8u15: 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=8u15 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8u15 OCA], [https://pdbe.org/8u15 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8u15 RCSB], [https://www.ebi.ac.uk/pdbsum/8u15 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8u15 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=8u15 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8u15 OCA], [https://pdbe.org/8u15 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8u15 RCSB], [https://www.ebi.ac.uk/pdbsum/8u15 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8u15 ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/SALL4_HUMAN SALL4_HUMAN] Acro-renal-ocular syndrome;IVIC syndrome;Okihiro syndrome due to 20q13 microdeletion;Okihiro syndrome due to a point mutation. 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.
== Function ==
[https://www.uniprot.org/uniprot/SALL4_HUMAN SALL4_HUMAN] Transcription factor with a key role in the maintenance and self-renewal of embryonic and hematopoietic stem cells.<ref>PMID:23012367</ref>
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== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
Retrieved from "https://proteopedia.org/8u15"