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Incidental Mutations
52
incidental mutations are currently displayed, and affect
52
genes.
4
are Possibly Damaging.
14
are Probably Damaging.
24
are Probably Benign.
7
are Probably Null.
1
create premature stop codons.
2
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
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
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
85742
0610010F05Rik
0.191
R1078
G1
225
Y
11
23611762 (GRCm38)
I358S
A
C
missense
Het
probably benign
0.450
0.090
2013-11-18
2
85723
9130230L23Rik
0.142
R1078
G1
225
Y
5
65988355 (GRCm38)
T138A
T
C
missense
Het
unknown
0.087
2013-11-18
3
85756
Abi3bp
0.079
R1078
G1
225
Y
16
56654081 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.949
2013-11-18
4
85731
Alpk3
0.283
R1078
G1
225
Y
7
81078600 (GRCm38)
M493L
A
T
missense
Het
probably benign
0.000
0.090
phenotype
2013-11-18
5
85757
Bace2
0.085
R1078
G1
114
Y
16
97356860 (GRCm38)
A20V
C
T
missense
Het
unknown
0.222
phenotype
2013-11-18
6
85728
Bms1
1.000
R1078
G1
225
Y
6
118405221 (GRCm38)
D452G
T
C
missense
Het
probably benign
0.001
0.090
phenotype
2013-11-18
7
85715
Ccdc187
0.075
R1078
G1
225
Y
2
26294377 (GRCm38)
T3A
T
C
missense
Het
probably damaging
0.979
0.459
2013-11-18
8
85734
Ctu2
1.000
R1078
G1
225
Y
8
122481499 (GRCm38)
V95A
T
C
missense
Het
possibly damaging
0.686
0.179
phenotype
2013-11-18
9
85730
Cyp2a5
0.058
R1078
G1
225
Y
7
26835541 (GRCm38)
K60E
A
G
missense
Het
probably benign
0.327
0.090
phenotype
2013-11-18
10
85760
Cyp4f13
0.095
R1078
G1
225
Y
17
32925568 (GRCm38)
H318R
T
C
missense
Het
probably damaging
1.000
0.837
phenotype
2013-11-18
11
85750
Dlgap5
0.758
R1078
G1
225
Y
14
47399566 (GRCm38)
T485M
G
A
missense
Het
probably damaging
1.000
0.647
phenotype
2013-11-18
12
85747
Dsp
1.000
R1078
G1
225
Y
13
38183106 (GRCm38)
C
T
splice site
Het
probably benign
phenotype
2013-11-18
13
85748
Ell2
0.000
R1078
G1
225
Y
13
75746419 (GRCm38)
T
C
splice site
Het
probably benign
2013-11-18
14
85729
Eml2
0.000
R1078
G1
225
Y
7
19179762 (GRCm38)
Y168F
A
T
missense
Het
probably benign
0.237
0.097
2013-11-18
15
85725
Ep400
1.000
R1078
G1
225
Y
5
110735522 (GRCm38)
C
T
unclassified
Het
probably benign
0.091
phenotype
2013-11-18
16
85755
Ercc4
0.969
R1078
G1
225
Y
16
13130197 (GRCm38)
A336D
C
A
missense
Het
probably benign
0.001
0.090
phenotype
2013-11-18
17
85762
Fam189a2
0.089
R1078
G1
225
Y
19
23973575 (GRCm38)
R547S
T
A
missense
Het
probably benign
0.012
0.072
2013-11-18
18
85720
Fat4
1.000
R1078
G1
225
Y
3
38983086 (GRCm38)
L3629S
T
C
missense
Het
probably benign
0.100
0.103
phenotype
2013-11-18
19
85721
Gabbr2
0.105
R1078
G1
207
Y
4
46664833 (GRCm38)
R925H
C
T
missense
Het
probably damaging
0.993
0.096
phenotype
2013-11-18
20
85716
Gfi1b
1.000
R1078
G1
225
Y
2
28613865 (GRCm38)
W108R
A
T
missense
Het
probably damaging
1.000
0.428
phenotype
2013-11-18
21
85753
Gtse1
0.075
R1078
G1
225
Y
15
85862307 (GRCm38)
P108L
C
T
missense
Het
probably damaging
0.980
0.199
phenotype
2013-11-18
22
85724
Hfm1
0.077
R1078
G1
225
Y
5
106878830 (GRCm38)
F140I
A
T
missense
Het
probably damaging
1.000
0.220
phenotype
2013-11-18
23
85736
Hyal2
1.000
R1078
G1
225
Y
9
107572246 (GRCm38)
H400Q
T
A
missense
Het
probably benign
0.000
0.092
phenotype
2013-11-18
24
85714
Igfn1
0.091
R1078
G1
225
Y
1
135974847 (GRCm38)
Y371H
A
G
missense
Het
probably damaging
0.996
0.264
2013-11-18
25
85740
Iltifb
0.058
R1078
G1
225
Y
10
118290151 (GRCm38)
*180C
T
G
makesense
Het
probably null
0.818
2013-11-18
26
85726
Kdm2b
1.000
R1078
G1
225
Y
5
122961541 (GRCm38)
T118A
T
C
missense
Het
possibly damaging
0.831
0.083
phenotype
2013-11-18
27
85719
Lama5
1.000
R1078
G1
225
Y
2
180179764 (GRCm38)
A
T
unclassified
Het
probably benign
phenotype
2013-11-18
28
85713
Lgr6
0.000
R1078
G1
225
Y
1
134994010 (GRCm38)
A199T
C
T
missense
Het
probably damaging
1.000
0.165
phenotype
2013-11-18
29
85752
Lmo7
0.172
R1078
G1
225
Y
14
101920474 (GRCm38)
C
T
splice site
Het
probably benign
0.090
phenotype
2013-11-18
30
85744
Lrrc37a
0.098
R1078
G1
225
Y
11
103497631 (GRCm38)
P2323T
G
T
missense
Het
unknown
0.087
2013-11-18
31
85722
Lrrc38
0.060
R1078
G1
168
Y
4
143350518 (GRCm38)
Y117C
A
G
missense
Het
probably benign
0.057
0.078
2013-11-18
32
85735
Myo1e
0.000
R1078
G1
225
Y
9
70383999 (GRCm38)
V1024A
T
C
missense
Het
probably benign
0.000
0.090
phenotype
2013-11-18
33
85739
Myrfl
0.000
R1078
G1
225
Y
10
116776732 (GRCm38)
N904S
T
C
missense
Het
possibly damaging
0.936
0.179
2013-11-18
34
85717
Olfr1015
0.223
R1078
G1
225
Y
2
85786093 (GRCm38)
V194A
T
C
missense
Het
possibly damaging
0.527
0.269
phenotype
2013-11-18
35
85761
Olfr103
0.062
R1078
G1
225
Y
17
37337026 (GRCm38)
I69F
T
A
missense
Het
probably damaging
0.980
0.428
phenotype
2013-11-18
36
85718
Olfr1297
0.085
R1078
G1
225
Y
2
111621345 (GRCm38)
H243R
T
C
missense
Het
probably damaging
1.000
0.156
phenotype
2013-11-18
37
85746
Pld4
0.000
R1078
G1
225
Y
12
112763442 (GRCm38)
I53F
A
T
missense
Het
probably benign
0.000
0.149
phenotype
2013-11-18
38
85733
Plekhg4
0.281
R1078
G1
225
Y
8
105381677 (GRCm38)
C1117*
T
A
nonsense
Het
probably null
0.976
phenotype
2013-11-18
39
85712
Prss39
0.074
R1078
G1
225
Y
1
34502086 (GRCm38)
E224K
G
A
missense
Het
probably benign
0.003
0.090
2013-11-18
40
85751
Psme1
0.000
R1078
G1
225
Y
14
55580650 (GRCm38)
G149V
G
T
missense
Het
probably damaging
1.000
0.968
phenotype
2013-11-18
41
85754
Soat2
0.094
R1078
G1
193
Y
15
102153138 (GRCm38)
T
A
splice site
Het
probably null
0.976
phenotype
2013-11-18
42
85738
Stab2
0.000
R1078
G1
225
Y
10
86907133 (GRCm38)
C
T
splice site
5 bp
Het
probably null
phenotype
2013-11-18
43
85763
Tcf7l2
1.000
R1078
G1
154
N
19
55743195 (GRCm38)
T127A
A
G
missense
Het
probably benign
0.192
phenotype
2013-11-18
44
85758
Tcp1
0.945
R1078
G1
214
Y
17
12923204 (GRCm38)
T
C
unclassified
Het
probably benign
phenotype
2013-11-18
45
85749
Thbs4
0.000
R1078
G1
194
Y
13
92762926 (GRCm38)
G
A
splice site
Het
probably benign
phenotype
2013-11-18
46
85727
Tmf1
0.160
R1078
G1
173
Y
6
97173300 (GRCm38)
D482G
T
C
missense
Het
probably damaging
0.999
0.131
phenotype
2013-11-18
47
85732
Trim66
0.166
R1078
G1
225
Y
7
109472319 (GRCm38)
P591H
G
T
missense
Het
probably damaging
0.999
0.096
2013-11-18
48
85759
Umodl1
0.000
R1078
G1
225
Y
17
30959373 (GRCm38)
S108P
T
C
missense
Het
probably benign
0.001
0.090
2013-11-18
49
85745
Unc79
1.000
R1078
G1
225
Y
12
103074853 (GRCm38)
M715R
T
G
missense
Het
probably benign
0.032
0.090
phenotype
2013-11-18
50
85741
Usp34
0.645
R1078
G1
225
Y
11
23433175 (GRCm38)
C
A
splice site
Het
probably benign
2013-11-18
51
85737
Utrn
0.000
R1078
G1
225
Y
10
12455566 (GRCm38)
T
G
critical splice acceptor site
Het
probably null
0.959
phenotype
2013-11-18
52
85743
Zfp830
1.000
R1078
G1
208
Y
11
82765339 (GRCm38)
T
C
splice site
Het
probably null
0.154
phenotype
2013-11-18
[records 1 to 52 of 52]