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"
641 to 650 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

641
Solute carrier family 25 member 3
OK/SW-cl.48, PHC, PTP, PiC
Hypertrophic cardiomyopathy, Mitochondrial disease

642
Solute carrier family 25 member 30
KMCP1
Gout

643
Solute carrier family 25 member 35
-
Cardiac arrhythmia, Glomerulonephritis, Uterine fibroid

644
Solute carrier family 25 member 36
HHF8, PNC2
Bipolar disorder, Hyperinsulinemic hypoglycemia

645
Solute carrier family 25 member 37
HT015, MFRN, MFRN1, MSC, MSCP, PRO1278, PRO1584, PRO2217
Anemia, Atrial fibrillation, Breast cancer, Estrogen-receptor negative breast cancer, Hypothyroidism, Major depressive disorder, Prostate cancer, Synovial disorder, Diabetes mellitus type 1, Diabetes mellitus type 2

646
Solute carrier family 25 member 38
SIDBA2
Sideroblastic anemia, Diverticulitis, X-linked sideroblastic anemia

647
Solute carrier family 25 member 4
AAC1, ANT, ANT 1, ANT1, MTDPS12, MTDPS12A, PEO2, PEO3, PEOA2, T1
Progressive external ophthalmoplegia, Bipolar disorder, Dilated cardiomyopathy, Sengers syndrome, Congenital cataract hypertrophic cardiomyopathy mitochondrial myopathy syndrome, Diabetic cardiomyopathy, Hypertrophic cardiomyopathy, Left ventricular disease, Leigh syndrome, Mitochondrial disease, Mitochondrial dna depletion syndrome, Mitochondrial myopathy, Myopia, Restrictive cardiomyopathy

648
Solute carrier family 25 member 42
MECREN
Mitochondrial myopathy

649
Solute carrier family 25 member 43
-
Gout

650
Solute carrier family 25 member 44
-
Breast cancer, Parkinson disease, Stroke, Testicular carcinoma, Testicular germ cell tumor