Health / Medical Topics |
PTEN Loss
A molecular abnormality referring to the loss of at least one copy of the PTEN gene (10q23). (NCI Thesaurus)
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A molecular genetic abnormality indicating the presence of an inactivating mutation in the PTEN gene on chromosome 10q23.
This gene plays a role in signal transduction and apoptosis. It is also involved in the regulation of cell cycle progression. …
A protein that helps control many cell functions, including cell division and cell death. Mutations (changes) in the gene that makes PTEN…
Human PTCH2 wild-type allele is located within 1p33-p34 and is approximately 21 kb in length. This allele, which encodes protein patched homolog…
This gene plays a role in intercellular communication, embryonic structure development, and in tumorigenesis.
Human PTCH1 wild-type allele is located in the vicinity of 9q22.3 and is approximately 65 kb in length. This allele, which encodes…