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Gene Expression Data
Assay Details
Assay
Reference: 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
Assay type: Immunohistochemistry
MGI Accession ID: MGI:5812445
Gene symbol: Cdh1
Gene name: cadherin 1
Antibody: Anti-E-cadherin (610405; clone 34)
Detection system: Secondary antibody coupled to Alexa Fluor 594
Results
Specimen S8B Diap1+/+: embryonic day 14.5 (more )
Note: Double labeled: red - Cdh1; green - Cdh2 (assay MGI:5812441).
Structure Level Pattern Image Note
TS22: brain Present Regionally restricted S8B Cdh1 Diap1+/+ , S8B Merge Diap1+/+ Expression was detected in lateral vertical wall.
Specimen S8B Diap1-/-: embryonic day 14.5; Diaph1tm1Asal/Diaph1tm1Asal (more )
Note: Double labeled: red - Cdh1; green - Cdh2 (assay MGI:5812441).
Structure Level Pattern Image Note
TS22: brain Present Regionally restricted S8B Cdh1 Diap1-/- , S8B Merge Diap1-/- Expression was detected in lateral vertical wall.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/30/2025
MGI 6.24 		The Jackson Laboratory