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Incidental Mutations
19
incidental mutations are currently displayed, and affect
19
genes.
2
are Possibly Damaging.
4
are Probably Damaging.
6
are Probably Benign.
6
are Probably Null.
5
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 19 of 19]
10
25
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Full List
ID
Source
UTSW
APN
Gene
E-score
Stock #
Gen
G0
G0'
G1
G2
G3
G3R
F1
F2
F3
C0
C1
C2
C3
D1
HES
IPS
A3
Quality
-
Vld
Y
N
?
Strain
Chr
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
X
Y
Position
Mutation
A
R
N
D
C
E
Q
G
H
I
L
K
M
F
P
S
T
W
Y
V
*
A
R
N
D
C
E
Q
G
H
I
L
K
M
F
P
S
T
W
Y
V
*
Ref
A
C
G
T
-
Var
A
C
G
T
-
Type
makesense
missense
nonsense
start codon destroyed
start gained
synonymous
splice acceptor site
splice donor site
critical splice acceptor site
critical splice donor site
splice site
large deletion
large insertion
rearrangement
small deletion
small insertion
exon
frame shift
intragenic
intron
utr 3 prime
utr 5 prime
unclassified
Exon Dist
Zygosity
Homo
Het
Hemi
Null
Predicted Effect
unknown
probably benign
probably null
possibly damaging
probably damaging
noncoding transcript
silent
not run
no transcript
PPH Score
-
Meta Score
MGI Phenotype
available
none listed
Posted
1
7615
1700123K08Rik
0.049
P0016
G1
Y
5
138562938
L154*
A
T
nonsense
Het
probably null
0.976
10/05/2012
2
7611
4930432E11Rik
0.069
P0016
G1
Y
7
29563112
T
C
unclassified
Het
noncoding transcript
10/05/2012
3
7571
Arap3
0.748
P0016
G1
Y
18
37984348
T892S
T
A
missense
Het
probably benign
0.001
0.090
phenotype
10/05/2012
4
7583
Ctnnd2
0.000
P0016
G1
Y
15
30966938
V987I
G
A
missense
Het
probably benign
0.001
0.060
phenotype
10/05/2012
5
7580
Dennd6b
0.099
P0016
G1
Y
15
89186977
I351V
T
C
missense
Het
probably benign
0.000
0.090
10/05/2012
6
7591
Kif27
0.157
P0016
G1
Y
13
58303452
Q1021*
G
A
nonsense
Het
probably null
0.976
phenotype
10/05/2012
7
7619
Klb
0.902
P0016
G1
Y
5
65379923
W865*
G
A
nonsense
Het
probably null
0.956
phenotype
10/05/2012
8
7569
Mbd1
0.000
P0016
G1
Y
18
74274538
R130*
C
T
nonsense
Het
probably null
0.976
phenotype
10/05/2012
9
7622
Mroh7
0.000
P0016
G1
Y
4
106707857
T
A
critical splice acceptor site
Het
probably null
0.949
10/05/2012
10
7609
Myo16
0.380
P0016
G1
Y
8
10400596
C
T
splice site
Het
probably benign
phenotype
10/05/2012
11
7570
Rbm22
1.000
P0016
G1
Y
18
60570770
T
A
splice site
Het
probably benign
phenotype
10/05/2012
12
7604
Rnaseh2a
0.966
P0016
G1
Y
8
84959800
D206H
C
G
missense
Het
probably damaging
0.999
0.208
phenotype
10/05/2012
13
7586
Slain1
0.152
P0016
G1
Y
14
103685674
T187A
A
G
missense
Het
probably benign
0.373
0.059
10/05/2012
14
7633
Slamf6
0.056
P0016
G1
Y
1
171936501
T154A
A
G
missense
Het
probably damaging
0.966
0.647
phenotype
10/05/2012
15
7596
Traip
1.000
P0016
G1
Y
9
107968656
D316G
A
G
missense
Het
possibly damaging
0.928
0.072
phenotype
10/05/2012
16
7630
Ttn
1.000
P0016
G1
Y
2
76811183
D5196G
T
C
missense
Het
probably damaging
0.997
0.242
phenotype
10/05/2012
17
7582
Ubr5
1.000
P0016
G1
Y
15
38000578
V1569M
C
T
missense
Het
probably damaging
0.996
0.187
phenotype
10/05/2012
18
7592
Zfp750
0.581
P0016
G1
Y
11
121513978
K24*
T
A
nonsense
Het
probably null
0.972
phenotype
10/05/2012
19
7573
Zfp799
0.111
P0016
G1
Y
17
32819357
E645G
T
C
missense
Het
possibly damaging
0.793
0.179
10/05/2012
[records 1 to 19 of 19]