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
12181 to 12190 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12181
Solute carrier family 29 member 1 (Augustine blood group)
AUG, ENT1, hENT1
Fetal erythroblastosis, Huntington disease, Pancreatic neoplasms

12182
Solute carrier family 29 member 3
ENT3, HCLAP, HJCD, PHID
Asthma, Congenital heart disease, Major depressive disorder, Desbuquois syndrome, Diabetes mellitus type 1, Digestive system neoplasms, Dyslipidemias, Hearing impairment, Hearing loss, Congenital heart defect, Hepatomegaly, Hypertrichosis, Hypogonadism, Obesity, Systemic lupus erythematosus
View all (1 more)

12183
Solute carrier family 29 member 4
ENT4, PMAT
Brain infarction, Cerebral amyloid angiopathy, Lewy body disease

12184
Solute carrier family 2 member 1
CSE, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT-1, GLUT1, GLUT1DS, HTLVR, PED, SDCHCN
Ataxia, Bell's palsy, Breast neoplasms, Ductal carcinoma, Hepatocellular carcinoma, Intraductal noninfiltrating carcinoma, Renal cell carcinoma, Cerebellar ataxia, Childhood absence epilepsy, Childhood-onset glut1 deficiency syndrome 2, Choreoathetosis, Chromosome 17q23.1-q23.2 deletion syndrome, Glucose transporter type 1 deficiency syndrome, Colonic neoplasms, Cryohydrocytosis
View all (25 more)

12185
Solute carrier family 2 member 10
ATORS, ATS, GLUT10
Alzheimer disease, Androgenetic alopecia, Aortic aneurysm, Arterial tortuosity syndrome, Astrocytoma, Auditory system disease, Bicuspid aortic valve, Breast neoplasms, Color vision deficiency, Congenital contractural arachnodactyly, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Marfan syndrome, Orofacial cleft

12186
Solute carrier family 2 member 11
GLUT10, GLUT11
Hypertrophic cardiomyopathy

12187
Solute carrier family 2 member 12
GLUT12, GLUT8
Coronary artery disease, Oligodendroglioma, Open angle glaucoma, Prostate cancer, Scoliosis

12188
Solute carrier family 2 member 13
HMIT
Alzheimer disease, Astrocytoma, Uinary system neoplasms, Colorectal cancer, Crohn disease, Inflammatory bowel disease, Insomnia, Leprosy, Parkinson disease, Progressive supranuclear palsy, Ulcerative colitis, Urogenital neoplasms

12189
Solute carrier family 2 member 14
GLUT14, SLC2A3P3
Autism, Brain aneurysm, Parkinson disease

12190
Solute carrier family 2 member 2
GLUT2
Breast neoplasms, Hepatocellular carcinoma, Experimental diabetes, Diabetes mellitus type 2, Diabetes mellitus permanent neonatal, Diabetic ketoacidosis, Long qt syndrome, Fanconi syndrome, Fanconi-bickel syndrome, Fatty liver, Fatty liver, alcoholic, Glycogen storage disease, Gout, Neonatal diabetes mellitus, Osteoarthritis