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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:5812433
Gene symbol: Cux1
Gene name: cut-like homeobox 1
Antibody: anti-Cux1 (CDP, M-222) (sc-13024)
Detection system: Secondary antibody coupled to Alexa Fluor 594
Results
Specimen S6A: postnatal day 0 (more )
Note: Double labeled: red - Cux1; green - Bcl11b (assay MGI:5812434).
Structure Level Pattern Image Note
TS27: cortical layer II Present S6A
TS27: cortical layer III Present S6A
TS27: cortical layer IV Present S6A
Specimen S6B: postnatal day 0; Diaph1tm1Asal/Diaph1tm1Asal (more )
Note: Double labeled: red - Cux1; green - Bcl11b (assay MGI:5812434).
Structure Level Pattern Image Note
TS27: cortical layer II Present S6B Expression was detected as in wild type.
TS27: cortical layer III Present S6B Expression was detected as in wild type.
TS27: cortical layer IV Present S6B Expression was detected as in wild type.
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