FAM123B

From Wikipedia, the free encyclopedia
Jump to: navigation, search
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[edit]

  1. ^ 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. PMID 17204608. doi:10.1126/science.1137509.