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Incidental Mutations
52
incidental mutations are currently displayed, and affect
50
genes.
12
are Possibly Damaging.
18
are Probably Damaging.
17
are Probably Benign.
4
are Probably Null.
1
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 52 of 52]
10
25
50
100
500
1000
per page
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
ABI
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
447182
Acpp
0.099
R5795
G1
225
N
9
104309489 (GRCm38)
V261A
A
G
missense
Het
probably benign
0.042
phenotype
2016-12-15
2
447151
Adipor1
0.000
R5795
G1
225
N
1
134424903 (GRCm38)
N137K
C
A
missense
Het
probably damaging
1.000
phenotype
2016-12-15
3
447203
Ahnak
0.260
R5795
G1
203
N
19
9012382 (GRCm38)
K3677*
A
T
nonsense
Het
probably null
phenotype
2016-12-15
4
447186
Ankrd24
0.664
R5795
G1
223
N
10
81645103 (GRCm38)
C
A
unclassified
Het
probably benign
2016-12-15
5
447191
Appl1
0.188
R5795
G1
225
N
14
26942816 (GRCm38)
P420Q
G
T
missense
Het
probably benign
0.012
phenotype
2016-12-15
6
447165
Bmp8b
0.112
R5795
G1
225
N
4
123121968 (GRCm38)
F249L
C
A
missense
Het
possibly damaging
0.590
phenotype
2016-12-15
7
447168
Brat1
0.256
R5795
G1
225
N
5
140713072 (GRCm38)
A275S
G
T
missense
Het
probably benign
0.006
phenotype
2016-12-15
8
447171
C5ar1
0.171
R5795
G1
225
N
7
16248394 (GRCm38)
K234E
T
C
missense
Het
possibly damaging
0.732
phenotype
2016-12-15
9
447202
Ccs
0.325
R5795
G1
225
N
19
4833339 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
2016-12-15
10
447162
Chmp5
1.000
R5795
G1
225
N
4
40950562 (GRCm38)
T
G
critical splice donor site
2 bp
Het
probably null
phenotype
2016-12-15
11
447181
Chrna3
0.305
R5795
G1
225
N
9
55015268 (GRCm38)
T419S
T
A
missense
Het
probably benign
0.168
phenotype
2016-12-15
12
447166
Crocc
0.153
R5795
G1
217
N
4
141041807 (GRCm38)
TCTGAGCTGCTGAGCTGC
TCTGAGCTGC
frame shift
Het
probably null
phenotype
2016-12-15
13
501524
Csf3
0.094
R5795
G1
143
N
11
98702027 (GRCm38)
C72F
G
T
missense
Het
probably damaging
0.999
phenotype
2017-12-01
14
447178
Dbndd1
0.066
R5795
G1
150
N
8
123509880 (GRCm38)
I83T
A
G
missense
Het
probably damaging
0.977
2016-12-15
15
447192
Ercc6
0.380
R5795
G1
225
N
14
32526352 (GRCm38)
K287E
A
G
missense
Het
probably damaging
0.976
phenotype
2016-12-15
16
447152
F5
1.000
R5795
G1
155
N
1
164152009 (GRCm38)
T16I
C
T
missense
Het
probably benign
0.089
phenotype
2016-12-15
17
447204
Gif
0.000
R5795
G1
225
N
19
11760376 (GRCm38)
T384A
A
G
missense
Het
probably damaging
0.989
phenotype
2016-12-15
18
447159
Gm14085
0.063
R5795
G1
225
N
2
122517994 (GRCm38)
M274T
T
C
missense
Het
possibly damaging
0.790
2016-12-15
19
447179
Hephl1
0.097
R5795
G1
225
N
9
15069760 (GRCm38)
G792E
C
T
missense
Het
probably damaging
0.987
2016-12-15
20
447188
Hmmr
0.000
R5795
G1
225
N
11
40721906 (GRCm38)
D158V
T
A
missense
Het
probably damaging
0.996
phenotype
2016-12-15
21
447155
Hsd11b1
0.244
R5795
G1
225
N
1
193240632 (GRCm38)
S76P
A
G
missense
Het
possibly damaging
0.852
phenotype
2016-12-15
22
447185
Ilvbl
0.087
R5795
G1
225
N
10
78577144 (GRCm38)
S167P
T
C
missense
Het
probably benign
0.007
phenotype
2016-12-15
23
447175
Irf7
0.000
R5795
G1
225
N
7
141265116 (GRCm38)
P118L
G
A
missense
Het
probably damaging
1.000
phenotype
2016-12-15
24
447200
Lama1
1.000
R5795
G1
225
N
17
67796727 (GRCm38)
N1981S
A
G
missense
Het
probably benign
0.017
phenotype
2016-12-15
25
447158
Lrp4
0.775
R5795
G1
139
N
2
91474471 (GRCm38)
D224G
A
G
missense
Het
probably benign
0.009
phenotype
2016-12-15
26
447189
Mink1
0.000
R5795
G1
225
N
11
70607790 (GRCm38)
Y594H
T
C
missense
Het
possibly damaging
0.861
phenotype
2016-12-15
27
447207
Minpp1
0.000
R5795
G1
225
N
19
32514157 (GRCm38)
V412M
G
A
missense
Het
probably damaging
0.998
phenotype
2016-12-15
28
447176
Muc5b
0.187
R5795
G1
225
N
7
141871741 (GRCm38)
V4708M
G
A
missense
Het
possibly damaging
0.956
phenotype
2016-12-15
29
447164
Mycl
0.000
R5795
G1
199
N
4
122996622 (GRCm38)
E34K
G
A
missense
Het
probably damaging
0.999
phenotype
2016-12-15
30
447180
Oaf
0.000
R5795
G1
225
N
9
43223944 (GRCm38)
D179V
T
A
missense
Het
probably damaging
0.992
2016-12-15
31
447167
Ogfod2
0.101
R5795
G1
225
N
5
124114761 (GRCm38)
G278D
G
A
missense
Het
probably damaging
0.999
2016-12-15
32
447206
Olfr1448
0.087
R5795
G1
225
N
19
12919824 (GRCm38)
F162L
A
G
missense
Het
possibly damaging
0.953
phenotype
2016-12-15
33
447198
Olfr91
0.084
R5795
G1
225
N
17
37093769 (GRCm38)
L35P
A
G
missense
Het
probably damaging
1.000
phenotype
2016-12-15
34
447172
Paf1
1.000
R5795
G1
225
N
7
28396618 (GRCm38)
M250R
T
G
missense
Het
probably damaging
0.971
phenotype
2016-12-15
35
447193
Pcdh8
0.000
R5795
G1
225
N
14
79770980 (GRCm38)
T48A
T
C
missense
Het
possibly damaging
0.953
phenotype
2016-12-15
36
447199
Pdzph1
0.138
R5795
G1
225
N
17
58885867 (GRCm38)
V1096A
A
G
missense
Het
possibly damaging
0.466
2016-12-15
37
501522
Polr3b
1.000
R5795
G1
225
N
10
84628252 (GRCm38)
E25D
A
T
missense
Het
probably benign
0.000
phenotype
2017-12-01
38
447187
Polr3b
1.000
R5795
G1
225
N
10
84677011 (GRCm38)
S586P
T
C
missense
Het
probably damaging
0.970
phenotype
2016-12-15
39
501523
Sfi1
0.243
R5795
G1
180
N
11
3153384 (GRCm38)
A
ATCTTCCCAAAGCCAGTGC
intron
Het
probably benign
2017-12-01
40
447163
Slc31a2
0.256
R5795
G1
225
N
4
62297052 (GRCm38)
V112A
T
C
missense
Het
probably damaging
1.000
2016-12-15
41
447201
Spire1
0.220
R5795
G1
225
N
18
67495195 (GRCm38)
S412T
A
T
missense
Het
probably benign
0.000
phenotype
2016-12-15
42
447157
Tanc1
0.000
R5795
G1
208
N
2
59807582 (GRCm38)
T876A
A
G
missense
Het
possibly damaging
0.620
phenotype
2016-12-15
43
447177
Tango6
1.000
R5795
G1
225
N
8
106718077 (GRCm38)
L538H
T
A
missense
Het
probably damaging
0.999
2016-12-15
44
447170
Tas2r125
0.057
R5795
G1
225
N
6
132909658 (GRCm38)
G3D
G
A
missense
Het
probably damaging
1.000
2016-12-15
45
447184
Tbc1d32
0.915
R5795
G1
225
N
10
56215062 (GRCm38)
M125K
A
T
missense
Het
possibly damaging
0.711
phenotype
2016-12-15
46
447154
Traf5
0.000
R5795
G1
225
N
1
191999846 (GRCm38)
S345G
T
C
missense
Het
probably benign
0.003
phenotype
2016-12-15
47
447153
Ush2a
0.527
R5795
G1
225
N
1
188443397 (GRCm38)
I1231F
A
T
missense
Het
probably benign
0.336
phenotype
2016-12-15
48
447195
Vmn2r104
0.118
R5795
G1
225
N
17
20030110 (GRCm38)
T633N
G
T
missense
Het
probably benign
0.017
2016-12-15
49
447196
Vmn2r104
0.118
R5795
G1
225
N
17
20030282 (GRCm38)
S576P
A
G
missense
Het
possibly damaging
0.890
2016-12-15
50
447197
Vmn2r105
0.000
R5795
G1
225
N
17
20228736 (GRCm38)
C60S
A
T
missense
Het
probably benign
0.001
2016-12-15
51
447169
Zfp316
0.144
R5795
G1
225
N
5
143262839 (GRCm38)
D217E
A
T
missense
Het
unknown
2016-12-15
52
447190
Zfp456
0.120
R5795
G1
225
N
13
67366920 (GRCm38)
D222E
A
T
missense
Het
probably benign
0.000
2016-12-15
[records 1 to 52 of 52]