Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | Notes | References

Symbol:	Rbp4tm1.1Mma
Name:	retinol binding protein 4, plasma; targeted mutation 1.1, Manuel Mark
MGI ID:	MGI:3625605
Synonyms:	Rbp4L-
Gene:	Rbp4  Location: Chr19:38105077-38113729 bp, - strand  Genetic Position: Chr19, 32.75 cM, cytoband D1
Alliance:	Rbp4tm1.1Mma page

Germline Transmission:	Earliest citation of germline transmission: J:108574
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: Crossing floxed mice with mice expressing cre recombinase in the germline resulted in the excision of exons 1-4. Western blot failed to detect protein in mutants. (J:108574)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

2 anatomical structure(s)

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 Rbp4 Mutation:	19 strains or lines available

Original:	J:108574 Ghyselinck NB, et al., Retinoids and spermatogenesis: Lessons from mutant mice lacking the plasma retinol binding protein. Dev Dyn. 2006 Jun;235(6):1608-1622
All:	2 reference(s)