nob10
Spontaneous Allele Detail

Summary

• Symbol: nob10
• Name: no b wave 10
• MGI ID: MGI:6423083
• Gene: nob10 Location: unknown Genetic Position: Chr19, Syntenic
• Alliance: nob10 page

Mutation origin

• Strain of Origin: B6.129S2-Oprk1^tm1Kff/J

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Undefined
• this recessive heritable phenotype arose spontaneously
• 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 nob10 Mutation: 1 strain or line available

References

• Original: J:287579 Chang B, et al., A new mouse model, nob10 , with no b wave and late onset retinal degeneration. Invest Ophthalmol Vis Sci. 2018;59(9):2345
• All: 1 reference(s)