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"
621 to 630 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

621
Solute carrier family 24 member 5
JSX, NCKX5, OCA6, SHEP4
Eye neoplasms, Melanoma, Glaucoma, Oculocutaneous albinism, Open angle glaucoma, Pulmonary arterial hypertension, Scoliosis, Skin cancer, Skin disease, Skin neoplasms, Skin hair eye pigmentation variation

622
Solute carrier family 25 member 1
CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3
Combined d-2- and l-2-hydroxyglutaric aciduria, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, D-2-hydroxyglutaric aciduria, Mitochondrial disease, Myasthenic syndrome, Presynaptic congenital myasthenic syndrome

623
Solute carrier family 25 member 10
DIC, MTDPS19
Carcinoma, Dental caries, Hearing loss, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial dna depletion syndrome

624
Solute carrier family 25 member 11
OGC, PGL6, PPGL6, SLC20A4
Metabolic syndrome, Pheochromocytoma/paraganglioma syndrome, Diabetes mellitus type 2

625
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

626
Solute carrier family 25 member 13
ARALAR2, CITRIN, CTLN2, NICCD
Citrin deficiency, Citrullinemia, Urea cycle disorder, Lung cancer, Osteoarthritis, Squamous cell carcinoma

627
Solute carrier family 25 member 15
D13S327, HHH, LNC-HC, ORC1, ORNT1
Amino acid metabolism disorder, Cardiac arrhythmia, Citrullinemia, Urea cycle disorder, Intellectual developmental disorder

628
Solute carrier family 25 member 16
D10S105E, GDA, GDC, HGT.1, ML7, hGP, hML7
Sarcoidosis, Secondary malignant neoplasm

629
Solute carrier family 25 member 17
PMP34
Bipolar disorder, Colorectal cancer, Insomnia, Neurotic disorder, Schizophrenia

630
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