Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12371 to 12380 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12371
SLCO1B3-SLCO1B7 readthrough
LST-3TM12, OATP1B3-1B7
Rotor syndrome, Scoliosis

12372
Solute carrier organic anion transporter family member 1C1
OATP-F, OATP-RP5, OATP1, OATP14, OATP1C1, OATPF, OATPRP5, SLC21A14
Alzheimer disease, Atrial fibrillation, Autism, Neurodevelopmental disorder, Dementia, Major depressive disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder

12373
Solute carrier organic anion transporter family member 2A1
MATR1, OATP2A1, PGT, PHOAD, PHOAR2, SLC21A2
Autism, Basal cell carcinoma, Enteropathy, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Desbuquois syndrome, Primary hypertrophic osteoarthropathy, Inflammatory bowel disease

12374
Solute carrier organic anion transporter family member 2B1
OATP-B, OATP2B1, OATPB, SLC21A9
Asthma

12375
Solute carrier organic anion transporter family member 3A1
OATP-D, OATP-RP3, OATP3A1, OATPD, OATPRP3, SLC21A11
Alzheimer disease, Candidemia, Lymphoblastic leukemia, Dementia, Hypertension, Immune system disease, Insomnia, Metabolic syndrome, Obesity, Open angle glaucoma, Willis-ekbom disease, Diabetes mellitus type 2

12376
Solute carrier organic anion transporter family member 4A1
OATP-E, OATP1, OATP4A1, OATPE, OATPRP1, POAT, SLC21A12
Diabetes mellitus, Oral cavity carcinoma, Schizophrenia, Diabetes mellitus type 2

12377
Solute carrier organic anion transporter family member 4C1
OATP-H, OATP-M1, OATP4C1, OATPX, PRO2176, SLC21A20
Ovarian epithelial cancer, Ovarian cancer, Preeclampsia, Willis-ekbom disease, Diabetes mellitus type 2

12378
Solute carrier organic anion transporter family member 5A1
OATP-J, OATP-RP4, OATP5A1, OATPJ, OATPRP4, SLC21A15
Cervical cancer, Desbuquois syndrome

12379
Solute carrier organic anion transporter family member 6A1
CT48, GST, OATP-I, OATP6A1, OATPY
Color vision deficiency, Diabetes mellitus, Metabolic syndrome, Orofacial cleft, Schizophrenia, Diabetes mellitus type 2

12380
SMC5/6 complex localization factor 2
ATELS1, C10orf6, FAM178A, hNSE6
Atelis syndrome, Lung cancer, Mosaic variegated aneuploidy, Nonalcoholic fatty liver disease, Squamous cell carcinoma, Diabetes mellitus type 2