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
12141 to 12150 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12141
Solute carrier family 25 member 21
MTDPS18, ODC, ODC1
Barrett esophagus, Breast cancer, Colorectal cancer, Coronary artery disease, Esophageal adenocarcinoma, Estrogen-receptor negative breast cancer, Migraine, Mitochondrial dna depletion syndrome, Ovarian cancer, Prostate cancer

12142
Solute carrier family 25 member 22
DEE3, EIEE3, GC-1, GC1, NET44
Developmental and epileptic encephalopathy, Developmental delay, Myoclonic encephalopathy, Epilepsy of infancy with migrating focal seizures, Malignant migrating partial seizures of infancy

12143
Solute carrier family 25 member 24
APC1, SCAMC-1, SCAMC1
Crohn disease, Dementia, Dental caries, Desbuquois syndrome, Eosinophilia, Heart failure, Inflammatory bowel disease, Liver cirrhosis, Ulcerative colitis

12144
Solute carrier family 25 member 25
MCSC, PCSCL, SCAMC-2, SCAMC2
Autism, Nephrolithiasis, Myopia

12145
Solute carrier family 25 member 26
COXPD28, SAMC
Appendicitis, Atrial fibrillation, Binge eating disorder, Bipolar disorder, Kidney disease, Colorectal adenoma, Colorectal cancer, Combined oxidative phosphorylation deficiency, Hyperuricemia, Lymphoid leukemia, Mitochondrial disease, Pulmonary hypertension, Sarcoidosis, Scoliosis, Diabetes mellitus type 2

12146
Solute carrier family 25 member 27
UCP4
Autoimmune thyroid disease, Graves disease, Hashimoto disease, Schizophrenia

12147
Solute carrier family 25 member 28
MFRN2, MRS3/4, MRS4L, NPD016
Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Colorectal adenoma, Colorectal cancer, Common variable immunodeficiency, Crohn disease, Diverticular disease, Glomerulonephritis, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Major depressive disorder, Psoriasis
View all (4 more)

12148
Solute carrier family 25 member 29
C14orf69, CACL, ORNT3
Alzheimer disease, Metabolic syndrome, Diabetes mellitus type 2

12149
Solute carrier family 25 member 3
OK/SW-cl.48, PHC, PTP, PiC
Hypertrophic cardiomyopathy, Mitochondrial disease

12150
Solute carrier family 25 member 30
KMCP1
Gout, Liver cirrhosis