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
12311 to 12320 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12311
Solute carrier family 5 member 5
NIS, TDH1
Breast neoplasms, Hepatocellular carcinoma, Cholangiocarcinoma, Congenital hypothyroidism, Thyroid dyshormonogenesis, Glioma, Kidney neoplasms, Melanoma, Ovarian neoplasms, Prostatic neoplasms, Thyroid neoplasms

12312
Solute carrier family 5 member 6
COMNB, NERIB, SMVT, SMVTD, hSMVT
Genetic neurodegenerative disease, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2, Uterine fibroid

12313
Solute carrier family 5 member 7
CHT, CHT1, CMS20, DHMNVP, HMN7A, HMND7, hCHT1
Charcot-marie-tooth disease, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Distal hereditary motor neuropathy, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Major depressive disorder, Mood disorder, Myasthenic syndrome, Presynaptic congenital myasthenic syndrome, Depression, Schizophrenia

12314
Solute carrier family 5 member 8
AIT, SMCT, SMCT1
Colonic neoplasms, Colorectal cancer, Hyperuricemia

12315
Solute carrier family 5 member 9
SGLT4
Gout

12316
Solute carrier family 66 member 1
LAAT-1, LAAT1, PQLC2
Hypothyroidism, Nephropathic cystinosis

12317
Solute carrier family 66 member 2
PQLC1
Dementia, Schizophrenia, Diabetes mellitus type 2

12318
Solute carrier family 66 member 3
C2orf22, PQLC3
Liver cirrhosis, Liver neoplasms, Hypertension, Uterine fibroid

12319
Solute carrier family 67 member 1
BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A18, SLC22A1L, TSSC5, p45-BWR1A
Breast cancer, Breast neoplasms, Embryonal nuclear cataract, Hereditary breast cancer, Lung cancer, Lung neoplasms, Rhabdomyosarcoma, Diabetes mellitus type 2

12320
Solute carrier family 6 member 1
GABATHG, GABATR, GAT1, MAE, hGAT-1
Alzheimer disease, Amyotrophic lateral sclerosis, Nonsyndromic intellectual disability, Bladder disease, Central nervous system cancer, Conduct disorder, Major depressive disorder, Developmental and epileptic encephalopathy, Epilepsy, Epilepsy with myoclonic atonic seizures, Rolandic epilepsy, Glioblastoma, Glioma, Global developmental delay, Intellectual developmental disorder
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