Gene Expression Data
Assay Details
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Assay
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Reference:
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J:189955
Star EN, et al., Regulation of retinal interneuron subtype identity by the Iroquois homeobox gene Irx6. Development. 2012 Dec;139(24):4644-55
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Assay type:
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In situ reporter (knock in)
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MGI Accession ID:
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MGI:6450114
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Gene symbol:
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Irx6
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Gene name:
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Iroquois homeobox 6
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Reporter:
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lacZ
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Direct Detection
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Results
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Specimen
2B:
embryonic day 12.5; Irx6tm1Chow/Irx6 +
(more  )
Specimen
2B:
(close  )
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Genetic Background:
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involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
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Mutant Allele(s):
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Irx6tm1Chow/Irx6+
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Age:
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embryonic day 12.5
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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
2C:
embryonic day 12.5; Irx6tm1Chow/Irx6 +
(more )
Specimen
2C:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
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Mutant Allele(s):
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Irx6tm1Chow/Irx6+
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Age:
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embryonic day 12.5
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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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Specimen
2D:
embryonic day 13.5; Irx6tm1Chow/Irx6 +
(more )
Specimen
2D:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
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Mutant Allele(s):
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Irx6tm1Chow/Irx6+
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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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| Structure |
Level |
Pattern |
Image |
Note |
| TS21: neural retina |
Weak |
Regionally restricted |
2D
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Faint X-gal staining was detected in the central ganglion cell region of the retina.
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Specimen
2E:
embryonic day 16.5; Irx6tm1Chow/Irx6 +
(more )
Specimen
2E:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
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Mutant Allele(s):
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Irx6tm1Chow/Irx6+
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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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Specimen
2G:
postnatal day 0; Irx6tm1Chow/Irx6 +
(more )
Specimen
2G:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
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Mutant Allele(s):
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Irx6tm1Chow/Irx6+
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Age:
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postnatal day 0
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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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Specimen
2H:
postnatal day 7; Irx6tm1Chow/Irx6 +
(more )
Specimen
2H:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
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Mutant Allele(s):
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Irx6tm1Chow/Irx6+
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Age:
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postnatal day 7
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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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Specimen
S1D:
postnatal day 0; Irx6tm1Chow/Irx6 +
(more )
Specimen
S1D:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
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Mutant Allele(s):
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Irx6tm1Chow/Irx6+
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Age:
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postnatal day 0
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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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| Structure |
Level |
Pattern |
Image |
Note |
| TS27: retina |
Present |
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S1D Xgal
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Onset and localization of reporter expression was consistent with the expression of Irx6 mRNA in the retina.
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Analysis Tools