rnv9
Spontaneous Allele Detail

Summary

• Symbol: rnv9
• Name: retinal neovascularization 9
• MGI ID: MGI:7735175
• Gene: rnv9 Location: unknown
• Alliance: rnv9 page

rnv9/rnv9 mice exhibit a strong retinal neovascularization phenotype by 4 weeks of age.

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

Mutation origin

• Strain of Origin: CWXS/Agl-Gja8^R205G/Boc

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Undefined
• This recessive heritable phenotypic marker has not been mapped. (J:354548)
• Inheritance: Recessive

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

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 rnv9 Mutation: 1 strain or line available

References

• Original: J:354548 Chang B, The retinal vascularization 9 (rnv9) model. MGI Direct Data Submission. 2024
• All: 1 reference(s)