SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions |
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RefSeq ID: | NM_002386 |
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Gene Symbol: | MC1R |
Description: | Homo sapiens melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) (MC1R), mRNA. |
Gene Location: | chr16(+):89984286-89987385 |
Browse Associations | |
Browse Pathways |
Mutation | Mutation ID | Sample Name | Cancer Type | ||||||
---|---|---|---|---|---|---|---|---|---|
chr16:g.89920464G>A | 8_1574 | 667720 | Myeloid leukemia | ||||||
miRNA Targets Table | |||||||||
miR ID | miRSite | Conservation | miRSeed | SeedClass | FuncClass | Wildtype CS+ | Mutant CS+ | PITA score change | |
hsa-miR-188-3p |
ggtTGTGGGAcctcaggct |
6 |
CUCCCACA | m7b | (m6b->m7b) | no TS | -0.085 |
-1.43 |
|
hsa-miR-4433-5p |
ggttGTGGGACctcaggct |
6 |
CGUCCCAC | m7b | Created | -0.101 | -0.288 |
-1.13 |
|
hsa-miR-4758-3p |
ggttGTGGGGCctcaggct |
6 |
UGCCCCAC | m7b | Disrupted | -0.208 | no TS |
2.86 |
|
hsa-miR-5008-5p |
ggttgtgGGGCCTCAggct |
5 |
UGAGGCCC | m8a | Disrupted | -0.73 | -0.398 |
0.75 |
Mutation | Mutation ID | Sample Name | Cancer Type | |||||
---|---|---|---|---|---|---|---|---|
chr16:g.89920872C>A | COSN1192653 | BN04T | [liver][NS][carcinoma][NS] | |||||
miRNA Targets Table | ||||||||
miR ID | miRSite | Conservation | miRSeed | SeedClass | FuncClass | Wildtype CS+ | Mutant CS+ | PITA score change |
hsa-miR-1228-5p |
tgcagcagtCGCCCAagca |
1 |
GUGGGCGG | m6b | Disrupted | -0.527000 | -0.315000 |
0.730000 |
hsa-miR-1273a |
tgcagcaGTCGCCCaagca |
0 | GGGCGACA | m7a | Disrupted | NA | NA |
2.450000 |
hsa-miR-4649-5p |
tgcagcagTCGCCCAagca |
1 |
UGGGCGAG | m7a | Disrupted | -0.230000 | no TS |
4.600000 |
hsa-miR-4674 |
tgcagcagtAGCCCAagca |
0 | CUGGGCUC | m6b | Created | no TS | -0.127000 |
-12.410000 |
hsa-miR-644b-5p |
tgcagcagTAGCCCAagca |
0 | UGGGCUAA | m7a | Created | no TS | -0.176000 |
-6.190000 |
hsa-miR-1228-5p |
tgcagcagtCGCCCAagca |
1 |
GUGGGCGG | m6b | Disrupted | -0.527000 | -0.315000 |
0.730000 |
hsa-miR-1273a |
tgcagcaGTCGCCCaagca |
0 | GGGCGACA | m7a | Disrupted | NA | NA |
2.450000 |
hsa-miR-4649-5p |
tgcagcagTCGCCCAagca |
1 |
UGGGCGAG | m7a | Disrupted | -0.230000 | no TS |
4.600000 |
hsa-miR-4674 |
tgcagcagtAGCCCAagca |
0 | CUGGGCUC | m6b | Created | no TS | -0.127000 |
-12.410000 |
hsa-miR-644b-5p |
tgcagcagTAGCCCAagca |
0 | UGGGCUAA | m7a | Created | no TS | -0.176000 |
-6.190000 |
hsa-miR-1228-5p |
tgcagcagtCGCCCAagca |
0 | GUGGGCGG | m6b | Disrupted | -0.527 | -0.315 |
0.73 |
hsa-miR-1273a |
tgcagcaGTCGCCCaagca |
0 | GGGCGACA | m7a | Disrupted | NA | NA |
2.45 |
hsa-miR-4649-5p |
tgcagcagTCGCCCAagca |
0 | UGGGCGAG | m7a | Disrupted | -0.23 | no TS |
4.6 |
hsa-miR-4674 |
tgcagcagtAGCCCAagca |
0 | CUGGGCUC | m6b | Created | no TS | -0.127 |
-12.41 |
hsa-miR-644b-5p |
tgcagcagTAGCCCAagca |
0 | UGGGCUAA | m7a | Created | no TS | -0.176 |
-6.19 |
Location | SNP ID | Ancestral Allele |
Allele | miR ID | Conservation | miRSite | FuncClass | Validation | context+ score change |
---|---|---|---|---|---|---|---|---|---|
89920519 | rs138058610 | G | G |
hsa-miR-1228-5p |
1 |
ttttCCGCCCAct |
Disrupted |
N |
-0.315 |
A |
hsa-miR-1293 hsa-miR-3148 hsa-miR-363-5p hsa-miR-4483 hsa-miR-6124 hsa-miR-6745 hsa-miR-6748-5p hsa-miR-6756-5p hsa-miR-6766-5p |
1 1 1 1 1 1 1 1 1 |
ttttCCACCCAct TTTTCCAcccact tttTCCACCCAct ttttCCACCCAct TTTTCCAcccact tttTCCACCCAct ttttcCACCCACt ttttCCACCCAct ttttCCACCCAct |
Created Created Created Created Created Created Created Created Created |
N N N N N N N N N |
-0.16 0.062 -0.399 -0.167 0.043 -0.42 -0.16 -0.13 -0.144 |
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89920793 | rs3212371 | G | A |
hsa-miR-1255b-2-3p hsa-miR-3189-5p |
0 |
AGTGGTAtggggc agtggtATGGGGC |
Created Created |
N N |
-0.077 -0.177 |
G |
hsa-miR-4758-3p |
3 |
agtggtGTGGGGC |
Disrupted |
N |
-0.206 |