Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12281 to 12290 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12281
Solute carrier family 46 member 1
G21, HCP1, HsPCFT, PCFT, hPCFT
Anemia, Congenital folate absorption defect, Hereditary folate malabsorption, Hyperhomocysteinemia, Intellectual developmental disorder, Liver cirrhosis, Malabsorption syndrome, Pancytopenia

12282
Solute carrier family 46 member 2
Ly110, TSCOT
Alzheimer disease

12283
Solute carrier family 46 member 3
FKSG16
Liver cirrhosis, Nonalcoholic fatty liver disease

12284
Solute carrier family 47 member 1
MATE1
Brain aneurysm, Kidney disease, Gout

12285
Solute carrier family 47 member 2
MATE2, MATE2-B, MATE2-K, MATE2K
Female infertility

12286
Solute carrier family 48 member 1
HRG, HRG-1, HRG1, hHRG-1
Gout, Hypothyroidism

12287
Solute carrier family 49 member 3
LP2561, MFSD7
Astrocytoma

12288
Solute carrier family 49 member 4
DIRC2, RCC4
Congenital heart malformation, Heart disease

12289
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

12290
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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