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
12291 to 12300 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12291
Solute carrier family 4 member 11
BTR1, CDPD1, CHED, CHED2, NABC1, dJ794I6.2
Congenital hereditary endothelial dystrophy, Corneal dystrophy, Corneal endothelial dystrophy, Fuchs endothelial dystrophy, Hereditary corneal dystrophy

12292
Solute carrier family 4 member 1 adaptor protein
HLC3
Alzheimer disease

12293
Solute carrier family 4 member 2
AE2, BND3L, EPB3L1, HKB3, NBND3, OPTB9
Polycystic kidney disease, Biliary cirrhosis, Cholecystolithiasis, Distal renal tubular acidosis, Liver cirrhosis, Osteopetrosis, Biliary cholangitis, Prostatic neoplasms

12294
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

12295
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

12296
Solute carrier family 4 member 5
NBC4, NBCe2
Post-traumatic stress disorder

12297
Solute carrier family 4 member 7
NBC2, NBC3, NBCN1, SBC2, SLC4A6
Breast cancer, Color vision deficiency, Cone-rod dystrophy, Hypertension, Retinitis pigmentosa, Uterine fibroid

12298
Solute carrier family 4 member 8
NBC3, NDCBE
Alzheimer disease, Major depressive disorder, Mood disorder, Peripheral arterial disease, Schizophrenia, Stomatitis

12299
Solute carrier family 4 member 9
AE4
Alzheimer disease, Metabolic syndrome, Diabetes mellitus type 2

12300
Solute carrier family 50 member 1
HsSWEET1, RAG1AP1, SCP, SWEET1, slv
Parkinson disease