Trpm1^nob11
Spontaneous Allele Detail

Summary

• Symbol: Trpm1^nob11
• Name: transient receptor potential cation channel, subfamily M, member 1; no b wave 11
• MGI ID: MGI:7620516
• Gene: Trpm1 Location: Chr7:63803583-63919523 bp, + strand Genetic Position: Chr7, Syntenic
• Alliance: Trpm1^nob11 page

Mutation origin

• Strain of Origin: STOCK Hcn4^{tm2.1(cre/ERT2)Sev}/J

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Undefined
• Mutation details: This heritable phenotype was proven an allele of Trpm1 by failed complementation with the rd15 allele (J:347037)
• Inheritance: Recessive

Disease models

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: 0 strains available Cell Lines: 0 lines available
• Carrying any Trpm1 Mutation: 101 strains or lines available

References

• Original: J:347037 Chang B, The no b wave 11 mutation. MGI Direct Data Submission. 2024
• All: 1 reference(s)