Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
541 to 550 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

541
Solute carrier family 12 member 4
CTC-479C5.17, KCC1, hKCC1
Bipolar disorder

542
Solute carrier family 12 member 5
DEE34, EIEE34, EIG14, KCC2, hKCC2
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Developmental and epileptic encephalopathy, Epilepsy, Epilepsy of infancy with migrating focal seizures, Idiopathic generalized epilepsy, Temporal lobe epilepsy, Hyperalgesia, Major depressive disorder, Malignant migrating partial seizures of infancy, Mood disorder, Movement disorder, Neurotic disorder, Psychiatric disorders
View all (4 more)

543
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

544
Solute carrier family 12 member 7
KCC4
Autism, Lung cancer, Major depressive disorder, Periodontitis, Squamous cell carcinoma, Urinary bladder neoplasms, Uterine fibroid

545
Solute carrier family 12 member 8
CCC9
Diabetes mellitus, Pharyngeal disorder, Respiratory system disease, Schizophrenia, Diabetes mellitus type 2, Upper respiratory tract disorder

546
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

547
Solute carrier family 13 member 3
ARLIAK, NADC3, NaC3, SDCT2
Astrocytoma, Kidney disease, Gout, Diabetes mellitus type 2

548
Solute carrier family 13 member 4
NAS2, SUT-1, SUT1
Autism, Juvenile idiopathic arthritis, Liver cirrhosis

549
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

550
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