Hnrnpf^tm1Jsdc
Targeted Allele Detail

Summary

• Symbol: Hnrnpf^tm1Jsdc
• Name: heterogeneous nuclear ribonucleoprotein F; targeted mutation 1, John SD Chan
• MGI ID: MGI:6391198
• Synonyms: Hnrnpf^fl
• Gene: Hnrnpf Location: Chr6:117877301-117902583 bp, + strand Genetic Position: Chr6, 55.66 cM
• Alliance: Hnrnpf^tm1Jsdc page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:284239
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: C57BL/6

Mutation description

• Allele Type: Targeted (Conditional ready)
• Mutation: Insertion
• Exon 4, containing both the ATG start codon and TAG stop codon, was flanked by loxP sites. (J:284239)

Disease models

Expression

In Structures Affected by this Mutation:

6 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 Hnrnpf Mutation: 104 strains or lines available

References

• Original: J:284239 Lo CS, et al., Tubular Deficiency of Heterogeneous Nuclear Ribonucleoprotein F Elevates Systolic Blood Pressure and Induces Glycosuria in Mice. Sci Rep. 2019 Oct 31;9(1):15765
• All: 1 reference(s)