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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 HSPA9 |
 Gene summary |
| Gene information | Gene symbol | HSPA9 | Gene ID | 3313 |
| Gene name | heat shock protein family A (Hsp70) member 9 | |
| Synonyms | CRP40|CSA|EVPLS|GRP-75|GRP75|HEL-S-124m|HSPA9B|MOT|MOT2|MTHSP75|PBP74|SAAN|SIDBA4 | |
| Cytomap | 5q31.2 | |
| Type of gene | protein-coding | |
| Description | stress-70 protein, mitochondrial75 kDa glucose-regulated proteincatecholamine-regulated protein 40epididymis secretory sperm binding protein Li 124mheat shock 70kD protein 9Bheat shock 70kDa protein 9 (mortalin)mortalin, perinuclearmortalin-2morta | |
| Modification date | 20180523 | |
| UniProtAcc | P38646 | |
| Context | PubMed: HSPA9 [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 HSPA9 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 HSPA9 |
| 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 HSPA9 |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_444591 | 5 | 137892140:137892281:137892462:137892555:137893090:137893185 | 137892462:137892555 | ENSG00000113013.8 | ENST00000297185.3 |
| exon_skip_444593 | 5 | 137893090:137893185:137893557:137893675:137894241:137894320 | 137893557:137893675 | ENSG00000113013.8 | ENST00000297185.3,ENST00000512328.1 |
| exon_skip_444594 | 5 | 137893557:137893675:137894241:137894346:137895552:137895780 | 137894241:137894346 | ENSG00000113013.8 | ENST00000297185.3 |
| exon_skip_444595 | 5 | 137894241:137894346:137895552:137895780:137897268:137897478 | 137895552:137895780 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1 |
| exon_skip_444599 | 5 | 137895686:137895780:137896469:137896620:137897268:137897478 | 137896469:137896620 | ENSG00000113013.8 | ENST00000523929.1 |
| exon_skip_444600 | 5 | 137895552:137895780:137897268:137897478:137902314:137902400 | 137897268:137897478 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1 |
| exon_skip_444602 | 5 | 137897268:137897478:137902314:137902407:137902689:137902852 | 137902314:137902407 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1 |
| exon_skip_444604 | 5 | 137903143:137903250:137903337:137903411:137904613:137904738 | 137903337:137903411 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1,ENST00000504902.1 |
| exon_skip_444605 | 5 | 137903337:137903411:137904613:137904738:137906648:137906830 | 137904613:137904738 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1,ENST00000504902.1 |
| exon_skip_444610 | 5 | 137909465:137909539:137909756:137909815:137910926:137911029 | 137909756:137909815 | ENSG00000113013.8 | ENST00000506477.1,ENST00000504902.1 |
| exon_skip_444611 | 5 | 137909465:137909539:137909756:137909858:137910926:137911029 | 137909756:137909858 | ENSG00000113013.8 | ENST00000507097.1,ENST00000507115.1 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for HSPA9 |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_444591 | 5 | 137892140:137892281:137892462:137892555:137893090:137893185 | 137892462:137892555 | ENSG00000113013.8 | ENST00000297185.3 |
| exon_skip_444593 | 5 | 137893090:137893185:137893557:137893675:137894241:137894320 | 137893557:137893675 | ENSG00000113013.8 | ENST00000297185.3,ENST00000512328.1 |
| exon_skip_444594 | 5 | 137893557:137893675:137894241:137894346:137895552:137895780 | 137894241:137894346 | ENSG00000113013.8 | ENST00000297185.3 |
| exon_skip_444595 | 5 | 137894241:137894346:137895552:137895780:137897268:137897478 | 137895552:137895780 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1 |
| exon_skip_444599 | 5 | 137895686:137895780:137896469:137896620:137897268:137897478 | 137896469:137896620 | ENSG00000113013.8 | ENST00000523929.1 |
| exon_skip_444600 | 5 | 137895552:137895780:137897268:137897478:137902314:137902400 | 137897268:137897478 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1 |
| exon_skip_444602 | 5 | 137897268:137897478:137902314:137902407:137902689:137902852 | 137902314:137902407 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1 |
| exon_skip_444604 | 5 | 137903143:137903250:137903337:137903411:137904613:137904738 | 137903337:137903411 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1,ENST00000504902.1 |
| exon_skip_444605 | 5 | 137903337:137903411:137904613:137904738:137906648:137906830 | 137904613:137904738 | ENSG00000113013.8 | ENST00000297185.3,ENST00000507097.1,ENST00000504902.1 |
| exon_skip_444610 | 5 | 137909465:137909539:137909756:137909815:137910926:137911029 | 137909756:137909815 | ENSG00000113013.8 | ENST00000504902.1,ENST00000506477.1 |
| exon_skip_444611 | 5 | 137909465:137909539:137909756:137909858:137910926:137911029 | 137909756:137909858 | ENSG00000113013.8 | ENST00000507097.1,ENST00000507115.1 |
| 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 HSPA9 |
| 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 |
| ENST00000297185 | 137893557 | 137893675 | Frame-shift |
| ENST00000297185 | 137903337 | 137903411 | Frame-shift |
| ENST00000297185 | 137904613 | 137904738 | Frame-shift |
| ENST00000297185 | 137892462 | 137892555 | In-frame |
| ENST00000297185 | 137894241 | 137894346 | In-frame |
| ENST00000297185 | 137895552 | 137895780 | In-frame |
| ENST00000297185 | 137897268 | 137897478 | In-frame |
| ENST00000297185 | 137902314 | 137902407 | 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 |
| ENST00000297185 | 137893557 | 137893675 | Frame-shift |
| ENST00000297185 | 137903337 | 137903411 | Frame-shift |
| ENST00000297185 | 137904613 | 137904738 | Frame-shift |
| ENST00000297185 | 137892462 | 137892555 | In-frame |
| ENST00000297185 | 137894241 | 137894346 | In-frame |
| ENST00000297185 | 137895552 | 137895780 | In-frame |
| ENST00000297185 | 137897268 | 137897478 | In-frame |
| ENST00000297185 | 137902314 | 137902407 | In-frame |
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Infer the effects of exon skipping event on protein functional features for HSPA9 |
| 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 |
| ENST00000297185 | 3338 | 679 | 137902314 | 137902407 | 1006 | 1098 | 293 | 324 |
| ENST00000297185 | 3338 | 679 | 137897268 | 137897478 | 1099 | 1308 | 324 | 394 |
| ENST00000297185 | 3338 | 679 | 137895552 | 137895780 | 1309 | 1536 | 394 | 470 |
| ENST00000297185 | 3338 | 679 | 137894241 | 137894346 | 1537 | 1641 | 470 | 505 |
| ENST00000297185 | 3338 | 679 | 137892462 | 137892555 | 1855 | 1947 | 576 | 607 |
| 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 |
| ENST00000297185 | 3338 | 679 | 137902314 | 137902407 | 1006 | 1098 | 293 | 324 |
| ENST00000297185 | 3338 | 679 | 137897268 | 137897478 | 1099 | 1308 | 324 | 394 |
| ENST00000297185 | 3338 | 679 | 137895552 | 137895780 | 1309 | 1536 | 394 | 470 |
| ENST00000297185 | 3338 | 679 | 137894241 | 137894346 | 1537 | 1641 | 470 | 505 |
| ENST00000297185 | 3338 | 679 | 137892462 | 137892555 | 1855 | 1947 | 576 | 607 |
| 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 |
| 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 |
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SNVs in the skipped exons for HSPA9 |
| - 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. |
HSPA9_KIRC_exon_skip_444602_psi_boxplot.png |
HSPA9_LIHC_exon_skip_444593_psi_boxplot.png |
| - 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-G3-A3CJ-01 | exon_skip_444593 | 137893558 | 137893675 | 137893625 | 137893625 | Frame_Shift_Del | A | - | p.F522fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_444595 | 137895553 | 137895780 | 137895754 | 137895754 | Frame_Shift_Del | A | - | p.F403fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_444595 | 137895553 | 137895780 | 137895754 | 137895754 | Frame_Shift_Del | A | - | p.F403fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_444604 | 137903338 | 137903411 | 137903384 | 137903384 | Frame_Shift_Del | T | - | p.N188fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_444604 | 137903338 | 137903411 | 137903384 | 137903384 | Frame_Shift_Del | T | - | p.N188fs |
| KIRP | TCGA-GL-8500-01 | exon_skip_444605 | 137904614 | 137904738 | 137904733 | 137904733 | Frame_Shift_Del | T | - | p.N139fs |
| CESC | TCGA-DS-A1OC-01 | exon_skip_444591 | 137892463 | 137892555 | 137892546 | 137892546 | Nonsense_Mutation | C | A | p.E580* |
| BLCA | TCGA-KQ-A41R-01 | exon_skip_444595 | 137895553 | 137895780 | 137895693 | 137895693 | Nonsense_Mutation | G | A | p.Q424* |
| COAD | TCGA-AA-3510-01 | exon_skip_444600 | 137897269 | 137897478 | 137897307 | 137897307 | Nonsense_Mutation | C | A | p.E382X |
| KIRC | TCGA-A3-3323-01 | exon_skip_444602 | 137902315 | 137902407 | 137902359 | 137902359 | Nonsense_Mutation | C | A | p.E310* |
| KIRC | TCGA-A3-3323-01 | exon_skip_444602 | 137902315 | 137902407 | 137902359 | 137902359 | Nonsense_Mutation | C | A | p.E310X |
| UCEC | TCGA-D1-A103-01 | exon_skip_444610 | 137909757 | 137909815 | 137909756 | 137909756 | Splice_Site | C | T | e2+1 |
| UCEC | TCGA-D1-A103-01 | exon_skip_444611 | 137909757 | 137909858 | 137909756 | 137909756 | Splice_Site | C | T | e2+1 |
| - Depth of coverage in the three exons composing exon skipping event |
| Depth of coverage in three exons | Mutation description |
 | Sample: TCGA-A3-3323-01 |
| Cancer type: KIRC | |
| ESID: exon_skip_444602 | |
| Skipped exon start: 137902315 | |
| Skipped exon end: 137902407 | |
| Mutation start: 137902359 | |
| Mutation end: 137902359 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E310X | |
| Sample: TCGA-A3-3323-01 |
| Cancer type: KIRC | |
| ESID: exon_skip_444602 | |
| Skipped exon start: 137902315 | |
| Skipped exon end: 137902407 | |
| Mutation start: 137902359 | |
| Mutation end: 137902359 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E310* | |
exon_skip_444602_KIRC_TCGA-A3-3323-01.png | |
 | Sample: TCGA-G3-A3CJ-01 |
| Cancer type: LIHC | |
| ESID: exon_skip_444593 | |
| Skipped exon start: 137893558 | |
| Skipped exon end: 137893675 | |
| Mutation start: 137893625 | |
| Mutation end: 137893625 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: A | |
| Mutation seq: - | |
| AAchange: p.F522fs | |
exon_skip_101516_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_106378_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_106524_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_109529_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_109778_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11286_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11289_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11349_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_113894_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_113898_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11611_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11615_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11638_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11641_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11926_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11933_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11937_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_11939_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_124065_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_124066_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_124693_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_126824_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_126833_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_126836_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_1268_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_1270_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_127101_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_1274_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_128729_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_13626_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_138373_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_138676_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_14564_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_153354_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_1873_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_24442_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_289275_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_289905_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_293221_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_300058_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_302253_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_331517_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_354387_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_365019_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_365023_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_371589_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_375393_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_380574_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_382000_LIHC_TCGA-G3-A3CJ-01.png | |
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exon_skip_385031_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_387684_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_421130_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_421131_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_421134_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_426528_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_426530_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_427391_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_430528_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_433436_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_433655_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_434375_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_43567_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_436327_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_436618_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_444593_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_445559_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_447600_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_452739_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_4535_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_457245_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_45824_LIHC_TCGA-G3-A3CJ-01.png | |
exon_skip_464169_LIHC_TCGA-G3-A3CJ-01.png | |
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| - 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 |
| SW480_LARGE_INTESTINE | 137903338 | 137903411 | 137903383 | 137903384 | Frame_Shift_Ins | - | T | p.N188fs |
| SNUC5_LARGE_INTESTINE | 137892463 | 137892555 | 137892501 | 137892501 | Missense_Mutation | T | C | p.K595E |
| DOV13_OVARY | 137892463 | 137892555 | 137892542 | 137892542 | Missense_Mutation | G | A | p.A581V |
| SNU1040_LARGE_INTESTINE | 137893558 | 137893675 | 137893567 | 137893567 | Missense_Mutation | C | T | p.E542K |
| CMK_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 137893558 | 137893675 | 137893573 | 137893573 | Missense_Mutation | C | T | p.G540R |
| KYSE270_OESOPHAGUS | 137893558 | 137893675 | 137893587 | 137893587 | Missense_Mutation | T | G | p.K535T |
| PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 137894242 | 137894346 | 137894247 | 137894247 | Missense_Mutation | T | C | p.T504A |
| OVCAR8_OVARY | 137895553 | 137895780 | 137895575 | 137895575 | Missense_Mutation | G | C | p.T463S |
| NUDUL1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 137895553 | 137895780 | 137895731 | 137895731 | Missense_Mutation | A | G | p.V411A |
| H2369_PLEURA | 137895553 | 137895780 | 137895747 | 137895747 | Missense_Mutation | C | A | p.A406S |
| KYSE270_OESOPHAGUS | 137895553 | 137895780 | 137895772 | 137895772 | Missense_Mutation | C | A | p.Q397H |
| ASH3_THYROID | 137897269 | 137897478 | 137897331 | 137897331 | Missense_Mutation | C | T | p.E374K |
| CW2_LARGE_INTESTINE | 137897269 | 137897478 | 137897393 | 137897393 | Missense_Mutation | C | A | p.G353V |
| CMLT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 137897269 | 137897478 | 137897453 | 137897453 | Missense_Mutation | G | A | p.T333I |
| NCIH1573_LUNG | 137903338 | 137903411 | 137903382 | 137903382 | Missense_Mutation | C | A | p.A189S |
| HT1376_URINARY_TRACT | 137904614 | 137904738 | 137904627 | 137904627 | Missense_Mutation | C | A | p.M174I |
| KYSE150_OESOPHAGUS | 137904614 | 137904738 | 137904685 | 137904685 | Missense_Mutation | T | C | p.E155G |
| RCC10RGB_KIDNEY | 137909757 | 137909815 | 137909793 | 137909793 | Missense_Mutation | T | A | p.H35L |
| RCC10RGB_KIDNEY | 137909757 | 137909858 | 137909793 | 137909793 | Missense_Mutation | T | A | p.H35L |
| TE14_OESOPHAGUS | 137895553 | 137895780 | 137895555 | 137895555 | Nonsense_Mutation | G | A | p.Q470* |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for HSPA9 |
| 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 HSPA9 |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for HSPA9 |
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RelatedDrugs for HSPA9 |
| 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 HSPA9 |
| Diseases associated with this gene. (DisGeNet 4.0) |
| Gene | Disease ID | Disease name | # pubmeds | Source |
| HSPA9 | C0004364 | Autoimmune Diseases | 1 | CTD_human |
| HSPA9 | C0007134 | Renal Cell Carcinoma | 1 | CTD_human |
| HSPA9 | C0019693 | HIV Infections | 1 | CTD_human |
| HSPA9 | C0030567 | Parkinson Disease | 1 | CTD_human |
| HSPA9 | C0036341 | Schizophrenia | 1 | PSYGENET |
| HSPA9 | C0042164 | Uveitis | 1 | CTD_human |
| HSPA9 | C0151744 | Myocardial Ischemia | 1 | CTD_human |
| HSPA9 | C0221765 | Chronic schizophrenia | 1 | PSYGENET |
| HSPA9 | C0376618 | Endotoxemia | 1 | CTD_human |
| HSPA9 | C0520459 | Necrotizing Enterocolitis | 1 | CTD_human |
| HSPA9 | C2239176 | Liver carcinoma | 1 | CTD_human |
| HSPA9 | C4225180 | EVEN-PLUS SYNDROME | 1 | UNIPROT |
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