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 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

541
Solute carrier family 11 member 1
LSH, NRAMP, NRAMP1
Juvenile arthritis, Rheumatoid arthritis, Behcet disease, Buruli ulcer, Ulcerative colitis, Crohn disease, Cystic fibrosis, Atopic dermatitis, Diabetes mellitus type 1, Inflammatory bowel disease, Juvenile idiopathic arthritis, Kidney failure, Leishmaniasis, Leprosy, Systemic lupus erythematosus
View all (6 more)

542
Solute carrier family 11 member 2
AHMIO1, DCT1, DMT1, NRAMP2
Amyotrophic lateral sclerosis, Anemia, Hypochromic microcytic anemia, Iron deficiency anemia, Hemochromatosis, Hypochromic anemia, Liver neoplasms, Microcytic anemia, Parkinson disease

543
Solute carrier family 12 member 1
BSC, BSC-1, BSC1, CCC2, NKCC2
Bartter syndrome, Eye neoplasms, Gitelman syndrome, Gout, Nephrolithiasis, Skin cancer, Skin neoplasms, Systemic lupus erythematosus

544
Solute carrier family 12 member 2
BSC, BSC-2, BSC2, CCC1, KILQS, NKCC1, PPP1R141, hNKCC1
Nonsyndromic intellectual disability, Breast cancer, Carcinoid tumor, Carcinoma, Cardiovascular disease, Deafness, Delpire-mcneill syndrome, Epilepsy, Temporal lobe epilepsy, Hearing loss, Hypertension, Intellectual developmental disorder, Lymphatic system disease, Movement disorder, Myopathy
View all (6 more)

545
Solute carrier family 12 member 3
NCC, NCCT, TSC
Bartter syndrome, Breast cancer, Hypertension, Hypokalemia-hypomagnesemia, Genetic renal tubular disease, Gitelman syndrome, Kidney disease, Lymphoid leukemia, Metabolic syndrome, Nephrolithiasis, Diabetes mellitus type 2, Vascular disease

546
Solute carrier family 12 member 4
CTC-479C5.17, KCC1, hKCC1
Bipolar disorder

547
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)

548
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

549
Solute carrier family 12 member 7
KCC4
Autism, Lung cancer, Major depressive disorder, Periodontitis, Squamous cell carcinoma, Urinary bladder neoplasms, Uterine fibroid

550
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