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Protein
Homologs
Fitness for 5 genes in
Escherichia coli ECOR38
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Top 29 experiments (either direction), sorted by average fitness
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500 nt
tsx and yajD are separated by 37 nucleotides
yajD and parE are separated by 87 nucleotides
parE and parD overlap by 8 nucleotides
parD and secF are separated by 151 nucleotides
HEPCGN_07110: tsx - nucleoside-specific channel-forming protein Tsx, at 155,119 to 156,003
tsx
HEPCGN_07115: yajD - HNH nuclease YajD, at 156,041 to 156,388
yajD
HEPCGN_07120: parE - type II toxin-antitoxin system RelE/ParE family toxin, at 156,476 to 156,757
parE
HEPCGN_07125: parD - Antitoxin ParD, at 156,750 to 156,992
parD
HEPCGN_07130: secF - Protein translocase subunit SecF, at 157,144 to 158,115
secF
Group
Condition
HEPCGN
_07110
HEPCGN
_07115
HEPCGN
_07120
HEPCGN
_07125
HEPCGN
_07130
tsx
yajD
parE
parD
secF
phage
Phi92
-1.3
-0.1
-0.1
-0.4
N.D.
phage
Phi92
-0.8
+0.3
-0.1
-1.1
N.D.
phage
K20
-0.2
+0.2
-0.1
-1.4
N.D.
phage
Bas48
+0.1
+0.3
-0.3
-1.2
N.D.
carbon source
Casamino-acids
+0.2
-0.3
-0.1
-0.8
N.D.
phage
RB23
-0.2
+0.2
-0.5
-0.6
N.D.
carbon source
Sodium-DL-Lactate
+0.4
-0.4
-0.3
-0.6
N.D.
phage
Bas48
-0.1
+0.1
-0.1
-0.9
N.D.
phage
Bas55
-0.0
+0.2
+0.1
-1.1
N.D.
phage
Bas19
+0.1
+0.1
-0.2
-0.9
N.D.
carbon source
L-Arabinose
+0.1
-0.1
-0.0
-0.8
N.D.
carbon source
L-Arabinose
+0.1
-0.5
+0.0
-0.5
N.D.
no phage control
Control_ECOR38
-0.1
-0.4
+0.1
-0.3
N.D.
phage
RB23
+0.2
-0.1
-0.1
-0.7
N.D.
carbon source
Sodium-DL-Lactate
+0.2
+0.2
-0.3
-0.7
N.D.
carbon source
D-Glucose
+0.1
-0.2
-0.2
-0.2
N.D.
carbon source
Casamino-acids
+0.2
+0.1
-0.2
-0.5
N.D.
phage
Bas39
+0.1
-0.1
+0.2
-0.4
N.D.
phage
RB68
+0.1
+0.6
+0.2
-1.0
N.D.
phage
K20
-0.1
-0.2
+0.3
-0.2
N.D.
no phage control
Control_ECOR38
-0.1
-0.2
+0.3
-0.0
N.D.
phage
Bas55
+0.1
+0.0
+0.1
-0.3
N.D.
phage
Bas19
+0.2
+0.4
+0.4
-0.9
N.D.
phage
Bas39
-0.0
+0.3
+0.3
-0.4
N.D.
phage
Bas51
+0.0
-0.1
+0.4
-0.0
N.D.
phage
Bas38
-0.0
+0.2
+0.4
-0.2
N.D.
phage
Bas38
+0.1
+0.0
+0.3
+0.1
N.D.
phage
TP7
+0.7
+0.6
-0.4
-0.2
N.D.
phage
TP7
+0.5
+0.1
+0.0
+0.2
N.D.
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