Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
781 to 790 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

781
Solute carrier family 4 member 1 (Diego blood group)
AE1, BND3, CD233, CHC, DI, EMPB3, EPB3, FR, RTA1A, SAO, SPH4, SW, WD, WD1, WR
Hemolytic anemia, Distal renal tubular acidosis, Cryohydrocytosis, Hereditary xerocytosis, Diverticular disease, Hereditary elliptocytosis, Gout, Hematologic disease, Obesity, Spherocytosis, Xerocytosis

782
Solute carrier family 4 member 10
NBCn2, NCBE
Attention deficit hyperactivity disorder, Bipolar disorder, Cognition disorder, Neurodevelopmental disorder, Connective tissue disease, Delirium, dementia, and cognitive disorders, Digestive system neoplasms, Epilepsy, Frontal lobe epilepsy, Intellectual developmental disorder, Intracranial hypertension, Migraine, Mixed connective tissue disease, Neurotic disorder, Non-specific syndromic intellectual disability
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783
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

784
Solute carrier family 4 member 1 adaptor protein
HLC3
Alzheimer disease

785
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

786
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

787
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, Oligodendroglioma, Scoliosis, Vascular dementia

788
Solute carrier family 4 member 5
NBC4, NBCe2
Post-traumatic stress disorder

789
Solute carrier family 4 member 7
NBC2, NBC3, NBCN1, SBC2, SLC4A6
Breast cancer, Color vision deficiency, Cone-rod dystrophy, Hypertension, Retinitis pigmentosa, Uterine fibroid

790
Solute carrier family 4 member 8
NBC3, NDCBE
Alzheimer disease, Major depressive disorder, Mood disorder, Peripheral arterial disease, Schizophrenia, Stomatitis