SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions |
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RefSeq ID: | NM_000207 |
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Gene Symbol: | INS |
Description: | Homo sapiens insulin (INS), transcript variant 1, mRNA. |
Gene Location: | chr11(-):2181008-2182439 |
Browse Associations | |
Browse Pathways |
Mutation | Mutation ID | Sample Name | Cancer Type | ||||||
---|---|---|---|---|---|---|---|---|---|
chr11:g.2159809G>A | COSN1080215 | TCGA-BS-A0UV-01 | [endometrium][NS][carcinoma][endometrioid_carcinoma] | ||||||
miRNA Targets Table | |||||||||
miR ID | miRSite | Conservation | miRSeed | SeedClass | FuncClass | Wildtype CS+ | Mutant CS+ | PITA score change | |
hsa-miR-1250 |
tcctGCACCGagagagatg |
0 | ACGGUGCU | m6b | Disrupted | -0.224000 | no TS |
19.500000 |
|
hsa-miR-3615 |
tcctgcaCCGAGAGAgatg |
0 | UCUCUCGG | m8a | Disrupted | -0.517000 | no TS |
14.550000 |
|
hsa-miR-1250 |
tcctGCACCGagagagatg |
0 | ACGGUGCU | m6b | Disrupted | -0.224 | no TS |
19.5 |
|
hsa-miR-3615 |
tcctgcaCCGAGAGAgatg |
0 | UCUCUCGG | m8a | Disrupted | -0.517 | no TS |
14.55 |
Mutation | Mutation ID | Sample Name | Cancer Type | |||||
---|---|---|---|---|---|---|---|---|
chr11:g.2159842G>A | COSN1080214 | TCGA-AX-A0J0-01 | [endometrium][NS][carcinoma][endometrioid_carcinoma] | |||||
miRNA Targets Table | ||||||||
miR ID | miRSite | Conservation | miRSeed | SeedClass | FuncClass | Wildtype CS+ | Mutant CS+ | PITA score change |
hsa-miR-1587 |
acgCAGCCCAcaggcagcc |
0 | UUGGGCUG | m7b | (m6c->m7b) | no TS | 0.000000 | No effect |
hsa-miR-4265 |
acgcaGCCCACAGgcagcc |
0 | CUGUGGGC | m8a | Created | no TS | 0.000000 |
-1.630000 |
hsa-miR-4296 |
acgcaGCCCACAggcagcc |
0 | AUGUGGGC | m7b | Created | no TS | 0.000000 |
-1.130000 |
hsa-miR-4322 |
acgcaGCCCACAGgcagcc |
0 | CUGUGGGC | m8a | Created | no TS | 0.000000 |
-1.530000 |
hsa-miR-4417 |
acgcAGCCCACaggcagcc |
0 | GGUGGGCU | m7b | Created | no TS | 0.000000 |
-0.330000 |
hsa-miR-4734 |
acgcagCCCGCAGgcagcc |
0 | GCUGCGGG | m7b | Disrupted | 0.000000 | no TS | No effect |
hsa-miR-4763-5p |
acgcagcccGCAGGCagcc |
0 | CGCCUGCC | m6b | Disrupted | 0.000000 | no TS | No effect |
hsa-miR-4767 |
acgcaGCCCGCaggcagcc |
0 | CGCGGGCG | m6b | Disrupted | 0.000000 | no TS | No effect |
hsa-miR-1587 |
acgCAGCCCAcaggcagcc |
0 | UUGGGCUG | m7b | (m6c->m7b) | no TS | 0 | No effect |
hsa-miR-4265 |
acgcaGCCCACAGgcagcc |
0 | CUGUGGGC | m8a | Created | no TS | 0 |
-1.63 |
hsa-miR-4296 |
acgcaGCCCACAggcagcc |
0 | AUGUGGGC | m7b | Created | no TS | 0 |
-1.13 |
hsa-miR-4322 |
acgcaGCCCACAGgcagcc |
0 | CUGUGGGC | m8a | Created | no TS | 0 |
-1.53 |
hsa-miR-4417 |
acgcAGCCCACaggcagcc |
0 | GGUGGGCU | m7b | Created | no TS | 0 |
-0.33 |
hsa-miR-4734 |
acgcagCCCGCAGgcagcc |
0 | GCUGCGGG | m7b | Disrupted | 0 | no TS | No effect |
hsa-miR-4763-5p |
acgcagcccGCAGGCagcc |
0 | CGCCUGCC | m6b | Disrupted | 0 | no TS | No effect |
hsa-miR-4767 |
acgcaGCCCGCaggcagcc |
0 | CGCGGGCG | m6b | Disrupted | 0 | no TS | No effect |
Location | SNP ID | Ancestral Allele |
Allele | miR ID | Conservation | miRSite | FuncClass | Validation | context+ score change |
---|---|---|---|---|---|---|---|---|---|
2159809 | rs192030414 | - | G |
hsa-miR-1250-5p hsa-miR-3615 hsa-miR-7110-3p hsa-miR-8088 |
0 |
tGCACCGAgagag tgcaCCGAGAGAg tgcaccGAGAGAG tgcACCGAGAgag |
Unknown Unknown Unknown Unknown |
N N N N |
-0.224 -0.517 -0.181 -0.207 |
2159843 | rs3842752 | - | C |
hsa-miR-4734 hsa-miR-4767 hsa-miR-6829-5p |
1 1 0 |
gcagCCCGCAGgc gcaGCCCGCAggc GCAGCCCgcaggc |
Unknown Unknown Unknown |
N N N |
No Change No Change No Change |
T |
hsa-miR-1205 hsa-miR-6511b-5p hsa-miR-6811-5p |
1 1 1 |
gcagCCTGCAGgc gcaGCCTGCAggc gcaGCCTGCAggc |
Unknown Unknown Unknown |
N N N |
No Change No Change No Change |