NSC identifier: |
NSC 208652
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Compound name: |
5-CHLORO-6-[[(3,4-DICHLOROPHENYL)AMINO]METHYL]-2,4-QUINOZOLINEDIAMINE |
CRmiRSNP:
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Records:14
Model : M1-Allele, M2-Recessive, M3-Additive, M4-Dominant
Total:1 Current:1
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SNP:
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Records:3268
Compound |
SNP |
Significance |
OR value |
Model |
NSC 208652 |
rs1429259 |
0.004761905 |
1.25 |
M2 |
NSC 208652 |
rs1429315 |
0.00024958 |
0.2222222 |
M3 |
NSC 208652 |
rs1429315 |
0.00024958 |
0.2222222 |
M4 |
NSC 208652 |
rs1429411 |
0.000297619 |
1.041667 |
M2 |
NSC 208652 |
rs1429559 |
0.000171999 |
1.028571 |
M2 |
NSC 208652 |
rs1430219 |
0.003185023 |
7.7 |
M2 |
NSC 208652 |
rs1430242 |
0.00097855 |
2.84375 |
M2 |
NSC 208652 |
rs1430530 |
1.24E-05 |
1.571429 |
M2 |
NSC 208652 |
rs1431553 |
0.0003663 |
0.9333333 |
M2 |
NSC 208652 |
rs1431638 |
0.01577578 |
0.3214286 |
M2 |
NSC 208652 |
rs1433200 |
0.00857942 |
0.225 |
M3 |
NSC 208652 |
rs1433200 |
0.00857942 |
0.225 |
M4 |
NSC 208652 |
rs1433526 |
0.03080916 |
0.5 |
M2 |
NSC 208652 |
rs1434539 |
0.000129105 |
3.375 |
M2 |
NSC 208652 |
rs1434539 |
0.01734091 |
4.407407 |
M1 |
Model : M1-Allele, M2-Recessive, M3-Additive, M4-Dominant
Total:218 Current:29
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miRNA:
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Records:61
Expression pattern: Sensitivity / Resistance
Total:5 Current:1
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Gene:
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Records:2671
Compound |
Gene |
Significance |
Expression pattern |
NSC 208652 |
AFG3L1P |
0.001 |
Down Regulated |
NSC 208652 |
CETN2 |
0.001 |
Up Regulated |
NSC 208652 |
RCC1 |
0.001 |
Down Regulated |
NSC 208652 |
CHD4 |
0.001 |
Down Regulated |
NSC 208652 |
COL12A1 |
0.001 |
Up Regulated |
NSC 208652 |
CSF2RB |
0.001 |
Down Regulated |
NSC 208652 |
CSNK2A1 |
0.001 |
Down Regulated |
NSC 208652 |
CSRP1 |
0.001 |
Up Regulated |
NSC 208652 |
CTRL |
0.001 |
Down Regulated |
NSC 208652 |
DAG1 |
0.001 |
Up Regulated |
NSC 208652 |
DAPK3 |
0.001 |
Up Regulated |
NSC 208652 |
DARS |
0.001 |
Down Regulated |
NSC 208652 |
DHX15 |
0.001 |
Down Regulated |
NSC 208652 |
DHODH |
0.001 |
Down Regulated |
NSC 208652 |
DMBT1 |
0.001 |
Up Regulated |
Expression pattern: Sensitivity / Resistance
Total:179 Current:1
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