FAM123B
| family with sequence similarity 123B | |
|---|---|
| Identifiers | |
| Symbol | FAM123B |
| Alt. symbols | WTX |
| Entrez | 139285 |
| HUGO | 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, et al. (February 2007). "An X chromosome gene, WTX, is commonly inactivated in Wilms tumor". Science 315 (5812): 642–645. doi:10.1126/science.1137509. PMID 17204608.
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