Gene Expression Data
Assay Details
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Assay
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Reference:
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J:75699
Albrecht AN, et al., The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements. Mech Dev. 2002 Mar;112(1-2):53-67
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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:5446482
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Gene symbol:
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Hoxd13
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Gene name:
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homeobox D13
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Probe:
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Hoxd13 probe17
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Probe preparation:
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Antisense labelled with P33 RNA
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Visualized with:
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Autoradiography
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Results
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Specimen
3 Hoxd13 13.5 wt:
embryonic day 13.5
(more  )
Specimen
3 Hoxd13 13.5 wt:
(close  )
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Genetic Background:
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involves: C3H * C57BL/6
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Age:
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embryonic day 13.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
3 Hoxd13 13.5 spdh/spdh:
(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 13.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
3 Hoxd13 14.5 wt:
embryonic day 14.5
(more )
Specimen
3 Hoxd13 14.5 wt:
(close )
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Genetic Background:
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involves: C3H * C57BL/6
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Age:
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embryonic day 14.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
3 Hoxd13 14.5 spdh/spdh:
(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 14.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
3 Hoxd13 16.5 wt:
embryonic day 16.5
(more )
Specimen
3 Hoxd13 16.5 wt:
(close )
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Genetic Background:
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involves: C3H * C57BL/6
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Age:
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embryonic day 16.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
3 Hoxd13 16.5 spdh/spdh:
(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 16.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
3 Hoxd13 Newborn wt:
postnatal newborn
(more )
Specimen
3 Hoxd13 Newborn wt:
(close )
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Genetic Background:
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involves: C3H * C57BL/6
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Age:
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postnatal newborn
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
3 Hoxd13 Newborn spdh/spdh:
(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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postnatal newborn
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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| Structure |
Level |
Pattern |
Image |
Note |
| TS27: hand bone |
Present |
Regionally restricted |
3_Hoxd13 Newborn spdh/spdh
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Expression in perichondrium and cartilage; No expression in hypertrophic chondrocytes. Authors state that expression was stronger in mutant compared with wildtype.
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| TS27: hand connective tissue |
Present |
Regionally restricted |
3_Hoxd13 Newborn spdh/spdh
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Expression in perichondrium and cartilage; No expression in hypertrophic chondrocytes. Authors state that expression was stronger in mutant compared with wildtype.
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| TS27: perichondrium |
Present |
Regionally restricted |
3_Hoxd13 Newborn spdh/spdh
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Expression in perichondrium and cartilage; No expression in hypertrophic chondrocytes. Authors state that expression was stronger in mutant compared with wildtype.
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Analysis Tools