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Incidental Mutations
46
incidental mutations are currently displayed, and affect
45
genes.
7
are Possibly Damaging.
19
are Probably Damaging.
14
are Probably Benign.
5
are Probably Null.
2
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 46 of 46]
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
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
485158
Agbl1
0.000
R6117
G1
225.01
N
7
76698786
Y625C
A
G
missense
Het
probably damaging
1.000
phenotype
08/16/2017
2
485144
Ankmy1
0.076
R6117
G1
225.01
N
1
92861274
A
G
unclassified
Het
probably benign
08/16/2017
3
485150
Apmap
0.000
R6117
G1
225.01
N
2
150600332
T41A
T
C
missense
Het
probably benign
0.131
08/16/2017
4
485161
Cacna1a
0.921
R6117
G1
225.01
N
8
84614721
Y1804C
A
G
missense
Het
probably damaging
1.000
phenotype
08/16/2017
5
485145
Cacna1e
0.130
R6117
G1
225.01
N
1
154561791
I333N
A
T
missense
Het
possibly damaging
0.675
phenotype
08/16/2017
6
485186
Cdsn
1.000
R6117
G1
181.01
N
17
35555034
S153R
C
A
missense
Het
unknown
phenotype
08/16/2017
7
485182
Celsr1
0.782
R6117
G1
225.01
N
15
85932411
M1777K
A
T
missense
Het
probably benign
0.043
phenotype
08/16/2017
8
485185
Cmtr1
0.966
R6117
G1
225.01
N
17
29682165
M249V
A
G
missense
Het
probably benign
0.431
08/16/2017
9
485176
Cmya5
0.324
R6117
G1
225.01
N
13
93095166
L1138P
A
G
missense
Het
probably damaging
0.976
08/16/2017
10
485187
Crim1
1.000
R6117
G1
225.01
N
17
78303088
D324A
A
C
missense
Het
probably damaging
1.000
phenotype
08/16/2017
11
485151
Dmap1
1.000
R6117
G1
178.01
N
4
117675535
T
A
intron
Het
probably null
phenotype
08/16/2017
12
485174
Dnah17
0.000
R6117
G1
215.01
N
11
118119571
Y307C
T
C
missense
Het
probably benign
0.002
phenotype
08/16/2017
13
485181
Dnah5
0.808
R6117
G1
225.01
N
15
28270420
L956H
T
A
missense
Het
probably damaging
0.989
phenotype
08/16/2017
14
485167
Enpp3
0.220
R6117
G1
225.01
N
10
24787852
S537N
C
T
missense
Het
probably damaging
0.998
phenotype
08/16/2017
15
485153
Eya3
0.810
R6117
G1
225.01
N
4
132711862
L323Q
T
A
missense
Het
probably damaging
1.000
phenotype
08/16/2017
16
485190
Fads3
0.000
R6117
G1
225.01
N
19
10054267
H226L
A
T
missense
Het
probably damaging
1.000
phenotype
08/16/2017
17
485149
Flrt3
1.000
R6117
G1
225.01
N
2
140660445
D421V
T
A
missense
Het
possibly damaging
0.461
phenotype
08/16/2017
18
485146
Frmd4a
0.156
R6117
G1
225.01
N
2
4602249
V370A
T
C
missense
Het
possibly damaging
0.660
phenotype
08/16/2017
19
485147
Gapvd1
1.000
R6117
G1
225.01
N
2
34690459
T
C
splice site
3 bp
Het
probably null
08/16/2017
20
485178
Gm2178
R6117
G1
225.01
N
14
26514840
T
C
intron
Het
probably benign
08/16/2017
21
485156
Gm5592
0.061
R6117
G1
225.01
N
7
41288464
N390S
A
G
missense
Het
probably benign
0.002
08/16/2017
22
485155
Hoxa10
0.000
R6117
G1
225.01
N
6
52234820
R39*
T
A
nonsense
Het
probably null
phenotype
08/16/2017
23
485165
Kcnj1
0.074
R6117
G1
225.01
N
9
32397182
T281A
A
G
missense
Het
probably damaging
0.999
phenotype
08/16/2017
24
485180
Myo10
0.000
R6117
G1
225.01
N
15
25805659
Y1709H
T
C
missense
Het
probably benign
0.005
phenotype
08/16/2017
25
485171
Nacad
0.000
R6117
G1
225.01
N
11
6599810
D1127G
T
C
missense
Het
probably benign
0.002
0.090
08/16/2017
26
485177
Naip1
0.000
R6117
G1
225.01
N
13
100444737
M1L
T
A
start codon destroyed
Het
probably damaging
0.989
phenotype
08/16/2017
27
485152
Olfr1331
0.055
R6117
G1
225.01
N
4
118869144
Y121F
A
T
missense
Het
probably benign
0.394
phenotype
08/16/2017
28
485169
Olfr811
0.056
R6117
G1
225.01
N
10
129801820
A235V
G
A
missense
Het
probably damaging
1.000
0.302
phenotype
08/16/2017
29
485170
Olfr811
0.056
R6117
G1
225.01
N
10
129801821
A235S
C
A
missense
Het
probably damaging
1.000
0.163
phenotype
08/16/2017
30
485189
Pcdhb12
0.061
R6117
G1
112.01
N
18
37435642
G
A
intron
Het
probably benign
08/16/2017
31
485184
Pde1b
0.000
R6117
G1
225.01
N
15
103521482
V134A
T
C
missense
Het
probably damaging
0.994
phenotype
08/16/2017
32
485183
Plxnb2
0.943
R6117
G1
225.01
N
15
89158000
D1600E
A
T
missense
Het
probably benign
0.043
phenotype
08/16/2017
33
485163
Prss54
0.055
R6117
G1
225.01
N
8
95565458
T
A
splice site
Het
probably null
phenotype
08/16/2017
34
485148
Ryr3
0.385
R6117
G1
225.01
N
2
112635396
I4757N
A
T
missense
Het
probably damaging
1.000
phenotype
08/16/2017
35
485168
Slc1a6
0.092
R6117
G1
225.01
N
10
78788988
Y76H
T
C
missense
Het
possibly damaging
0.723
phenotype
08/16/2017
36
485157
Slco3a1
0.234
R6117
G1
225.01
N
7
74318506
D489N
C
T
missense
Het
probably benign
0.019
0.084
08/16/2017
37
485172
Sox15
0.000
R6117
G1
225.01
N
11
69655890
G173V
G
T
missense
Het
possibly damaging
0.903
phenotype
08/16/2017
38
485173
Stard3
0.000
R6117
G1
225.01
N
11
98372262
S48P
T
C
missense
Het
probably damaging
1.000
phenotype
08/16/2017
39
485160
Stk32c
0.000
R6117
G1
225.01
N
7
139122923
Q67*
G
A
nonsense
Het
probably null
phenotype
08/16/2017
40
485188
Svil
0.217
R6117
G1
225.01
N
18
5116016
W2101R
T
A
missense
Het
probably damaging
1.000
phenotype
08/16/2017
41
485166
Taar7e
0.105
R6117
G1
225.01
N
10
24038529
Y306N
T
A
missense
Het
probably damaging
0.976
08/16/2017
42
485164
Tarbp1
0.000
R6117
G1
225.01
N
8
126427541
M1485L
T
A
missense
Het
probably benign
0.002
phenotype
08/16/2017
43
485175
Togaram1
0.563
R6117
G1
225.01
N
12
64967487
D504G
A
G
missense
Het
probably damaging
0.999
08/16/2017
44
485154
Trrap
1.000
R6117
G1
225.01
N
5
144802961
L1091S
T
C
missense
Het
possibly damaging
0.777
phenotype
08/16/2017
45
485143
Unc80
0.891
R6117
G1
225.01
N
1
66675067
E2856G
A
G
missense
Het
possibly damaging
0.719
phenotype
08/16/2017
46
485159
Usp47
0.688
R6117
G1
225.01
N
7
112087932
T699M
C
T
missense
Het
probably damaging
0.976
phenotype
08/16/2017
[records 1 to 46 of 46]