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RB1 mutants (E2F binding) [nucleoplasm]
Stable Identifier
R-HSA-9659785
Type
Set [CandidateSet]
Species
Homo sapiens
Compartment
nucleoplasm
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of mitotic cell cycle (Homo sapiens)
Aberrant regulation of mitotic cell cycle due to RB1 defects (Homo sapiens)
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects (Homo sapiens)
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) (Homo sapiens)
Defective RB1 does not bind E2F1,(E2F2,E2F3) (Homo sapiens)
RB1 mutants (E2F binding) [nucleoplasm] (Homo sapiens)
Participants
members
RB1 N480del [nucleoplasm]
(Homo sapiens)
RB1 R661W [nucleoplasm]
(Homo sapiens)
RB1 C706F [nucleoplasm]
(Homo sapiens)
RB1 T738_R775del [nucleoplasm]
(Homo sapiens)
candidates
RB1 R661Q [nucleoplasm]
(Homo sapiens)
RB1 C706Y [nucleoplasm]
(Homo sapiens)
RB1 I703_E737del [nucleoplasm]
(Homo sapiens)
Participates
as an input of
Defective RB1 does not bind E2F1,(E2F2,E2F3) (Homo sapiens)
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