| Name: palladin, cytoskeletal associated protein |
| Aliases: 2410003B16Rik, RIKEN cDNA 2410003B16 gene |
| Description: PHENOTYPE: All homozygous null embryos die around E15.5 displaying exencephaly derived from neural tube closure defects, and herniation of the intestine and liver due to ventral closure defects. Mutant MEFs show impaired formation of actin stress fibers, reduced migration and decreased adhesion to fibronectin. [provided by MGI curators] |
| Crossreferences: MGI:1919583, ENSEMBL:ENSMUSG00000058056, UniProtKB:Q9ET54, UniProtKB:Q9ET53, UniProtKB:K0BWC3, UniProtKB:D3Z1J5, NCBI_Gene:72333 |
| This information is supplied by the AllianceGenome.org API. |
| Compared To: | Log2fold: | SEM: | Adjusted p-value: |
|---|---|---|---|
| EV-GFPneg Tumor Microglia | 0.139 | 0.674 | 1 |
| EV-GFPpos Tumor Microglia | -0.75 | 0.67 | 0.49482447 |
| Compared To: | Log2fold: | SEM: | Adjusted p-value: |
|---|---|---|---|
| Control microglia | -0.139 | 0.674 | 1 |
| EV-GFPpos Tumor Microglia | -0.889 | 0.67 | 0.48310128 |
| Compared To: | Log2fold: | SEM: | Adjusted p-value: |
|---|---|---|---|
| Control Microglia | 0.75 | 0.67 | 0.49482447 |
| EV-GFPneg Tumor Microglia | 0.889 | 0.67 | 0.48310128 |