Fhod1^{Gt(IST13553G8)Tigm}
Gene trapped Allele Detail

Summary

• Symbol: Fhod1^{Gt(IST13553G8)Tigm}
• Name: formin homology 2 domain containing 1; gene trap Fhod1Gt(IST13553G8)Tigm, Texas Institute for Genomic Medicine
• MGI ID: MGI:7281451
• Gene: Fhod1 Location: Chr8:106055795-106074585 bp, - strand Genetic Position: Chr8, 53.04 cM
• Alliance: Fhod1^{Gt(IST13553G8)Tigm} page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:324742
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: C57BL/6

Mutation description

• Allele Type: Gene trapped (Null/knockout)
• Mutation: Insertion of gene trap vector

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: 1 line available
• Carrying any Fhod1 Mutation: 55 strains or lines available

References

• Original: J:324742 Zuidscherwoude M, et al., Loss of mDia1 and Fhod1 impacts platelet formation but not platelet function. Platelets. 2021 Nov 17;32(8):1051-1062
• All: 1 reference(s)