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Incidental Mutations
71
incidental mutations are currently displayed, and affect
69
genes.
13
are Possibly Damaging.
25
are Probably Damaging.
20
are Probably Benign.
7
are Probably Null.
3
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 71 of 71]
10
25
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100
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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
655885
4930512M02Rik
0.188
R8511
G1
225.01
N
11
11590056 (GRCm38)
H186R
T
C
missense
Het
unknown
2020-10-20
2
655859
4931409K22Rik
0.157
R8511
G1
225.01
N
5
24545908 (GRCm38)
H559L
T
A
missense
Het
possibly damaging
0.954
2020-10-20
3
655876
6430548M08Rik
0.136
R8511
G1
225.01
N
8
120152562 (GRCm38)
N233S
A
G
missense
Het
probably benign
0.294
2020-10-20
4
655872
Acan
1.000
R8511
G1
225.01
N
7
79097935 (GRCm38)
D818G
A
G
missense
Het
possibly damaging
0.944
phenotype
2020-10-20
5
655858
Adam22
1.000
R8511
G1
225.01
N
5
8134558 (GRCm38)
T478I
G
A
missense
Het
probably damaging
0.979
phenotype
2020-10-20
6
655890
Agmo
0.069
R8511
G1
225.01
N
12
37244397 (GRCm38)
*115R
T
A
makesense
Het
probably null
phenotype
2020-10-20
7
655910
Ahnak
0.260
R8511
G1
225.01
N
19
9012355 (GRCm38)
K3668E
A
G
missense
Het
unknown
phenotype
2020-10-20
8
655894
Aldh6a1
0.248
R8511
G1
225.01
N
12
84433971 (GRCm38)
T430I
G
A
missense
Het
possibly damaging
0.931
phenotype
2020-10-20
9
655877
Ankrd11
1.000
R8511
G1
225.01
N
8
122899729 (GRCm38)
D17G
T
C
missense
Het
phenotype
2020-10-20
10
655897
Apol10b
0.000
R8511
G1
225.01
N
15
77585010 (GRCm38)
E322D
C
G
missense
Het
probably benign
0.029
2020-10-20
11
655898
Apol10b
0.000
R8511
G1
225.01
N
15
77585011 (GRCm38)
E322G
T
C
missense
Het
probably benign
0.428
2020-10-20
12
655899
Apol8
0.000
R8511
G1
225.01
N
15
77750073 (GRCm38)
G101E
C
T
missense
Het
probably benign
0.002
phenotype
2020-10-20
13
655852
Arhgef26
0.173
R8511
G1
225.01
N
3
62428929 (GRCm38)
M630L
A
T
missense
Het
probably damaging
0.983
phenotype
2020-10-20
14
655842
Aspm
0.000
R8511
G1
225.01
N
1
139457308 (GRCm38)
L230P
T
C
missense
Het
probably damaging
0.999
phenotype
2020-10-20
15
655901
Atg101
0.229
R8511
G1
225.01
N
15
101290622 (GRCm38)
S203P
T
C
missense
Het
probably damaging
0.999
2020-10-20
16
655844
Baz2b
0.412
R8511
G1
225.01
N
2
59901814 (GRCm38)
T1996S
T
A
missense
Het
probably benign
0.000
phenotype
2020-10-20
17
655904
Brwd1
0.000
R8511
G1
225.01
N
16
96058738 (GRCm38)
M350K
A
T
missense
Het
probably damaging
0.998
0.387
phenotype
2020-10-20
18
655860
Cad
0.966
R8511
G1
225.01
N
5
31075821 (GRCm38)
K1869R
A
G
missense
Het
probably benign
0.002
phenotype
2020-10-20
19
655907
Caskin1
0.105
R8511
G1
225.01
N
17
24505936 (GRCm38)
I1233F
A
T
missense
Het
probably benign
0.116
2020-10-20
20
655846
Ckap5
1.000
R8511
G1
225.01
N
2
91615147 (GRCm38)
L1770I
T
A
missense
Het
possibly damaging
0.946
phenotype
2020-10-20
21
655862
Clip1
0.000
R8511
G1
225.01
N
5
123653906 (GRCm38)
N67S
T
C
missense
Het
possibly damaging
0.505
phenotype
2020-10-20
22
655856
Csmd2
0.151
R8511
G1
225.01
N
4
128368899 (GRCm38)
N626S
A
G
missense
Het
2020-10-20
23
655911
Cuedc2
0.264
R8511
G1
225.01
N
19
46330919 (GRCm38)
C
A
critical splice donor site
1 bp
Het
probably null
2020-10-20
24
655874
Dmbt1
0.338
R8511
G1
225.01
N
7
131102012 (GRCm38)
N1275Y
A
T
missense
Het
unknown
phenotype
2020-10-20
25
655843
Dnm3
0.000
R8511
G1
225.01
N
1
162286042 (GRCm38)
V483A
A
G
missense
Het
possibly damaging
0.692
phenotype
2020-10-20
26
655895
Dock9
0.000
R8511
G1
225.01
N
14
121627389 (GRCm38)
H718Q
A
T
missense
Het
probably benign
0.402
2020-10-20
27
655896
Dock9
0.000
R8511
G1
225.01
N
14
121681435 (GRCm38)
D50G
T
C
missense
Het
probably damaging
1.000
2020-10-20
28
655886
Egfr
0.938
R8511
G1
225.01
N
11
16896949 (GRCm38)
I782S
T
G
missense
Het
probably damaging
1.000
phenotype
2020-10-20
29
655879
Elmod1
0.000
R8511
G1
225.01
N
9
53912811 (GRCm38)
F298I
A
T
missense
Het
probably damaging
1.000
phenotype
2020-10-20
30
655900
Enthd1
0.084
R8511
G1
225.01
N
15
80474227 (GRCm38)
Q364R
T
C
missense
Het
probably damaging
0.999
2020-10-20
31
655887
Fat2
0.000
R8511
G1
225.01
N
11
55309237 (GRCm38)
S1004C
T
A
missense
Het
probably damaging
0.989
phenotype
2020-10-20
32
655853
Fga
0.447
R8511
G1
225.01
N
3
83031757 (GRCm38)
K480*
A
T
nonsense
Het
probably null
phenotype
2020-10-20
33
655909
Fhod3
1.000
R8511
G1
225.01
N
18
25132937 (GRCm38)
T1561A
A
G
missense
Het
probably damaging
0.989
phenotype
2020-10-20
34
655891
Foxg1
1.000
R8511
G1
225.01
N
12
49385085 (GRCm38)
Y200*
T
A
nonsense
Het
probably null
phenotype
2020-10-20
35
655868
Foxj2
0.456
R8511
G1
225.01
N
6
122831445 (GRCm38)
R115*
C
T
nonsense
Het
probably null
2020-10-20
36
655889
Ggnbp2
0.918
R8511
G1
225.01
N
11
84837989 (GRCm38)
C
T
critical splice acceptor site
Het
probably null
phenotype
2020-10-20
37
655869
Gm15922
0.051
R8511
G1
225.01
N
7
3739348 (GRCm38)
L60P
A
G
missense
Het
probably damaging
1.000
2020-10-20
38
655854
Gpsm2
0.837
R8511
G1
225.01
N
3
108682083 (GRCm38)
S580P
A
G
missense
Het
probably benign
0.001
phenotype
2020-10-20
39
655892
Hectd1
1.000
R8511
G1
225.01
N
12
51787871 (GRCm38)
S870P
A
G
missense
Het
probably benign
0.011
phenotype
2020-10-20
40
655902
Hic2
0.629
R8511
G1
225.01
N
16
17258010 (GRCm38)
N234K
T
A
missense
Het
possibly damaging
0.841
phenotype
2020-10-20
41
655864
Ica1
0.208
R8511
G1
225.01
N
6
8754726 (GRCm38)
F15L
A
G
missense
Het
probably benign
0.002
phenotype
2020-10-20
42
655847
Immp1l
0.317
R8511
G1
225.01
N
2
105930755 (GRCm38)
R3H
G
A
missense
Het
probably benign
0.081
phenotype
2020-10-20
43
655875
Jak3
0.689
R8511
G1
225.01
N
8
71685550 (GRCm38)
Y882N
T
A
missense
Het
probably damaging
1.000
phenotype
2020-10-20
44
655870
Klk1b1
0.063
R8511
G1
225.01
N
7
43970343 (GRCm38)
R109C
C
T
missense
Het
possibly damaging
0.858
phenotype
2020-10-20
45
655857
Luzp1
0.861
R8511
G1
225.01
N
4
136541339 (GRCm38)
D291G
A
G
missense
Het
probably damaging
1.000
phenotype
2020-10-20
46
655841
Map3k19
0.101
R8511
G1
225.01
N
1
127847418 (GRCm38)
E61K
C
T
missense
Het
possibly damaging
0.707
2020-10-20
47
655867
Mical3
0.173
R8511
G1
225.01
N
6
121038552 (GRCm38)
I175T
A
G
missense
Het
possibly damaging
0.782
2020-10-20
48
655903
Nectin3
0.220
R8511
G1
225.01
N
16
46464000 (GRCm38)
P107L
G
A
missense
Het
probably damaging
1.000
phenotype
2020-10-20
49
655878
Olfr975
0.055
R8511
G1
225.01
N
9
39950159 (GRCm38)
V204A
A
G
missense
Het
probably benign
0.206
phenotype
2020-10-20
50
655866
Polr1a
1.000
R8511
G1
225.01
N
6
71920520 (GRCm38)
H207N
C
A
missense
Het
probably benign
0.012
phenotype
2020-10-20
51
655849
Prokr2
0.237
R8511
G1
225.01
N
2
132381502 (GRCm38)
V40A
A
G
missense
Het
probably benign
0.001
phenotype
2020-10-20
52
655880
Prtg
0.764
R8511
G1
225.01
N
9
72890874 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
2020-10-20
53
655908
Ptprs
1.000
R8511
G1
225.01
N
17
56447440 (GRCm38)
T200I
G
A
missense
Het
probably damaging
0.999
phenotype
2020-10-20
54
655884
Ramp3
0.076
R8511
G1
225.01
N
11
6676709 (GRCm38)
R139C
C
T
missense
Het
probably benign
0.005
phenotype
2020-10-20
55
655861
Scfd2
0.158
R8511
G1
225.01
N
5
74212288 (GRCm38)
V642A
A
G
missense
Het
possibly damaging
0.843
2020-10-20
56
655881
Scn11a
0.087
R8511
G1
225.01
N
9
119789915 (GRCm38)
K787R
T
C
missense
Het
probably damaging
0.994
phenotype
2020-10-20
57
655871
Slco3a1
0.134
R8511
G1
225.01
N
7
74303242 (GRCm38)
V523A
A
G
missense
Het
probably benign
0.329
2020-10-20
58
655865
Smo
1.000
R8511
G1
225.01
N
6
29755532 (GRCm38)
Y401C
A
G
missense
Het
probably damaging
0.999
phenotype
2020-10-20
59
655851
Spata5
1.000
R8511
G1
225.01
N
3
37436748 (GRCm38)
M481V
A
G
missense
Het
probably damaging
0.994
phenotype
2020-10-20
60
655850
Stmn2
0.770
R8511
G1
225.01
N
3
8509555 (GRCm38)
A
G
start gained
Het
probably benign
phenotype
2020-10-20
61
655855
Stra6l
0.000
R8511
G1
225.01
N
4
45885347 (GRCm38)
G605V
G
T
missense
Het
probably benign
0.001
2020-10-20
62
655893
Syne2
0.259
R8511
G1
225.01
N
12
76008873 (GRCm38)
I4170V
A
G
missense
Het
probably benign
0.031
phenotype
2020-10-20
63
655848
Tgm7
0.068
R8511
G1
225.01
N
2
121093660 (GRCm38)
I594F
T
A
missense
Het
probably damaging
0.991
phenotype
2020-10-20
64
655882
Tle2
0.210
R8511
G1
225.01
N
10
81587996 (GRCm38)
L648P
T
C
missense
Het
probably damaging
0.999
2020-10-20
65
655905
Tmprss2
0.000
R8511
G1
225.01
N
16
97568462 (GRCm38)
L371I
G
T
missense
Het
possibly damaging
0.941
phenotype
2020-10-20
66
655845
Ttn
1.000
R8511
G1
225.01
N
2
76749522 (GRCm38)
R23676G
T
C
missense
Het
probably damaging
1.000
phenotype
2020-10-20
67
655888
Tvp23b
0.000
R8511
G1
225.01
N
11
62883737 (GRCm38)
I69T
T
C
missense
Het
possibly damaging
0.905
2020-10-20
68
655873
Vmn2r66
0.089
R8511
G1
225.01
N
7
85006818 (GRCm38)
I330N
A
T
missense
Het
probably damaging
0.988
2020-10-20
69
655906
Vmn2r99
0.125
R8511
G1
225.01
N
17
19394181 (GRCm38)
D721V
A
T
missense
Het
probably damaging
1.000
2020-10-20
70
655863
Zan
0.078
R8511
G1
225.01
N
5
137446846 (GRCm38)
V1717E
A
T
missense
Het
unknown
phenotype
2020-10-20
71
655883
Zmiz2
1.000
R8511
G1
225.01
N
11
6403190 (GRCm38)
H658Y
C
T
missense
Het
probably damaging
0.994
phenotype
2020-10-20
[records 1 to 71 of 71]