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FAM123B is a human gene, also referred to as WTX.
| family with sequence similarity 123B | |
|---|---|
| Identifiers | |
| Symbol | FAM123B |
| Alt. symbols | WTX |
| NCBI gene | 139285 |
| HGNC | 26837 |
| OMIM | 300647 |
| RefSeq | NM_152424 |
| Other data | |
| Locus | Chr. X q11.1 |
It has been associated with Wilms tumor.[1]
References
edit- ^ 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 (February 2007). "An X chromosome gene, WTX, is commonly inactivated in Wilms tumor". Science. 315 (5812): 642–5. Bibcode:2007Sci...315..642R. doi:10.1126/science.1137509. PMID 17204608. S2CID 38928453.
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