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Fancd2Gt(OST57859)Lex
Gene trapped Allele Detail
Nomenclature
Symbol: Fancd2Gt(OST57859)Lex
Name: Fanconi anemia, complementation group D2; gene trap OST57859, Lexicon Genetics
MGI ID: MGI:3530554
Synonyms: Fancd2-, Fancd2Gt(IRESBetageo)479Lex
Gene: Fancd2  Location: Chr6:113531682-113597017 bp, + strand  Genetic Position: Chr6, 52.78 cM, cytoband E3
Mutation
origin
Mutant Cell Line:  OST57859 (Lexicon Genetics)
Germline Transmission:  Earliest citation of germline transmission: J:146616
Parent Cell Line:  Lex-1 (ES Cell)
Strain of Origin:  129S5/SvEvBrd
Project Collection: Lexicon
Mutation
description
Allele Type:    Gene trapped
Mutation:    Insertion of gene trap vector
    A genetrap insertion resulted in a null allele. (J:94338)
Sequence Tags: 
Sequence tag details (1 tag)
Genome Context: 
Genome Browser view of this mutation
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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 Fancd2 Mutation:  15 strains or lines available
References
Original:  J:146616 Kim JM, et al., Inactivation of murine Usp1 results in genomic instability and a Fanconi anemia phenotype. Dev Cell. 2009 Feb;16(2):314-20
All:  5 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/18/2014
MGI 5.20
The Jackson Laboratory