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Incidental Mutations
33
incidental mutations are currently displayed, and affect
33
genes.
3
are Possibly Damaging.
17
are Probably Damaging.
9
are Probably Benign.
4
are Probably Null.
1
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33]
10
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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
518787
Arc
1.000
R6436
G1
133.01
Y
15
74672249
V42L
C
A
missense
Het
possibly damaging
0.475
phenotype
05/24/2018
2
538067
Clip1
0.000
R6436
G1
56.01
Y
5
123641785
E433K
C
T
missense
Het
probably damaging
1.000
phenotype
10/19/2018
3
518784
Cmya5
0.378
R6436
G1
225.01
Y
13
93089215
T3122A
T
C
missense
Het
probably damaging
0.983
0.103
05/24/2018
4
518777
Ctf2
0.076
R6436
G1
152.01
Y
7
127719431
A92E
G
T
missense
Het
probably damaging
1.000
0.633
05/24/2018
5
518792
Ctsw
0.000
R6436
G1
225.01
Y
19
5466294
R184S
G
T
missense
Het
possibly damaging
0.909
0.079
phenotype
05/24/2018
6
518783
D130043K22Rik
0.000
R6436
G1
117.01
Y
13
24877935
E629G
A
G
missense
Het
probably damaging
0.998
phenotype
05/24/2018
7
518779
Dmbt1
0.266
R6436
G1
225.01
Y
7
131116641
V1523A
T
C
missense
Het
probably benign
0.008
0.085
phenotype
05/24/2018
8
518773
Eml2
0.000
R6436
G1
220.01
Y
7
19201163
V432I
G
A
missense
Het
probably damaging
1.000
0.253
05/24/2018
9
518775
Fanci
0.709
R6436
G1
225.01
Y
7
79440698
I982T
T
C
missense
Het
probably benign
0.025
0.085
phenotype
05/24/2018
10
518767
Fnbp1
0.623
R6436
G1
225.01
Y
2
31096127
D3G
T
C
missense
Het
probably damaging
0.999
phenotype
05/24/2018
11
518768
Gm10770
0.121
R6436
G1
225.01
Y
2
150178910
T229I
G
A
missense
Het
probably benign
0.067
05/24/2018
12
518771
Gm35315
0.084
R6436
G1
225.01
Y
5
110078712
T287I
G
A
missense
Het
probably benign
0.000
05/24/2018
13
518782
Itgb3
0.861
R6436
G1
225.01
Y
11
104633492
D151E
T
A
missense
Het
probably damaging
0.994
0.871
phenotype
05/24/2018
14
518766
Lcn8
0.056
R6436
G1
225.01
Y
2
25654978
A
T
splice site
Het
probably null
phenotype
05/24/2018
15
518769
Ninl
0.000
R6436
G1
150.01
Y
2
150966178
L310P
A
G
missense
Het
probably damaging
1.000
0.386
phenotype
05/24/2018
16
518772
Nop2
0.967
R6436
G1
160.01
Y
6
125137311
D215G
A
G
missense
Het
probably benign
0.012
0.086
phenotype
05/24/2018
17
518793
Olfr1426
0.081
R6436
G1
225.01
Y
19
12087935
T286A
T
C
missense
Het
probably benign
0.238
phenotype
05/24/2018
18
518781
Olfr788
0.081
R6436
G1
225.01
Y
10
129472904
T71A
A
G
missense
Het
probably damaging
0.978
phenotype
05/24/2018
19
518786
Parg
1.000
R6436
G1
202.01
Y
14
32271677
W289R
T
C
missense
Het
probably damaging
1.000
phenotype
05/24/2018
20
538068
Pdcd4
0.317
R6436
G1
57.01
Y
19
53926931
A
G
splice site
Het
probably null
phenotype
10/19/2018
21
518785
Plk2
1.000
R6436
G1
225.01
Y
13
110396036
E95*
G
T
nonsense
Het
probably null
0.975
phenotype
05/24/2018
22
518774
Pold1
0.971
R6436
G1
198.01
Y
7
44538778
R559C
G
A
missense
Het
probably damaging
1.000
phenotype
05/24/2018
23
518764
Ptprc
0.000
R6436
G1
225.01
Y
1
138083639
D560G
T
C
missense
Het
possibly damaging
0.766
0.077
phenotype
05/24/2018
24
518790
Rasal3
0.063
R6436
G1
225.01
Y
17
32397504
Y290C
T
C
missense
Het
probably damaging
0.999
phenotype
05/24/2018
25
518765
Rcsd1
0.058
R6436
G1
225.01
Y
1
165657615
S90C
T
A
missense
Het
probably damaging
1.000
0.146
05/24/2018
26
518791
Rttn
1.000
R6436
G1
193.01
Y
18
89110729
L1935P
T
C
missense
Het
probably damaging
1.000
phenotype
05/24/2018
27
518788
Smc1b
0.737
R6436
G1
225.01
Y
15
85092031
R825Q
C
T
missense
Het
probably benign
0.032
0.090
phenotype
05/24/2018
28
538066
Srsf11
1.000
R6436
G1
222
Y
3
158023344
C
T
unclassified
Homo
probably benign
0.090
phenotype
10/19/2018
29
518776
Tmc3
0.000
R6436
G1
225.01
Y
7
83598487
Y230H
T
C
missense
Het
probably damaging
1.000
0.631
05/24/2018
30
518770
Tnfrsf25
0.000
R6436
G1
183.01
Y
4
152119627
A
T
splice site
4237 bp
Het
probably null
0.971
phenotype
05/24/2018
31
518780
Ubl7
0.161
R6436
G1
225.01
Y
9
57920510
L160P
T
C
missense
Het
probably damaging
1.000
0.583
05/24/2018
32
518789
Vmn2r106
0.117
R6436
G1
225.01
Y
17
20268463
C558Y
C
T
missense
Het
probably damaging
1.000
0.647
05/24/2018
33
518778
Zfp646
0.234
R6436
G1
225.01
Y
7
127879941
V430E
T
A
missense
Het
probably benign
0.005
0.085
05/24/2018
[records 1 to 33 of 33]