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Mycbp2mgln
Chemically induced Allele Detail
Summary
Symbol: Mycbp2mgln
Name: MYC binding protein 2, E3 ubiquitin protein ligase; Magellan
MGI ID: MGI:3777464
Synonyms: Phr1Mag
Gene: Mycbp2  Location: Chr14:103350847-103584250 bp, - strand  Genetic Position: Chr14, 51.79 cM
Alliance: Mycbp2mgln page
Mutation
origin
Strain of Origin:  (BALB/c x C57BL/6)F1 X DBA/2J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced an G to T transition in exon 63 that resulted in a premature termination codon. The presence of a truncated protein lacking the C-terminal RING finger domain was confirmed by western blot analysis. (J:132726)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Mycbp2 Mutation:  224 strains or lines available
Notes
ENU exposed DBA/2J males were mated with (BALB/c x C57BL/6)F1 females carrying the Tg(Isl1-EGFP*)1Slp reporter.
References
Original:  J:132726 Lewcock JW, et al., The ubiquitin ligase Phr1 regulates axon outgrowth through modulation of microtubule dynamics. Neuron. 2007 Nov 21;56(4):604-20
All:  3 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
10/29/2024
MGI 6.24
The Jackson Laboratory