pendrin

pendrin
pen·drin (penґdrin) a glycoprotein found on the apical surface of thyroid follicular cells, acting as a transport protein for iodide to leave the cell and aid in formation of thyroxine; mutations in the gene specifying pendrin cause Pendred syndrome (see under syndrome).

Medical dictionary. 2011.

Игры ⚽ Нужно решить контрольную?

Look at other dictionaries:

  • Pendrin — also known as solute carrier family 26, member 4 or SLC26A4, is a human gene.cite web | title = Entrez Gene: SLC26A4 solute carrier family 26, member 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5172|… …   Wikipedia

  • pendrin — noun A protein involved in the exchange of chloride and iodide ions across biological membranes …   Wiktionary

  • Pendred syndrome — Classification and external resources OMIM 274600 DiseasesDB 9771 GeneReviews …   Wikipedia

  • Cystic fibrosis — Classification and external resources A breathing treatment for cystic fibrosis, using a mask nebuliser and a ThAIRapy Vest ICD 10 E …   Wikipedia

  • Collecting duct system — Scheme of renal tubule and its vascular supply. Latin tubulus renalis colligens Gray s …   Wikipedia

  • Renal physiology — This illustration demonstrates the normal kidney physiology. It also includes illustrations showing where some types of diuretics act, and what they do. Renal physiology (Latin rēnēs, kidney ) is the study of the physiology of the kidney. This… …   Wikipedia

  • Thyroid peroxidase — protein Name = thyroid peroxidase caption = width = HGNCid = 12015 Symbol = TPO AltSymbols = EntrezGene = 7173 OMIM = 606765 RefSeq = NM 175722 UniProt = P07202 PDB = ECnumber = 1.11.1.8 Chromosome = 2 Arm = Band = LocusSupplementaryData = pter… …   Wikipedia

  • Diiodotyrosine transaminase — Identifiers EC number 2.6.1.24 CAS number 9033 18 5 …   Wikipedia

  • SLC4A2 — Solute carrier family 4, anion exchanger, member 2 (erythrocyte membrane protein band 3 like 1), also known as SLC4A2, is a human gene.cite web | title = Entrez Gene: SLC4A2 solute carrier family 4, anion exchanger, member 2 (erythrocyte membrane …   Wikipedia

  • SLC4A3 — Solute carrier family 4, anion exchanger, member 3, also known as SLC4A3, is a human gene.cite web | title = Entrez Gene: SLC4A3 solute carrier family 4, anion exchanger, member 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”