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DAXX Truncation Mutants (N-terminus) [nucleoplasm]
Stable Identifier
R-HSA-9670611
Type
Set [CandidateSet]
Species
Homo sapiens
Compartment
nucleoplasm
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of mitotic cell cycle (Homo sapiens)
Diseases of Telomere Maintenance (Homo sapiens)
Alternative Lengthening of Telomeres (ALT) (Homo sapiens)
Defective Inhibition of DNA Recombination at Telomere (Homo sapiens)
Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations (Homo sapiens)
Defective DAXX does not bind ATRX (Homo sapiens)
DAXX Truncation Mutants (N-terminus) [nucleoplasm] (Homo sapiens)
Participants
candidates
DAXX H26Tfs*118 [nucleoplasm]
(Homo sapiens)
DAXX A36Qfs*108 [nucleoplasm]
(Homo sapiens)
DAXX R48Vfs*93 [nucleoplasm]
(Homo sapiens)
DAXX K56* [nucleoplasm]
(Homo sapiens)
DAXX E72Nfs*72 [nucleoplasm]
(Homo sapiens)
DAXX C74* [nucleoplasm]
(Homo sapiens)
DAXX L98Vfs*13 [nucleoplasm]
(Homo sapiens)
DAXX A103Sfs*40 [nucleoplasm]
(Homo sapiens)
DAXX E104* [nucleoplasm]
(Homo sapiens)
DAXX C106* [nucleoplasm]
(Homo sapiens)
DAXX S138* [nucleoplasm]
(Homo sapiens)
Participates
as an input of
Defective DAXX does not bind ATRX (Homo sapiens)
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