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
12061 to 12070 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12061
Solute carrier family 15 member 2
PEPT2
Asthma, Autoimmune disease, Melanoma, Multiple sclerosis

12062
Solute carrier family 15 member 3
OCTP, PHT2, PTR3, hPHT2
Conotruncal cardiac defect, Liver cirrhosis, Prostate cancer, Diabetes mellitus type 1, Diabetes mellitus type 2

12063
Solute carrier family 15 member 4
FP12591, PHT1, PTR4
Systemic lupus erythematosus

12064
Solute carrier family 15 member 5
-
Dementia, Large artery stroke, Major depressive disorder, Scoliosis

12065
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

12066
Solute carrier family 16 member 10
MCT10, PRO0813, TAT1
Atypical femoral fracture, Color vision deficiency, Dental caries, Gout, Psoriasis, Psoriatic arthritis

12067
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

12068
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

12069
Solute carrier family 16 member 13
MCT13
Astrocytoma, Diabetes mellitus type 2

12070
Solute carrier family 16 member 14
MCT14
Esophageal squamous cell carcinoma, Obsessive-compulsive disorder