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"
551 to 560 of 1624 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

551
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)

552
Solute carrier family 15 member 1
HPECT1, HPEPT1, PEPT1
Colorectal cancer, Coronary artery disease, Myocardial infarction, Oligodendroglioma

553
Solute carrier family 15 member 2
PEPT2
Asthma, Autoimmune disease, Melanoma, Multiple sclerosis

554
Solute carrier family 15 member 3
OCTP, PHT2, PTR3, hPHT2
Conotruncal cardiac defect, Prostate cancer, Diabetes mellitus type 1, Diabetes mellitus type 2

555
Solute carrier family 15 member 4
FP12591, PHT1, PTR4
Systemic lupus erythematosus

556
Solute carrier family 15 member 5
-
Dementia, Large artery stroke, Major depressive disorder, Scoliosis

557
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

558
Solute carrier family 16 member 10
MCT10, PRO0813, TAT1
Atypical femoral fracture, Color vision deficiency, Dental caries, Gout, Psoriasis, Psoriatic arthritis

559
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

560
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