Home
Phenotypic Mutations
Incidental Mutations
Engineered Mutations
Candidate Explorer
Protocols
Mutation Statistics
About
Contact
Links
Request Mice
Beutler Lab
APN
Strains @ MMRRC
Search Phenotypes
NEW
Candidate Explorer
Staff Login
Download
Incidental Mutations
36
incidental mutations are currently displayed, and affect
36
genes.
5
are Possibly Damaging.
13
are Probably Damaging.
14
are Probably Benign.
3
are Probably Null.
1
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
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
85961
4922502D21Rik
0.050
R1065
G1
225
Y
6
129323050
I155T
A
G
missense
Het
possibly damaging
0.834
0.179
11/18/2013
2
85972
Cd300ld2
0.000
R1065
G1
225
Y
11
115013760
T94A
T
C
missense
Het
probably damaging
1.000
0.647
11/18/2013
3
85984
Cdc42bpg
0.386
R1065
G1
225
Y
19
6322826
S1515N
G
A
missense
Het
probably damaging
0.996
0.064
11/18/2013
4
85973
Ckb
0.000
R1065
G1
225
Y
12
111671247
E150G
T
C
missense
Het
probably benign
0.066
0.616
phenotype
11/18/2013
5
85970
Cobl
0.000
R1065
G1
225
Y
11
12254327
M785L
T
A
missense
Het
possibly damaging
0.666
0.116
phenotype
11/18/2013
6
85968
Col6a5
0.849
R1065
G1
225
Y
9
105881783
N2075D
T
C
missense
Het
probably damaging
0.993
0.158
phenotype
11/18/2013
7
85955
Commd7
0.199
R1065
G1
225
Y
2
153619527
G
C
splice site
Het
probably benign
0.090
11/18/2013
8
85958
Corin
0.196
R1065
G1
225
Y
5
72301650
R927*
G
A
nonsense
Het
probably null
0.976
phenotype
11/18/2013
9
85960
Ift122
1.000
R1065
G1
225
Y
6
115875325
A
T
splice site
3 bp
Het
probably null
0.976
phenotype
11/18/2013
10
85953
Il1b
0.115
R1065
G1
225
Y
2
129368007
T83I
G
A
missense
Het
probably benign
0.005
0.113
phenotype
11/18/2013
11
85965
Ints4
0.964
R1065
G1
225
Y
7
97507892
T
C
critical splice donor site
2 bp
Het
probably null
0.950
phenotype
11/18/2013
12
85981
Msh6
1.000
R1065
G1
225
Y
17
87988463
T
G
unclassified
Het
probably benign
0.090
phenotype
11/18/2013
13
85969
Mtmr3
0.000
R1065
G1
225
Y
11
4492859
K392E
T
C
missense
Het
probably damaging
1.000
0.130
phenotype
11/18/2013
14
85951
Olfr1094
0.208
R1065
G1
225
Y
2
86829544
H264R
A
G
missense
Het
probably damaging
0.982
0.346
phenotype
11/18/2013
15
85963
Pde3a
0.246
R1065
G1
225
Y
6
141476732
T
C
splice site
Het
probably benign
phenotype
11/18/2013
16
85962
Pde6h
0.078
R1065
G1
225
Y
6
136959370
K37T
A
C
missense
Het
probably damaging
0.999
0.190
phenotype
11/18/2013
17
85966
Plat
0.000
R1065
G1
225
Y
8
22776863
D290E
C
A
missense
Het
probably damaging
0.989
0.647
phenotype
11/18/2013
18
85976
Polk
0.146
R1065
G1
225
Y
13
96508252
L122R
A
C
missense
Het
probably damaging
1.000
0.647
phenotype
11/18/2013
19
85975
Ppp1r3g
0.080
R1065
G1
225
Y
13
35969435
D279E
T
A
missense
Het
probably benign
0.074
0.108
11/18/2013
20
85957
Ptpru
0.000
R1065
G1
225
Y
4
131808340
E370G
T
C
missense
Het
possibly damaging
0.487
0.118
phenotype
11/18/2013
21
85954
Ralgapa2
0.215
R1065
G1
225
Y
2
146450558
Y187C
T
C
missense
Het
probably benign
0.003
0.060
phenotype
11/18/2013
22
85979
Rps6ka2
0.418
R1065
G1
225
Y
17
7281758
C
T
splice site
Het
probably benign
0.090
phenotype
11/18/2013
23
85971
Slit3
0.893
R1065
G1
155
Y
11
35121635
S41P
T
C
missense
Het
possibly damaging
0.856
0.188
phenotype
11/18/2013
24
85967
Smarca5
1.000
R1065
G1
159
Y
8
80704714
L958Q
A
T
missense
Het
probably damaging
1.000
0.647
phenotype
11/18/2013
25
85978
Snx9
0.827
R1065
G1
225
Y
17
5902361
T
C
splice site
Het
probably benign
0.090
phenotype
11/18/2013
26
85950
Stkld1
0.069
R1065
G1
225
Y
2
26940038
N72I
A
T
missense
Het
probably damaging
0.970
0.283
11/18/2013
27
85952
Strc
0.325
R1065
G1
225
Y
2
121366651
D1532Y
C
A
missense
Het
probably damaging
1.000
0.124
phenotype
11/18/2013
28
85977
Sucla2
0.941
R1065
G1
225
Y
14
73560634
C
T
unclassified
Het
probably benign
0.090
phenotype
11/18/2013
29
85982
Svil
0.149
R1065
G1
225
Y
18
5063777
T
G
splice site
Het
probably benign
phenotype
11/18/2013
30
85949
Traf3ip1
1.000
R1065
G1
225
Y
1
91500784
D122E
T
A
missense
Het
unknown
0.087
phenotype
11/18/2013
31
85956
Vmn2r7
0.077
R1065
G1
225
Y
3
64707138
D509E
A
T
missense
Het
possibly damaging
0.818
0.179
11/18/2013
32
85980
Vps52
1.000
R1065
G1
225
Y
17
33961239
Q306K
C
A
missense
Het
probably benign
0.019
0.062
phenotype
11/18/2013
33
85974
Wdr60
1.000
R1065
G1
225
Y
12
116256076
R82H
C
T
missense
Het
probably damaging
0.978
0.119
phenotype
11/18/2013
34
85983
Zfp407
1.000
R1065
G1
225
Y
18
84559773
A1072T
C
T
missense
Het
probably benign
0.139
0.090
phenotype
11/18/2013
35
85964
Zfp418
0.088
R1065
G1
225
Y
7
7181562
Q175K
C
A
missense
Het
probably benign
0.177
0.247
11/18/2013
36
85959
Zxdc
0.139
R1065
G1
225
Y
6
90378903
S465P
T
C
missense
Het
probably damaging
0.998
0.251
11/18/2013
[records 1 to 36 of 36]