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rnv5
Spontaneous Allele Detail
Summary
Symbol: rnv5
Name: retinal neovascularization 5
MGI ID: MGI:7707431
Gene: rnv5  Location: unknown  
Alliance: rnv5 page
Significant retinal neovascularization in Crb1rd8/Crb1rd8 \AlleleSymbolMGI(7707431|0)/rnv5+ mice by 4 weeks of age

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  (C3A.BLiA-Pde6b+/J x C57BL/6NJ)F2
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
    This dominant modifier of Crb1 has not been mapped
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 rnv5 Mutation:  1 strain or line available
References
Original:  J:352529 Chang B, The retinal neovascularization 5 (rnv5) model. MGI Direct Data Submission. 2024;
All:  1 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
09/03/2024
MGI 6.24
The Jackson Laboratory