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
12001 to 12010 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12001
Solute carrier family 14 member 2
HUT2, UT-A2, UT2, UTA, UTR, hUT-A6
Alzheimer disease, Androgenetic alopecia, Astrocytoma, Attention deficit hyperactivity disorder, Breast cancer, Central nervous system cancer, Obstructive pulmonary disease, Color vision deficiency, Cor pulmonale, Coronary artery disease, Estrogen-receptor negative breast cancer, Gastroesophageal reflux disease, Glioblastoma, Glioma, Gout
View all (8 more)

12002
Solute carrier family 15 member 1
HPECT1, HPEPT1, PEPT1
Colorectal cancer, Coronary artery disease, Myocardial infarction, Oligodendroglioma

12003
Solute carrier family 15 member 2
PEPT2
Asthma, Autoimmune disease, Melanoma, Multiple sclerosis

12004
Solute carrier family 15 member 3
OCTP, PHT2, PTR3, hPHT2
Conotruncal cardiac defect, Prostate cancer, Diabetes mellitus type 1, Diabetes mellitus type 2

12005
Solute carrier family 15 member 4
FP12591, PHT1, PTR4
Systemic lupus erythematosus

12006
Solute carrier family 15 member 5
-
Dementia, Large artery stroke, Major depressive disorder, Scoliosis

12007
Solute carrier family 16 member 1
HHF7, MCT, MCT1, MCT1D
Autism, Colonic neoplasms, Fatty acid and ketone body metabolism disorder, Fatty acid oxidation and ketone body metabolism disorder, Erythrocyte lactate transporter defect, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Osteoarthritis

12008
Solute carrier family 16 member 10
MCT10, PRO0813, TAT1
Atypical femoral fracture, Color vision deficiency, Dental caries, Gout, Psoriasis, Psoriatic arthritis

12009
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

12010
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