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Incidental Mutations
37
incidental mutations are currently displayed, and affect
37
genes.
9
are Possibly Damaging.
13
are Probably Damaging.
10
are Probably Benign.
3
are Probably Null.
2
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 37 of 37]
10
25
50
100
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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
245288
4930415L06Rik
0.160
R2299
G1
222
Y
X
89932399
M64T
A
G
missense
Het
possibly damaging
0.719
0.179
10/30/2014
2
245256
4933434E20Rik
1.000
R2299
G1
225
Y
3
90064538
N68S
A
G
missense
Het
possibly damaging
0.879
0.179
10/30/2014
3
245279
5031439G07Rik
0.097
R2299
G1
225
Y
15
84953285
F276V
A
C
missense
Het
possibly damaging
0.590
0.080
10/30/2014
4
245249
Abca12
1.000
R2299
G1
225
Y
1
71258222
V2370I
C
T
missense
Het
probably damaging
0.996
0.106
phenotype
10/30/2014
5
245250
Acsl3
0.426
R2299
G1
225
Y
1
78699110
C469W
T
G
missense
Het
probably damaging
1.000
0.685
phenotype
10/30/2014
6
245267
Adgrg5
0.000
R2299
G1
225
Y
8
94938576
I372F
A
T
missense
Het
possibly damaging
0.884
0.179
phenotype
10/30/2014
7
245263
Ankrd42
0.096
R2299
G1
219
Y
7
92590254
I442T
A
G
missense
Het
probably benign
0.332
0.088
10/30/2014
8
245286
Arsi
0.078
R2299
G1
225
Y
18
60916651
G202E
G
A
missense
Het
probably benign
0.068
0.063
phenotype
10/30/2014
9
245257
Bmpr1b
0.663
R2299
G1
225
Y
3
141845202
R376L
C
A
missense
Het
probably damaging
1.000
0.615
phenotype
10/30/2014
10
245278
C1qtnf6
0.000
R2299
G1
225
Y
15
78525342
T102S
T
A
missense
Het
probably benign
0.002
0.090
10/30/2014
11
245268
Chordc1
1.000
R2299
G1
225
Y
9
18302108
L85P
T
C
missense
Het
probably damaging
0.994
0.062
phenotype
10/30/2014
12
245260
Clec2j
0.068
R2299
G1
225
Y
6
128655236
T
A
unclassified
Het
noncoding transcript
0.087
10/30/2014
13
245251
Copa
0.971
R2299
G1
225
Y
1
172121725
I1223T
T
C
missense
Het
probably benign
0.105
0.127
phenotype
10/30/2014
14
245280
Crygs
0.000
R2299
G1
225
Y
16
22805551
G102D
C
T
missense
Het
possibly damaging
0.927
0.179
phenotype
10/30/2014
15
245273
Cyfip2
1.000
R2299
G1
179
Y
11
46286131
E74V
T
A
missense
Het
probably benign
0.017
0.189
phenotype
10/30/2014
16
245284
Dsg1a
0.095
R2299
G1
186
Y
18
20340150
D760V
A
T
missense
Het
probably damaging
1.000
0.851
phenotype
10/30/2014
17
245264
Folr1
1.000
R2299
G1
225
Y
7
101863992
L32P
A
G
missense
Het
probably damaging
1.000
0.830
phenotype
10/30/2014
18
245253
Galnt13
0.182
R2299
G1
225
Y
2
55060583
R425S
A
T
missense
Het
possibly damaging
0.612
0.098
phenotype
10/30/2014
19
245266
Gm4559
0.157
R2299
G1
205
Y
7
142273835
C177S
A
T
missense
Het
unknown
0.087
10/30/2014
20
245252
H3f3a
0.453
R2299
G1
171
N
1
180803138
R117H
C
T
missense
Het
probably benign
0.002
phenotype
10/30/2014
21
245274
Hist1h2bh
0.257
R2299
G1
210
Y
13
23543184
S57P
A
G
missense
Het
probably damaging
1.000
0.179
phenotype
10/30/2014
22
245248
Kansl1l
0.198
R2299
G1
225
Y
1
66773477
D459G
T
C
missense
Het
probably damaging
1.000
0.117
10/30/2014
23
245270
Limd1
0.359
R2299
G1
225
Y
9
123516877
K574*
A
T
nonsense
Het
probably null
0.976
phenotype
10/30/2014
24
245259
Mmrn1
0.000
R2299
G1
225
Y
6
60976441
K569E
A
G
missense
Het
probably damaging
0.994
0.065
phenotype
10/30/2014
25
245265
Olfr583
0.139
R2299
G1
225
Y
7
103051582
W95R
T
C
missense
Het
probably damaging
0.991
0.732
phenotype
10/30/2014
26
245275
Ppwd1
0.957
R2299
G1
225
Y
13
104220063
M315V
T
C
missense
Het
probably benign
0.000
0.058
10/30/2014
27
245281
Prss21
0.054
R2299
G1
225
Y
17
23869589
E176G
A
G
missense
Het
probably benign
0.184
0.189
phenotype
10/30/2014
28
245269
Ptpn23
1.000
R2299
G1
225
Y
9
110392513
I173T
A
G
missense
Het
possibly damaging
0.718
0.212
phenotype
10/30/2014
29
245255
Rit1
0.122
R2299
G1
225
Y
3
88726070
T
A
critical splice donor site
2 bp
Het
probably null
0.950
phenotype
10/30/2014
30
245285
Rnf14
0.707
R2299
G1
225
Y
18
38308085
A176V
C
T
missense
Het
probably benign
0.033
0.090
phenotype
10/30/2014
31
245277
Sema5a
1.000
R2299
G1
225
Y
15
32562776
V311E
T
A
missense
Het
possibly damaging
0.950
0.082
phenotype
10/30/2014
32
245254
Slc28a2
0.066
R2299
G1
225
Y
2
122441778
Q34*
C
T
nonsense
Het
probably null
0.976
10/30/2014
33
245287
Spire1
0.272
R2299
G1
225
Y
18
67530423
L36R
A
C
missense
Het
probably damaging
1.000
0.661
phenotype
10/30/2014
34
245258
Usp33
0.820
R2299
G1
225
Y
3
152374621
V463E
T
A
missense
Het
probably damaging
0.994
0.271
phenotype
10/30/2014
35
245247
Vcpip1
0.371
R2299
G1
225
Y
1
9745719
L813S
A
G
missense
Het
possibly damaging
0.712
0.103
phenotype
10/30/2014
36
245261
Vmn1r174
0.058
R2299
G1
196
Y
7
23754004
I32F
A
T
missense
Het
probably benign
0.076
0.090
10/30/2014
37
245271
Zbtb24
1.000
R2299
G1
123
Y
10
41464581
V536M
G
A
missense
Het
probably damaging
1.000
0.647
phenotype
10/30/2014
[records 1 to 37 of 37]