SLC22A11 Products

Description

The protein encoded by the SLC22A11 gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and is found mainly in the kidney and in the placenta, where it may act to prevent potentially harmful organic anions from reaching the fetus. [provided by RefSeq]

Bioinformatics

Entrez	55867 Human
Uniprot	NP_060954.1 Human Q9NSA0 Human
Product By Gene ID	55867
Alternate Names	MGC34282 solute carrier family 22 member 11 Organic anion transporter 4 OAT4solute carrier family 22 (organic anion/cation transporter), member 11 hOAT4 solute carrier family 22 (organic anion/urate transporter), member 11

Diseases related to SLC22A11

Discover more about diseases related to SLC22A11.

Malignant Neoplasms
Gout
Hyperuricemia
Malignant Neoplasm Of Breast
Cardiovascular Diseases
Malignant Tumor Of Colon
Diabetes Mellitus
Kidney Diseases
Cholangiocarcinoma
Coronary Heart Disease
Infarction
Neurodegenerative Disorders
Teratogenic Effect
Coronary Artery Disease
Carcinoma
Injury To Kidney
Insulin Resistance
Immunologic Deficiency Syndromes
Myocardial Infarction

Pathways for SLC22A11

View related products by pathway and learn more about each of the pathways below.

Transport
Excretion
Secretion
Anion Transport
Organic Anion Transport
Localization
Glomerular Filtration
Gene Silencing
Renal Tubular Secretion
Aging
Dna Methylation
Glycosylation
Endocytosis
Response To Drug
Transepithelial Transport
Methylation
Cell Death
Protein Folding
Urate Transport
Acid Secretion

PTMs for SLC22A11

Learn more about PTMs related to SLC22A11.

Carboxylation
Glycosylation
Methylation

Bioinformatics Tool for SLC22A11

Discover related pathways, diseases and genes to SLC22A11. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.