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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 ADAM32 |
 Gene summary |
| Gene information | Gene symbol | ADAM32 | Gene ID | 203102 |
| Gene name | ADAM metallopeptidase domain 32 | |
| Synonyms | - | |
| Cytomap | 8p11.22 | |
| Type of gene | protein-coding | |
| Description | disintegrin and metalloproteinase domain-containing protein 32a disintegrin and metalloprotease domain 32a disintegrin and metalloproteinase domain 32metalloproteinase 12-like proteintesticular tissue protein Li 13 | |
| Modification date | 20180519 | |
| UniProtAcc | Q8TC27 | |
| Context | PubMed: ADAM32 [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 |
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Exon skipping events across known transcript of Ensembl for ADAM32 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 ADAM32 |
| 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 ADAM32 |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_483026 | 8 | 38965291:38965352:38975604:38975684:38994175:38994237 | 38975604:38975684 | ENSG00000197140.10 | ENST00000522506.1,ENST00000399831.3,ENST00000379907.4,ENST00000519315.1 |
| exon_skip_483028 | 8 | 38965291:38965352:38994175:38994237:39004648:39004724 | 38994175:38994237 | ENSG00000197140.10 | ENST00000437682.2 |
| exon_skip_483029 | 8 | 38975640:38975684:38987494:38987616:38994175:38994237 | 38987494:38987616 | ENSG00000197140.10 | ENST00000518259.1 |
| exon_skip_483030 | 8 | 38975640:38975684:38994175:38994237:39004648:39004724 | 38994175:38994237 | ENSG00000197140.10 | ENST00000523400.1,ENST00000521741.1,ENST00000522506.1,ENST00000399831.3,ENST00000379907.4,ENST00000519315.1 |
| exon_skip_483031 | 8 | 39009018:39009067:39018415:39018484:39022282:39022311 | 39018415:39018484 | ENSG00000197140.10 | ENST00000437682.2,ENST00000518259.1,ENST00000379907.4,ENST00000519315.1 |
| exon_skip_483037 | 8 | 39022548:39022715:39027434:39027516:39044427:39044564 | 39027434:39027516 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483039 | 8 | 39022548:39022715:39027434:39027516:39079128:39079221 | 39027434:39027516 | ENSG00000197140.10 | ENST00000437682.2,ENST00000519315.1 |
| exon_skip_483046 | 8 | 39027434:39027516:39044427:39044564:39068662:39068843 | 39044427:39044564 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483049 | 8 | 39044427:39044564:39068662:39068843:39079128:39079221 | 39068662:39068843 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483050 | 8 | 39068662:39068843:39079128:39079221:39080558:39080757 | 39079128:39079221 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483051 | 8 | 39103601:39103685:39111932:39112035:39114705:39114756 | 39111932:39112035 | ENSG00000197140.10 | ENST00000437682.2,ENST00000520691.1,ENST00000379907.4,ENST00000519315.1 |
| exon_skip_483057 | 8 | 39128394:39128433:39131830:39131869:39133346:39133385 | 39131830:39131869 | ENSG00000197140.10 | ENST00000517416.1,ENST00000437682.2,ENST00000379907.4,ENST00000524303.1 |
| exon_skip_483061 | 8 | 39131830:39131869:39133346:39133385:39138654:39138693 | 39133346:39133385 | ENSG00000197140.10 | ENST00000437682.2,ENST00000379907.4 |
| exon_skip_483063 | 8 | 39133346:39133385:39138654:39138693:39141104:39141143 | 39138654:39138693 | ENSG00000197140.10 | ENST00000437682.2,ENST00000379907.4 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for ADAM32 |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_483026 | 8 | 38965291:38965352:38975604:38975684:38994175:38994237 | 38975604:38975684 | ENSG00000197140.10 | ENST00000399831.3,ENST00000519315.1,ENST00000379907.4,ENST00000522506.1 |
| exon_skip_483028 | 8 | 38965291:38965352:38994175:38994237:39004648:39004724 | 38994175:38994237 | ENSG00000197140.10 | ENST00000437682.2 |
| exon_skip_483029 | 8 | 38975640:38975684:38987494:38987616:38994175:38994237 | 38987494:38987616 | ENSG00000197140.10 | ENST00000518259.1 |
| exon_skip_483030 | 8 | 38975640:38975684:38994175:38994237:39004648:39004724 | 38994175:38994237 | ENSG00000197140.10 | ENST00000523400.1,ENST00000399831.3,ENST00000519315.1,ENST00000379907.4,ENST00000522506.1,ENST00000521741.1 |
| exon_skip_483031 | 8 | 39009018:39009067:39018415:39018484:39022282:39022311 | 39018415:39018484 | ENSG00000197140.10 | ENST00000437682.2,ENST00000519315.1,ENST00000379907.4,ENST00000518259.1 |
| exon_skip_483037 | 8 | 39022548:39022715:39027434:39027516:39044427:39044564 | 39027434:39027516 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483039 | 8 | 39022548:39022715:39027434:39027516:39079128:39079221 | 39027434:39027516 | ENSG00000197140.10 | ENST00000437682.2,ENST00000519315.1 |
| exon_skip_483046 | 8 | 39027434:39027516:39044427:39044564:39068662:39068843 | 39044427:39044564 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483049 | 8 | 39044427:39044564:39068662:39068843:39079128:39079221 | 39068662:39068843 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483050 | 8 | 39068662:39068843:39079128:39079221:39080558:39080757 | 39079128:39079221 | ENSG00000197140.10 | ENST00000379907.4 |
| exon_skip_483051 | 8 | 39103601:39103685:39111932:39112035:39114705:39114756 | 39111932:39112035 | ENSG00000197140.10 | ENST00000437682.2,ENST00000519315.1,ENST00000379907.4,ENST00000520691.1 |
| exon_skip_483057 | 8 | 39128394:39128433:39131830:39131869:39133346:39133385 | 39131830:39131869 | ENSG00000197140.10 | ENST00000437682.2,ENST00000379907.4,ENST00000524303.1,ENST00000517416.1 |
| exon_skip_483061 | 8 | 39131830:39131869:39133346:39133385:39138654:39138693 | 39133346:39133385 | ENSG00000197140.10 | ENST00000437682.2,ENST00000379907.4 |
| exon_skip_483063 | 8 | 39133346:39133385:39138654:39138693:39141104:39141143 | 39138654:39138693 | ENSG00000197140.10 | ENST00000437682.2,ENST00000379907.4 |
| 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 ADAM32 |
| 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 |
| ENST00000379907 | 38975604 | 38975684 | Frame-shift |
| ENST00000379907 | 38994175 | 38994237 | Frame-shift |
| ENST00000379907 | 39027434 | 39027516 | Frame-shift |
| ENST00000379907 | 39044427 | 39044564 | Frame-shift |
| ENST00000379907 | 39068662 | 39068843 | Frame-shift |
| ENST00000379907 | 39111932 | 39112035 | Frame-shift |
| ENST00000379907 | 39018415 | 39018484 | In-frame |
| ENST00000379907 | 39079128 | 39079221 | In-frame |
| ENST00000379907 | 39131830 | 39131869 | In-frame |
| ENST00000379907 | 39133346 | 39133385 | In-frame |
| ENST00000379907 | 39138654 | 39138693 | 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 |
| ENST00000379907 | 38975604 | 38975684 | Frame-shift |
| ENST00000379907 | 38994175 | 38994237 | Frame-shift |
| ENST00000379907 | 39027434 | 39027516 | Frame-shift |
| ENST00000379907 | 39044427 | 39044564 | Frame-shift |
| ENST00000379907 | 39068662 | 39068843 | Frame-shift |
| ENST00000379907 | 39111932 | 39112035 | Frame-shift |
| ENST00000379907 | 39018415 | 39018484 | In-frame |
| ENST00000379907 | 39079128 | 39079221 | In-frame |
| ENST00000379907 | 39131830 | 39131869 | In-frame |
| ENST00000379907 | 39133346 | 39133385 | In-frame |
| ENST00000379907 | 39138654 | 39138693 | In-frame |
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Infer the effects of exon skipping event on protein functional features for ADAM32 |
| 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 |
| ENST00000379907 | 2618 | 787 | 39018415 | 39018484 | 653 | 721 | 175 | 198 |
| ENST00000379907 | 2618 | 787 | 39079128 | 39079221 | 1361 | 1453 | 411 | 442 |
| ENST00000379907 | 2618 | 787 | 39131830 | 39131869 | 2329 | 2367 | 734 | 746 |
| ENST00000379907 | 2618 | 787 | 39133346 | 39133385 | 2368 | 2406 | 747 | 759 |
| ENST00000379907 | 2618 | 787 | 39138654 | 39138693 | 2407 | 2445 | 760 | 772 |
| 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 |
| ENST00000379907 | 2618 | 787 | 39018415 | 39018484 | 653 | 721 | 175 | 198 |
| ENST00000379907 | 2618 | 787 | 39079128 | 39079221 | 1361 | 1453 | 411 | 442 |
| ENST00000379907 | 2618 | 787 | 39131830 | 39131869 | 2329 | 2367 | 734 | 746 |
| ENST00000379907 | 2618 | 787 | 39133346 | 39133385 | 2368 | 2406 | 747 | 759 |
| ENST00000379907 | 2618 | 787 | 39138654 | 39138693 | 2407 | 2445 | 760 | 772 |
| 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 |
| Q8TC27 | 175 | 198 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 175 | 198 | 186 | 383 | Domain | Note=Peptidase M12B;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00276 |
| Q8TC27 | 175 | 198 | 175 | 682 | Topological domain | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 411 | 442 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 411 | 442 | 391 | 479 | Domain | Note=Disintegrin;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00068 |
| Q8TC27 | 411 | 442 | 175 | 682 | Topological domain | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 734 | 746 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 734 | 746 | 704 | 787 | Topological domain | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 747 | 759 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 747 | 759 | 704 | 787 | Topological domain | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 760 | 772 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 760 | 772 | 704 | 787 | Topological domain | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| 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 |
| Q8TC27 | 175 | 198 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 175 | 198 | 186 | 383 | Domain | Note=Peptidase M12B;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00276 |
| Q8TC27 | 175 | 198 | 175 | 682 | Topological domain | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 411 | 442 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 411 | 442 | 391 | 479 | Domain | Note=Disintegrin;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00068 |
| Q8TC27 | 411 | 442 | 175 | 682 | Topological domain | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 734 | 746 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 734 | 746 | 704 | 787 | Topological domain | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 747 | 759 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 747 | 759 | 704 | 787 | Topological domain | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
| Q8TC27 | 760 | 772 | 175 | 787 | Chain | ID=PRO_0000029139;Note=Disintegrin and metalloproteinase domain-containing protein 32 |
| Q8TC27 | 760 | 772 | 704 | 787 | Topological domain | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 |
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SNVs in the skipped exons for ADAM32 |
| - 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 |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_483026 | 38975605 | 38975684 | 38975643 | 38975643 | Frame_Shift_Del | A | - | p.K33fs |
| LIHC | TCGA-G3-A3CJ-01 | exon_skip_483026 | 38975605 | 38975684 | 38975643 | 38975643 | Frame_Shift_Del | A | - | p.K33fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_483031 | 39018416 | 39018484 | 39018476 | 39018476 | Frame_Shift_Del | A | - | p.K196fs |
| SKCM | TCGA-EE-A20F-06 | exon_skip_483037 exon_skip_483039 | 39027435 | 39027516 | 39027453 | 39027453 | Frame_Shift_Del | T | - | p.R284fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_483049 | 39068663 | 39068843 | 39068713 | 39068713 | Frame_Shift_Del | A | - | p.Q368fs |
| ESCA | TCGA-L5-A4OI-01 | exon_skip_483049 | 39068663 | 39068843 | 39068767 | 39068767 | Frame_Shift_Del | A | - | p.K388fs |
| ESCA | TCGA-L5-A4OI-01 | exon_skip_483049 | 39068663 | 39068843 | 39068767 | 39068767 | Frame_Shift_Del | A | - | p.Q386fs |
| LIHC | TCGA-DD-A116-01 | exon_skip_483049 | 39068663 | 39068843 | 39068767 | 39068767 | Frame_Shift_Del | A | - | p.Q386fs |
| UCEC | TCGA-BG-A0M3-01 | exon_skip_483049 | 39068663 | 39068843 | 39068767 | 39068767 | Frame_Shift_Del | A | - | p.Q386fs |
| UCEC | TCGA-BS-A0TE-01 | exon_skip_483049 | 39068663 | 39068843 | 39068767 | 39068767 | Frame_Shift_Del | A | - | p.Q386fs |
| UCS | TCGA-N7-A4Y0-01 | exon_skip_483049 | 39068663 | 39068843 | 39068767 | 39068767 | Frame_Shift_Del | A | - | p.Q386fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_483050 | 39079129 | 39079221 | 39079155 | 39079155 | Frame_Shift_Del | T | - | p.D420fs |
| KIRP | TCGA-DW-7836-01 | exon_skip_483049 | 39068663 | 39068843 | 39068760 | 39068760 | Nonsense_Mutation | C | T | p.Q384X |
| DLBC | TCGA-G8-6909-01 | exon_skip_483046 | 39044428 | 39044564 | 39044565 | 39044565 | Splice_Site | G | A | . |
| - 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 |
| DG75_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 39068663 | 39068843 | 39068766 | 39068767 | Frame_Shift_Ins | - | A | p.Q386fs |
| WM278_SKIN | 38975605 | 38975684 | 38975628 | 38975628 | Missense_Mutation | A | T | p.I28F |
| MDAMB436_BREAST | 38975605 | 38975684 | 38975658 | 38975658 | Missense_Mutation | A | G | p.T38A |
| MG63_BONE | 38994176 | 38994237 | 38994203 | 38994203 | Missense_Mutation | G | T | p.D56Y |
| NCIH1836_LUNG | 39018416 | 39018484 | 39018464 | 39018464 | Missense_Mutation | A | G | p.I192V |
| NCIH1568_LUNG | 39018416 | 39018484 | 39018470 | 39018470 | Missense_Mutation | G | T | p.V194L |
| NCIH1435_LUNG | 39027435 | 39027516 | 39027461 | 39027461 | Missense_Mutation | G | T | p.G287V |
| L540_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 39044428 | 39044564 | 39044435 | 39044435 | Missense_Mutation | A | T | p.K308M |
| OC316_OVARY | 39044428 | 39044564 | 39044467 | 39044467 | Missense_Mutation | G | A | p.V319I |
| HEC108_ENDOMETRIUM | 39044428 | 39044564 | 39044494 | 39044494 | Missense_Mutation | G | A | p.G328R |
| MFE296_ENDOMETRIUM | 39044428 | 39044564 | 39044509 | 39044509 | Missense_Mutation | G | C | p.D333H |
| NCIH740_LUNG | 39068663 | 39068843 | 39068728 | 39068728 | Missense_Mutation | A | G | p.N373S |
| SNU81_LARGE_INTESTINE | 39068663 | 39068843 | 39068750 | 39068750 | Missense_Mutation | G | T | p.Q380H |
| OC316_OVARY | 39068663 | 39068843 | 39068762 | 39068762 | Missense_Mutation | A | C | p.Q384H |
| OC314_OVARY | 39068663 | 39068843 | 39068762 | 39068762 | Missense_Mutation | A | C | p.Q384H |
| HUTU80_SMALL_INTESTINE | 39068663 | 39068843 | 39068765 | 39068766 | Missense_Mutation | GC | TG | p.385_386MQ>IE |
| NALM19_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 39068663 | 39068843 | 39068788 | 39068788 | Missense_Mutation | T | C | p.V393A |
| IGR1_SKIN | 39068663 | 39068843 | 39068799 | 39068799 | Missense_Mutation | G | A | p.G397S |
| SNGM_ENDOMETRIUM | 39079129 | 39079221 | 39079133 | 39079133 | Missense_Mutation | G | A | p.C413Y |
| HCC2998_LARGE_INTESTINE | 39079129 | 39079221 | 39079147 | 39079147 | Missense_Mutation | T | C | p.C418R |
| PLCPRF5_LIVER | 39079129 | 39079221 | 39079160 | 39079160 | Missense_Mutation | G | A | p.R422Q |
| EB3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 39079129 | 39079221 | 39079160 | 39079160 | Missense_Mutation | G | A | p.R422Q |
| BL70_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 39079129 | 39079221 | 39079211 | 39079211 | Missense_Mutation | A | T | p.K439I |
| RPMI2650_UPPER_AERODIGESTIVE_TRACT | 39111933 | 39112035 | 39111936 | 39111936 | Missense_Mutation | T | C | p.C636R |
| NO10_CENTRAL_NERVOUS_SYSTEM | 39111933 | 39112035 | 39111996 | 39111996 | Missense_Mutation | C | T | p.R656C |
| SW480_LARGE_INTESTINE | 39111933 | 39112035 | 39112015 | 39112015 | Missense_Mutation | T | C | p.I662T |
| SW620_LARGE_INTESTINE | 39111933 | 39112035 | 39112015 | 39112015 | Missense_Mutation | T | C | p.I662T |
| MAC2A_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 39111933 | 39112035 | 39112017 | 39112017 | Missense_Mutation | T | C | p.F663L |
| TK10_KIDNEY | 39111933 | 39112035 | 39112021 | 39112021 | Missense_Mutation | C | T | p.P664L |
| NCIH1573_LUNG | 39138655 | 39138693 | 39138657 | 39138657 | Missense_Mutation | C | T | p.S761F |
| SNUC2A_LARGE_INTESTINE | 39138655 | 39138693 | 39138670 | 39138670 | Missense_Mutation | T | A | p.D765E |
| SNUC2B_LARGE_INTESTINE | 39138655 | 39138693 | 39138670 | 39138670 | Missense_Mutation | T | A | p.D765E |
| SNU81_LARGE_INTESTINE | 38975605 | 38975684 | 38975679 | 38975679 | Nonsense_Mutation | G | T | p.E45* |
| HCC2998_LARGE_INTESTINE | 39079129 | 39079221 | 39079159 | 39079159 | Nonsense_Mutation | C | T | p.R422* |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ADAM32 |
| 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 ADAM32 |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ADAM32 |
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RelatedDrugs for ADAM32 |
| 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 ADAM32 |
| Diseases associated with this gene. (DisGeNet 4.0) |
| Gene | Disease ID | Disease name | # pubmeds | Source |
Copyright 2018-Present -The University of Texas Health Science Center at Houston (UTHealth)
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