Gene Expression Data
Assay Details
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Assay
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Reference:
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J:166923
Wang B, et al., Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B. Hum Mol Genet. 2011 Jan 15;20(2):271-85
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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:5755277
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Gene symbol:
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Fgf8
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Gene name:
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fibroblast growth factor 8
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Results
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Specimen
5J/K:
embryonic day 13.5
(more  )
Specimen
5J/K:
(close  )
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Genetic Background:
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Not Specified
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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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whole mount
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Fixation:
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4% Paraformaldehyde
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| Structure |
Level |
Pattern |
Image |
Note |
| TS21: forelimb digit |
Present |
Regionally restricted |
5J left
,
5K
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Expressed in the distal region of each digit primordial.
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Specimen
5J/L:
(close )
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Genetic Background:
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involves: A
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Mutant Allele(s):
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Vangl2Lp/Vangl2Lp
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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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whole mount
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Fixation:
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4% Paraformaldehyde
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Specimen
S2 left:
embryonic day 13.5
(more )
Specimen
S2 left:
(close )
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Genetic Background:
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Not Specified
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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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whole mount
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Fixation:
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4% Paraformaldehyde
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| Structure |
Level |
Pattern |
Image |
Note |
| TS21: forelimb digit |
Present |
Regionally restricted |
S2_left
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Expressed in the distal region of each digit primordial.
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Specimen
S2 right:
(close )
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Genetic Background:
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involves: 129S7/SvEvBrd
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Mutant Allele(s):
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Wnt5atm1Amc/Wnt5atm1Amc
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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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whole mount
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Fixation:
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4% Paraformaldehyde
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Analysis Tools
