Lama1^tm1.1Olf
Targeted Allele Detail

Nomenclature

• Symbol: Lama1^tm1.1Olf
• Name: laminin, alpha 1; targeted mutation 1.1, Olivier Lefebvre
• MGI ID: MGI:3611213
• Synonyms: Lama1^delta
• Gene: Lama1 Location: Chr17:67697265-67822645 bp, + strand Genetic Position: Chr17, 38.8 cM

Lama1^nmf223/Lama1^tm1.1Olf mice experience vitreal fibroplasia and vessel tortuosity

Show the 1 phenotype image(s) involving this allele.

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:102740
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: 129S2/SvPas

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutation: Intragenic deletion
• Mutation details: The loxP-flanked region encompassing part of the promoter region, the transcription start site, and the first exon was excised in the germline. (J:102740)

Expression

In Structures Affected by this Mutation:

6 anatomical structures

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 Lama1 Mutation: 97 strains or lines available

References

• Original: J:102740 Alpy F, et al., Generation of a conditionally null allele of the laminin alpha1 gene. Genesis. 2005 Oct;43(2):59-70
• All: 4 reference(s)