SomamiR DB 2.0
Somatic mutations altering microRNA-ceRNA interactions
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PolymiRTS Database
Prediction criteria: TargetScan sites only     All 6mer or longer seed matches
Transcript ID: NM_001040664
Gene Symbol: PPAN-P2RY11

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr19:g.10110803G>A COSM1524109 TCGA-55-6982-01 [lung][right_lower_lobe][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6853-3p ggacgatAATGAACa UGUUCAUU m7b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-136-3p ggaCGATGATGaaca CAUCAUCG m8a Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4528 ggacgATAATGAaca UCAUUAUA m7a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6853-3p ggacgatAATGAACa UGUUCAUU m7b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-136-3p ggaCGATGATGaaca CAUCAUCG m8a Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4528 ggacgATAATGAaca UCAUUAUA m7a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374

Mutation Mutation ID Sample Name Cancer Type
chr19:g.10110800G>A COSM1390002 TCGA-AD-6889-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6852-3p tGAGGACAatgatga UGUCCUCU m7a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-676-3p tgAGGACAatgatga CUGUCCUA m6b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4289 tgaggACAATGatga GCAUUGUG m6b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-3909 tGAGGACAatgatga UGUCCUCU m7a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-2355-3p tgAGGACAATgatga AUUGUCCU m8a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-136-3p tgaggaCGATGATGa CAUCAUCG m8a Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-136-3p tgaggaCGATGATGa CAUCAUCG m8a Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-2355-3p tgAGGACAATgatga AUUGUCCU m8a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-3909 tGAGGACAatgatga UGUCCUCU m7a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4289 tgaggACAATGatga GCAUUGUG m6b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-676-3p tgAGGACAatgatga CUGUCCUA m6b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6852-3p tGAGGACAatgatga UGUCCUCU m7a Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374

Mutation Mutation ID Sample Name Cancer Type
chr19:g.10110768C>A COSM3422366 TCGA-F5-6814-01 [large_intestine][rectum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-7856-5p atcCCTTAAAggacg UUUUAAGG m7b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4635 atccCTTCAAGgacg UCUUGAAG m7b Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-7856-5p atcCCTTAAAggacg UUUUAAGG m7b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6892-5p aTCCCTTAaaggacg GUAAGGGA m7b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6864-5p atCCCTTCAAggacg UUGAAGGG m8a Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6126 atcCCTTCAaggacg GUGAAGGC m6b Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4477b atcCCTTAAaggacg AUUAAGGA m6b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-3179 atCCCTTCaaggacg AGAAGGGG m6b Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6892-5p aTCCCTTAaaggacg GUAAGGGA m7b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6864-5p atCCCTTCAAggacg UUGAAGGG m8a Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-6126 atcCCTTCAaggacg GUGAAGGC m6b Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4635 atccCTTCAAGgacg UCUUGAAG m7b Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-4477b atcCCTTAAaggacg AUUAAGGA m6b Created HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374
hsa-miR-3179 atCCCTTCaaggacg AGAAGGGG m6b Disrupted HHHNE_14000_PPAN-P2RY11|NM_001040664|exon_CDS|-2.05628151001042|-1.23864671066374

*By default, only target sites identified by TargetScan are displayed. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.

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