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

Symbol:	Efnb1tm1.1Rha
Name:	ephrin B1; targeted mutation 1.1, Ralf H Adams
MGI ID:	MGI:3653700
Synonyms:	ephrinB1KO
Gene:	Efnb1  Location: ChrX:98179736-98192597 bp, + strand  Genetic Position: ChrX, 43.22 cM, cytoband D
Alliance:	Efnb1tm1.1Rha page

Germline Transmission:	Earliest citation of germline transmission: J:110732
Parent Cell Line:	E14.1 (ES Cell)
Strain of Origin:	129P2/OlaHsd

Allele Type:    Targeted (Null/knockout) Mutation:    Intragenic deletion     Exon 2 was removed via cre-mediated recombination. Western blot failed to detect protein in mutants. (J:110732)

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

In Structures Affected by this Mutation:

1 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 Efnb1 Mutation:	15 strains or lines available

Original:	J:110732 Compagni A, et al., Control of skeletal patterning by ephrinB1-EphB interactions. Dev Cell. 2003 Aug;5(2):217-30
All:	3 reference(s)