Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12131 to 12140 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12131
Solute carrier family 25 member 10
DIC, MTDPS19
Carcinoma, Dental caries, Hearing loss, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial dna depletion syndrome

12132
Solute carrier family 25 member 11
OGC, PGL6, PPGL6, SLC20A4
Metabolic syndrome, Pheochromocytoma/paraganglioma syndrome, Diabetes mellitus type 2

12133
Solute carrier family 25 member 12
AGC1, ARALAR, DEE39, EIEE39
Rheumatoid arthritis, Asperger syndrome, Autism, Developmental and epileptic encephalopathy, Major depressive disorder, Mitochondrial disease, Schizophrenia, Amyotrophic lateral sclerosis, Diabetes mellitus type 2

12134
Solute carrier family 25 member 13
ARALAR2, CITRIN, CTLN2, NICCD
Citrin deficiency, Citrullinemia, Disorder of the urea cycle metabolism, Liver cirrhosis, Lung cancer, Osteoarthritis, Squamous cell carcinoma

12135
Solute carrier family 25 member 15
D13S327, HHH, LNC-HC, ORC1, ORNT1
Amino acid metabolism disorder, Cardiac arrhythmia, Citrullinemia, Disorder of the urea cycle metabolism, Intellectual developmental disorder

12136
Solute carrier family 25 member 16
D10S105E, GDA, GDC, HGT.1, ML7, hGP, hML7
Sarcoidosis, Secondary malignant neoplasm

12137
Solute carrier family 25 member 17
PMP34
Bipolar disorder, Colorectal cancer, Insomnia, Neurotic disorder, Schizophrenia

12138
Solute carrier family 25 member 19
DNC, MCPHA, MTPPT, MUP1, THMD3, THMD4, TPC
Amish lethal microcephaly, Leigh syndrome, Microcephaly, Systemic lupus erythematosus, Thiamine metabolism dysfunction syndrome

12139
Solute carrier family 25 member 2
ORC2, ORNT2
Obesity

12140
Solute carrier family 25 member 20
CAC, CACT
Autism, Carnitine acetyltransferase deficiency, Insomnia