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
12161 to 12170 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

12161
Solute carrier family 25 member 47
C14orf68, HDCMP, HDMCP, HMFN1655
Hepatocellular carcinoma

12162
Solute carrier family 25 member 48
-
Coronary aneurysm, Duchenne muscular dystrophy, Obesity, Prostate cancer, Schizophrenia, Scoliosis

12163
Solute carrier family 25 member 5
2F1, AAC2, ANT2, T2, T3
Gout, Intellectual developmental disorder

12164
Solute carrier family 26 member 1
CAON, CAON1, EDM4, HYSULF, SAT-1, SAT1
Alzheimer disease, Developmental and epileptic encephalopathy, Hyperoxaluria, Mucopolysaccharidosis, Nephrolithiasis, Pfaundler-hurler syndrome, Polymyositis, Urolithiasis

12165
Solute carrier family 26 member 11
-
Mucopolysaccharidosis, Stroke

12166
Solute carrier family 26 member 2
D5S1708, DTD, DTDST, EDM4, MST153, MSTP157
Achondrogenesis, Atelosteogenesis, Bone disease, Brachydactyly, Carnevale syndrome, Congenital cartilage disorder, Connective tissue disease, Craniofacial abnormalities, De la chapelle dysplasia, Desbuquois syndrome, Diastrophic dysplasia, Diastrophic dysplasia, broad bone-platyspondylic variant, Ear disease, Epiphyseal dysplasia, Juvenile idiopathic arthritis
View all (4 more)

12167
Solute carrier family 26 member 3
CLD, DRA
Cholecystolithiasis, Ulcerative colitis, Congenital chloride diarrhea, Congenital secretory diarrhea, Dysentery, Hydrops fetalis, Intestinal obstruction

12168
Solute carrier family 26 member 4
DFNB4, EVA, PDS, TDH2B
Congenital hypothyroidism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Thyroid agenesis, Congenital ear anomaly, Congenital hypothyroidism due to absence of thyroid gland, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Pendred syndrome, Prostatic neoplasms, Wolff-parkinson-white syndrome

12169
Solute carrier family 26 member 5
DFNB61, PRES
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing impairment, Hearing loss, Nonsyndromic hearing loss

12170
Solute carrier family 26 member 6
-
Hepatocellular carcinoma, Hyperoxaluria