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WNT7A gene

Known as: proto-oncogene Wnt7a protein, WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 7A, WNT7A 
This gene plays a role in signal transduction and intercellular communication. It is involved in limb development.
National Institutes of Health

Related topics

Related topics

7 relations
Cell Fate ControlIntercellular Communication ProcessLimb DevelopmentMorphogenesis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
WNT7A Expression is Downregulated in T Lymphocytes after T-Cell Receptor Activation Due to Histone Modifications and in T-ALL by DNA Methylation
WNT signaling pathway regulates several processes involved in the homeostasis of normal cells. Its dysregulation is associated… 
2017
2017
Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation.
2017
2017
Santos syndrome is caused by mutation in the WNT7A gene
We have recently described a family with a condition (Santos syndrome (SS; MIM 613005)) characterized by fibular agenesis… 
2016
2016
A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus.
2016
2016
Effect of WNT5a and WNT7a on chondrogenesis during limb development
2015
2015
Expression of WNT genes in cervical cancer-derived cells: Implication of WNT7A in cell proliferation and migration.
2011
2011
Al‐Awadi–Raas‐Rothschild (limb/pelvis/uterus–hypoplasia/aplasia) syndrome and WNT7A mutations: Genetic homogeneity and nosological delineation
The Al‐Awadi–Raas‐Rothschild syndrome (AARRS; OMIM 276820) and the Fuhrmann syndrome (FS; OMIM 228930) are distinct limb… 
2010
2010
A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al‐Awadi/Raas‐Rothschild/Schinzel phocomelia syndrome
Al‐Awadi/Raas‐Rothschild/Schinzel phocomelia (AARRS) syndrome, a rare autosomal recessive disorder, comprises malformations of… 
2006
2006
Mutational analyses of WNT7A and HDAC11 as candidate tumour suppressor genes in sporadic malignant pancreatic endocrine tumours
Objective  We and others have reported loss of heterozygosity (LOH) on chromosome 3p25 in sporadic malignant pancreatic endocrine… 
2005
2005
Comparative genomics on Wnt7a orthologs.
WNT and Hedgehog signaling pathways network together during carcinogenesis and embryogenesis. WNT7A mRNA is expressed in human… 
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