FAM123B
| 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; 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.
{{cite journal}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help)
 | This genetics article is a stub. You can help Wikipedia by expanding it. |