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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 MAP3K19 |
 Gene summary |
| Gene information | Gene symbol | MAP3K19 | Gene ID | 80122 |
| Gene name | mitogen-activated protein kinase kinase kinase 19 | |
| Synonyms | RCK|YSK4 | |
| Cytomap | 2q21.3 | |
| Type of gene | protein-coding | |
| Description | mitogen-activated protein kinase kinase kinase 19SPS1/STE20-related protein kinase YSK4YSK4 Sps1/Ste20-related kinase homologregulated in COPD kinaseregulated in COPD, protein kinaseyeast Sps1/Ste20-related kinase 4 | |
| Modification date | 20180523 | |
| UniProtAcc | Q56UN5 | |
| Context | PubMed: MAP3K19 [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 MAP3K19 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 MAP3K19 |
| 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 MAP3K19 |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_343714 | 2 | 135738390:135739088:135740749:135740901:135741245:135741395 | 135740749:135740901 | ENSG00000176601.7 | ENST00000315513.3,ENST00000392915.1 |
| exon_skip_343715 | 2 | 135738390:135739088:135741245:135741395:135743369:135744611 | 135741245:135741395 | ENSG00000176601.7 | ENST00000437365.1,ENST00000358371.4,ENST00000375845.3 |
| exon_skip_343720 | 2 | 135741277:135741395:135743369:135745823:135749106:135749150 | 135743369:135745823 | ENSG00000176601.7 | ENST00000315513.3,ENST00000358371.4,ENST00000392915.1,ENST00000375845.3 |
| exon_skip_343721 | 2 | 135743369:135745823:135749106:135749150:135756307:135756567 | 135749106:135749150 | ENSG00000176601.7 | ENST00000315513.3,ENST00000392915.1,ENST00000375845.3 |
| exon_skip_343722 | 2 | 135763090:135763101:135779284:135779400:135797932:135798072 | 135779284:135779400 | ENSG00000176601.7 | ENST00000414343.1 |
| exon_skip_343724 | 2 | 135779284:135779400:135787881:135788070:135797932:135798069 | 135787881:135788070 | ENSG00000176601.7 | ENST00000468155.1 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for MAP3K19 |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_343714 | 2 | 135738390:135739088:135740749:135740901:135741245:135741395 | 135740749:135740901 | ENSG00000176601.7 | ENST00000392915.1,ENST00000315513.3 |
| exon_skip_343715 | 2 | 135738390:135739088:135741245:135741395:135743369:135744611 | 135741245:135741395 | ENSG00000176601.7 | ENST00000375845.3,ENST00000358371.4,ENST00000437365.1 |
| exon_skip_343720 | 2 | 135741277:135741395:135743369:135745823:135749106:135749150 | 135743369:135745823 | ENSG00000176601.7 | ENST00000375845.3,ENST00000358371.4,ENST00000392915.1,ENST00000315513.3 |
| exon_skip_343721 | 2 | 135743369:135745823:135749106:135749150:135756307:135756567 | 135749106:135749150 | ENSG00000176601.7 | ENST00000375845.3,ENST00000392915.1,ENST00000315513.3 |
| exon_skip_343724 | 2 | 135779284:135779400:135787881:135788070:135797932:135798069 | 135787881:135788070 | ENSG00000176601.7 | ENST00000468155.1 |
| 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 MAP3K19 |
| 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 |
| ENST00000392915 | 135740749 | 135740901 | Frame-shift |
| ENST00000375845 | 135749106 | 135749150 | Frame-shift |
| ENST00000392915 | 135749106 | 135749150 | Frame-shift |
| ENST00000375845 | 135741245 | 135741395 | In-frame |
| ENST00000375845 | 135743369 | 135745823 | In-frame |
| ENST00000392915 | 135743369 | 135745823 | 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 |
| ENST00000392915 | 135740749 | 135740901 | Frame-shift |
| ENST00000375845 | 135749106 | 135749150 | Frame-shift |
| ENST00000392915 | 135749106 | 135749150 | Frame-shift |
| ENST00000375845 | 135741245 | 135741395 | In-frame |
| ENST00000375845 | 135743369 | 135745823 | In-frame |
| ENST00000392915 | 135743369 | 135745823 | In-frame |
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Infer the effects of exon skipping event on protein functional features for MAP3K19 |
| 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 |
| ENST00000375845 | 4394 | 1328 | 135743369 | 135745823 | 650 | 3103 | 206 | 1024 |
| ENST00000392915 | 4367 | 1328 | 135743369 | 135745823 | 790 | 3243 | 223 | 1041 |
| ENST00000375845 | 4394 | 1328 | 135741245 | 135741395 | 3104 | 3253 | 1024 | 1074 |
| 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 |
| ENST00000375845 | 4394 | 1328 | 135743369 | 135745823 | 650 | 3103 | 206 | 1024 |
| ENST00000392915 | 4367 | 1328 | 135743369 | 135745823 | 790 | 3243 | 223 | 1041 |
| ENST00000375845 | 4394 | 1328 | 135741245 | 135741395 | 3104 | 3253 | 1024 | 1074 |
| 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 MAP3K19 |
| - 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-G3-A3CJ-01 | exon_skip_343714 | 135740750 | 135740901 | 135740810 | 135740810 | Frame_Shift_Del | T | - | p.K1122fs |
| STAD | TCGA-FP-A4BE-01 | exon_skip_343720 | 135743370 | 135745823 | 135743471 | 135743471 | Frame_Shift_Del | T | - | p.M991fs |
| SARC | TCGA-IS-A3K6-01 | exon_skip_343720 | 135743370 | 135745823 | 135744087 | 135744087 | Frame_Shift_Del | G | - | p.M786fs |
| SARC | TCGA-IS-A3K6-01 | exon_skip_343720 | 135743370 | 135745823 | 135744087 | 135744087 | Frame_Shift_Del | G | - | p.P785fs |
| LIHC | TCGA-G3-A3CJ-01 | exon_skip_343720 | 135743370 | 135745823 | 135744281 | 135744281 | Frame_Shift_Del | T | - | p.T721fs |
| LIHC | TCGA-G3-A3CJ-01 | exon_skip_343720 | 135743370 | 135745823 | 135744786 | 135744786 | Frame_Shift_Del | A | - | p.F552fs |
| LIHC | TCGA-G3-A3CJ-01 | exon_skip_343720 | 135743370 | 135745823 | 135745522 | 135745522 | Frame_Shift_Del | T | - | p.N307fs |
| SKCM | TCGA-EE-A3JA-06 | exon_skip_343714 | 135740750 | 135740901 | 135740840 | 135740840 | Nonsense_Mutation | C | T | p.W1112* |
| SKCM | TCGA-EE-A3AG-06 | exon_skip_343714 | 135740750 | 135740901 | 135740892 | 135740892 | Nonsense_Mutation | G | A | p.Q1095* |
| STAD | TCGA-BR-8680-01 | exon_skip_343715 | 135741246 | 135741395 | 135741299 | 135741299 | Nonsense_Mutation | C | A | p.E1057X |
| CESC | TCGA-IR-A3LA-01 | exon_skip_343720 | 135743370 | 135745823 | 135744028 | 135744028 | Nonsense_Mutation | G | C | p.S805* |
| UCS | TCGA-N8-A4PN-01 | exon_skip_343720 | 135743370 | 135745823 | 135745259 | 135745259 | Nonsense_Mutation | G | A | p.Q395* |
| UCS | TCGA-N8-A4PN-01 | exon_skip_343720 | 135743370 | 135745823 | 135745259 | 135745259 | Nonsense_Mutation | G | A | p.Q395X |
| LGG | TCGA-CS-5395-01 | exon_skip_343720 | 135743370 | 135745823 | 135745373 | 135745373 | Nonsense_Mutation | G | A | p.R357* |
| LGG | TCGA-CS-5395-01 | exon_skip_343720 | 135743370 | 135745823 | 135745373 | 135745373 | Nonsense_Mutation | G | A | p.R357X |
| THCA | TCGA-ET-A25J-01 | exon_skip_343720 | 135743370 | 135745823 | 135745373 | 135745373 | Nonsense_Mutation | G | A | p.R357* |
| THCA | TCGA-ET-A25J-01 | exon_skip_343720 | 135743370 | 135745823 | 135745373 | 135745373 | Nonsense_Mutation | G | A | p.R357X |
| UCS | TCGA-N9-A4Q4-01 | exon_skip_343720 | 135743370 | 135745823 | 135745373 | 135745373 | Nonsense_Mutation | G | A | p.R357* |
| UCS | TCGA-N9-A4Q4-01 | exon_skip_343720 | 135743370 | 135745823 | 135745373 | 135745373 | Nonsense_Mutation | G | A | p.R357X |
| KIRC | TCGA-B8-A8YJ-01 | exon_skip_343720 | 135743370 | 135745823 | 135745518 | 135745518 | Nonsense_Mutation | C | T | p.W308X |
| SKCM | TCGA-FR-A8YC-06 | exon_skip_343720 | 135743370 | 135745823 | 135745518 | 135745518 | Nonsense_Mutation | C | T | p.W308* |
| KIRP | TCGA-2Z-A9JQ-01 | exon_skip_343722 | 135779285 | 135779400 | 135779307 | 135779307 | Nonsense_Mutation | A | T | p.L39X |
| - 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 |
| IMR32_AUTONOMIC_GANGLIA | 135741246 | 135741395 | 135741265 | 135741265 | Frame_Shift_Del | C | - | p.G1068fs |
| OVK18_OVARY | 135743370 | 135745823 | 135743471 | 135743471 | Frame_Shift_Del | T | - | p.M991fs |
| 253J_URINARY_TRACT | 135743370 | 135745823 | 135743731 | 135743734 | Frame_Shift_Del | GTAA | - | p.LT903fs |
| 253JBV_URINARY_TRACT | 135743370 | 135745823 | 135743731 | 135743734 | Frame_Shift_Del | GTAA | - | p.LT903fs |
| SNU119_OVARY | 135743370 | 135745823 | 135743940 | 135743953 | Frame_Shift_Del | GAGGCTTGTGGTGA | - | p.LTTSL830fs |
| KMS21BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135744280 | 135744281 | Frame_Shift_Ins | - | T | p.T721fs |
| HUH1_LIVER | 135779285 | 135779400 | 135779321 | 135779322 | Frame_Shift_Ins | - | T | p.N34fs |
| DU145_PROSTATE | 135741246 | 135741395 | 135741313 | 135741313 | Missense_Mutation | C | T | p.S1052N |
| DM3_FIBROBLAST | 135741246 | 135741395 | 135741367 | 135741367 | Missense_Mutation | T | A | p.D1034V |
| LS411N_LARGE_INTESTINE | 135743370 | 135745823 | 135743410 | 135743410 | Missense_Mutation | G | T | p.P1011Q |
| SW684_SOFT_TISSUE | 135743370 | 135745823 | 135743428 | 135743428 | Missense_Mutation | C | T | p.R1005K |
| MDAPCA2B_PROSTATE | 135743370 | 135745823 | 135743452 | 135743452 | Missense_Mutation | G | T | p.P997H |
| SJSA1_BONE | 135743370 | 135745823 | 135743504 | 135743504 | Missense_Mutation | G | T | p.L980I |
| HEC251_ENDOMETRIUM | 135743370 | 135745823 | 135743586 | 135743586 | Missense_Mutation | A | C | p.I952M |
| LI7_LIVER | 135743370 | 135745823 | 135743605 | 135743605 | Missense_Mutation | A | G | p.L946S |
| MFE296_ENDOMETRIUM | 135743370 | 135745823 | 135743683 | 135743683 | Missense_Mutation | T | C | p.Y920C |
| WM88_SKIN | 135743370 | 135745823 | 135743698 | 135743698 | Missense_Mutation | G | A | p.A915V |
| HEC1A_ENDOMETRIUM | 135743370 | 135745823 | 135743698 | 135743698 | Missense_Mutation | G | A | p.A915V |
| HEC251_ENDOMETRIUM | 135743370 | 135745823 | 135743788 | 135743788 | Missense_Mutation | C | T | p.R885Q |
| MEWO_SKIN | 135743370 | 135745823 | 135743788 | 135743788 | Missense_Mutation | C | T | p.R885Q |
| SNU81_LARGE_INTESTINE | 135743370 | 135745823 | 135743788 | 135743788 | Missense_Mutation | C | T | p.R885Q |
| DSH1_URINARY_TRACT | 135743370 | 135745823 | 135743851 | 135743851 | Missense_Mutation | G | T | p.S864Y |
| FTC238_THYROID | 135743370 | 135745823 | 135743863 | 135743863 | Missense_Mutation | C | A | p.S860I |
| MRKNU1_BREAST | 135743370 | 135745823 | 135743887 | 135743887 | Missense_Mutation | G | A | p.S852L |
| EFM192A_BREAST | 135743370 | 135745823 | 135743914 | 135743914 | Missense_Mutation | A | C | p.L843R |
| SW684_SOFT_TISSUE | 135743370 | 135745823 | 135744037 | 135744037 | Missense_Mutation | G | A | p.P802L |
| MCAS_OVARY | 135743370 | 135745823 | 135744092 | 135744092 | Missense_Mutation | G | T | p.H784N |
| PACADD137_PANCREAS | 135743370 | 135745823 | 135744167 | 135744167 | Missense_Mutation | C | A | p.G759C |
| CA922_UPPER_AERODIGESTIVE_TRACT | 135743370 | 135745823 | 135744197 | 135744197 | Missense_Mutation | C | G | p.V749L |
| NB13_AUTONOMIC_GANGLIA | 135743370 | 135745823 | 135744261 | 135744261 | Missense_Mutation | C | A | p.K727N |
| LS411N_LARGE_INTESTINE | 135743370 | 135745823 | 135744265 | 135744265 | Missense_Mutation | G | A | p.P726L |
| EW3_BONE | 135743370 | 135745823 | 135744273 | 135744273 | Missense_Mutation | C | T | p.M723I |
| SNU899_UPPER_AERODIGESTIVE_TRACT | 135743370 | 135745823 | 135744277 | 135744277 | Missense_Mutation | T | C | p.H722R |
| ISHIKAWAHERAKLIO02ER_ENDOMETRIUM | 135743370 | 135745823 | 135744304 | 135744304 | Missense_Mutation | C | A | p.R713I |
| HEC251_ENDOMETRIUM | 135743370 | 135745823 | 135744343 | 135744343 | Missense_Mutation | T | C | p.K700R |
| CI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135744357 | 135744357 | Missense_Mutation | T | G | p.R695S |
| L33_PANCREAS | 135743370 | 135745823 | 135744434 | 135744434 | Missense_Mutation | C | T | p.V670I |
| MDAMB231_BREAST | 135743370 | 135745823 | 135744526 | 135744526 | Missense_Mutation | A | C | p.L639R |
| YT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135744535 | 135744535 | Missense_Mutation | T | C | p.E636G |
| RERFLCKJ_LUNG | 135743370 | 135745823 | 135744554 | 135744554 | Missense_Mutation | G | A | p.L630F |
| HCT15_LARGE_INTESTINE | 135743370 | 135745823 | 135744598 | 135744598 | Missense_Mutation | G | T | p.P615H |
| MM370_SKIN | 135743370 | 135745823 | 135744670 | 135744670 | Missense_Mutation | T | A | p.Q591L |
| SNU719_STOMACH | 135743370 | 135745823 | 135744836 | 135744836 | Missense_Mutation | T | A | p.S536C |
| SW48_LARGE_INTESTINE | 135743370 | 135745823 | 135744838 | 135744838 | Missense_Mutation | C | A | p.R535M |
| MHHPREB1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135744838 | 135744838 | Missense_Mutation | C | T | p.R535K |
| HEC251_ENDOMETRIUM | 135743370 | 135745823 | 135744917 | 135744917 | Missense_Mutation | T | C | p.K509E |
| JEKO1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135744968 | 135744968 | Missense_Mutation | C | A | p.D492Y |
| RERFLCMS_LUNG | 135743370 | 135745823 | 135745024 | 135745024 | Missense_Mutation | C | T | p.R473K |
| KYSE520_OESOPHAGUS | 135743370 | 135745823 | 135745066 | 135745066 | Missense_Mutation | C | T | p.C459Y |
| ECC12_STOMACH | 135743370 | 135745823 | 135745066 | 135745066 | Missense_Mutation | C | T | p.C459Y |
| AGS_STOMACH | 135743370 | 135745823 | 135745123 | 135745123 | Missense_Mutation | A | G | p.L440P |
| SW684_SOFT_TISSUE | 135743370 | 135745823 | 135745166 | 135745166 | Missense_Mutation | C | T | p.E426K |
| KE39_STOMACH | 135743370 | 135745823 | 135745237 | 135745237 | Missense_Mutation | A | T | p.I402K |
| SNU81_LARGE_INTESTINE | 135743370 | 135745823 | 135745274 | 135745274 | Missense_Mutation | T | C | p.I390V |
| JHUEM7_ENDOMETRIUM | 135743370 | 135745823 | 135745361 | 135745361 | Missense_Mutation | C | T | p.E361K |
| LAN6_AUTONOMIC_GANGLIA | 135743370 | 135745823 | 135745372 | 135745372 | Missense_Mutation | C | A | p.R357L |
| HS616T_FIBROBLAST | 135743370 | 135745823 | 135745375 | 135745375 | Missense_Mutation | G | A | p.T356M |
| CROAP3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135745424 | 135745424 | Missense_Mutation | T | C | p.N340D |
| G361_SKIN | 135743370 | 135745823 | 135745570 | 135745570 | Missense_Mutation | G | A | p.S291F |
| RD_SOFT_TISSUE | 135743370 | 135745823 | 135745633 | 135745633 | Missense_Mutation | T | A | p.K270M |
| JHUEM7_ENDOMETRIUM | 135743370 | 135745823 | 135745645 | 135745645 | Missense_Mutation | C | T | p.G266E |
| GP5D_LARGE_INTESTINE | 135743370 | 135745823 | 135745654 | 135745654 | Missense_Mutation | T | C | p.E263G |
| JHUEM7_ENDOMETRIUM | 135743370 | 135745823 | 135745655 | 135745655 | Missense_Mutation | C | T | p.E263K |
| HEC251_ENDOMETRIUM | 135743370 | 135745823 | 135745789 | 135745789 | Missense_Mutation | C | T | p.R218Q |
| SNU81_LARGE_INTESTINE | 135743370 | 135745823 | 135745789 | 135745789 | Missense_Mutation | C | T | p.R218Q |
| HEC108_ENDOMETRIUM | 135743370 | 135745823 | 135745792 | 135745792 | Missense_Mutation | G | A | p.T217M |
| CA46_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135745817 | 135745817 | Missense_Mutation | G | T | p.L209M |
| MZ7MEL_SKIN | 135749107 | 135749150 | 135749120 | 135749120 | Missense_Mutation | C | T | p.G202D |
| JHUEM7_ENDOMETRIUM | 135779285 | 135779400 | 135779352 | 135779352 | Missense_Mutation | G | T | p.S24Y |
| HELA_CERVIX | 135779285 | 135779400 | 135779394 | 135779394 | Missense_Mutation | T | G | p.H10P |
| SNU81_LARGE_INTESTINE | 135741246 | 135741395 | 135741338 | 135741338 | Nonsense_Mutation | C | A | p.E1044* |
| SNU81_LARGE_INTESTINE | 135743370 | 135745823 | 135743579 | 135743579 | Nonsense_Mutation | C | A | p.E955* |
| NCIH526_LUNG | 135743370 | 135745823 | 135743681 | 135743681 | Nonsense_Mutation | G | A | p.Q921* |
| 639V_URINARY_TRACT | 135743370 | 135745823 | 135744338 | 135744338 | Nonsense_Mutation | G | A | p.R702* |
| EMCBAC2_LUNG | 135743370 | 135745823 | 135744728 | 135744728 | Nonsense_Mutation | G | A | p.Q572* |
| NCIH2591_PLEURA | 135743370 | 135745823 | 135745373 | 135745373 | Nonsense_Mutation | G | A | p.R357* |
| L1236_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 135743370 | 135745823 | 135745736 | 135745736 | Nonsense_Mutation | T | A | p.R236* |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for MAP3K19 |
| 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 MAP3K19 |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for MAP3K19 |
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RelatedDrugs for MAP3K19 |
| 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 |
| Q56UN5 | DB12010 | Fostamatinib | Mitogen-activated protein kinase kinase kinase 19 | small molecule | approved|investigational |
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RelatedDiseases for MAP3K19 |
| Diseases associated with this gene. (DisGeNet 4.0) |
| Gene | Disease ID | Disease name | # pubmeds | Source |
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