GeneProduct annotation
| Name: | WRN |
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| Identifier: | ENSG00000165392 |
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| Database: | Ensembl |
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| Description: | Werner syndrome, RecQ helicase-like [Source:HGNC Symbol;Acc:12791] |
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| Chromosome: | 8 |
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Expression data
| Identifier | WRN |
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| ENSEMBL.ID | ENST00000298139 |
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| biotype | protein_coding |
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| coordinates | chr8:30891317-31031285:1 |
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| tlength | 5180.0 |
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| Blastocyst.CTR3.12ctr3.1 | 3.581781845 |
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| Blastocyst.CTR3.12ctr3.2 | 3.578389394 |
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| Blastocyst.CTR5.12ctr5.1 | -0.147473158 |
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| Blastocyst.CTR5.12ctr5.2 | -0.124668865 |
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| Blastocyst.F1.6ctr1 | 0.087358786 |
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| Blastocyst.F2.6ctr2 | 5.662095716 |
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| Blastocyst.F3.6ctr3 | 6.354039022 |
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| Blastocyst.F4.6ctr4 | 0.015691626 |
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| Blastocyst.F5.6ctr5 | 0.697642953 |
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| Blastocyst.F6.6ctr6 | -0.358904055 |
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| Naive.ESC.1 | 6.036213313 |
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| Naive.ESC.2 | 5.443783089 |
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| EpiLC.D2.1 | 5.511947452 |
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| EpiLC.D2.2 | 5.81247882 |
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| PGCLC.D4.1 | 5.619511673 |
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| PGCLC.D4.2 | 5.241568343 |
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| PGCLC_Average | 5.430540008 |
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| TCam2.1 | 4.967470671 |
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| TCam2.2 | 5.20256432 |
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| hPGC_wk4 | 5.846456662 |
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| hPGC.E39_M | 5.979540981 |
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| hPGC.E45_M | 5.693322448 |
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| hPGC.E48_M | 6.184101012 |
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| hPGC.E47_F | 5.694100586 |
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| hPGC.E48_F | 5.989710654 |
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| hPGC.E51_F | 5.421167369 |
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| hPGC.E60_M.1 | 5.941330254 |
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| hPGC.E60_M.2 | 6.230825432 |
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| hPGC.E60_F | 5.954237617 |
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| hPGC.E63_F | 6.021613934 |
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| hSoma_wk4 | 5.908047702 |
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| hSoma.E46_M | 5.544172037 |
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| hSoma.E48_M | 5.912685773 |
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| hSoma.E47_F | 5.238192739 |
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| hSoma.E48_F | 5.287972347 |
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| hSoma.E51_F | 5.109168384 |
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| hPGC_wk4__Blastocyst.F.log2FoldChange | 1.334317368 |
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| hPGC_wk4__Blastocyst.F.pval | 0.641089284 |
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| PGCLC__Blastocyst.F.log2FoldChange | 0.930741728 |
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| PGCLC__Blastocyst.F.pval | 0.864932487 |
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| Blastocyst.F__Blastocyst.CTR3.log2FoldChange | 0.932052678 |
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| Blastocyst.F__Blastocyst.CTR3.pval | 0.921602111 |
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| hPGC_wk4__PGCLC.log2FoldChange | 0.403575639 |
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| hPGC_wk4__PGCLC.pval | 0.732493566 |
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Cross references