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Incidental Mutations
36
incidental mutations are currently displayed, and affect
35
genes.
9
are Possibly Damaging.
14
are Probably Damaging.
8
are Probably Benign.
4
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 36 of 36]
10
25
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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
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
526545
4930430A15Rik
0.052
R6654
G1
225.01
Y
2
111171884 (GRCm38)
M154L
T
A
missense
Het
unknown
2018-07-23
2
543619
Akr1b3
0.301
R6654
G1
74.01
Y
6
34310004 (GRCm38)
V206M
C
T
missense
Het
possibly damaging
0.561
0.075
phenotype
2019-04-03
3
526557
Armc6
0.153
R6654
G1
225.01
Y
8
70231375 (GRCm38)
E9G
T
C
missense
Het
probably damaging
0.993
phenotype
2018-07-23
4
526552
Bhlhe40
0.000
R6654
G1
217.47
Y
6
108664857 (GRCm38)
254
TG
TGG
frame shift
Het
probably null
0.976
phenotype
2018-07-23
5
526564
Ddc
1.000
R6654
G1
225.01
Y
11
11880452 (GRCm38)
I64N
A
T
missense
Het
probably damaging
1.000
phenotype
2018-07-23
6
526546
Exd1
0.000
R6654
G1
225.01
Y
2
119524717 (GRCm38)
T
A
critical splice acceptor site
Het
probably null
phenotype
2018-07-23
7
526544
Gm13757
0.060
R6654
G1
225.01
Y
2
88446672 (GRCm38)
T89P
T
G
missense
Het
possibly damaging
0.796
2018-07-23
8
526553
Gm15922
0.051
R6654
G1
225.01
N
7
3735929 (GRCm38)
S560T
A
T
missense
Het
probably benign
0.185
2018-07-23
9
526542
Gm4847
0.108
R6654
G1
225.01
Y
1
166630387 (GRCm38)
G466C
C
A
missense
Het
probably damaging
1.000
0.647
2018-07-23
10
526565
Gm5431
0.059
R6654
G1
225.01
Y
11
48894600 (GRCm38)
D316G
T
C
missense
Het
possibly damaging
0.912
2018-07-23
11
526561
Gsta4
0.000
R6654
G1
225.01
Y
9
78209099 (GRCm38)
F197L
T
C
missense
Het
probably damaging
0.980
0.647
phenotype
2018-07-23
12
526556
Irs2
0.612
R6654
G1
225.01
Y
8
11006486 (GRCm38)
Y649H
A
G
missense
Het
probably damaging
1.000
phenotype
2018-07-23
13
526547
Kif16b
1.000
R6654
G1
225.01
Y
2
142701277 (GRCm38)
T
C
intron
Het
probably benign
phenotype
2018-07-23
14
526563
Krtap12-1
0.075
R6654
G1
225.01
Y
10
77720703 (GRCm38)
T
C
unclassified
Het
probably benign
0.090
2018-07-23
15
526571
Ktn1
0.000
R6654
G1
225.01
Y
14
47690000 (GRCm38)
S537N
G
A
missense
Het
probably damaging
1.000
0.115
phenotype
2018-07-23
16
526549
Med12l
0.238
R6654
G1
225.01
Y
3
59262292 (GRCm38)
G1626W
G
T
missense
Het
probably damaging
1.000
0.164
phenotype
2018-07-23
17
526572
Mfng
0.205
R6654
G1
225.01
N
15
78759339 (GRCm38)
T223S
T
A
missense
Het
probably damaging
1.000
phenotype
2018-07-23
18
526570
Msh3
0.287
R6654
G1
225.01
Y
13
92345042 (GRCm38)
T321A
T
C
missense
Het
probably benign
0.006
phenotype
2018-07-23
19
526576
Myo7b
0.000
R6654
G1
107.01
Y
18
31990269 (GRCm38)
I672V
T
C
missense
Het
possibly damaging
0.464
0.179
phenotype
2018-07-23
20
526566
Nbas
1.000
R6654
G1
225.01
Y
12
13483874 (GRCm38)
Q1837*
C
T
nonsense
Het
probably null
phenotype
2018-07-23
21
526575
Nlrc4
0.110
R6654
G1
225.01
Y
17
74445528 (GRCm38)
A620V
G
A
missense
Het
possibly damaging
0.553
phenotype
2018-07-23
22
526567
Nubpl
1.000
R6654
G1
225.01
Y
12
52310733 (GRCm38)
V310E
T
A
missense
Het
probably damaging
0.999
phenotype
2018-07-23
23
526543
Olfr1109
0.057
R6654
G1
225.01
Y
2
87093050 (GRCm38)
S116P
A
G
missense
Het
probably benign
0.232
phenotype
2018-07-23
24
526548
P2ry12
0.099
R6654
G1
225.01
Y
3
59218020 (GRCm38)
L78P
A
G
missense
Het
probably damaging
0.997
phenotype
2018-07-23
25
526559
Pkd1l3
0.000
R6654
G1
225.01
Y
8
109624283 (GRCm38)
S587A
T
G
missense
Het
probably benign
0.230
phenotype
2018-07-23
26
526550
Prkacb
0.663
R6654
G1
225.01
Y
3
146750543 (GRCm38)
V145A
A
G
missense
Het
possibly damaging
0.768
0.401
phenotype
2018-07-23
27
526558
Rpgrip1l
1.000
R6654
G1
225.01
Y
8
91220205 (GRCm38)
E1256G
T
C
missense
Het
probably benign
0.364
phenotype
2018-07-23
28
526562
Rsph4a
0.150
R6654
G1
225.01
Y
10
33912992 (GRCm38)
Q611R
A
G
missense
Het
probably benign
0.000
0.090
phenotype
2018-07-23
29
526560
Sorl1
0.366
R6654
G1
225.01
Y
9
41980645 (GRCm38)
D1903G
T
C
missense
Het
possibly damaging
0.472
0.161
phenotype
2018-07-23
30
526551
Tmem39b
0.291
R6654
G1
225.01
Y
4
129686826 (GRCm38)
V291D
A
T
missense
Het
probably damaging
0.996
0.824
2018-07-23
31
526568
Unc79
1.000
R6654
G1
173.01
Y
12
103079048 (GRCm38)
K685Q
A
C
missense
Het
probably damaging
0.994
0.074
phenotype
2018-07-23
32
526569
Unc79
1.000
R6654
G1
175.01
Y
12
103079049 (GRCm38)
K685I
A
T
missense
Het
probably damaging
0.998
0.068
phenotype
2018-07-23
33
526573
Vmn2r111
0.071
R6654
G1
225.01
Y
17
22559051 (GRCm38)
N549S
T
C
missense
Het
possibly damaging
0.502
0.179
2018-07-23
34
526574
Vmn2r112
0.151
R6654
G1
225.01
Y
17
22603469 (GRCm38)
S376I
G
T
missense
Het
possibly damaging
0.891
2018-07-23
35
526555
Zfp850
0.069
R6654
G1
225.01
Y
7
27985215 (GRCm38)
C35*
A
T
nonsense
Het
probably null
2018-07-23
36
526554
Zfp974
0.060
R6654
G1
225.01
Y
7
27926403 (GRCm38)
V14A
A
G
missense
Het
probably damaging
1.000
2018-07-23
[records 1 to 36 of 36]