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Gene Expression Data
Assay Details
Assay
Reference: J:344968 Leslie JS, et al., Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities. Genet Med. 2022 Nov;24(11):2249-2261
Assay type: RNA in situ
MGI Accession ID: MGI:7611838
Gene symbol: Daw1
Gene name: dynein assembly factor with WDR repeat domains 1
Probe: Daw1 probe
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Results
Specimen S5 A: embryonic day 7.5 (more )
Note: Early headfold stage embryo.
Structure Level Pattern Image Note
TS11: node Present S5A
Specimen S5B: embryonic day 8.0 (more )
Note: 2-somite stage embryo.
Structure Level Pattern Image Note
TS12: node Strong S5B
Specimen S5C: embryonic day 8.0 (more )
Note: 6-somite stage embryo.
Structure Level Pattern Image Note
TS12: node Weak S5C
Specimen S5 D: embryonic day 7.5 (more )
Note: Early headfold stage embryo.
Structure Level Pattern Image Note
TS11: node Present S5D
Specimen S5 E: embryonic day 8.0 (more )
Note: 3-somite stage embryo.
Structure Level Pattern Image Note
TS12: node Present Regionally restricted S5E Expression is in the ventral node.
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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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory