GeneProduct annotation
Name: | NPHS1 |
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Identifier: | ENSG00000161270 |
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Database: | Ensembl |
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Description: | nephrosis 1, congenital, Finnish type (nephrin) [Source:HGNC Symbol;Acc:7908] |
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Chromosome: | 19 |
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Expression data
Identifier | NPHS1 |
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ENSEMBL.ID | ENST00000378910 |
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biotype | protein_coding |
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coordinates | chr19:36316866-36342739:-1 |
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tlength | 4247.0 |
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Blastocyst.CTR3.12ctr3.1 | 2.369483977 |
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Blastocyst.CTR3.12ctr3.2 | 2.565337101 |
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Blastocyst.CTR5.12ctr5.1 | 2.139034832 |
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Blastocyst.CTR5.12ctr5.2 | 1.746801625 |
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Blastocyst.F1.6ctr1 | 3.69579487 |
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Blastocyst.F2.6ctr2 | 3.170996126 |
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Blastocyst.F3.6ctr3 | 2.536210351 |
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Blastocyst.F4.6ctr4 | 5.346593734 |
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Blastocyst.F5.6ctr5 | 6.598860787 |
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Blastocyst.F6.6ctr6 | 4.571460124 |
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Naive.ESC.1 | 0.282307033 |
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Naive.ESC.2 | -0.761562018 |
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EpiLC.D2.1 | 0.239488149 |
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EpiLC.D2.2 | -0.013713323 |
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PGCLC.D4.1 | 0.348024209 |
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PGCLC.D4.2 | 0.64355355 |
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PGCLC_Average | 0.4957888795 |
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TCam2.1 | -0.610207485 |
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TCam2.2 | -0.451765619 |
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hPGC_wk4 | 1.143406398 |
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hPGC.E39_M | 0.718297549 |
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hPGC.E45_M | 0.202849164 |
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hPGC.E48_M | 0.594650266 |
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hPGC.E47_F | 0.201874331 |
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hPGC.E48_F | 0.497245523 |
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hPGC.E51_F | 0.5410938 |
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hPGC.E60_M.1 | 0.631648487 |
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hPGC.E60_M.2 | 1.26372227 |
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hPGC.E60_F | 1.213560777 |
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hPGC.E63_F | 0.997509142 |
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hSoma_wk4 | 0.205871005 |
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hSoma.E46_M | 0.487690316 |
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hSoma.E48_M | 2.223004723 |
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hSoma.E47_F | 2.248133167 |
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hSoma.E48_F | 1.635880881 |
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hSoma.E51_F | 2.927227881 |
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hPGC_wk4__Blastocyst.F.log2FoldChange | -3.83510201 |
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hPGC_wk4__Blastocyst.F.pval | 1.0 |
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PGCLC__Blastocyst.F.log2FoldChange | -4.475165497 |
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PGCLC__Blastocyst.F.pval | 0.753636816 |
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Blastocyst.F__Blastocyst.CTR3.log2FoldChange | 2.507776912 |
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Blastocyst.F__Blastocyst.CTR3.pval | 0.961791536 |
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hPGC_wk4__PGCLC.log2FoldChange | 0.640063486 |
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hPGC_wk4__PGCLC.pval | 0.705088589 |
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Cross references