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"
561 to 570 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

561
Solute carrier family 15 member 5
-
Dementia, Large artery stroke, Major depressive disorder, Scoliosis

562
Solute carrier family 16 member 1
HHF7, MCT, MCT1, MCT1D
Autism, Colonic neoplasms, Disorder of fatty acid and ketone body metabolism, Disorder of fatty acid oxidation and ketone body metabolism, Erythrocyte lactate transporter defect, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Osteoarthritis

563
Solute carrier family 16 member 10
MCT10, PRO0813, TAT1
Atypical femoral fracture, Color vision deficiency, Dental caries, Gout, Psoriasis, Psoriatic arthritis

564
Solute carrier family 16 member 11
MCT 11, MCT11
Crohn disease, Diabetes mellitus, Diabetic ketoacidosis, Inflammatory bowel disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

565
Solute carrier family 16 member 12
CJMG, CRT2, CTRCT47, MCT12
Atrial fibrillation, Cataract, Cataract-microcornea-metabolic syndrome, Central nervous system cancer, Congenital cataract, Congenital ocular coloboma, Glioblastoma, Glioma

566
Solute carrier family 16 member 13
MCT13
Astrocytoma, Diabetes mellitus type 2

567
Solute carrier family 16 member 14
MCT14
Esophageal squamous cell carcinoma, Obsessive-compulsive disorder

568
Solute carrier family 16 member 2
AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT
Allan-herndon-dudley syndrome, Autism, Cholelithiasis, Hypothyroidism, Intellectual developmental disorder, Spastic paraplegia, Hereditary spastic paraplegia

569
Solute carrier family 16 member 3
MCT 3, MCT 4, MCT-3, MCT-4, MCT3, MCT4
Breast neoplasms, Kidney disease, Peripheral arterial disease, Stomach neoplasms

570
Solute carrier family 16 member 4
MCT4, MCT5
Scoliosis