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
12101 to 12110 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12101
Solute carrier family 25 member 45
-
Melanoma

12102
Solute carrier family 25 member 46
HMSN6B, PCH1E
Asthma, Astrocytoma, Eczema, Charcot-marie-tooth disease, Congenital pontocerebellar hypoplasia, Hereditary motor and sensory neuropathies, Leigh syndrome, Major depressive disorder, Hereditary motor and sensory neuropathy, Optic atrophy, Pontocerebellar hypoplasia, Respiratory system disease, Retinitis pigmentosa, Seasonal allergic rhinitis, Spastic ataxia

12103
Solute carrier family 25 member 47
C14orf68, HDCMP, HDMCP, HMFN1655
Hepatocellular carcinoma

12104
Solute carrier family 25 member 48
-
Coronary aneurysm, Duchenne muscular dystrophy, Obesity, Prostate cancer, Schizophrenia, Scoliosis

12105
Solute carrier family 25 member 5
2F1, AAC2, ANT2, T2, T3
Gout, Intellectual developmental disorder

12106
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

12107
Solute carrier family 26 member 11
-
Mucopolysaccharidosis, Stroke

12108
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
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12109
Solute carrier family 26 member 3
CLD, DRA
Cholecystolithiasis, Ulcerative colitis, Congenital chloride diarrhea, Congenital secretory diarrhea, Hydrops fetalis, Intestinal obstruction

12110
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