FAM123B
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 | This article needs additional citations for verification. (January 2024) |
| 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 |
FAM123B is a human gene, also referred to as WTX.
It has been associated with Wilms tumor.[1]
References
- ^ 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.
 | This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it. |
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