Crizotinib


Curated chemical-gene interactions from CTD
Entrez gene IDGene symbolInteraction typeReference
10018 BCL2L11 Increases expression PMID:22729845
1399 CRKL Increases expression PMID:22683780
1576 CYP3A4 Increases expression PMID:23129213
2152 F3 Increases expression PMID:25569083
2194 FASN Increases expression PMID:23707608
238 ALK Decreases activity PMID:21030459; PMID:21812414; PMID:22072639; PMID:26144315; PMID:21767331; PMID:21838707; PMID:22072639; PMID:22912387; PMID:21838707; PMID:23104988
25 ABL1 Decreases activity PMID:21812414
3082 HGF Increases expression PMID:22683780
3156 HMGCR Increases expression PMID:23707608
3157 HMGCS1 Increases expression PMID:23707608
329 BIRC2 Decreases expression PMID:22729845
331 XIAP Decreases expression PMID:22729845
332 BIRC5 Decreases expression PMID:22729845
3638 INSIG1 Increases expression PMID:23707608
3757 KCNH2 Decreases activity PMID:23707608
3932 LCK Decreases activity PMID:21812414
4072 EPCAM Decreases expression PMID:22973962
4233 MET Decreases activity PMID:21266357; PMID:21405128; PMID:21812414; PMID:22948846
4233 MET Increases expression PMID:22683780
4486 MST1R Decreases activity PMID:21812414
5243 ABCB1 Decreases activity PMID:28369651
5594 MAPK1 Increases expression PMID:22683780
5595 MAPK3 Increases expression PMID:22683780
6331 SCN5A Decreases activity PMID:23707608
6721 SREBF2 Increases expression PMID:23707608
6774 STAT3 Increases expression PMID:22683780
7010 TEK Decreases activity PMID:21812414
7431 VIM Decreases expression PMID:22973962
775 CACNA1C Decreases activity PMID:23707608
836 CASP3 Increases activity PMID:23707608
840 CASP7 Increases activity PMID:23707608
8842 PROM1 Decreases expression PMID:22973962
9415 FADS2 Increases expression PMID:23707608
9429 ABCG2 Decreases activity PMID:28369651
960 CD44 Decreases expression PMID:22973962
978 CDA Decreases expression PMID:22973962

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We have built a comprehensive resource which compiles potential endocrine disrupting chemicals (EDCs) based on the observed adverse effects or endocrine-mediated endpoints in published experiments on humans or rodents to support basic research. We are not responsible for any errors or omissions in the published research articles or supporting literature on potential EDCs compiled in this resource. Users are advised to exercise their own judgement on the weight of evidence for potential EDCs compiled in this resource. Importantly, our sole goal to build this resource on potential EDCs is to enable future basic research towards better understanding of the systems-level perturbations upon chemical exposure rather than influencing regulatory advice on chemical use.