Gene Expression Data
Assay Details
Assay
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Reference:
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J:144432
Hajihosseini MK, et al., Evidence that Fgf10 contributes to the skeletal and visceral defects of an apert syndrome mouse model. Dev Dyn. 2009 Feb;238(2):376-85
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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:6402556
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Gene symbol:
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Foxa2
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Gene name:
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forkhead box A2
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Probe:
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Foxa2 probe25
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Probe preparation:
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Antisense labelled with digoxigenin RNA
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Visualized with:
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Alkaline phosphatase
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Results
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Specimen
4J left:
embryonic day 11.5
(more )
Specimen
4J left:
(close )
Genetic Background:
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involves: 129 * 129X1/SvJ * C57BL/6J
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Age:
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embryonic day 11.5
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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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Specimen
4J middle:
embryonic day 11.5; Fgfr2tm2.3Dsn/Fgfr2 +
(more )
Specimen
4J middle:
(close )
Genetic Background:
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involves: 129 * 129X1/SvJ * C57BL/6J
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Mutant Allele(s):
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Fgfr2tm2.3Dsn/Fgfr2+
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Age:
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embryonic day 11.5
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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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Specimen
4J right:
(close )
Genetic Background:
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involves: 129 * 129X1/SvJ * C57BL/6J
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Mutant Allele(s):
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Fgf10tm1Wss/Fgf10+ Fgfr2tm2.3Dsn/Fgfr2+
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Age:
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embryonic day 11.5
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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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