Gene Expression Data
Assay Details
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Assay
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Reference:
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J:228552
Ercan-Sencicek AG, et al., Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. Eur J Hum Genet. 2015 Feb;23(2):165-72
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:5812437
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Gene symbol:
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Ctnnb1
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Gene name:
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catenin beta 1
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Results
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Specimen
S8A Diap1+/+:
embryonic day 14.5
(more  )
Specimen
S8A Diap1<+/+>:
(close  )
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Genetic Background:
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Not Specified
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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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| Structure |
Level |
Pattern |
Image |
Note |
| TS22: brain |
Present |
Regionally restricted |
S8A Ctnnb1 Diap1+/+
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Expression was detected in lateral vertical wall.
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Specimen
S8A Diap1<-/->:
(close )
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Genetic Background:
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involves: 129S1/Sv * C57BL/6
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Mutant Allele(s):
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Diaph1tm1Asal/Diaph1tm1Asal
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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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| Structure |
Level |
Pattern |
Image |
Note |
| TS22: brain |
Present |
Regionally restricted |
S8A Ctnnb1 Diap1-/-
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Expression was detected in lateral vertical wall.
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Analysis Tools
