| Symbol: | CUTC | 
	  
      
  	  | Description: | cutC copper transporter homolog (E. coli) [Source:HGNC Symbol;Acc:24271] | 
      
  	  | Location: | Chr10:101462315-101515891[+] | 
	  
         
	   
       | CRmiRSNP:
	   
		
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      		Records:null
      		 
      			
      			
      				| Compound | CRmiRSNP | SNP_sig | Model | Molecule | Mol_sig | Type |  
      			Model : M1-Allele, M2-Recessive, M3-Additive, M4-DominantTotal:0 Current:1 
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       | Compound:
	    
		
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      		Records:251			
      		 
      			
      				| Gene | Compound | Gen_sig | Exp_pattern |  
				    | CUTC | NSC 13713 | 0.02 | Down |  
				    | CUTC | Ethanesulfonic acid, compd. with 2-[m-(4,6-diamino-2,2-dimethyl-s-triazin-1(2H)-yl)phenyl]acetanilide (1:1) | 0.015 | Down |  
				    | CUTC | TZT | 0.001 | Down |  
				    | CUTC | as-Triazine-3,5(2H,4H)-dione, 2-.beta.-D-ribofuranosyl-3-thio- | 0.001 | Down |  
				    | CUTC | OLENDRIGENIN | 0.001 | Down |  
				    | CUTC | Phosphinic amide, P,P-bis(1-aziridinyl)-N-tricyclo[3.3.1.1(3.7)]dec-1-yl- | 0.006 | Down |  
				    | CUTC | 7H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 4-amino-6-hydrazino-7-.beta.-D-ribofuranosyl- | 0.028 | Down |  
				    | CUTC | L-Aspartic acid, N-[4-[[(2-amino-4-hydroxy-6-quinazolinyl)methyl]amino]benzoyl]-, monohydrate | 0.001 | Down |  
				    | CUTC | NSC 175296 | 0.001 | Down |  
				    | CUTC | 9-METHOXYCAMPTOTHECIN | 0.025 | Down |  
				    | CUTC | 1H-Indol-2-one, 5-bromo-2,3-dihydro-3-[[(4-methoxyphenyl) carbonyl]methylene]- | 0.035 | Down |  
				    | CUTC | 5-CHLORO-6-[[(3,4-DICHLOROPHENYL)AMINO]METHYL]-2,4-QUINOZOLINEDIAMINE | 0.016 | Down |  
				    | CUTC | NSC 212446 | 0.006 | Down |  
				    | CUTC | 1,8-Octanediamine, N,N'-di-9-acridinyl- | 0.001 | Down |  
				    | CUTC | NSC 227265 | 0.002 | Down |  
			 Expression pattern: Sensitivity / Resistance 
      			Total:17 Current:2 
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       | SNP:
	   
		
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      		Records:8
      		 
      			Total:1 Current:1 
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       | miRNA:
	   
		
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      		Records:70
      		 
      			Total:5 Current:1 
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