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
12011 to 12020 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12011
Solute carrier family 16 member 13
MCT13
Astrocytoma, Diabetes mellitus type 2

12012
Solute carrier family 16 member 14
MCT14
Esophageal squamous cell carcinoma, Obsessive-compulsive disorder

12013
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

12014
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

12015
Solute carrier family 16 member 4
MCT4, MCT5
Scoliosis

12016
Solute carrier family 16 member 6
MCT6, MCT7
Endometriosis

12017
Solute carrier family 16 member 7
MCT2
Colorectal cancer, Insomnia, Major depressive disorder, Kawasaki disease, Non-small cell lung carcinoma, Obesity, Proliferative diabetic retinopathy, Scoliosis

12018
Solute carrier family 16 member 8
MCT3, REMP
Atrophic macular degeneration, Central nervous system cancer, Glaucoma, Glioblastoma, Glioma, Macular degeneration, Age-related macular degeneration

12019
Solute carrier family 16 member 9
C10orf36, MCT9
Alzheimer disease, Central nervous system cancer, Glioblastoma, Glioma, Gout

12020
Solute carrier family 17 member 1
NAPI-1, NPT-1, NPT1
Alzheimer disease, Celiac disease, Dental caries, Gout, Insomnia, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus type 2