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FAM123B wt Allele

Known as: FLJ39827, RP11-403E24.2, Family with Sequence Similarity 123B wt Allele 
Human FAM123B wild-type allele is located in the vicinity of Xq11.1 and is approximately 21 kb in length. This allele, which encodes protein FAM123B… 
National Institutes of Health

Related topics

Related topics

5 relations

Broader (1)

AMER1 gene
NephroblastomaProtein FAM123BSignal TransductionXq11.1

Papers overview

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2016
2016
Expression of WTX gene in hepatocellular carcinoma and cell lines and its clinical significance
Objective: Wilms’ tumor gene on the X chromosome (WTX) was reported to be a tumor-suppression gene for various cancers. The… 
2013
2013
Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locus
Osteopathia striata congenita with cranial sclerosis (OSCS) is a skeletal dysplasia caused by germline deletions of or truncating… 
Review
2012
Review
2012
Molecular Cell Previews WTX : An Unexpected Regulator for p 53
Wilms tumor is an embryonic kidney tumor that affects 1 in 10,000 of live births and represents the most common solid organ tumor… 
2011
2011
Kidney cancer: An enigma remains
The tumour suppressor WTX regulates mesenchymal progenitor cell fate and lineage specification. 
2010
2010
Abstract 3426: The lower incidence of loss of IGF2 imprinting, but not that of WT1, WTX or CTNNB1 abnormality may cause different incidence rates of Wilms tumor between Japanese and Caucasian…
Incidence rates of Wilms tumor (WT) markedly differ among ethnic groups; the epidemiological studies showed that the incidence of… 
2010
2010
OSTEOPATIA ESTRIADA COM ESCLEROSE CRANIANA
Apresentamos uma crianca do sexo feminino com atraso do crescimento, laringotraqueomalacia, surdez de conducao e dismorfia facial…