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

Symbol:	Aplnrtm1Dgen
Name:	apelin receptor; targeted mutation 1, Deltagen
MGI ID:	MGI:5433631
Gene:	Aplnr  Location: Chr2:84966704-84970267 bp, + strand  Genetic Position: Chr2, 49.45 cM, cytoband E1
Alliance:	Aplnrtm1Dgen page

Germline Transmission:	Earliest citation of germline transmission: J:186909
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified
Project Collection:	Deltagen

Allele Type:    Targeted (Null/knockout) Mutation:    Not Specified   Mutation details: In situ hybridization histochemistry confirmed the absence of protein expression in peripheral tissues from homozygous mice. (J:186909)

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 Aplnr Mutation:	28 strains or lines available

Original:	J:186909 Roberts EM, et al., Abnormal fluid homeostasis in apelin receptor knockout mice. J Endocrinol. 2009 Sep;202(3):453-62
All:	4 reference(s)