| 词条 | FAM123B |
| 释义 |
|name=family with sequence similarity 123B |caption= |image= |width= |HGNCid=26837 |Symbol=FAM123B |AltSymbols=WTX |EntrezGene=139285 |OMIM=300647 |RefSeq=NM_152424 |UniProt= |PDB= |ECnumber= |Chromosome=X |Arm=q |Band=11.1 |LocusSupplementaryData= }} FAM123B is a human gene, also referred to as WTX. It has been associated with Wilms tumor.[1] References1. ^{{cite journal | vauthors = Rivera MN, Kim WJ, Wells J, Driscoll DR, Brannigan BW, Han M, Kim JC, Feinberg AP, Gerald WL, Vargas SO, Chin L, Iafrate AJ, Bell DW, Haber DA | title = An X chromosome gene, WTX, is commonly inactivated in Wilms tumor | journal = Science | volume = 315 | issue = 5812 | pages = 642–5 | date = February 2007 | pmid = 17204608 | doi = 10.1126/science.1137509 | url = http://www.sciencemag.org/cgi/pmidlookup?view=long&pmid=17204608 }} {{gene-X-stub}} |
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