B9d1tm1c(EUCOMM)Wtsi
Targeted Allele Detail
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Symbol: |
B9d1tm1c(EUCOMM)Wtsi |
Name: |
B9 protein domain 1; targeted mutation 1c, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:5301331 |
Synonyms: |
B9d1flox |
Gene: |
B9d1 Location: Chr11:61395970-61403757 bp, + strand Genetic Position: Chr11, 37.96 cM
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Alliance: |
B9d1tm1c(EUCOMM)Wtsi page
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IMPC: |
B9d1 gene page |
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Germline Transmission: |
Earliest citation of germline transmission:
J:178421
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
C57BL/6N
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Project Collection: |
EUCOMM
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Allele Type: |
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Targeted (Conditional ready) |
Mutation: |
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Insertion
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Flp-mediated recombination removed the reporter and selection cassettes and left exon 3 floxed. (J:178421)
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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 B9d1 Mutation: |
14 strains or lines available
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Original: |
J:178421 Dowdle WE, et al., Disruption of a ciliary B9 protein complex causes Meckel syndrome. Am J Hum Genet. 2011 Jul 15;89(1):94-110 |
All: |
2 reference(s) |
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