7y35: Difference between revisions

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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7y35 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7y35 OCA], [https://pdbe.org/7y35 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7y35 RCSB], [https://www.ebi.ac.uk/pdbsum/7y35 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7y35 ProSAT]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7y35 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7y35 OCA], [https://pdbe.org/7y35 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7y35 RCSB], [https://www.ebi.ac.uk/pdbsum/7y35 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7y35 ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
 
[https://www.uniprot.org/uniprot/PTH1R_HUMAN PTH1R_HUMAN] Blomstrand lethal chondrodysplasia;Dental ankylosis;Eiken syndrome;Metaphyseal chondrodysplasia, Jansen type;Enchondromatosis. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  The disease may be caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.
==See Also==
== Function ==
*[[Transducin 3D structures|Transducin 3D structures]]
[https://www.uniprot.org/uniprot/PTH1R_HUMAN PTH1R_HUMAN] This is a receptor for parathyroid hormone and for parathyroid hormone-related peptide. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase and also a phosphatidylinositol-calcium second messenger system.<ref>PMID:18611381</ref> <ref>PMID:20172855</ref>
== References ==
<references/>
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