Gene Expression Data
Assay Details
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Assay
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Reference:
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J:71694
Bruneau S, et al., The mouse hoxd13(spdh) mutation, a polyalanine expansion similar to human type ii synpolydactyly (spd), disrupts the function but not the expression of other hoxd genes. Dev Biol. 2001 Sep 15;237(2):345-53
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Assay type:
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RNA in situ
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MGI Accession ID:
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MGI:2153102
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Gene symbol:
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Hoxd11
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Gene name:
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homeobox D11
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Results
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Specimen
3I, +/+:
embryonic day 11.5
(more  )
Specimen
3I, +/+:
(close  )
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Genetic Background:
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Not Specified
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Age:
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embryonic day 11.5
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Age Note:
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Age of embryo at noon of plug day not specified in reference.
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Sex:
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Not Specified
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Type:
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whole mount
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Specimen
3I, -/-:
(close )
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Genetic Background:
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B6C3Fe a/a-Hoxd13spdh/J
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Mutant Allele(s):
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Hoxd13spdh/Hoxd13spdh
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Age:
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embryonic day 11.5
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Age Note:
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Age of embryo at noon of plug day not specified in reference.
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Sex:
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Not Specified
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Type:
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whole mount
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| Structure |
Level |
Pattern |
Image |
Note |
| TS19: limb |
Present |
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3I Hoxd11 right
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Expression in this mutant is the same as in wild-type embryos.
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Analysis Tools
