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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 HAUS6 |
 Gene summary |
| Gene information | Gene symbol | HAUS6 | Gene ID | 54801 |
| Gene name | HAUS augmin like complex subunit 6 | |
| Synonyms | Dgt6|FAM29A | |
| Cytomap | 9p22.1 | |
| Type of gene | protein-coding | |
| Description | HAUS augmin-like complex subunit 6dim gamma-tubulin homologfamily with sequence similarity 29, member A | |
| Modification date | 20180519 | |
| UniProtAcc | Q7Z4H7 | |
| Context | PubMed: HAUS6 [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 HAUS6 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 HAUS6 |
| 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 HAUS6 |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENSG00000147874.6 | ENST00000380502.3 |
| exon_skip_502787 | 9 | 19063005:19063191:19063511:19063578:19070216:19070298 | 19063511:19063578 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502789 | 9 | 19076599:19076702:19078173:19078300:19080476:19080670 | 19078173:19078300 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502792 | 9 | 19078173:19078300:19080476:19080670:19082870:19083041 | 19080476:19080670 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502793 | 9 | 19080476:19080670:19082870:19083041:19086731:19086780 | 19082870:19083041 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502795 | 9 | 19087088:19087154:19089409:19089557:19093168:19093211 | 19089409:19089557 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for HAUS6 |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENSG00000147874.6 | ENST00000380502.3 |
| exon_skip_502787 | 9 | 19063005:19063191:19063511:19063578:19070216:19070298 | 19063511:19063578 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502789 | 9 | 19076599:19076702:19078173:19078300:19080476:19080670 | 19078173:19078300 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502792 | 9 | 19078173:19078300:19080476:19080670:19082870:19083041 | 19080476:19080670 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502793 | 9 | 19080476:19080670:19082870:19083041:19086731:19086780 | 19082870:19083041 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| exon_skip_502795 | 9 | 19087088:19087154:19089409:19089557:19093168:19093211 | 19089409:19089557 | ENSG00000147874.6 | ENST00000380502.3,ENST00000380496.1 |
| 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 HAUS6 |
| 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 |
| ENST00000380502 | 19063511 | 19063578 | Frame-shift |
| ENST00000380502 | 19076599 | 19076702 | Frame-shift |
| ENST00000380502 | 19078173 | 19078300 | Frame-shift |
| ENST00000380502 | 19080476 | 19080670 | Frame-shift |
| ENST00000380502 | 19089409 | 19089557 | Frame-shift |
| ENST00000380502 | 19057958 | 19058999 | In-frame |
| ENST00000380502 | 19082870 | 19083041 | 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 |
| ENST00000380502 | 19063511 | 19063578 | Frame-shift |
| ENST00000380502 | 19076599 | 19076702 | Frame-shift |
| ENST00000380502 | 19078173 | 19078300 | Frame-shift |
| ENST00000380502 | 19080476 | 19080670 | Frame-shift |
| ENST00000380502 | 19089409 | 19089557 | Frame-shift |
| ENST00000380502 | 19057958 | 19058999 | In-frame |
| ENST00000380502 | 19082870 | 19083041 | In-frame |
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Infer the effects of exon skipping event on protein functional features for HAUS6 |
| 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 |
| ENST00000380502 | 6553 | 955 | 19082870 | 19083041 | 1168 | 1338 | 233 | 290 |
| ENST00000380502 | 6553 | 955 | 19057958 | 19058999 | 2234 | 3274 | 588 | 935 |
| 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 |
| ENST00000380502 | 6553 | 955 | 19082870 | 19083041 | 1168 | 1338 | 233 | 290 |
| ENST00000380502 | 6553 | 955 | 19057958 | 19058999 | 2234 | 3274 | 588 | 935 |
| 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 HAUS6 |
| - 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. |
HAUS6_CESC_exon_skip_502793_psi_boxplot.png |
HAUS6_STAD_exon_skip_502793_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-DD-A1EG-01 | exon_skip_502784 | 19057959 | 19058999 | 19058461 | 19058461 | Frame_Shift_Del | A | - | p.F768fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_502784 | 19057959 | 19058999 | 19058461 | 19058461 | Frame_Shift_Del | A | - | p.F768fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_502784 | 19057959 | 19058999 | 19058941 | 19058941 | Frame_Shift_Del | T | - | p.K608fs |
| LIHC | TCGA-DD-A1EG-01 | 19076600 | 19076702 | 19076672 | 19076672 | Frame_Shift_Del | G | - | p.L408fs | |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_502789 | 19078174 | 19078300 | 19078191 | 19078191 | Frame_Shift_Del | T | - | p.I392fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_502792 | 19080477 | 19080670 | 19080524 | 19080524 | Frame_Shift_Del | T | - | p.K339fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_502792 | 19080477 | 19080670 | 19080524 | 19080524 | Frame_Shift_Del | T | - | p.K339fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_502793 | 19082871 | 19083041 | 19082998 | 19082998 | Frame_Shift_Del | A | - | p.L248fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_502793 | 19082871 | 19083041 | 19082998 | 19082998 | Frame_Shift_Del | A | - | p.L248fs |
| LIHC | TCGA-G3-A3CJ-01 | exon_skip_502793 | 19082871 | 19083041 | 19082998 | 19082998 | Frame_Shift_Del | A | - | p.L248fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_502795 | 19089410 | 19089557 | 19089455 | 19089455 | Frame_Shift_Del | A | - | p.L180fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_502795 | 19089410 | 19089557 | 19089464 | 19089464 | Frame_Shift_Del | A | - | p.L177fs |
| BLCA | TCGA-MV-A51V-01 | exon_skip_502784 | 19057959 | 19058999 | 19058381 | 19058381 | Nonsense_Mutation | G | C | p.S795* |
| UCEC | TCGA-B5-A11E-01 | exon_skip_502784 | 19057959 | 19058999 | 19058868 | 19058868 | Nonsense_Mutation | C | A | p.E633* |
| UCEC | TCGA-BS-A0UV-01 | exon_skip_502784 | 19057959 | 19058999 | 19058868 | 19058868 | Nonsense_Mutation | C | A | p.E633* |
| READ | TCGA-F5-6814-01 | exon_skip_502789 | 19078174 | 19078300 | 19078221 | 19078221 | Nonsense_Mutation | C | A | p.E382X |
| UCEC | TCGA-D1-A17Q-01 | exon_skip_502789 | 19078174 | 19078300 | 19078225 | 19078225 | Nonsense_Mutation | C | T | p.W380* |
| KIRP | TCGA-SX-A71S-01 | exon_skip_502792 | 19080477 | 19080670 | 19080609 | 19080609 | Nonsense_Mutation | A | T | p.L311X |
| CESC | TCGA-EK-A2R8-01 | exon_skip_502793 | 19082871 | 19083041 | 19082873 | 19082873 | Nonsense_Mutation | G | A | p.Q290* |
| LUAD | TCGA-05-4410-01 | exon_skip_502789 | 19078174 | 19078300 | 19078172 | 19078172 | Splice_Site | A | C | p.P397_splice |
| STAD | TCGA-CG-5721-01 | exon_skip_502793 | 19082871 | 19083041 | 19083042 | 19083042 | Splice_Site | C | A | . |
| STAD | TCGA-CG-5721-01 | exon_skip_502793 | 19082871 | 19083041 | 19083042 | 19083042 | Splice_Site | C | A | p.V234_splice |
| PAAD | TCGA-IB-7651-01 | exon_skip_502795 | 19089410 | 19089557 | 19089409 | 19089409 | Splice_Site | C | A | . |
| - Depth of coverage in the three exons composing exon skipping event |
| Depth of coverage in three exons | Mutation description |
 | Sample: TCGA-CG-5721-01 |
| Cancer type: STAD | |
| ESID: exon_skip_502793 | |
| Skipped exon start: 19082871 | |
| Skipped exon end: 19083041 | |
| Mutation start: 19083042 | |
| Mutation end: 19083042 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: . | |
| Sample: TCGA-CG-5721-01 |
| Cancer type: STAD | |
| ESID: exon_skip_502793 | |
| Skipped exon start: 19082871 | |
| Skipped exon end: 19083041 | |
| Mutation start: 19083042 | |
| Mutation end: 19083042 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.V234_splice | |
exon_skip_107493_STAD_TCGA-CG-5721-01.png | |
exon_skip_107867_STAD_TCGA-CG-5721-01.png | |
exon_skip_123973_STAD_TCGA-CG-5721-01.png | |
exon_skip_124728_STAD_TCGA-CG-5721-01.png | |
exon_skip_20583_STAD_TCGA-CG-5721-01.png | |
exon_skip_284550_STAD_TCGA-CG-5721-01.png | |
exon_skip_287086_STAD_TCGA-CG-5721-01.png | |
exon_skip_287092_STAD_TCGA-CG-5721-01.png | |
exon_skip_328008_STAD_TCGA-CG-5721-01.png | |
exon_skip_347989_STAD_TCGA-CG-5721-01.png | |
exon_skip_360357_STAD_TCGA-CG-5721-01.png | |
exon_skip_360359_STAD_TCGA-CG-5721-01.png | |
exon_skip_361242_STAD_TCGA-CG-5721-01.png | |
exon_skip_363554_STAD_TCGA-CG-5721-01.png | |
exon_skip_370065_STAD_TCGA-CG-5721-01.png | |
exon_skip_377240_STAD_TCGA-CG-5721-01.png | |
exon_skip_378735_STAD_TCGA-CG-5721-01.png | |
exon_skip_41850_STAD_TCGA-CG-5721-01.png | |
exon_skip_425098_STAD_TCGA-CG-5721-01.png | |
exon_skip_443908_STAD_TCGA-CG-5721-01.png | |
exon_skip_449553_STAD_TCGA-CG-5721-01.png | |
exon_skip_452918_STAD_TCGA-CG-5721-01.png | |
exon_skip_454809_STAD_TCGA-CG-5721-01.png | |
exon_skip_462689_STAD_TCGA-CG-5721-01.png | |
exon_skip_482821_STAD_TCGA-CG-5721-01.png | |
exon_skip_482822_STAD_TCGA-CG-5721-01.png | |
exon_skip_487878_STAD_TCGA-CG-5721-01.png | |
exon_skip_502793_STAD_TCGA-CG-5721-01.png | |
exon_skip_508189_STAD_TCGA-CG-5721-01.png | |
exon_skip_516607_STAD_TCGA-CG-5721-01.png | |
exon_skip_54935_STAD_TCGA-CG-5721-01.png | |
exon_skip_96977_STAD_TCGA-CG-5721-01.png | |
| - 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 |
| MPP89_PLEURA | 19057959 | 19058999 | 19058872 | 19058875 | Frame_Shift_Del | TTGA | - | p.NQ630fs |
| EN_ENDOMETRIUM | 19057959 | 19058999 | 19058353 | 19058354 | Frame_Shift_Ins | - | T | p.N804fs |
| ES2_OVARY | 19076600 | 19076702 | 19076628 | 19076630 | In_Frame_Del | AAT | - | p.I422del |
| HT115_LARGE_INTESTINE | 19057959 | 19058999 | 19058009 | 19058009 | Missense_Mutation | C | A | p.R919I |
| 647V_URINARY_TRACT | 19057959 | 19058999 | 19058019 | 19058019 | Missense_Mutation | C | T | p.V916M |
| PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19057959 | 19058999 | 19058036 | 19058036 | Missense_Mutation | A | G | p.L910P |
| SNU201_CENTRAL_NERVOUS_SYSTEM | 19057959 | 19058999 | 19058055 | 19058055 | Missense_Mutation | T | G | p.K904Q |
| HTCC3_THYROID | 19057959 | 19058999 | 19058055 | 19058055 | Missense_Mutation | T | G | p.K904Q |
| ESS1_ENDOMETRIUM | 19057959 | 19058999 | 19058057 | 19058057 | Missense_Mutation | C | A | p.R903I |
| JHUEM7_ENDOMETRIUM | 19057959 | 19058999 | 19058127 | 19058127 | Missense_Mutation | T | G | p.N880H |
| MYM12_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19057959 | 19058999 | 19058273 | 19058273 | Missense_Mutation | T | G | p.Q831P |
| T3M10_LUNG | 19057959 | 19058999 | 19058349 | 19058349 | Missense_Mutation | G | C | p.P806A |
| SKNO1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19057959 | 19058999 | 19058358 | 19058358 | Missense_Mutation | G | A | p.P803S |
| HCC2998_LARGE_INTESTINE | 19057959 | 19058999 | 19058458 | 19058458 | Missense_Mutation | T | G | p.K769N |
| YKG1_CENTRAL_NERVOUS_SYSTEM | 19057959 | 19058999 | 19058702 | 19058702 | Missense_Mutation | T | G | p.N688T |
| MC116_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19057959 | 19058999 | 19058790 | 19058790 | Missense_Mutation | T | A | p.I659F |
| WIL2NS_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19063512 | 19063578 | 19063522 | 19063522 | Missense_Mutation | A | G | p.V478A |
| MOLT16_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19076600 | 19076702 | 19076674 | 19076674 | Missense_Mutation | G | A | p.P407L |
| RKO_LARGE_INTESTINE | 19078174 | 19078300 | 19078271 | 19078271 | Missense_Mutation | A | G | p.I365T |
| PATU8902_PANCREAS | 19078174 | 19078300 | 19078272 | 19078272 | Missense_Mutation | T | C | p.I365V |
| NCIH2110_LUNG | 19078174 | 19078300 | 19078284 | 19078284 | Missense_Mutation | C | A | p.D361Y |
| HEC251_ENDOMETRIUM | 19078174 | 19078300 | 19078290 | 19078290 | Missense_Mutation | T | G | p.K359Q |
| CCRFCEM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19080477 | 19080670 | 19080479 | 19080479 | Missense_Mutation | C | T | p.M354I |
| JHUEM7_ENDOMETRIUM | 19080477 | 19080670 | 19080537 | 19080537 | Missense_Mutation | T | C | p.H335R |
| RCK8_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 19080477 | 19080670 | 19080551 | 19080551 | Missense_Mutation | C | G | p.L330F |
| MFE319_ENDOMETRIUM | 19082871 | 19083041 | 19082990 | 19082990 | Missense_Mutation | C | T | p.E251K |
| JHH2_LIVER | 19082871 | 19083041 | 19082998 | 19082998 | Missense_Mutation | A | C | p.L248W |
| HEC59_ENDOMETRIUM | 19089410 | 19089557 | 19089480 | 19089480 | Missense_Mutation | C | T | p.A172T |
| HEC251_ENDOMETRIUM | 19089410 | 19089557 | 19089522 | 19089522 | Missense_Mutation | T | G | p.K158Q |
| HEC251_ENDOMETRIUM | 19057959 | 19058999 | 19058898 | 19058898 | Nonsense_Mutation | C | A | p.E623* |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for HAUS6 |
| 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 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | COAD | rs13286328 | chr9:19076673 | G/C | 1.82e-05 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | COAD | rs13286328 | chr9:19076673 | G/C | 1.82e-05 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | BRCA | rs13286328 | chr9:19076673 | G/C | 4.70e-10 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | BRCA | rs13286328 | chr9:19076673 | G/C | 4.71e-10 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | LGG | rs13286328 | chr9:19076673 | G/C | 2.60e-04 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | LGG | rs13286328 | chr9:19076673 | G/C | 2.61e-04 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | KIRC | rs13286328 | chr9:19076673 | G/C | 3.80e-04 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | KIRC | rs13286328 | chr9:19076673 | G/C | 3.81e-04 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | LUAD | rs13286328 | chr9:19076673 | G/C | 1.53e-04 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | LUAD | rs13286328 | chr9:19076673 | G/C | 1.53e-04 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | PRAD | rs13286328 | chr9:19076673 | G/C | 2.53e-03 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | PRAD | rs13286328 | chr9:19076673 | G/C | 2.53e-03 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | TGCT | rs13286328 | chr9:19076673 | G/C | 2.37e-04 |
| exon_skip_502788 | 9 | 19070216:19070298:19076599:19076702:19078173:19078300 | 19076599:19076702 | ENST00000380502.3,ENST00000380496.1 | TGCT | rs13286328 | chr9:19076673 | G/C | 2.37e-04 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | COAD | rs150852615 | chr9:19058483 | C/A | 1.68e-05 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | COAD | rs150852615 | chr9:19058483 | C/A | 1.68e-05 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | COAD | rs62622380 | chr9:19058921 | G/A | 1.40e-04 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | COAD | rs62622380 | chr9:19058921 | G/A | 1.40e-04 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | ESCA | rs150852615 | chr9:19058483 | C/A | 4.30e-04 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | ESCA | rs150852615 | chr9:19058483 | C/A | 4.30e-04 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | BRCA | rs150852615 | chr9:19058483 | C/A | 4.12e-12 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | BRCA | rs150852615 | chr9:19058483 | C/A | 4.12e-12 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | BRCA | rs10511670 | chr9:19058743 | C/G | 4.68e-05 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | BRCA | rs10511670 | chr9:19058743 | C/G | 4.68e-05 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | BRCA | rs10511671 | chr9:19058821 | A/G | 1.68e-04 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | BRCA | rs10511671 | chr9:19058821 | A/G | 1.68e-04 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | KIRP | rs11515236 | chr9:19058425 | G/A | 1.99e-05 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | KIRP | rs11515236 | chr9:19058425 | G/A | 2.00e-05 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | KIRC | rs150852615 | chr9:19058483 | C/A | 4.58e-09 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | KIRC | rs150852615 | chr9:19058483 | C/A | 4.61e-09 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | KIRC | rs62622380 | chr9:19058921 | G/A | 6.68e-09 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | KIRC | rs62622380 | chr9:19058921 | G/A | 6.73e-09 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | LUAD | rs150852615 | chr9:19058483 | C/A | 3.01e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | LUAD | rs150852615 | chr9:19058483 | C/A | 3.01e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | OV | rs10511671 | chr9:19058821 | A/G | 2.10e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | OV | rs10511671 | chr9:19058821 | A/G | 2.11e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | OV | rs150852615 | chr9:19058483 | C/A | 2.11e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | OV | rs150852615 | chr9:19058483 | C/A | 2.12e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | THCA | rs150852615 | chr9:19058483 | C/A | 1.51e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | THCA | rs150852615 | chr9:19058483 | C/A | 1.51e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | THCA | rs62622380 | chr9:19058921 | G/A | 1.55e-03 |
| exon_skip_502784 | 9 | 19053140:19056402:19057958:19058999:19060085:19060221 | 19057958:19058999 | ENST00000380502.3 | THCA | rs62622380 | chr9:19058921 | G/A | 1.55e-03 |
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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for HAUS6 |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for HAUS6 |
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RelatedDrugs for HAUS6 |
| 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 HAUS6 |
| 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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