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Pou4f3ddl
Spontaneous Allele Detail
Summary
Symbol: Pou4f3ddl
Name: POU domain, class 4, transcription factor 3; dreidel
MGI ID: MGI:1857795
Synonyms: ddl
Gene: Pou4f3  Location: Chr18:42527662-42529158 bp, + strand  Genetic Position: Chr18, 22.58 cM, cytoband B3-E1
Alliance: Pou4f3ddl page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThe molecular mutation of this allele is a TG dinucleotide deletion (nt #841-842 from GenBank accession number S69352) resulting in premature stop codon upstream of the POU box and homeodomains of the encoded protein. (J:55448)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 21 assay results
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Pou4f3 Mutation:  25 strains or lines available
References
Original:  J:55448 Frankel WN, et al., The mutant mouse dreidel (ddl) contains a mutation in the Pou4f3 gene. Personal Communication. 1999;
All:  5 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