Fitness for 5 genes in Escherichia coli Nissle 1917

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500 ntECOLIN_RS02970 and ECOLIN_RS02975 are separated by 59 nucleotidesECOLIN_RS02975 and ECOLIN_RS02980 are separated by 55 nucleotidesECOLIN_RS02980 and ECOLIN_RS02985 are separated by 21 nucleotidesECOLIN_RS02985 and ECOLIN_RS02990 are separated by 128 nucleotides ECOLIN_RS02970: ECOLIN_RS02970 - putative allantoin permease, at 611,650 to 613,104 _RS02970 ECOLIN_RS02975: ECOLIN_RS02975 - allantoinase AllB, at 613,164 to 614,525 _RS02975 ECOLIN_RS02980: ECOLIN_RS02980 - uracil/xanthine transporter, at 614,581 to 615,882 _RS02980 ECOLIN_RS02985: ECOLIN_RS02985 - glycerate 3-kinase, at 615,904 to 617,049 _RS02985 ECOLIN_RS02990: ECOLIN_RS02990 - (S)-ureidoglycine aminohydrolase, at 617,178 to 617,963 _RS02990
Group Condition ECOLIN_RS02970 ECOLIN_RS02975 ECOLIN_RS02980 ECOLIN_RS02985 ECOLIN_RS02990
carbon source D-Glucose -0.6 -0.3 -0.8 -0.1 N.D.
phage RB68 -0.1 -0.2 -0.2 -1.3 N.D.
phage Bas63 -0.4 -0.2 -0.1 -1.1 N.D.
phage Bas45 -0.2 -0.7 -0.3 -0.5 N.D.
phage Bas05 +0.1 -0.2 -0.9 -0.5 N.D.
carbon source D-Glucose -0.3 -0.3 -0.9 +0.0 N.D.
carbon source L-Arabinose +0.2 -0.2 -0.6 -0.7 N.D.
no phage control Control_Nissle +0.7 +0.3 +0.5 -2.6 N.D.
phage Bas38 -0.1 +0.5 -0.4 -1.1 N.D.
phage Bas48 -0.5 -0.4 +0.9 -0.8 N.D.
phage Bas10 -0.2 -0.1 -1.2 +0.7 N.D.
phage Bas21 -0.5 -0.2 -0.4 +0.3 N.D.
phage JK38 -0.6 +0.3 -0.5 +0.2 N.D.
phage TP7 -1.3 +0.1 -0.1 +0.8 N.D.
phage Bas21 +0.1 -0.4 -0.6 +0.4 N.D.
carbon source L-Rhamnose +0.0 +0.4 +0.4 -1.3 N.D.
phage Bas52 -0.7 +0.1 +0.7 -0.4 N.D.
phage Bas68 +0.1 -0.3 +0.5 -0.6 N.D.
phage K25 -0.8 -0.1 +0.8 -0.0 N.D.
phage Bas10 +0.3 -0.2 -0.6 +0.6 N.D.
phage Bas31 +0.2 -0.1 -0.6 +0.7 N.D.
phage EV219 +0.4 -0.2 -0.4 +0.5 N.D.
carbon source L-Rhamnose +0.4 -0.2 -1.0 +1.0 N.D.
phage Bas63 +0.5 -0.1 +0.4 -0.5 N.D.
phage Bas05 -0.3 -0.3 +0.3 +0.7 N.D.
phage Bas27 +0.3 -0.2 -0.3 +0.6 N.D.
phage CEV1 -0.3 -0.3 +0.5 +0.7 N.D.
phage Bas52 +0.2 +0.0 +0.8 +0.4 N.D.
phage Phi92 +0.2 +0.5 +0.4 +0.4 N.D.
phage Bas04 +0.4 +0.1 +0.5 +0.7 N.D.
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