- AMN (gene)
Amnionless homolog (mouse), also known as AMN, is a human
gene .PBB_Summary
section_title =
summary_text = The protein encoded by this gene is a type I transmembrane protein. It is thought to modulate bone morphogenetic protein (BMP) receptor function by serving as an accessory or coreceptor, and thus facilitates or hinders BMP binding. It is known that the mouse AMN gene is expressed in the extraembryonic visceral endoderm layer during gastrulation, but it is found to be mutated in amnionless mouse. The encoded protein has sequence similarity to short gastrulation (Sog) and procollagen IIA proteins in Drosophila.cite web | title = Entrez Gene: AMN amnionless homolog (mouse)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=81693| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Kozyraki R, Gofflot F |title=Multiligand endocytosis and congenital defects: roles of cubilin, megalin and amnionless. |journal=Curr. Pharm. Des. |volume=13 |issue= 29 |pages= 3038–46 |year= 2008 |pmid= 17979745 |doi=10.2174/138161207782110507
*cite journal | author=Wang X, Bornslaeger EA, Haub O, "et al." |title=A candidate gene for the amnionless gastrulation stage mouse mutation encodes a TRAF-related protein. |journal=Dev. Biol. |volume=177 |issue= 1 |pages= 274–90 |year= 1996 |pmid= 8660894 |doi= 10.1006/dbio.1996.0162
*cite journal | author=Tomihara-Newberger C, Haub O, Lee HG, "et al." |title=The amn gene product is required in extraembryonic tissues for the generation of middle primitive streak derivatives. |journal=Dev. Biol. |volume=204 |issue= 1 |pages= 34–54 |year= 1999 |pmid= 9851841 |doi= 10.1006/dbio.1998.9034
*cite journal | author=Dunn NR, Hogan BL |title=How does the mouse get its trunk? |journal=Nat. Genet. |volume=27 |issue= 4 |pages= 351–2 |year= 2001 |pmid= 11279507 |doi= 10.1038/86829
*cite journal | author=Kalantry S, Manning S, Haub O, "et al." |title=The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domain. |journal=Nat. Genet. |volume=27 |issue= 4 |pages= 412–6 |year= 2001 |pmid= 11279523 |doi= 10.1038/86912
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Tanner SM, Aminoff M, Wright FA, "et al." |title=Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia. |journal=Nat. Genet. |volume=33 |issue= 3 |pages= 426–9 |year= 2003 |pmid= 12590260 |doi= 10.1038/ng1098
*cite journal | author=Clark HF, Gurney AL, Abaya E, "et al." |title=The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. |journal=Genome Res. |volume=13 |issue= 10 |pages= 2265–70 |year= 2003 |pmid= 12975309 |doi= 10.1101/gr.1293003
*cite journal | author=Fyfe JC, Madsen M, Højrup P, "et al." |title=The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. |journal=Blood |volume=103 |issue= 5 |pages= 1573–9 |year= 2004 |pmid= 14576052 |doi= 10.1182/blood-2003-08-2852
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Tsang HT, Connell JW, Brown SE, "et al." |title=A systematic analysis of human CHMP protein interactions: additional MIT domain-containing proteins bind to multiple components of the human ESCRT III complex. |journal=Genomics |volume=88 |issue= 3 |pages= 333–46 |year= 2006 |pmid= 16730941 |doi= 10.1016/j.ygeno.2006.04.003PBB_Controls
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