7jsl: Difference between revisions

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

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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=7jsl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7jsl OCA], [https://pdbe.org/7jsl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7jsl RCSB], [https://www.ebi.ac.uk/pdbsum/7jsl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7jsl ProSAT]</span></td></tr>
 </table>
-== Disease ==
-[https://www.uniprot.org/uniprot/ERF_HUMAN ERF_HUMAN] Non-syndromic sagittal craniosynostosis;Crouzon syndrome. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
-== Function ==
-[https://www.uniprot.org/uniprot/ERF_HUMAN ERF_HUMAN] Potent transcriptional repressor that binds to the H1 element of the Ets2 promoter. May regulate other genes involved in cellular proliferation. Required for extraembryonic ectoderm differentiation, ectoplacental cone cavity closure, and chorioallantoic attachment (By similarity). May be important for regulating trophoblast stem cell differentiation (By similarity).
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 == Publication Abstract from PubMed ==