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Incidental Mutations
52
incidental mutations are currently displayed, and affect
52
genes.
11
are Possibly Damaging.
20
are Probably Damaging.
12
are Probably Benign.
9
are Probably Null.
1
create premature stop codons.
4
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 52 of 52]
10
25
50
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
80582
2010300C02Rik
0.000
R0928
G1
81
N
1
37624582
D745G
T
C
missense
Het
possibly damaging
0.845
11/07/2013
2
80640
4931406P16Rik
0.000
R0928
G1
208
N
7
34248246
A
T
splice site
Het
probably null
11/07/2013
3
80586
Abca12
1.000
R0928
G1
197
N
1
71349174
D179V
T
A
missense
Het
probably benign
0.060
phenotype
11/07/2013
4
80693
Abcc1
0.117
R0928
G1
225
N
16
14389985
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
11/07/2013
5
80618
Adad1
0.370
R0928
G1
187
N
3
37076740
G
A
critical splice donor site
1 bp
Het
probably null
phenotype
11/07/2013
6
80594
Apobec4
0.090
R0928
G1
225
N
1
152756277
Y19H
T
C
missense
Het
probably damaging
0.999
phenotype
11/07/2013
7
80662
Bco2
0.067
R0928
G1
225
N
9
50545931
T104S
T
A
missense
Het
probably damaging
1.000
phenotype
11/07/2013
8
80644
Bnc1
0.000
R0928
G1
144
N
7
81973502
V659A
A
G
missense
Het
probably benign
0.000
phenotype
11/07/2013
9
80616
Ccdc144b
0.065
R0928
G1
225
N
3
36025366
N258K
A
C
missense
Het
possibly damaging
0.828
11/07/2013
10
80703
Ccs
0.327
R0928
G1
225
N
19
4825960
E184G
T
C
missense
Het
probably damaging
0.997
phenotype
11/07/2013
11
80686
Cfap70
0.064
R0928
G1
225
N
14
20443919
K97N
T
G
missense
Het
probably damaging
0.997
11/07/2013
12
80699
Daam2
0.000
R0928
G1
225
N
17
49488227
I313V
T
C
missense
Het
probably benign
0.296
Daam1 conditional KO
increases the severity of the heart phenotype (abnormal ventricular morphology and pressure) of the Daam1 single KO. [provided by MGI curators] (source: MGI)">phenotype
11/07/2013
13
80690
Dach1
1.000
R0928
G1
185
N
14
97915832
S467G
T
C
missense
Het
probably damaging
0.979
phenotype
11/07/2013
14
80678
Dnah11
0.638
R0928
G1
225
N
12
118045562
S2122P
A
G
missense
Het
probably damaging
0.999
phenotype
11/07/2013
15
80648
Dnah3
0.083
R0928
G1
225
N
7
120030051
D1427V
T
A
missense
Het
probably damaging
1.000
phenotype
11/07/2013
16
80622
Dnaic1
0.504
R0928
G1
184
N
4
41602566
F97L
T
C
missense
Het
possibly damaging
0.569
phenotype
11/07/2013
17
80701
Dsc1
0.085
R0928
G1
225
N
18
20110249
A
T
splice site
Het
probably null
phenotype
11/07/2013
18
80632
En2
0.667
R0928
G1
225
N
5
28170331
K291*
A
T
nonsense
Het
probably null
phenotype
11/07/2013
19
80626
Eps15
0.000
R0928
G1
225
N
4
109312963
V154A
T
C
missense
Het
possibly damaging
0.952
phenotype
11/07/2013
20
80638
Etnk1
0.000
R0928
G1
150
N
6
143184703
I183V
A
G
missense
Het
probably benign
0.004
phenotype
11/07/2013
21
80597
Fcrlb
0.000
R0928
G1
88
N
1
170907940
V255D
A
T
missense
Het
possibly damaging
0.871
phenotype
11/07/2013
22
80634
Fry
0.716
R0928
G1
225
N
5
150437084
E52V
A
T
missense
Het
probably damaging
1.000
11/07/2013
23
80584
Gm8251
0.079
R0928
G1
225
N
1
44057228
S1570I
C
A
missense
Het
possibly damaging
0.734
11/07/2013
24
80695
Gtf2h4
0.968
R0928
G1
223
N
17
35670885
Y152C
T
C
missense
Het
probably damaging
0.999
phenotype
11/07/2013
25
80612
Hao1
0.075
R0928
G1
217
N
2
134505616
L256F
C
A
missense
Het
possibly damaging
0.542
phenotype
11/07/2013
26
80672
Helz
0.000
R0928
G1
225
N
11
107626693
I685K
T
A
missense
Het
probably damaging
0.989
phenotype
11/07/2013
27
80588
Hjurp
0.902
R0928
G1
217
N
1
88266524
GT
GTT
nonsense
Het
probably null
0.976
11/07/2013
28
80642
Izumo2
0.000
R0928
G1
225
N
7
44715423
I171F
A
T
missense
Het
possibly damaging
0.915
11/07/2013
29
80692
Krt83
0.073
R0928
G1
178
N
15
101491280
C57F
C
A
missense
Het
probably benign
0.004
11/07/2013
30
80609
Mapkbp1
0.000
R0928
G1
225
N
2
120015368
H400R
A
G
missense
Het
probably benign
0.001
11/07/2013
31
80630
Megf6
0.000
R0928
G1
207
N
4
154177047
V43E
T
A
missense
Het
probably damaging
0.995
11/07/2013
32
80697
Mut
1.000
R0928
G1
218
N
17
40937283
I67T
T
C
missense
Het
probably benign
0.237
phenotype
11/07/2013
33
80615
Ninl
0.000
R0928
G1
173
N
2
150963475
V396E
A
T
missense
Het
probably damaging
0.994
phenotype
11/07/2013
34
80599
Nvl
0.960
R0928
G1
225
N
1
181093902
V844E
A
T
missense
Het
probably benign
0.002
phenotype
11/07/2013
35
80680
Olfr11
0.193
R0928
G1
225
N
13
21638956
C189Y
C
T
missense
Het
probably damaging
1.000
phenotype
11/07/2013
36
80607
P2rx3
0.115
R0928
G1
163
N
2
85035298
M1K
A
T
start codon destroyed
Het
probably null
0.979
phenotype
11/07/2013
37
80656
Pabpn1l
0.000
R0928
G1
196
N
8
122622619
T20A
T
C
missense
Het
probably benign
0.029
11/07/2013
38
80624
Ppp3r2
0.076
R0928
G1
211
N
4
49681439
C
A
critical splice donor site
1 bp
Het
probably null
phenotype
11/07/2013
39
80620
Prmt6
0.000
R0928
G1
156
N
3
110250682
G97D
C
T
missense
Het
probably damaging
0.999
phenotype
11/07/2013
40
80654
Prmt9
0.172
R0928
G1
225
N
8
77581176
V823A
T
C
missense
Het
probably damaging
1.000
11/07/2013
41
80628
Skint11
0.060
R0928
G1
225
N
4
114244601
D79E
C
A
missense
Het
possibly damaging
0.947
11/07/2013
42
80666
Slc17a8
0.000
R0928
G1
225
N
10
89598683
H194L
T
A
missense
Het
probably damaging
0.999
phenotype
11/07/2013
43
80590
Slco6c1
0.000
R0928
G1
225
N
1
97104848
I293F
T
A
missense
Het
possibly damaging
0.883
11/07/2013
44
80676
Tcl1b4
0.080
R0928
G1
216
N
12
105202606
H43L
A
T
missense
Het
probably benign
0.014
11/07/2013
45
80688
Tm9sf1
0.137
R0928
G1
225
N
14
55636457
D528G
T
C
missense
Het
probably damaging
1.000
11/07/2013
46
80682
Tpbpb
0.031
R0928
G1
225
N
13
60902175
V47I
C
T
missense
Het
probably benign
0.059
11/07/2013
47
80684
Ttc37
0.480
R0928
G1
225
N
13
76113592
L142W
T
G
missense
Het
probably damaging
1.000
phenotype
11/07/2013
48
80604
Ttn
1.000
R0928
G1
225
N
2
76907532
G
T
intron
Het
probably benign
phenotype
11/07/2013
49
80660
Usp28
0.000
R0928
G1
225
N
9
49030891
S341A
T
G
missense
Het
possibly damaging
0.601
phenotype
11/07/2013
50
80658
Vwa5a
0.000
R0928
G1
225
N
9
38728007
Y345H
T
C
missense
Het
probably damaging
1.000
11/07/2013
51
80650
Wdr11
0.118
R0928
G1
225
N
7
129606653
D377E
C
A
missense
Het
probably damaging
1.000
phenotype
11/07/2013
52
80600
Zer1
0.128
R0928
G1
133
N
2
30101763
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
11/07/2013
[records 1 to 52 of 52]