NSC identifier: |
NSC 172599
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Compound name: |
7H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 4-amino-6-hydrazino-7-.beta.-D-ribofuranosyl- |
CRmiRSNP:
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Records:13
Model : M1-Allele, M2-Recessive, M3-Additive, M4-Dominant
Total:1 Current:1
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SNP:
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Records:3697
Compound |
SNP |
Significance |
OR value |
Model |
NSC 172599 |
rs967436 |
0.000204248 |
0.9142857 |
M3 |
NSC 172599 |
rs967436 |
0.000204248 |
0.9142857 |
M4 |
NSC 172599 |
rs967582 |
0.02107152 |
3.52 |
M1 |
NSC 172599 |
rs967582 |
7.86E-05 |
2.892857 |
M2 |
NSC 172599 |
rs967778 |
2.29E-05 |
1.2 |
M2 |
NSC 172599 |
rs969607 |
0.001289683 |
5 |
M2 |
NSC 172599 |
rs970039 |
1.05E-05 |
1.05 |
M2 |
NSC 172599 |
rs970337 |
1.09E-05 |
0.2857143 |
M2 |
NSC 172599 |
rs970522 |
0.000161463 |
2.285714 |
M3 |
NSC 172599 |
rs970522 |
0.000161463 |
2.285714 |
M4 |
NSC 172599 |
rs972742 |
0.000245098 |
0.84375 |
M2 |
NSC 172599 |
rs973128 |
0.03161415 |
0.3888889 |
M3 |
NSC 172599 |
rs973128 |
0.03161415 |
0.3888889 |
M4 |
NSC 172599 |
rs974283 |
0.02885464 |
0.5333333 |
M2 |
NSC 172599 |
rs974597 |
0.000757576 |
1.428571 |
M3 |
Model : M1-Allele, M2-Recessive, M3-Additive, M4-Dominant
Total:247 Current:243
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miRNA:
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Records:52
Expression pattern: Sensitivity / Resistance
Total:4 Current:1
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Gene:
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Records:2812
Compound |
Gene |
Significance |
Expression pattern |
NSC 172599 |
CLK2 |
0.001 |
Down Regulated |
NSC 172599 |
COL6A1 |
0.001 |
Up Regulated |
NSC 172599 |
COX15 |
0.001 |
Down Regulated |
NSC 172599 |
DAD1 |
0.001 |
Up Regulated |
NSC 172599 |
DDB1 |
0.001 |
Down Regulated |
NSC 172599 |
DHX9 |
0.001 |
Down Regulated |
NSC 172599 |
HBEGF |
0.001 |
Up Regulated |
NSC 172599 |
EIF4B |
0.001 |
Down Regulated |
NSC 172599 |
EMX1 |
0.001 |
Down Regulated |
NSC 172599 |
EPHX2 |
0.001 |
Down Regulated |
NSC 172599 |
ETS1 |
0.001 |
Up Regulated |
NSC 172599 |
EWSR1 |
0.001 |
Down Regulated |
NSC 172599 |
F3 |
0.001 |
Up Regulated |
NSC 172599 |
FANCC |
0.001 |
Down Regulated |
NSC 172599 |
FLOT2 |
0.001 |
Down Regulated |
Expression pattern: Sensitivity / Resistance
Total:188 Current:1
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