Trpm1^rd15
Spontaneous Allele Detail

Summary

• Symbol: Trpm1^rd15
• Name: transient receptor potential cation channel, subfamily M, member 1; retinal degeneration 15
• MGI ID: MGI:4867502
• Gene: Trpm1 Location: Chr7:63803583-63919523 bp, + strand Genetic Position: Chr7, Syntenic
• Alliance: Trpm1^rd15 page

Mutation origin

• Strain of Origin: Not Specified

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Nucleotide substitutions
• This spontaneous C to A transversion in exon 17 causes an A725D substitution (J:346902)

Disease models

Expression

In Structures Affected by this Mutation:

2 anatomical structure(s)

Find Mice (IMSR)

• 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 Trpm1 Mutation: 101 strains or lines available

References

• Original: J:167193 Hawes NL, et al., A New Mouse Model of Retinal Degeneration (rd15) With Retinal Outer Plexiform Dystrophy. Invest Ophthalmol Vis Sci. 2005;46(13):3175
• All: 4 reference(s)