| 词条 | Fibrocystin |
| 释义 |
| Symbol = Fibrocystin | Name = Fibrocystin | image = | width = | caption = | Pfam= | InterPro= IPR029927 | SMART= | Prosite = | SCOP = | TCDB = | OPM family= | OPM protein= | PDB= | Membranome superfamily = 632 }}{{infobox protein |Name=polycystic kidney and hepatic disease 1 (autosomal recessive) |caption= |image= |width= |HGNCid=9016 |Symbol=PKHD1 |AltSymbols=TIGM1 |EntrezGene=5314 |OMIM=606702 |RefSeq=NM_138694 |UniProt=Q8TCZ9 |PDB= |ECnumber= |Chromosome=6 |Arm=p |Band=21.2 |LocusSupplementaryData=-p12 }}Fibrocystin is a large, receptor-like protein that is thought to be involved in the tubulogenesis and/or maintenance of duct-lumen architecture of epithelium.[1] FPC associates with the primary cilia of epithelial cells and co-localizes with the Pkd2 gene product polycystin-2 (PC2), suggesting that these two proteins may function in a common molecular pathway. PathologyMutations of its encoding gene (chromosomal locus 6p12.2) can cause autosomal recessive polycystic kidney disease. References1. ^{{cite journal | vauthors = Zhang M, Mai W, Li C, Cho S, Hao C, Moeckel G, Zhao R, Kim I, Wang J, Xiong H, Wang H, Sato Y, Wu Y, Nakanuma Y, Lilova M, Pei Y, Harris R, Li S, Coffey R, Sun L, Wu D, Chen X, Breyer M, Zhao Z, McKanna J, Wu G | title = PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells. | journal = Proc Natl Acad Sci USA | volume = 101 | issue = 8 | pages = 2311–6 | year = 2004 | pmid = 14983006 | url=http://www.pnas.org/cgi/content/full/101/8/2311 | doi = 10.1073/pnas.0400073101 | pmc = 356947}} External links
1 : Single-pass transmembrane proteins |
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