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"
771 to 780 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

771
Solute carrier family 44 member 2 (CTL2 blood group)
CTL2, PP1292
Bipolar disorder, Thromboembolic pulmonary hypertension, Congenital heart disease, Cor pulmonale, Hyperlipidemia, Heart disease, Liver cirrhosis, Multiple sclerosis, Osteoarthritis, Stroke, Systemic lupus erythematosus, Venous thromboembolism

772
Solute carrier family 44 member 3
CTL3
Dementia

773
Solute carrier family 44 member 4
C6orf29, CTL4, DFNA72, NG22, TPPT, hTPPT1
Asthma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing loss, Hypertension, Lung cancer, Parkinson disease, Psoriasis, Sarcoidosis, Squamous cell carcinoma, Systemic lupus erythematosus, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm, Vitiligo
View all (1 more)

774
Solute carrier family 44 member 5
CTL5
Alzheimer disease, Major depressive disorder, Mood disorder, Neurotic disorder

775
Solute carrier family 45 member 1
DNB5, IDDNPF, PAST-A
Eczema, Nonsyndromic intellectual disability, Inflammatory skin disease, Intellectual developmental disorder neuropsychiatric, Migraine, Psoriasis, Schizophrenia, Diabetes mellitus type 1

776
Solute carrier family 45 member 2
1A1, AIM1, MATP, OCA4, SHEP5
Basal cell carcinoma, Skin neoplasms, Biliary tract cancer, Breast cancer, Cancer, Squamous cell carcinoma, Cervical cancer, Colorectal cancer, Melanoma, Cutaneous squamous cell carcinoma, Endometrial cancer, Erythematosquamous dermatosis, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer
View all (20 more)

777
Solute carrier family 45 member 4
-
Bipolar disorder, Osteoarthritis

778
Solute carrier family 46 member 1
G21, HCP1, HsPCFT, PCFT, hPCFT
Anemia, Congenital folate absorption defect, Hereditary folate malabsorption, Hyperhomocysteinemia, Intellectual developmental disorder, Liver cirrhosis, Malabsorption syndrome, Pancytopenia

779
Solute carrier family 46 member 2
Ly110, TSCOT
Alzheimer disease

780
Solute carrier family 46 member 3
FKSG16
Liver cirrhosis, Nonalcoholic fatty liver disease