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
12051 to 12060 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12051
Solute carrier family 12 member 6
ACCPN, CMT2II, KCC3, KCC3A, KCC3B
Agenesis of corpus callosum, Barrett esophagus, Bipolar disorder, Charcot-marie-tooth disease, Clinodactyly, Corpus callosum agenesis neuronopathy syndrome, Dejerine-sottas disease, Hereditary motor and sensory neuropathies, Hypertension, Hypertrophic neuropathy, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome

12052
Solute carrier family 12 member 7
KCC4
Autism, Lung cancer, Major depressive disorder, Periodontitis, Squamous cell carcinoma, Urinary bladder neoplasms, Uterine fibroid

12053
Solute carrier family 12 member 8
CCC9
Diabetes mellitus, Disorder of pharynx, Respiratory system disease, Schizophrenia, Tonsillitis, Diabetes mellitus type 2, Upper respiratory tract disorder

12054
Solute carrier family 12 member 9
CCC6, CIP1, WO3.3, hCCC6
Bipolar disorder, Capillary malformation-arteriovenous malformation, Cataract, Neurodevelopmental disorder, Hypertension, Non-specific syndromic intellectual disability

12055
Solute carrier family 13 member 3
ARLIAK, NADC3, NaC3, SDCT2
Astrocytoma, Kidney disease, Gout, Diabetes mellitus type 2

12056
Solute carrier family 13 member 4
NAS2, SUT-1, SUT1
Autism, Juvenile idiopathic arthritis, Liver cirrhosis

12057
Solute carrier family 13 member 5
DEE25, EIEE25, INDY, NACT, mIndy
Amelocerebrohypohidrotic syndrome, Kidney disease, Developmental and epileptic encephalopathy, Pyridoxine dependent epilepsy, Fatty liver, Fatty liver, alcoholic, Global developmental delay, Insomnia, Depression

12058
Solute carrier family 14 member 1 (Kidd blood group)
HUT11, HUT11A, HsT1341, JK, Jk(a), Jk(b), RACH1, RACH2, UT-B1, UT1, UTE
Hemolytic anemia, Autoimmune hemolytic anemia, Urinary bladder cancer

12059
Solute carrier family 14 member 2
HUT2, UT-A2, UT2, UTA, UTR, hUT-A6
Alzheimer disease, Androgenetic alopecia, Astrocytoma, Attention deficit hyperactivity disorder, Breast cancer, Central nervous system cancer, Obstructive pulmonary disease, Color vision deficiency, Cor pulmonale, Coronary artery disease, Estrogen-receptor negative breast cancer, Gastroesophageal reflux disease, Glioblastoma, Glioma, Gout
View all (8 more)

12060
Solute carrier family 15 member 1
HPECT1, HPEPT1, PEPT1
Colorectal cancer, Coronary artery disease, Myocardial infarction, Oligodendroglioma