Lama1tm1.1Olf
Targeted Allele Detail
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Symbol: |
Lama1tm1.1Olf |
Name: |
laminin, alpha 1; targeted mutation 1.1, Olivier Lefebvre |
MGI ID: |
MGI:3611213 |
Synonyms: |
Lama1delta |
Gene: |
Lama1 Location: Chr17:67697265-67822645 bp, + strand Genetic Position: Chr17, 38.8 cM
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Lama1nmf223/Lama1tm1.1Olf mice experience vitreal fibroplasia and vessel tortuosity
Show the 1 phenotype image(s) involving this allele.
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Germline Transmission: |
Earliest citation of germline transmission:
J:102740
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
129S2/SvPas |
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Allele Type: |
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Targeted (Null/knockout) |
Mutation: |
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Intragenic deletion
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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)
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View phenotypes and curated references for all genotypes (concatenated display).
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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
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Carrying any Lama1 Mutation: |
97 strains or lines available
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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) |
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