Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2022-07-13

AUTHORS

Mingzhu Miao, Shoulian Lu, Xiao Sun, Meng Zhao, Jue Wang, Xiaotan Su, Bai Jin, Lizhou Sun

ABSTRACT

BackgroundTumor protein p63 is an important transcription factor regulating epithelial morphogenesis. Variants associated with the TP63 gene are known to cause multiple disorders. In this study, we determined the genetic cause of split-hand/foot malformation in a Chinese pedigree.MethodsFor this study, we have recruited a Chinese family and collected samples from affected and normal individuals of the family (three affected and two normal). Whole exome sequencing was performed to detect the underlying genetic defect in this family. The potential variant was validated using the Sanger sequencing approach.ResultsUsing whole-exome and Sanger sequencing, we identified a novel heterozygous pathogenic missense variant in TP63 (NM_003722.5: c.921G > T; p.Met307Ile). This variant resulted in the substitution of methionine with isoleucine. Structural analysis suggested a resulting change in the structure of a key functional domain of the p63 protein.ConclusionThis novel missense variant expands the TP63 variant spectrum and provides a basis for genetic counseling and prenatal diagnosis of families with split-hand/foot malformation or other TP63-related diseases. More... »

PAGES

157

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1186/s12920-022-01311-y

DOI

http://dx.doi.org/10.1186/s12920-022-01311-y

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https://app.dimensions.ai/details/publication/pub.1149448378

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/35831859


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