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Phf13Gt(XB691)Byg
Gene trapped Allele Detail
Summary
Symbol: Phf13Gt(XB691)Byg
Name: PHD finger protein 13; gene trap XB691, BayGenomics
MGI ID: MGI:3836461
Gene: Phf13  Location: Chr4:152074088-152080636 bp, - strand  Genetic Position: Chr4, 82.81 cM
Alliance: Phf13Gt(XB691)Byg page
Mutation
origin
Mutant Cell Line:  XB691
Germline Transmission:  Earliest citation of germline transmission: J:185876
Parent Cell Line:  Other (see notes) (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Gene trapped (Null/knockout, Reporter)
Mutation:    Insertion of gene trap vector     Vector: pGT0pfs     Vector Type: gene trap
    The integration site of the gene trap is located in intron 1. (J:185876)
Sequence Tags: 
Sequence tag details (1 tag)
Genome Context: 
Genome Browser view of this mutation
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 4 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 Phf13 Mutation:  17 strains or lines available
Notes
All BayGenomics gene trap mutations were generated in either CGR8 or E14TG2a (129P2/OlaHsd) parental ES cell lines, with the majority in subline E14TG2a.4. The specific ES cell line in which each mutation was made is not specified.
References
Original:  J:185876 Bordlein A, et al., SPOC1 (PHF13) is required for spermatogonial stem cell differentiation and sustained spermatogenesis. J Cell Sci. 2011 Sep 15;124(Pt 18):3137-48
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
04/16/2024
MGI 6.23
The Jackson Laboratory