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
12151 to 12160 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12151
Solute carrier family 25 member 35
-
Cardiac arrhythmia, Glomerulonephritis, Uterine fibroid

12152
Solute carrier family 25 member 36
HHF8, PNC2
Bipolar disorder, Hyperinsulinemic hypoglycemia

12153
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

12154
Solute carrier family 25 member 38
SIDBA2
Sideroblastic anemia, Diverticulitis, X-linked sideroblastic anemia

12155
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, Liver cirrhosis, Mitochondrial disease, Mitochondrial dna depletion syndrome, Mitochondrial myopathy, Myopia, Restrictive cardiomyopathy

12156
Solute carrier family 25 member 42
MECREN
Mitochondrial myopathy

12157
Solute carrier family 25 member 43
-
Gout

12158
Solute carrier family 25 member 44
-
Breast cancer, Parkinson disease, Stroke, Testicular carcinoma, Testicular germ cell tumor

12159
Solute carrier family 25 member 45
-
Melanoma

12160
Solute carrier family 25 member 46
HMSN6B, PCH1E
Asthma, Astrocytoma, Eczema, Charcot-marie-tooth disease, Congenital pontocerebellar hypoplasia, Hereditary motor and sensory neuropathies, Leigh syndrome, Major depressive disorder, Hereditary motor and sensory neuropathy, Optic atrophy, Pontocerebellar hypoplasia, Respiratory system disease, Retinitis pigmentosa, Seasonal allergic rhinitis, Spastic ataxia