rs556182426

This variant is located in the WNT10A gene.

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ClinVar annotation

Likely Benign★☆☆☆

1 submitter

Schöpf-Schulz-Passarge syndrome; Selective tooth agenesis; Odonto-onycho-dermal dysplasia

About WNT10A

The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is strongly expressed in the cell lines of promyelocytic leukemia and Burkitt's lymphoma. In addition, it and another family member, the WNT6 gene, are strongly coexpressed in colorectal cancer cell lines. The gene overexpression may play key roles in carcinogenesis through activation of the WNT-beta-catenin-TCF signaling pathway. This gene and the WNT6 gene are clustered in the chromosome 2q35 region. [provided by RefSeq, Jul 2008]

View all WNT10A variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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