PTEN, phosphatase and tensin homolog, 5728

N. diseases: 1349; N. variants: 384
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.040 GeneticVariation disease BEFREE A total of 5 tagging single-nucleotide polymorphisms (rs2299941 of PTEN, rs2735385, rs6999227, rs1805812, and rs1061302 of Nijmegen breakage syndrome 1) were tightly associated with breast cancer risk in sporadic cases, and 5 other tagging single-nucleotide polymorphisms (rs1042522 of TP53, rs2735343 of PTEN, rs7220719, rs16945628, and rs11871753 of BRCA1-interacting protein 1) were tightly associated with breast cancer risk in familial and early-onset cases. 30799775 2018
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.040 GeneticVariation disease BEFREE Genetic testing revealed the patient to have the familial germline PTEN mutation. 19622968 2009
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.040 Biomarker disease BEFREE PTEN is an important tumor suppressor implicated in the pathogenesis of a number of familial and sporadic cancers. 11891178 2002
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.040 GeneticVariation disease BEFREE Additionally, germ-line mutations of PTEN/MMAC1 are responsible for several familial neoplastic disorders, including Cowden disease and Bannayan-Zonana syndrome. 9354433 1997