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Gene | ATM |
Variant | N2326_K2363del |
Impact List | deletion |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | ATM N2326_K2363del results in the deletion of 38 amino acids in the FAT domain of the Atm protein from amino acids 2326 to 2363 (UniProt.org). N2326_K2363del results in failure to induce expression of TP53 target genes upon DNA damage in patient-derived cells in culture (PMID: 23585524), and therefore, is predicted to lead to a loss of Atm protein function. |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM N2326_K2363del |
Transcript | NM_000051.4 |
gDNA | chr11:g.108327645_108327758del114 |
cDNA | c.6976_7089del114 |
Protein | p.N2326_K2363del38 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011542842.4 | chr11:g.108329073_108329186del114 | c.6977_7090del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_047426978.1 | chr11:g.108329073_108329186del114 | c.6977_7090del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_047426977.1 | chr11:g.108329073_108329186del114 | c.6977_7090del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_011542844.4 | chr11:g.108334979_108335092del114 | c.6977_7090del114 | p.T2326_E2363del38 | RefSeq | GRCh38/hg38 |
XM_047426979.1 | chr11:g.108329073_108329186del114 | c.6977_7090del114 | p.N2326_K2363del38 | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108327645_108327758del114 | c.6976_7089del114 | p.N2326_K2363del | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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