Unknown annotation
| Name: | MKS1 |
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| Identifier: | ENSG00000011143 |
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| Database: | Ensembl |
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| Description: | Meckel syndrome, type 1 [Source:HGNC Symbol;Acc:7121] |
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| Chromosome: | 17 |
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Expression data
| Identifier | MKS1 |
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| ENSEMBL.ID | ENST00000393119 |
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| biotype | protein_coding |
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| coordinates | chr17:56282803-56296666:-1 |
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| tlength | 2374.0 |
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| Blastocyst.CTR3.12ctr3.1 | 4.988826943 |
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| Blastocyst.CTR3.12ctr3.2 | 5.418267075 |
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| Blastocyst.CTR5.12ctr5.1 | 0.978159005 |
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| Blastocyst.CTR5.12ctr5.2 | 1.000963298 |
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| Blastocyst.F1.6ctr1 | 7.79795345 |
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| Blastocyst.F2.6ctr2 | 1.202765378 |
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| Blastocyst.F3.6ctr3 | 1.05340643 |
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| Blastocyst.F4.6ctr4 | 1.141323789 |
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| Blastocyst.F5.6ctr5 | 1.823275116 |
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| Blastocyst.F6.6ctr6 | 0.766728108 |
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| Naive.ESC.1 | 4.246962089 |
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| Naive.ESC.2 | 4.031758466 |
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| EpiLC.D2.1 | 4.129238395 |
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| EpiLC.D2.2 | 3.82541085 |
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| PGCLC.D4.1 | 4.745143836 |
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| PGCLC.D4.2 | 4.804605819 |
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| PGCLC_Average | 4.7748748275 |
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| TCam2.1 | 4.783505541 |
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| TCam2.2 | 4.510740971 |
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| hPGC_wk4 | 5.882003696 |
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| hPGC.E39_M | 4.245477716 |
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| hPGC.E45_M | 4.996169648 |
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| hPGC.E48_M | 5.417286317 |
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| hPGC.E47_F | 5.412557368 |
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| hPGC.E48_F | 4.180718826 |
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| hPGC.E51_F | 5.196134909 |
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| hPGC.E60_M.1 | 3.718700174 |
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| hPGC.E60_M.2 | 5.502017537 |
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| hPGC.E60_F | 5.060504455 |
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| hPGC.E63_F | 4.312366746 |
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| hSoma_wk4 | 4.999191489 |
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| hSoma.E46_M | 4.193547959 |
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| hSoma.E48_M | 4.062128897 |
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| hSoma.E47_F | 4.694939918 |
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| hSoma.E48_F | 4.576543081 |
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| hSoma.E51_F | 3.97446025 |
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| hPGC_wk4__Blastocyst.F.log2FoldChange | 0.59433236 |
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| hPGC_wk4__Blastocyst.F.pval | 0.61786027 |
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| PGCLC__Blastocyst.F.log2FoldChange | -0.512490183 |
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| PGCLC__Blastocyst.F.pval | 0.991313732 |
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| Blastocyst.F__Blastocyst.CTR3.log2FoldChange | 0.068204298 |
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| Blastocyst.F__Blastocyst.CTR3.pval | 1.0 |
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| hPGC_wk4__PGCLC.log2FoldChange | 1.106822543 |
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| hPGC_wk4__PGCLC.pval | 0.607576248 |
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Cross references