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
Showing genes starting with "S"
791 to 800 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

791
Solute carrier family 4 member 3
AE3, CAE3/BAE3, SLC2C, SQT7
Distal renal tubular acidosis, Cardiac arrhythmia, Congenital short qt syndrome, Heart disease, Short qt syndrome

792
Solute carrier family 4 member 4
HNBC1, KNBC, NBC1, NBC2, NBCe1, NBCe1-A, PRTAO, SLC4A5, hhNMC, kNBC1, pNBC
Atrial fibrillation, Proximal renal tubular acidosis, Cataract, Central nervous system cancer, Corneal opacity, Dental enamel hypoplasia, Developmental disability, Glaucoma, Glioblastoma, Glioma, Liver cirrhosis, Oligodendroglioma, Scoliosis, Vascular dementia

793
Solute carrier family 4 member 5
NBC4, NBCe2
Post-traumatic stress disorder

794
Solute carrier family 4 member 7
NBC2, NBC3, NBCN1, SBC2, SLC4A6
Breast cancer, Color vision deficiency, Cone-rod dystrophy, Hypertension, Retinitis pigmentosa, Uterine fibroid

795
Solute carrier family 4 member 8
NBC3, NDCBE
Alzheimer disease, Major depressive disorder, Mood disorder, Peripheral arterial disease, Schizophrenia, Stomatitis

796
Solute carrier family 4 member 9
AE4
Alzheimer disease, Metabolic syndrome, Diabetes mellitus type 2

797
Solute carrier family 50 member 1
HsSWEET1, RAG1AP1, SCP, SWEET1, slv
Parkinson disease

798
Solute carrier family 51 member A
OSTA, OSTalpha, PFIC6, SLC51A1
Biliary cirrhosis, Cholelithiasis, Cognition disorder, Complications of diabetes mellitus, Delirium, dementia, and cognitive disorders, Diabetes complications, Liver cirrhosis, Biliary cholangitis, Progressive intrahepatic cholestasis

799
SLC51 subunit beta
OSTB, OSTBETA, PBAM2, SLC51A1BP
Bile acid malabsorption, Biliary cirrhosis, Cholelithiasis, Cognition disorder, Complications of diabetes mellitus, Delirium, dementia, and cognitive disorders, Diabetes complications, Liver cirrhosis, Biliary cholangitis

800
Solute carrier family 52 member 1
GPCR42, GPR172B, PAR2, RBFVD, RFT1, RFVT1, hRFT1, huPAR-2
Alzheimer disease, Lung cancer, Ovarian epithelial cancer, Ovarian cancer, Peptic ulcer disease, Riboflavin deficiency, Riboflavin transporter deficiency, Diabetes mellitus type 2