Fatty liver, Fatty liver, alcoholic, Gallstones, Gastroesophageal reflux disease, Hirschsprung disease, Iga nephropathy, Kidney failure
View all (9 more)

12735
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

12736
SREK1 interacting protein 1
P18SRP, SFRS12IP1
Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Glioblastoma, Glioma

12737
Serum response factor
MCM1
Cardiomyopathy, Congenital heart disease, Tetralogy of fallot

12738
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, Aortic dissection, Thoracic aortic aneurysm and aortic dissection, Myocardial infarction, Venous thromboembolism

12739
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

12740
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