Gene Expression Data
Assay Details
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Assay
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Reference:
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J:82084
Van de Putte T, et al., Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome. Am J Hum Genet. 2003 Feb;72(2):465-70
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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:7310105
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Gene symbol:
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Sox3
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Gene name:
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SRY (sex determining region Y)-box 3
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Results
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Specimen
4C:
embryonic day 8.5
(more  )
Specimen
4C:
(close  )
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Genetic Background:
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Not Specified
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Age:
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embryonic day 8.5
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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
4D:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129X1/SvJ * CD-1
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Mutant Allele(s):
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Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
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Age:
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embryonic day 8.5
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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 |
| TS13: neural ectoderm |
Present |
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4D
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Expression unaffected compared with wild type.
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Analysis Tools
