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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 CAMK2G |
 Gene summary |
| Gene information | Gene symbol | CAMK2G | Gene ID | 818 |
| Gene name | calcium/calmodulin dependent protein kinase II gamma | |
| Synonyms | CAMK|CAMK-II|CAMKG | |
| Cytomap | 10q22.2 | |
| Type of gene | protein-coding | |
| Description | calcium/calmodulin-dependent protein kinase type II subunit gammacaMK-II subunit gammacalcium/calmodulin-dependent protein kinase (CaM kinase) II gamma | |
| Modification date | 20180527 | |
| UniProtAcc | Q13555 | |
| Context | PubMed: CAMK2G [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 |
| CAMK2G | GO:0051259 | protein complex oligomerization | 20668654 |
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Exon skipping events across known transcript of Ensembl for CAMK2G 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 CAMK2G |
| 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 CAMK2G |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_51211 | 10 | 75574958:75575005:75576780:75576875:75577236:75577312 | 75576780:75576875 | ENSG00000148660.16 | ENST00000305762.7,ENST00000351293.3,ENST00000472912.1,ENST00000474131.1,ENST00000423381.1,ENST00000441192.1,ENST00000322680.3,ENST00000372765.1,ENST00000433289.1,ENST00000394762.2,ENST00000322635.3 |
| exon_skip_51213 | 10 | 75577236:75577312:75577966:75578653:75579289:75579375 | 75577966:75578653 | ENSG00000148660.16 | ENST00000472912.1 |
| exon_skip_51215 | 10 | 75577236:75577312:75579289:75579375:75581439:75581488 | 75579289:75579375 | ENSG00000148660.16 | ENST00000474131.1 |
| exon_skip_51216 | 10 | 75577236:75577312:75579289:75579403:75581439:75581488 | 75579289:75579403 | ENSG00000148660.16 | ENST00000423381.1,ENST00000441192.1,ENST00000322680.3,ENST00000394762.2 |
| exon_skip_51218 | 10 | 75581439:75581488:75583797:75583842:75585036:75585105 | 75583797:75583842 | ENSG00000148660.16 | ENST00000305762.7,ENST00000472912.1,ENST00000444854.2,ENST00000423381.1,ENST00000441192.1,ENST00000322680.3,ENST00000433289.1 |
| exon_skip_51219 | 10 | 75581439:75581488:75583797:75583842:75587846:75587879 | 75583797:75583842 | ENSG00000148660.16 | ENST00000322635.3 |
| exon_skip_51220 | 10 | 75581439:75581488:75583797:75583842:75597225:75597269 | 75583797:75583842 | ENSG00000148660.16 | ENST00000351293.3,ENST00000372765.1,ENST00000394762.2 |
| exon_skip_51228 | 10 | 75583797:75583842:75585036:75585105:75587846:75587879 | 75585036:75585105 | ENSG00000148660.16 | ENST00000305762.7,ENST00000423381.1 |
| exon_skip_51230 | 10 | 75583797:75583842:75585036:75585105:75597225:75597269 | 75585036:75585105 | ENSG00000148660.16 | ENST00000472912.1,ENST00000444854.2,ENST00000441192.1,ENST00000322680.3,ENST00000433289.1 |
| exon_skip_51233 | 10 | 75583797:75583842:75585078:75585105:75597225:75597269 | 75585078:75585105 | ENSG00000148660.16 | ENST00000474131.1 |
| exon_skip_51234 | 10 | 75583797:75583842:75587846:75587879:75597225:75597269 | 75587846:75587879 | ENSG00000148660.16 | ENST00000322635.3 |
| exon_skip_51236 | 10 | 75585078:75585105:75587846:75587879:75597225:75597269 | 75587846:75587879 | ENSG00000148660.16 | ENST00000305762.7,ENST00000423381.1 |
| exon_skip_51238 | 10 | 75597225:75597269:75599296:75599359:75601926:75601969 | 75599296:75599359 | ENSG00000148660.16 | ENST00000472912.1,ENST00000423381.1,ENST00000372765.1,ENST00000322635.3 |
| exon_skip_51239 | 10 | 75602215:75602299:75606982:75607105:75607745:75607770 | 75606982:75607105 | ENSG00000148660.16 | ENST00000305762.7,ENST00000351293.3,ENST00000472912.1,ENST00000492020.1,ENST00000423381.1,ENST00000441192.1,ENST00000322680.3,ENST00000372765.1,ENST00000433289.1,ENST00000394762.2,ENST00000322635.3 |
| exon_skip_51243 | 10 | 75606982:75607105:75607745:75607840:75608283:75608367 | 75607745:75607840 | ENSG00000148660.16 | ENST00000477652.1,ENST00000305762.7,ENST00000351293.3,ENST00000472912.1,ENST00000423381.1,ENST00000322680.3,ENST00000372765.1,ENST00000433289.1,ENST00000394762.2,ENST00000322635.3 |
| exon_skip_51247 | 10 | 75607745:75607840:75608283:75608367:75608770:75608873 | 75608283:75608367 | ENSG00000148660.16 | ENST00000477652.1,ENST00000305762.7,ENST00000351293.3,ENST00000472912.1,ENST00000423381.1,ENST00000322680.3,ENST00000372765.1,ENST00000433289.1,ENST00000394762.2,ENST00000322635.3 |
| exon_skip_51248 | 10 | 75609018:75609091:75612011:75612077:75612949:75613004 | 75612011:75612077 | ENSG00000148660.16 | ENST00000305762.7,ENST00000351293.3,ENST00000423381.1,ENST00000322680.3,ENST00000372765.1,ENST00000433289.1,ENST00000394762.2,ENST00000322635.3 |
| exon_skip_51251 | 10 | 75612011:75612077:75612949:75613004:75620587:75620612 | 75612949:75613004 | ENSG00000148660.16 | ENST00000305762.7,ENST00000351293.3,ENST00000423381.1,ENST00000322680.3,ENST00000372765.1,ENST00000433289.1,ENST00000394762.2,ENST00000322635.3 |
| exon_skip_51257 | 10 | 75632746:75632841:75633147:75633281:75634154:75634219 | 75633147:75633281 | ENSG00000148660.16 | ENST00000472912.1 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for CAMK2G |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_51211 | 10 | 75574958:75575005:75576780:75576875:75577236:75577312 | 75576780:75576875 | ENSG00000148660.16 | ENST00000351293.3,ENST00000322635.3,ENST00000423381.1,ENST00000322680.3,ENST00000394762.2,ENST00000433289.1,ENST00000305762.7,ENST00000372765.1,ENST00000441192.1,ENST00000472912.1,ENST00000474131.1 |
| exon_skip_51213 | 10 | 75577236:75577312:75577966:75578653:75579289:75579375 | 75577966:75578653 | ENSG00000148660.16 | ENST00000472912.1 |
| exon_skip_51215 | 10 | 75577236:75577312:75579289:75579375:75581439:75581488 | 75579289:75579375 | ENSG00000148660.16 | ENST00000474131.1 |
| exon_skip_51216 | 10 | 75577236:75577312:75579289:75579403:75581439:75581488 | 75579289:75579403 | ENSG00000148660.16 | ENST00000423381.1,ENST00000322680.3,ENST00000394762.2,ENST00000441192.1 |
| exon_skip_51218 | 10 | 75581439:75581488:75583797:75583842:75585036:75585105 | 75583797:75583842 | ENSG00000148660.16 | ENST00000423381.1,ENST00000322680.3,ENST00000433289.1,ENST00000305762.7,ENST00000441192.1,ENST00000472912.1,ENST00000444854.2 |
| exon_skip_51219 | 10 | 75581439:75581488:75583797:75583842:75587846:75587879 | 75583797:75583842 | ENSG00000148660.16 | ENST00000322635.3 |
| exon_skip_51220 | 10 | 75581439:75581488:75583797:75583842:75597225:75597269 | 75583797:75583842 | ENSG00000148660.16 | ENST00000351293.3,ENST00000394762.2,ENST00000372765.1 |
| exon_skip_51228 | 10 | 75583797:75583842:75585036:75585105:75587846:75587879 | 75585036:75585105 | ENSG00000148660.16 | ENST00000423381.1,ENST00000305762.7 |
| exon_skip_51230 | 10 | 75583797:75583842:75585036:75585105:75597225:75597269 | 75585036:75585105 | ENSG00000148660.16 | ENST00000322680.3,ENST00000433289.1,ENST00000441192.1,ENST00000472912.1,ENST00000444854.2 |
| exon_skip_51233 | 10 | 75583797:75583842:75585078:75585105:75597225:75597269 | 75585078:75585105 | ENSG00000148660.16 | ENST00000474131.1 |
| exon_skip_51234 | 10 | 75583797:75583842:75587846:75587879:75597225:75597269 | 75587846:75587879 | ENSG00000148660.16 | ENST00000322635.3 |
| exon_skip_51236 | 10 | 75585078:75585105:75587846:75587879:75597225:75597269 | 75587846:75587879 | ENSG00000148660.16 | ENST00000423381.1,ENST00000305762.7 |
| exon_skip_51238 | 10 | 75597225:75597269:75599296:75599359:75601926:75601969 | 75599296:75599359 | ENSG00000148660.16 | ENST00000322635.3,ENST00000423381.1,ENST00000372765.1,ENST00000472912.1 |
| exon_skip_51239 | 10 | 75602215:75602299:75606982:75607105:75607745:75607770 | 75606982:75607105 | ENSG00000148660.16 | ENST00000351293.3,ENST00000322635.3,ENST00000423381.1,ENST00000322680.3,ENST00000394762.2,ENST00000433289.1,ENST00000305762.7,ENST00000372765.1,ENST00000441192.1,ENST00000472912.1,ENST00000492020.1 |
| exon_skip_51243 | 10 | 75606982:75607105:75607745:75607840:75608283:75608367 | 75607745:75607840 | ENSG00000148660.16 | ENST00000351293.3,ENST00000322635.3,ENST00000423381.1,ENST00000322680.3,ENST00000394762.2,ENST00000433289.1,ENST00000305762.7,ENST00000372765.1,ENST00000472912.1,ENST00000477652.1 |
| exon_skip_51247 | 10 | 75607745:75607840:75608283:75608367:75608770:75608873 | 75608283:75608367 | ENSG00000148660.16 | ENST00000351293.3,ENST00000322635.3,ENST00000423381.1,ENST00000322680.3,ENST00000394762.2,ENST00000433289.1,ENST00000305762.7,ENST00000372765.1,ENST00000472912.1,ENST00000477652.1 |
| exon_skip_51248 | 10 | 75609018:75609091:75612011:75612077:75612949:75613004 | 75612011:75612077 | ENSG00000148660.16 | ENST00000351293.3,ENST00000322635.3,ENST00000423381.1,ENST00000322680.3,ENST00000394762.2,ENST00000433289.1,ENST00000305762.7,ENST00000372765.1 |
| exon_skip_51251 | 10 | 75612011:75612077:75612949:75613004:75620587:75620612 | 75612949:75613004 | ENSG00000148660.16 | ENST00000351293.3,ENST00000322635.3,ENST00000423381.1,ENST00000322680.3,ENST00000394762.2,ENST00000433289.1,ENST00000305762.7,ENST00000372765.1 |
| exon_skip_51257 | 10 | 75632746:75632841:75633147:75633281:75634154:75634219 | 75633147:75633281 | ENSG00000148660.16 | ENST00000472912.1 |
| 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 CAMK2G |
| 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 |
| ENST00000423381 | 75576780 | 75576875 | Frame-shift |
| ENST00000423381 | 75607745 | 75607840 | Frame-shift |
| ENST00000423381 | 75612949 | 75613004 | Frame-shift |
| ENST00000423381 | 75579289 | 75579403 | In-frame |
| ENST00000423381 | 75583797 | 75583842 | In-frame |
| ENST00000423381 | 75585036 | 75585105 | In-frame |
| ENST00000423381 | 75587846 | 75587879 | In-frame |
| ENST00000423381 | 75599296 | 75599359 | In-frame |
| ENST00000423381 | 75606982 | 75607105 | In-frame |
| ENST00000423381 | 75608283 | 75608367 | In-frame |
| ENST00000423381 | 75612011 | 75612077 | 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 |
| ENST00000423381 | 75576780 | 75576875 | Frame-shift |
| ENST00000423381 | 75607745 | 75607840 | Frame-shift |
| ENST00000423381 | 75612949 | 75613004 | Frame-shift |
| ENST00000423381 | 75579289 | 75579403 | In-frame |
| ENST00000423381 | 75583797 | 75583842 | In-frame |
| ENST00000423381 | 75585036 | 75585105 | In-frame |
| ENST00000423381 | 75587846 | 75587879 | In-frame |
| ENST00000423381 | 75599296 | 75599359 | In-frame |
| ENST00000423381 | 75606982 | 75607105 | In-frame |
| ENST00000423381 | 75608283 | 75608367 | In-frame |
| ENST00000423381 | 75612011 | 75612077 | In-frame |
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Infer the effects of exon skipping event on protein functional features for CAMK2G |
| 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 |
| ENST00000423381 | 3925 | 558 | 75612011 | 75612077 | 400 | 465 | 92 | 113 |
| ENST00000423381 | 3925 | 558 | 75608283 | 75608367 | 642 | 725 | 172 | 200 |
| ENST00000423381 | 3925 | 558 | 75606982 | 75607105 | 821 | 943 | 232 | 273 |
| ENST00000423381 | 3925 | 558 | 75599296 | 75599359 | 1071 | 1133 | 315 | 336 |
| ENST00000423381 | 3925 | 558 | 75587846 | 75587879 | 1178 | 1210 | 351 | 362 |
| ENST00000423381 | 3925 | 558 | 75585036 | 75585105 | 1211 | 1279 | 362 | 385 |
| ENST00000423381 | 3925 | 558 | 75583797 | 75583842 | 1280 | 1324 | 385 | 400 |
| ENST00000423381 | 3925 | 558 | 75579289 | 75579403 | 1374 | 1487 | 416 | 454 |
| 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 |
| ENST00000423381 | 3925 | 558 | 75612011 | 75612077 | 400 | 465 | 92 | 113 |
| ENST00000423381 | 3925 | 558 | 75608283 | 75608367 | 642 | 725 | 172 | 200 |
| ENST00000423381 | 3925 | 558 | 75606982 | 75607105 | 821 | 943 | 232 | 273 |
| ENST00000423381 | 3925 | 558 | 75599296 | 75599359 | 1071 | 1133 | 315 | 336 |
| ENST00000423381 | 3925 | 558 | 75587846 | 75587879 | 1178 | 1210 | 351 | 362 |
| ENST00000423381 | 3925 | 558 | 75585036 | 75585105 | 1211 | 1279 | 362 | 385 |
| ENST00000423381 | 3925 | 558 | 75583797 | 75583842 | 1280 | 1324 | 385 | 400 |
| ENST00000423381 | 3925 | 558 | 75579289 | 75579403 | 1374 | 1487 | 416 | 454 |
| 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 CAMK2G |
| - 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. |
CAMK2G_COAD_exon_skip_51251_psi_boxplot.png |
CAMK2G_SARC_exon_skip_51238_psi_boxplot.png |
CAMK2G_STAD_exon_skip_51251_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_51228 exon_skip_51233 exon_skip_51230 | 75585037 | 75585105 | 75585086 | 75585086 | Frame_Shift_Del | T | - | p.N369fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_51228 exon_skip_51233 exon_skip_51230 | 75585079 | 75585105 | 75585086 | 75585086 | Frame_Shift_Del | T | - | p.N369fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_51247 | 75608284 | 75608367 | 75608352 | 75608352 | Frame_Shift_Del | G | - | p.P178fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_51247 | 75608284 | 75608367 | 75608363 | 75608363 | Frame_Shift_Del | A | - | p.F174fs |
| SARC | TCGA-3B-A9HT-01 | exon_skip_51238 | 75599297 | 75599359 | 75599351 | 75599351 | Nonsense_Mutation | G | A | p.Q319* |
| UCEC | TCGA-B5-A11H-01 | exon_skip_51239 | 75606983 | 75607105 | 75606989 | 75606989 | Nonsense_Mutation | C | T | p.W271* |
| SKCM | TCGA-EE-A20H-06 | exon_skip_51239 | 75606983 | 75607105 | 75607051 | 75607051 | Nonsense_Mutation | G | A | p.Q251* |
| SKCM | TCGA-EE-A20H-06 | exon_skip_51239 | 75606983 | 75607105 | 75607051 | 75607051 | Nonsense_Mutation | G | A | p.Q251X |
| UCEC | TCGA-AP-A056-01 | exon_skip_51239 | 75606983 | 75607105 | 75607064 | 75607064 | Nonsense_Mutation | C | A | p.E25* |
| UCEC | TCGA-BG-A0M4-01 | exon_skip_51228 exon_skip_51233 exon_skip_51230 | 75585037 | 75585105 | 75585106 | 75585106 | Splice_Site | C | T | e14-1 |
| UCEC | TCGA-BG-A0M4-01 | exon_skip_51228 exon_skip_51233 exon_skip_51230 | 75585037 | 75585105 | 75585106 | 75585106 | Splice_Site | C | T | p.P323_splice |
| UCEC | TCGA-BG-A0M4-01 | exon_skip_51228 exon_skip_51233 exon_skip_51230 | 75585079 | 75585105 | 75585106 | 75585106 | Splice_Site | C | T | e14-1 |
| UCEC | TCGA-BG-A0M4-01 | exon_skip_51228 exon_skip_51233 exon_skip_51230 | 75585079 | 75585105 | 75585106 | 75585106 | Splice_Site | C | T | p.P323_splice |
| STAD | TCGA-CG-4441-01 | exon_skip_51251 | 75612950 | 75613004 | 75612948 | 75612948 | Splice_Site | A | G | p.L84_splice |
| COAD | TCGA-AA-3713-01 | exon_skip_51251 | 75612950 | 75613004 | 75613005 | 75613005 | Splice_Site | C | T | . |
| - Depth of coverage in the three exons composing exon skipping event |
| Depth of coverage in three exons | Mutation description |
 | Sample: TCGA-AA-3713-01 |
| Cancer type: COAD | |
| ESID: exon_skip_51251 | |
| Skipped exon start: 75612950 | |
| Skipped exon end: 75613004 | |
| Mutation start: 75613005 | |
| Mutation end: 75613005 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
exon_skip_133096_COAD_TCGA-AA-3713-01.png | |
exon_skip_26067_COAD_TCGA-AA-3713-01.png | |
exon_skip_37475_COAD_TCGA-AA-3713-01.png | |
exon_skip_450406_COAD_TCGA-AA-3713-01.png | |
exon_skip_461886_COAD_TCGA-AA-3713-01.png | |
exon_skip_468121_COAD_TCGA-AA-3713-01.png | |
exon_skip_489166_COAD_TCGA-AA-3713-01.png | |
exon_skip_49506_COAD_TCGA-AA-3713-01.png | |
exon_skip_51251_COAD_TCGA-AA-3713-01.png | |
exon_skip_517478_COAD_TCGA-AA-3713-01.png | |
exon_skip_62245_COAD_TCGA-AA-3713-01.png | |
exon_skip_73552_COAD_TCGA-AA-3713-01.png | |
 | Sample: TCGA-3B-A9HT-01 |
| Cancer type: SARC | |
| ESID: exon_skip_51238 | |
| Skipped exon start: 75599297 | |
| Skipped exon end: 75599359 | |
| Mutation start: 75599351 | |
| Mutation end: 75599351 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q319* | |
exon_skip_141552_SARC_TCGA-3B-A9HT-01.png | |
exon_skip_286384_SARC_TCGA-3B-A9HT-01.png | |
exon_skip_377825_SARC_TCGA-3B-A9HT-01.png | |
exon_skip_51238_SARC_TCGA-3B-A9HT-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 |
| HT55_LARGE_INTESTINE | 75576781 | 75576875 | 75576826 | 75576826 | Missense_Mutation | T | A | p.N404Y |
| SU8686_PANCREAS | 75579290 | 75579375 | 75579349 | 75579349 | Missense_Mutation | C | A | p.R435L |
| SU8686_PANCREAS | 75579290 | 75579403 | 75579349 | 75579349 | Missense_Mutation | C | A | p.R435L |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75579290 | 75579375 | 75579353 | 75579353 | Missense_Mutation | A | G | p.S434P |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75579290 | 75579403 | 75579353 | 75579353 | Missense_Mutation | A | G | p.S434P |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75579290 | 75579375 | 75579373 | 75579373 | Missense_Mutation | G | A | p.S427L |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75579290 | 75579403 | 75579373 | 75579373 | Missense_Mutation | G | A | p.S427L |
| SUPM2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 75579290 | 75579403 | 75579394 | 75579394 | Missense_Mutation | A | G | p.L420P |
| HCC1569_BREAST | 75583798 | 75583842 | 75583804 | 75583804 | Missense_Mutation | C | G | p.D167H |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75583798 | 75583842 | 75583816 | 75583816 | Missense_Mutation | G | A | p.R163C |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75583798 | 75583842 | 75583828 | 75583828 | Missense_Mutation | A | G | p.C159R |
| MESSA_SOFT_TISSUE | 75583798 | 75583842 | 75583836 | 75583836 | Missense_Mutation | G | C | p.Q333E |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75583798 | 75583842 | 75583840 | 75583840 | Missense_Mutation | C | T | p.A155T |
| SNU1040_LARGE_INTESTINE | 75585037 | 75585105 | 75585056 | 75585056 | Missense_Mutation | G | A | p.A358V |
| NCIH524_LUNG | 75585037 | 75585105 | 75585057 | 75585057 | Missense_Mutation | C | T | p.A358T |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75585037 | 75585105 | 75585058 | 75585058 | Missense_Mutation | G | A | p.R147C |
| DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 75585037 | 75585105 | 75585058 | 75585058 | Missense_Mutation | G | A | p.R147C |
| DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 75585037 | 75585105 | 75585058 | 75585058 | Missense_Mutation | G | A | p.R147C |
| FTC133_THYROID | 75599297 | 75599359 | 75599324 | 75599324 | Missense_Mutation | C | T | p.A328T |
| HEC1A_ENDOMETRIUM | 75599297 | 75599359 | 75599336 | 75599336 | Missense_Mutation | C | T | p.A324T |
| HEC1B_ENDOMETRIUM | 75599297 | 75599359 | 75599336 | 75599336 | Missense_Mutation | C | T | p.A324T |
| LNCAPCLONEFGC_PROSTATE | 75606983 | 75607105 | 75607006 | 75607006 | Missense_Mutation | C | T | p.A266T |
| SNU1040_LARGE_INTESTINE | 75612012 | 75612077 | 75612070 | 75612070 | Missense_Mutation | C | T | p.G95S |
| SNU1040_LARGE_INTESTINE | 75612950 | 75613004 | 75613001 | 75613001 | Missense_Mutation | C | T | p.R75H |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 75583798 | 75583842 | 75583819 | 75583819 | Nonsense_Mutation | G | A | p.Q162* |
| MEWO_SKIN | 75576781 | 75576875 | 75576781 | 75576781 | Splice_Site | G | A | p.L419F |
| HPBALL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 75608284 | 75608367 | 75608285 | 75608285 | Splice_Site | G | A | p.C200C |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for CAMK2G |
| 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 CAMK2G |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for CAMK2G |
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RelatedDrugs for CAMK2G |
| 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 |
| Q13555 | DB06616 | Bosutinib | Calcium/calmodulin-dependent protein kinase type II subunit gamma | small molecule | approved | |
| Q13555 | DB12010 | Fostamatinib | Calcium/calmodulin-dependent protein kinase type II subunit gamma | small molecule | approved|investigational |
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RelatedDiseases for CAMK2G |
| Diseases associated with this gene. (DisGeNet 4.0) |
| Gene | Disease ID | Disease name | # pubmeds | Source |
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