Rhbdf2^Uncv
Spontaneous Allele Detail

Summary

• Symbol: Rhbdf2^Uncv
• Name: rhomboid 5 homolog 2; uncovered
• MGI ID: MGI:2387311
• Synonyms: iRhom2^Uncv
• Gene: Rhbdf2 Location: Chr11:116488991-116517786 bp, - strand Genetic Position: Chr11, Syntenic
• Alliance: Rhbdf2^Uncv page

Mutation origin

• Strain of Origin: BALB/c

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• Mutation details: A spontaneous mouse mutation that arose at The Institute of Jinfeng Medical Laboratory Animal, Beijing, China. Sequence capture array and sequencing platform identified a non-frameshift 309 bp deletion mutation in the N-terminal cytoplasmic domain of Rhbdf2. (J:52604, J:228844)
• Inheritance: Semidominant

Expression

In Mice Carrying this Mutation:	1 RNA-Seq or microarray experiment(s)
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 Rhbdf2 Mutation: 84 strains or lines available

References

• Original: J:52604 Li SR, et al., Uncv (uncovered): a new mutation causing hairloss on mouse chromosome 11. Genet Res. 1999 Jun;73(3):233-8
• All: 4 reference(s)