Fnip1^m2Btlr
Chemically induced Allele Detail

Summary

• Symbol: Fnip1^m2Btlr
• Name: folliculin interacting protein 1; mutation 2, Bruce Beutler
• MGI ID: MGI:6199692
• Synonyms: hamel2
• Gene: Fnip1 Location: Chr11:54329025-54409061 bp, + strand Genetic Position: Chr11, 32.13 cM
• Alliance: Fnip1^m2Btlr page

Mutation origin

• Strain of Origin: C57BL/6J
• Project Collection: Beutler Mutagenetix

Mutation description

• Allele Type: Chemically induced (ENU) (Not Specified)
• Mutation: Single point mutation
• Mutation details: ENU-induced G to T transversion at base pair 54,502,271 (v38) on chromosome 11, or base pair 64,127 in the GenBank genomic region NC_000077. The mutation corresponds to residue 1,650 in the mRNA sequence NM_173753 within exon 14 of 18 total exons. The mutation results in a glycine to valine substitution at position 511 (G511V) in the FNIP1 protein. (J:265134)
• Inheritance: Recessive

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 Fnip1 Mutation: 60 strains or lines available

References

• Original: J:265134 Zhong X, et al., Mutagenetix entry for hamel2. MGI Direct Data Submission. 2018
• All: 1 reference(s)