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Incidental Mutations
32
incidental mutations are currently displayed, and affect
32
genes.
8
are Possibly Damaging.
11
are Probably Damaging.
9
are Probably Benign.
3
are Probably Null.
0
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 32 of 32]
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
416067
A930011G23Rik
0.098
IGL03295
5
99243056
A
T
splice site
Het
probably benign
08/02/2016
2
416045
Adamts5
0.222
IGL03295
16
85877945
T444A
T
C
missense
Het
probably damaging
0.997
phenotype
08/02/2016
3
416060
Aldh18a1
1.000
IGL03295
19
40562942
E522G
T
C
missense
Het
probably damaging
0.998
phenotype
08/02/2016
4
416053
Bbx
0.000
IGL03295
16
50224564
T437A
T
C
missense
Het
probably damaging
0.998
phenotype
08/02/2016
5
416069
Bsx
0.000
IGL03295
9
40874447
A
G
splice site
Het
probably benign
phenotype
08/02/2016
6
416064
C330027C09Rik
0.953
IGL03295
16
48994341
S22P
T
C
missense
Het
probably damaging
1.000
phenotype
08/02/2016
7
416047
Cdc42bpa
0.591
IGL03295
1
180150204
N729S
A
G
missense
Het
probably benign
0.005
phenotype
08/02/2016
8
416061
Cdk1
1.000
IGL03295
10
69342543
H162Q
G
T
missense
Het
possibly damaging
0.877
phenotype
08/02/2016
9
416056
Chrac1
0.281
IGL03295
15
73093596
A
G
intron
Het
probably benign
phenotype
08/02/2016
10
416050
Ddx60
0.126
IGL03295
8
61956121
D397V
A
T
missense
Het
possibly damaging
0.823
phenotype
08/02/2016
11
416054
Edn2
1.000
IGL03295
4
120161981
C56S
T
A
missense
Het
probably damaging
1.000
phenotype
08/02/2016
12
416038
Gm13103
0.072
IGL03295
4
143853189
C448Y
G
A
missense
Het
probably damaging
1.000
08/02/2016
13
416039
Gm4952
0.063
IGL03295
19
12618327
V27A
T
C
missense
Het
probably benign
0.394
08/02/2016
14
416046
Herc1
0.000
IGL03295
9
66396703
S763T
T
A
missense
Het
possibly damaging
0.561
phenotype
08/02/2016
15
416051
Hspd1
1.000
IGL03295
1
55080175
T381I
G
A
missense
Het
probably benign
0.004
phenotype
08/02/2016
16
416057
Krt2
0.142
IGL03295
15
101816429
I249F
T
A
missense
Het
probably damaging
0.988
phenotype
08/02/2016
17
416042
Lman2l
0.699
IGL03295
1
36438811
D148G
T
C
missense
Het
probably damaging
0.998
phenotype
08/02/2016
18
416068
Lrp1b
0.000
IGL03295
2
40678987
C
T
splice site
5 bp
Het
probably null
phenotype
08/02/2016
19
416043
Mier3
0.757
IGL03295
13
111703681
T51K
C
A
missense
Het
probably benign
0.001
08/02/2016
20
416062
Ppp1r36
0.288
IGL03295
12
76438418
P305L
C
T
missense
Het
probably damaging
0.966
08/02/2016
21
416049
Prdm1
1.000
IGL03295
10
44439870
I790V
T
C
missense
Het
probably damaging
0.993
phenotype
08/02/2016
22
416055
Sephs2
0.708
IGL03295
7
127272769
E384G
T
C
missense
Het
possibly damaging
0.600
phenotype
08/02/2016
23
416059
Sipa1l1
0.000
IGL03295
12
82432940
W1466R
T
A
missense
Het
probably damaging
0.996
08/02/2016
24
416041
Snai2
0.857
IGL03295
16
14706774
L48P
T
C
missense
Het
possibly damaging
0.642
phenotype
08/02/2016
25
416065
Stt3a
0.943
IGL03295
9
36763331
A
G
splice site
6 bp
Het
probably null
phenotype
08/02/2016
26
416058
Synj1
1.000
IGL03295
16
90938430
N1545I
T
A
missense
Het
probably benign
0.143
phenotype
08/02/2016
27
416052
Vav2
0.464
IGL03295
2
27275029
S607T
A
T
missense
Het
possibly damaging
0.903
phenotype
08/02/2016
28
416063
Wdr27
0.125
IGL03295
17
14934575
K27E
T
C
missense
Het
possibly damaging
0.710
phenotype
08/02/2016
29
416048
Xcl1
IGL03295
1
164935435
V19E
A
T
missense
Het
unknown
phenotype
08/02/2016
30
416066
Xlr3c
IGL03295
X
73257634
A
T
critical splice donor site
2 bp
Het
probably null
08/02/2016
31
416044
Zbtb44
0.350
IGL03295
9
31053457
D54E
T
A
missense
Het
probably benign
0.003
08/02/2016
32
416040
Zscan21
0.000
IGL03295
5
138125278
D73G
A
G
missense
Het
possibly damaging
0.845
phenotype
08/02/2016
[records 1 to 32 of 32]