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| Open reading frame (ORF) annotation in the exon skipping event |
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| Splicing Quantitative Trait Loci (sQTLs) in the skipped exons |
| Splicing Quantitative Trait Methylation (sQTM) in the skipped exon |
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Gene summary for NUP155 |
 Gene summary |
| Gene information | Gene symbol | NUP155 | Gene ID | 9631 |
| Gene name | nucleoporin 155 | |
| Synonyms | ATFB15|N155 | |
| Cytomap | 5p13.2 | |
| Type of gene | protein-coding | |
| Description | nuclear pore complex protein Nup155155 kDa nucleoporinnucleoporin 155kDnucleoporin 155kDa | |
| Modification date | 20180523 | |
| UniProtAcc | O75694 | |
| Context | PubMed: NUP155 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract] - Title (PMID) |
| Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Gene | GO ID | GO term | PubMed ID |
| NUP155 | GO:0006998 | nuclear envelope organization | 19070573 |
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Exon skipping events across known transcript of Ensembl for NUP155 from UCSC genome browser |
| Skipped exons in TCGA and GTEx based on Ensembl gene isoform structure. * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Gene isoform structures and expression levels for NUP155 |
| Expression levels of gene isoforms across TCGA. |
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| Expression levels of gene isoforms across GTEx. |
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Exon skipping events with PSIs in TCGA for NUP155 |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_441621 | 5 | 37292001:37292140:37292980:37293087:37294430:37294567 | 37292980:37293087 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2,ENST00000502533.1 |
| exon_skip_441624 | 5 | 37292980:37293087:37294430:37294567:37298969:37299080 | 37294430:37294567 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2,ENST00000502533.1 |
| exon_skip_441625 | 5 | 37298969:37299080:37299549:37299670:37301538:37301652 | 37299549:37299670 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2,ENST00000502533.1 |
| exon_skip_441626 | 5 | 37299549:37299670:37301538:37301652:37302880:37303010 | 37301538:37301652 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2,ENST00000502533.1 |
| exon_skip_441627 | 5 | 37305158:37305312:37307398:37307534:37309230:37309369 | 37307398:37307534 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2,ENST00000502533.1 |
| exon_skip_441628 | 5 | 37309230:37309369:37309505:37309674:37310653:37310770 | 37309505:37309674 | ENSG00000113569.11 | ENST00000502533.1 |
| exon_skip_441629 | 5 | 37309230:37309369:37310653:37310845:37314299:37314428 | 37310653:37310845 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2 |
| exon_skip_441631 | 5 | 37318089:37318187:37324093:37324209:37326002:37326069 | 37324093:37324209 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2 |
| exon_skip_441632 | 5 | 37326002:37326069:37327730:37327878:37328459:37328522 | 37327730:37327878 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2 |
| exon_skip_441634 | 5 | 37330139:37330234:37331786:37331897:37333564:37333735 | 37331786:37331897 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2 |
| exon_skip_441635 | 5 | 37331786:37331897:37333564:37333735:37337919:37338020 | 37333564:37333735 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2 |
| exon_skip_441636 | 5 | 37337919:37338020:37341191:37341344:37342650:37342748 | 37341191:37341344 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2 |
| exon_skip_441637 | 5 | 37341191:37341344:37342650:37342748:37348606:37348698 | 37342650:37342748 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2 |
| exon_skip_441638 | 5 | 37351291:37351458:37352838:37352931:37358182:37358253 | 37352838:37352931 | ENSG00000113569.11 | ENST00000231498.3,ENST00000513532.1,ENST00000381843.2 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for NUP155 |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_441621 | 5 | 37292001:37292140:37292980:37293087:37294430:37294567 | 37292980:37293087 | ENSG00000113569.11 | ENST00000231498.3,ENST00000502533.1,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441624 | 5 | 37292980:37293087:37294430:37294567:37298969:37299080 | 37294430:37294567 | ENSG00000113569.11 | ENST00000231498.3,ENST00000502533.1,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441625 | 5 | 37298969:37299080:37299549:37299670:37301538:37301652 | 37299549:37299670 | ENSG00000113569.11 | ENST00000231498.3,ENST00000502533.1,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441626 | 5 | 37299549:37299670:37301538:37301652:37302880:37303010 | 37301538:37301652 | ENSG00000113569.11 | ENST00000231498.3,ENST00000502533.1,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441627 | 5 | 37305158:37305312:37307398:37307534:37309230:37309369 | 37307398:37307534 | ENSG00000113569.11 | ENST00000231498.3,ENST00000502533.1,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441628 | 5 | 37309230:37309369:37309505:37309674:37310653:37310770 | 37309505:37309674 | ENSG00000113569.11 | ENST00000502533.1 |
| exon_skip_441629 | 5 | 37309230:37309369:37310653:37310845:37314299:37314428 | 37310653:37310845 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2 |
| exon_skip_441631 | 5 | 37318089:37318187:37324093:37324209:37326002:37326069 | 37324093:37324209 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441632 | 5 | 37326002:37326069:37327730:37327878:37328459:37328522 | 37327730:37327878 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441634 | 5 | 37330139:37330234:37331786:37331897:37333564:37333735 | 37331786:37331897 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441635 | 5 | 37331786:37331897:37333564:37333735:37337919:37338020 | 37333564:37333735 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441636 | 5 | 37337919:37338020:37341191:37341344:37342650:37342748 | 37341191:37341344 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441637 | 5 | 37341191:37341344:37342650:37342748:37348606:37348698 | 37342650:37342748 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2,ENST00000513532.1 |
| exon_skip_441638 | 5 | 37351291:37351458:37352838:37352931:37358182:37358253 | 37352838:37352931 | ENSG00000113569.11 | ENST00000231498.3,ENST00000381843.2,ENST00000513532.1 |
| PSI values of skipped exons in GTEx. |
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| * Skipped exon sequences. |
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Open reading frame (ORF) annotation in the exon skipping event for NUP155 |
| Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms. |
| ENST | Start of skipped exon | End of skipped exon | ORF |
| ENST00000231498 | 37292980 | 37293087 | Frame-shift |
| ENST00000231498 | 37294430 | 37294567 | Frame-shift |
| ENST00000231498 | 37299549 | 37299670 | Frame-shift |
| ENST00000231498 | 37307398 | 37307534 | Frame-shift |
| ENST00000231498 | 37324093 | 37324209 | Frame-shift |
| ENST00000231498 | 37327730 | 37327878 | Frame-shift |
| ENST00000231498 | 37342650 | 37342748 | Frame-shift |
| ENST00000231498 | 37301538 | 37301652 | In-frame |
| ENST00000231498 | 37310653 | 37310845 | In-frame |
| ENST00000231498 | 37331786 | 37331897 | In-frame |
| ENST00000231498 | 37333564 | 37333735 | In-frame |
| ENST00000231498 | 37341191 | 37341344 | In-frame |
| ENST00000231498 | 37352838 | 37352931 | In-frame |
| Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms. |
| ENST | Start of skipped exon | End of skipped exon | ORF |
| ENST00000231498 | 37292980 | 37293087 | Frame-shift |
| ENST00000231498 | 37294430 | 37294567 | Frame-shift |
| ENST00000231498 | 37299549 | 37299670 | Frame-shift |
| ENST00000231498 | 37307398 | 37307534 | Frame-shift |
| ENST00000231498 | 37324093 | 37324209 | Frame-shift |
| ENST00000231498 | 37327730 | 37327878 | Frame-shift |
| ENST00000231498 | 37342650 | 37342748 | Frame-shift |
| ENST00000231498 | 37301538 | 37301652 | In-frame |
| ENST00000231498 | 37310653 | 37310845 | In-frame |
| ENST00000231498 | 37331786 | 37331897 | In-frame |
| ENST00000231498 | 37333564 | 37333735 | In-frame |
| ENST00000231498 | 37341191 | 37341344 | In-frame |
| ENST00000231498 | 37352838 | 37352931 | In-frame |
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Infer the effects of exon skipping event on protein functional features for NUP155 |
| Exon skipping at the protein sequence level and followed lost functional features. * Click on the image to enlarge it in a new window. |
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| Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases. |
| ENST | Length of mRNA | Length of AA seq. | Genomic start | Genomic end | mRNA start | mRNA end | AA start | AA end |
| ENST00000231498 | 8160 | 1391 | 37352838 | 37352931 | 668 | 760 | 154 | 185 |
| ENST00000231498 | 8160 | 1391 | 37341191 | 37341344 | 1298 | 1450 | 364 | 415 |
| ENST00000231498 | 8160 | 1391 | 37333564 | 37333735 | 1552 | 1722 | 449 | 506 |
| ENST00000231498 | 8160 | 1391 | 37331786 | 37331897 | 1723 | 1833 | 506 | 543 |
| ENST00000231498 | 8160 | 1391 | 37310653 | 37310845 | 2641 | 2832 | 812 | 876 |
| ENST00000231498 | 8160 | 1391 | 37301538 | 37301652 | 3652 | 3765 | 1149 | 1187 |
| Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases. |
| ENST | Length of mRNA | Length of AA seq. | Genomic start | Genomic end | mRNA start | mRNA end | AA start | AA end |
| ENST00000231498 | 8160 | 1391 | 37352838 | 37352931 | 668 | 760 | 154 | 185 |
| ENST00000231498 | 8160 | 1391 | 37341191 | 37341344 | 1298 | 1450 | 364 | 415 |
| ENST00000231498 | 8160 | 1391 | 37333564 | 37333735 | 1552 | 1722 | 449 | 506 |
| ENST00000231498 | 8160 | 1391 | 37331786 | 37331897 | 1723 | 1833 | 506 | 543 |
| ENST00000231498 | 8160 | 1391 | 37310653 | 37310845 | 2641 | 2832 | 812 | 876 |
| ENST00000231498 | 8160 | 1391 | 37301538 | 37301652 | 3652 | 3765 | 1149 | 1187 |
| Lost protein functional features of individual exon skipping events in TCGA. |
| UniProt acc. | Start of exon skipping (AA) | End of exon skipping (AA) | Protein feature start (AA) | Protein feature end (AA) | Category of protein feature | Description of feature |
| O75694 | 154 | 185 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 364 | 415 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 364 | 415 | 391 | 391 | Natural variant | ID=VAR_071762;Note=In ATFB15%3B fails to accumulate at various foci of the nuclear envelope and is diffusely distributed in the cytoplasm%3B shows significantly reduced permeability of the nuclear envelope compared to wild-type. R->H;Ontology_term=ECO:000 |
| O75694 | 449 | 506 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 506 | 543 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 506 | 543 | 526 | 526 | Glycosylation | Note=O-linked (GlcNAc) serine;Ontology_term=ECO:0000250;evidence=ECO:0000250 |
| O75694 | 812 | 876 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 1149 | 1187 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| Lost protein functional features of individual exon skipping events in GTEx. |
| UniProt acc. | Start of exon skipping (AA) | End of exon skipping (AA) | Protein feature start (AA) | Protein feature end (AA) | Category of protein feature | Description of feature |
| O75694 | 154 | 185 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 364 | 415 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 364 | 415 | 391 | 391 | Natural variant | ID=VAR_071762;Note=In ATFB15%3B fails to accumulate at various foci of the nuclear envelope and is diffusely distributed in the cytoplasm%3B shows significantly reduced permeability of the nuclear envelope compared to wild-type. R->H;Ontology_term=ECO:000 |
| O75694 | 449 | 506 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 506 | 543 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 506 | 543 | 526 | 526 | Glycosylation | Note=O-linked (GlcNAc) serine;Ontology_term=ECO:0000250;evidence=ECO:0000250 |
| O75694 | 812 | 876 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
| O75694 | 1149 | 1187 | 2 | 1391 | Chain | ID=PRO_0000204844;Note=Nuclear pore complex protein Nup155 |
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SNVs in the skipped exons for NUP155 |
| - Lollipop plot for presenting exon skipping associated SNVs. * Click on the image to enlarge it in a new window. |
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| - Differential PSIs between mutated versus non-mutated samples. |
| - Non-synonymous mutations located in the skipped exons in TCGA. |
| Cancer type | Sample | ESID | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| BLCA | TCGA-XF-A9SG-01 | exon_skip_441621 | 37292981 | 37293087 | 37293010 | 37293010 | Frame_Shift_Del | C | - | p.E1336fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_441624 | 37294431 | 37294567 | 37294549 | 37294549 | Frame_Shift_Del | A | - | p.L1271fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_441627 | 37307399 | 37307534 | 37307482 | 37307482 | Frame_Shift_Del | T | - | p.K940fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_441629 | 37310654 | 37310845 | 37310789 | 37310789 | Frame_Shift_Del | T | - | p.K831fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_441631 | 37324094 | 37324209 | 37324203 | 37324203 | Frame_Shift_Del | T | - | p.S701fs |
| HNSC | TCGA-CV-7245-01 | exon_skip_441634 | 37331787 | 37331897 | 37331833 | 37331833 | Frame_Shift_Del | A | - | p.V528fs |
| COAD | TCGA-F4-6856-01 | exon_skip_441635 | 37333565 | 37333735 | 37333653 | 37333653 | Frame_Shift_Del | T | - | p.N418fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_441637 | 37342651 | 37342748 | 37342695 | 37342695 | Frame_Shift_Del | T | - | p.N350fs |
| LUSC | TCGA-66-2794-01 | exon_skip_441625 | 37299550 | 37299670 | 37299569 | 37299569 | Nonsense_Mutation | C | T | p.W1221* |
| COAD | TCGA-CA-6717-01 | exon_skip_441635 | 37333565 | 37333735 | 37333656 | 37333656 | Nonsense_Mutation | A | C | p.L476X |
| CESC | TCGA-EK-A3GK-01 | exon_skip_441636 | 37341192 | 37341344 | 37341221 | 37341221 | Nonsense_Mutation | G | C | p.S406* |
| STAD | TCGA-HU-A4H8-01 | exon_skip_441638 | 37352839 | 37352931 | 37352911 | 37352911 | Nonsense_Mutation | G | A | p.R162* |
| COAD | TCGA-CA-6717-01 | exon_skip_441624 | 37294431 | 37294567 | 37294429 | 37294429 | Splice_Site | A | G | . |
| - Depth of coverage in the three exons composing exon skipping event |
| Depth of coverage in three exons | Mutation description |
| - Non-synonymous mutations located in the skipped exons in CCLE. |
| Sample | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| HS819T_FIBROBLAST | 37301539 | 37301652 | 37301601 | 37301601 | Frame_Shift_Del | G | - | p.H1168fs |
| NCIH1417_LUNG | 37292981 | 37293087 | 37292987 | 37292987 | Missense_Mutation | C | T | p.C1344Y |
| CL34_LARGE_INTESTINE | 37292981 | 37293087 | 37293015 | 37293015 | Missense_Mutation | C | G | p.V1335L |
| ESS1_ENDOMETRIUM | 37292981 | 37293087 | 37293053 | 37293053 | Missense_Mutation | T | C | p.H1322R |
| HT1376_URINARY_TRACT | 37294431 | 37294567 | 37294435 | 37294435 | Missense_Mutation | G | A | p.S1309L |
| PC9_LUNG | 37294431 | 37294567 | 37294527 | 37294527 | Missense_Mutation | C | G | p.L1278F |
| HS766T_PANCREAS | 37294431 | 37294567 | 37294547 | 37294547 | Missense_Mutation | C | G | p.E1272Q |
| RERFLCFM_LUNG | 37299550 | 37299670 | 37299592 | 37299592 | Missense_Mutation | G | C | p.P1214A |
| JVM2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 37299550 | 37299670 | 37299642 | 37299642 | Missense_Mutation | T | A | p.K1197I |
| PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 37301539 | 37301652 | 37301558 | 37301558 | Missense_Mutation | T | C | p.E1181G |
| CCK81_LARGE_INTESTINE | 37307399 | 37307534 | 37307498 | 37307498 | Missense_Mutation | G | A | p.T935M |
| COLO684_ENDOMETRIUM | 37310654 | 37310845 | 37310689 | 37310689 | Missense_Mutation | G | A | p.L865F |
| CI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 37310654 | 37310845 | 37310696 | 37310696 | Missense_Mutation | G | C | p.I862M |
| REH_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 37310654 | 37310845 | 37310779 | 37310779 | Missense_Mutation | C | A | p.G835W |
| GP2D_LARGE_INTESTINE | 37310654 | 37310845 | 37310793 | 37310793 | Missense_Mutation | T | A | p.D830V |
| GP5D_LARGE_INTESTINE | 37310654 | 37310845 | 37310793 | 37310793 | Missense_Mutation | T | A | p.D830V |
| SNU324_PANCREAS | 37324094 | 37324209 | 37324118 | 37324118 | Missense_Mutation | G | A | p.A728V |
| SNGM_ENDOMETRIUM | 37324094 | 37324209 | 37324190 | 37324190 | Missense_Mutation | C | T | p.C704Y |
| WM2664_SKIN | 37331787 | 37331897 | 37331801 | 37331801 | Missense_Mutation | A | G | p.F539L |
| KYSE410_OESOPHAGUS | 37331787 | 37331897 | 37331870 | 37331870 | Missense_Mutation | G | A | p.P516S |
| KYSE140_OESOPHAGUS | 37333565 | 37333735 | 37333648 | 37333648 | Missense_Mutation | C | A | p.D479Y |
| HT1376_URINARY_TRACT | 37333565 | 37333735 | 37333687 | 37333687 | Missense_Mutation | C | T | p.E466K |
| MRKNU1_BREAST | 37341192 | 37341344 | 37341218 | 37341218 | Missense_Mutation | T | A | p.K407I |
| SNUC4_LARGE_INTESTINE | 37341192 | 37341344 | 37341227 | 37341227 | Missense_Mutation | T | C | p.K404R |
| JHUEM7_ENDOMETRIUM | 37341192 | 37341344 | 37341243 | 37341243 | Missense_Mutation | A | G | p.S399P |
| A204_SOFT_TISSUE | 37341192 | 37341344 | 37341287 | 37341287 | Missense_Mutation | G | T | p.T384K |
| TTC642_SOFT_TISSUE | 37341192 | 37341344 | 37341287 | 37341287 | Missense_Mutation | G | T | p.T384K |
| LNCAPCLONEFGC_PROSTATE | 37341192 | 37341344 | 37341291 | 37341291 | Missense_Mutation | T | C | p.N383D |
| NCIH835_LUNG | 37341192 | 37341344 | 37341317 | 37341317 | Missense_Mutation | G | T | p.P374Q |
| SNU1040_LARGE_INTESTINE | 37342651 | 37342748 | 37342737 | 37342737 | Missense_Mutation | C | T | p.R336H |
| NCIH720_LUNG | 37352839 | 37352931 | 37352869 | 37352869 | Missense_Mutation | G | C | p.L176V |
| IM95_STOMACH | 37352839 | 37352931 | 37352883 | 37352883 | Missense_Mutation | A | G | p.V171A |
| A101D_SKIN | 37331787 | 37331897 | 37331810 | 37331810 | Nonsense_Mutation | C | A | p.E536* |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for NUP155 |
| sQTL information located at the skipped exons. |
| Exon skip ID | Chromosome | Three exons | Skippped exon | ENST | Cancer type | SNP id | Location | DNA change (ref/var) | P-value |
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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for NUP155 |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for NUP155 |
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RelatedDrugs for NUP155 |
| Approved drugs targeting this gene. (DrugBank Version 5.1.0 2018-04-02) |
| Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for NUP155 |
| Diseases associated with this gene. (DisGeNet 4.0) |
| Gene | Disease ID | Disease name | # pubmeds | Source |
| NUP155 | C4014269 | ATRIAL FIBRILLATION, FAMILIAL, 15 | 1 | UNIPROT |
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