Atmin^m1H
Chemically induced Allele Detail

Summary

• Symbol: Atmin^m1H
• Name: ATM interactor; mutation 1, Harwell
• MGI ID: MGI:5620361
• Synonyms: Atmin^H210Q
• Gene: Atmin Location: Chr8:117670132-117687184 bp, + strand Genetic Position: Chr8, 63.37 cM
• Alliance: Atmin^m1H page

Mutation origin

• Strain of Origin: BALB/c

Mutation description

• Allele Type: Chemically induced (ENU) (Not Applicable)
• Mutation: Single point mutation
• Mutation details: ENU mutagenesis induced a point mutation that results in the amino acid substitution of glutamine for histidine at position 210 (H210Q) in the fourth zinc finger. This mutation is predicted to interfer with zinc chelation. (J:217609)
• Inheritance: Recessive

Expression

In Structures Affected by this Mutation:

7 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 Atmin Mutation: 38 strains or lines available

References

• Original: J:217609 Goggolidou P, et al., ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis. Development. 2014 Oct;141(20):3966-77
• All: 2 reference(s)