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Gene | TET2 |
Variant | K1171fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TET2 K1171fs results in a change in the amino acid sequence of the Tet2 protein beginning at aa 1171 of 2002, likely resulting in premature truncation of the functional protein (UniProt.org). K1171fs has not been characterized however, due to the effects of other truncation mutations downstream of K1171 (PMID: 24994606), is predicted to lead to a loss of Tet2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TET2 mutant TET2 inact mut TET2 K1171fs |
Transcript | NM_001127208.3 |
gDNA | chr4:g.(105242843_105242844) |
cDNA | c.(3511_3510) |
Protein | p.K1171fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_024454102.1 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
NM_001127208.3 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
NM_001127208 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
XM_005263082.3 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
XM_047415840.1 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
NM_001127208.2 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
XM_005263082.4 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
XM_024454103.1 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
XM_024454102.2 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
XM_005263082 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
XM_024454103.2 | chr4:g.(105242843_105242844) | c.(3511_3510) | p.K1171fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
TET2 mutant | acute myeloid leukemia | predicted - sensitive | Azacitidine | Phase I | Actionable | In a retrospective analysis, presence of a TET2 mutation correlated with higher overall response rate (ORR) in patients with myelodysplastic syndrome and acute myeloid leukemia following treatment with Vidaza (azacitidine), with an ORR of 85% (11/3) in TET2-mutated patients, compared to 47% (34/47) in patients with wild-type TET2, but did not correlate with overall survival (PMID: 21494260). | 21494260 |
TET2 mutant | myelofibrosis | not applicable | N/A | Guideline | Diagnostic | TET2 mutations aid in the diagnosis of primary myelofibrosis in the absence of JAK2, CALR, or MPL mutations (NCCN.org). | detail... |
TET2 mutant | acute myeloid leukemia | sensitive | Olaparib | Preclinical - Patient cell culture | Actionable | In a preclinical study, Lynparza (olaparib) treatment inhibited colony formation in patient-derived acute myeloid leukemia cells harboring a TET2 mutation along with FLT3-ITD and NPM1 mutation in culture (PMID: 34215619). | 34215619 |
TET2 mutant | angioimmunoblastic T-cell lymphoma | not applicable | N/A | Guideline | Diagnostic | TET2 mutations aid in the diagnosis of angioimmunoblastic T-cell lymphoma (NCCN.org). | detail... |
TET2 mutant | acute myeloid leukemia | not applicable | N/A | Clinical Study | Prognostic | In multiple clinical studies, including a meta-analysis, TET2 mutations were associated with shorter overall survival in patients with acute myeloid leukemia (PMID: 24524305, PMID: 25412851, PMID: 24994606). | 24524305 25412851 24994606 |