GeneProduct annotation
| Name: | MECP2 |
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| Identifier: | ENSG00000169057 |
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| Database: | Ensembl |
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| Description: | methyl CpG binding protein 2 (Rett syndrome) [Source:HGNC Symbol;Acc:6990] |
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| Chromosome: | X |
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Expression data
| Identifier | MECP2 |
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| ENSEMBL.ID | ENST00000303391 |
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| biotype | protein_coding |
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| coordinates | chrX:153287024-153363212:-1 |
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| tlength | 10501.0 |
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| Blastocyst.CTR3.12ctr3.1 | 1.347266236 |
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| Blastocyst.CTR3.12ctr3.2 | 1.018318295 |
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| Blastocyst.CTR5.12ctr5.1 | -1.166975875 |
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| Blastocyst.CTR5.12ctr5.2 | -1.144171582 |
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| Blastocyst.F1.6ctr1 | 3.460173491 |
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| Blastocyst.F2.6ctr2 | -0.942369503 |
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| Blastocyst.F3.6ctr3 | -1.091728451 |
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| Blastocyst.F4.6ctr4 | 6.166113909 |
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| Blastocyst.F5.6ctr5 | -0.321859765 |
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| Blastocyst.F6.6ctr6 | -1.378406773 |
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| Naive.ESC.1 | 3.459379213 |
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| Naive.ESC.2 | 3.199213816 |
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| EpiLC.D2.1 | 3.364527259 |
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| EpiLC.D2.2 | 3.965678188 |
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| PGCLC.D4.1 | 4.148212906 |
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| PGCLC.D4.2 | 4.665009121 |
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| PGCLC_Average | 4.4066110135 |
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| TCam2.1 | 4.261201346 |
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| TCam2.2 | 4.440493302 |
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| hPGC_wk4 | 5.186804522 |
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| hPGC.E39_M | 3.582211843 |
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| hPGC.E45_M | 4.224765293 |
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| hPGC.E48_M | 3.711850989 |
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| hPGC.E47_F | 4.315402516 |
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| hPGC.E48_F | 3.813952238 |
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| hPGC.E51_F | 4.726936189 |
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| hPGC.E60_M.1 | 4.86285618 |
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| hPGC.E60_M.2 | 4.980079375 |
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| hPGC.E60_F | 4.970827902 |
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| hPGC.E63_F | 4.920317125 |
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| hSoma_wk4 | 3.916668585 |
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| hSoma.E46_M | 4.449567864 |
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| hSoma.E48_M | 4.221644119 |
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| hSoma.E47_F | 4.149717879 |
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| hSoma.E48_F | 4.318554861 |
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| hSoma.E51_F | 4.172627115 |
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| hPGC_wk4__Blastocyst.F.log2FoldChange | 1.36254637 |
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| hPGC_wk4__Blastocyst.F.pval | 0.616343791 |
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| PGCLC__Blastocyst.F.log2FoldChange | 0.605370759 |
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| PGCLC__Blastocyst.F.pval | 0.909150089 |
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| Blastocyst.F__Blastocyst.CTR3.log2FoldChange | 2.632110725 |
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| Blastocyst.F__Blastocyst.CTR3.pval | 0.61908732 |
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| hPGC_wk4__PGCLC.log2FoldChange | 0.75717561 |
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| hPGC_wk4__PGCLC.pval | 0.6717131 |
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Cross references