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Rb1tm3Fad
Targeted Allele Detail
Summary
Symbol: Rb1tm3Fad
Name: RB transcriptional corepressor 1; targeted mutation 3, Frederick A Dick
MGI ID: MGI:5638883
Synonyms: RbdeltaS, RbS
Gene: Rb1  Location: Chr14:73430298-73563446 bp, - strand  Genetic Position: Chr14, 38.73 cM, cytoband D3
Alliance: Rb1tm3Fad page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:217849
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsA codon change from TTT to GCT introduced the amino acid substitution of alanine for phenylalanine at position 832 (F832A) in exon 24. A loxP-flanked PGK-Neo cassette was inserted downstream of the mutation and was removed via Cre-mediated recombination. This mutation abolishes binding to E2F1. (J:217849, J:249124)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Rb1 Mutation:  106 strains or lines available
References
Original:  J:217849 Coschi CH, et al., Haploinsufficiency of an RB-E2F1-Condensin II complex leads to aberrant replication and aneuploidy. Cancer Discov. 2014 Jul;4(7):840-53
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory