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Incidental Mutations
54
incidental mutations are currently displayed, and affect
54
genes.
8
are Possibly Damaging.
21
are Probably Damaging.
15
are Probably Benign.
7
are Probably Null.
3
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 54 of 54]
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
429768
Acox2
0.126
R5397
G1
225
N
14
8243803 (GRCm38)
T518A
T
C
missense
Het
probably benign
0.021
phenotype
2016-09-06
2
429772
Acvr1b
1.000
R5397
G1
225
N
15
101198964 (GRCm38)
V254D
T
A
missense
Het
probably damaging
0.990
phenotype
2016-09-06
3
429732
Adar
1.000
R5397
G1
225
N
3
89735319 (GRCm38)
I169T
T
C
missense
Het
probably benign
0.000
phenotype
2016-09-06
4
429775
Afg3l2
1.000
R5397
G1
225
N
18
67421259 (GRCm38)
L458M
G
T
missense
Het
probably damaging
1.000
0.387
phenotype
2016-09-06
5
429744
Arap1
0.000
R5397
G1
225
N
7
101384912 (GRCm38)
Q187L
A
T
missense
Het
possibly damaging
0.951
phenotype
2016-09-06
6
429759
Atad5
1.000
R5397
G1
225
N
11
80111493 (GRCm38)
M1037K
T
A
missense
Het
probably damaging
0.999
phenotype
2016-09-06
7
429753
Bsg
0.920
R5397
G1
225
N
10
79708795 (GRCm38)
W56R
T
A
missense
Het
probably damaging
1.000
phenotype
2016-09-06
8
429770
C1qtnf3
0.000
R5397
G1
225
N
15
10978541 (GRCm38)
T276A
A
G
missense
Het
probably damaging
0.989
phenotype
2016-09-06
9
429725
Capn2
1.000
R5397
G1
225
N
1
182470706 (GRCm38)
C665R
A
G
missense
Het
probably damaging
1.000
phenotype
2016-09-06
10
429767
Cast
0.000
R5397
G1
225
N
13
74720937 (GRCm38)
S248P
A
G
missense
Het
possibly damaging
0.827
phenotype
2016-09-06
11
429758
Cd68
0.300
R5397
G1
225
N
11
69665658 (GRCm38)
V108I
C
T
missense
Het
probably benign
0.003
phenotype
2016-09-06
12
429771
Cyp2d11
0.155
R5397
G1
225
N
15
82392078 (GRCm38)
W131R
A
T
missense
Het
probably damaging
1.000
2016-09-06
13
429762
Dhx58
0.180
R5397
G1
225
N
11
100703920 (GRCm38)
V50A
A
G
missense
Het
probably damaging
0.998
phenotype
2016-09-06
14
429769
Fam124a
0.063
R5397
G1
225
N
14
62606389 (GRCm38)
S449G
A
G
missense
Het
probably benign
0.000
2016-09-06
15
429738
Flnc
1.000
R5397
G1
225
N
6
29441161 (GRCm38)
M371I
G
A
missense
Het
possibly damaging
0.866
phenotype
2016-09-06
16
429755
Gad1-ps
0.186
R5397
G1
225
N
10
99445147 (GRCm38)
G
A
exon
Het
noncoding transcript
0.291
2016-09-06
17
429764
Gm4787
0.061
R5397
G1
225
N
12
81377830 (GRCm38)
T518S
G
C
missense
Het
probably benign
0.008
0.090
2016-09-06
18
429776
Gm7102
0.128
R5397
G1
225
N
19
61175926 (GRCm38)
G24R
C
T
missense
Het
unknown
0.109
2016-09-06
19
429730
Gpr149
0.083
R5397
G1
225
N
3
62530805 (GRCm38)
S644P
A
G
missense
Het
probably damaging
1.000
phenotype
2016-09-06
20
429731
Gucy1b1
0.877
R5397
G1
225
N
3
82044151 (GRCm38)
T274I
G
A
missense
Het
possibly damaging
0.915
phenotype
2016-09-06
21
429721
Kcnq5
0.528
R5397
G1
225
N
1
21405856 (GRCm38)
V541A
A
G
missense
Het
probably damaging
1.000
phenotype
2016-09-06
22
429723
Kdm5b
0.452
R5397
G1
225
N
1
134622098 (GRCm38)
G
A
splice site
5 bp
Het
probably null
0.976
phenotype
2016-09-06
23
429747
Lig4
1.000
R5397
G1
225
N
8
9972644 (GRCm38)
R379S
G
T
missense
Het
probably benign
0.011
phenotype
2016-09-06
24
429750
Map7
0.468
R5397
G1
209
N
10
20273321 (GRCm38)
R514Q
G
A
missense
Het
unknown
phenotype
2016-09-06
25
429728
Mertk
0.121
R5397
G1
225
N
2
128771464 (GRCm38)
F467I
T
A
missense
Het
possibly damaging
0.860
phenotype
2016-09-06
26
429774
Mettl4
0.226
R5397
G1
225
N
17
94727277 (GRCm38)
Y463*
A
T
nonsense
Het
probably null
2016-09-06
27
429766
Nme8
0.128
R5397
G1
225
N
13
19694379 (GRCm38)
D70G
T
C
missense
Het
probably damaging
0.999
phenotype
2016-09-06
28
429749
Npat
1.000
R5397
G1
225
N
9
53570474 (GRCm38)
N1161D
A
G
missense
Het
probably damaging
0.998
2016-09-06
29
429727
Olfr1283
0.582
R5397
G1
225
N
2
111368940 (GRCm38)
C103S
T
A
missense
Het
probably benign
0.001
phenotype
2016-09-06
30
429745
Olfr616
0.118
R5397
G1
225
N
7
103564506 (GRCm38)
I258F
T
A
missense
Het
probably damaging
0.994
phenotype
2016-09-06
31
429756
Olfr813
0.118
R5397
G1
225
N
10
129856710 (GRCm38)
F64S
T
C
missense
Het
probably damaging
1.000
phenotype
2016-09-06
32
478333
Paxip1
1.000
R5397
G1
225
N
5
27772004 (GRCm38)
A
T
unclassified
Het
probably benign
phenotype
2017-06-23
33
429737
Peg10
1.000
R5397
G1
217
N
6
4756453 (GRCm38)
C
CTCG
small insertion
Het
probably benign
phenotype
2016-09-06
34
429754
Plxnc1
0.252
R5397
G1
225
N
10
94843752 (GRCm38)
T923A
T
C
missense
Het
probably benign
0.077
phenotype
2016-09-06
35
429722
Pms1
0.000
R5397
G1
225
N
1
53192120 (GRCm38)
K857*
T
A
nonsense
Het
probably null
phenotype
2016-09-06
36
429761
Ppp1r9b
0.000
R5397
G1
202
N
11
95002110 (GRCm38)
E260G
A
G
missense
Het
probably damaging
0.997
phenotype
2016-09-06
37
429734
Prpf3
1.000
R5397
G1
225
N
3
95853579 (GRCm38)
S4T
A
T
missense
Het
probably benign
0.087
phenotype
2016-09-06
38
429763
Rdh14
0.076
R5397
G1
225
N
12
10394869 (GRCm38)
V240D
T
A
missense
Het
probably damaging
0.992
2016-09-06
39
429777
Ripply1
0.000
R5397
G1
116
N
X
139779850 (GRCm38)
TTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCT
TTCCTCCTCCTCCTCCTCCTCCTCCTCCT
small deletion
Het
probably benign
0.090
phenotype
2016-09-06
40
429733
S100a1
R5397
G1
225
N
3
90512135 (GRCm38)
M1K
A
T
start codon destroyed
Het
probably null
0.999
phenotype
2016-09-06
41
429736
Slc2a5
0.094
R5397
G1
225
N
4
150139823 (GRCm38)
G
A
splice site
5 bp
Het
probably null
phenotype
2016-09-06
42
478334
Slc5a5
0.000
R5397
G1
225
N
8
70891179 (GRCm38)
T160A
T
C
missense
Het
probably damaging
0.996
phenotype
2017-06-23
43
429746
Srcap
0.956
R5397
G1
225
N
7
127553296 (GRCm38)
T
G
critical splice donor site
2 bp
Het
probably null
phenotype
2016-09-06
44
429765
Tcrg-V5
0.089
R5397
G1
225
N
13
19192558 (GRCm38)
E42D
A
C
missense
Het
possibly damaging
0.845
2016-09-06
45
429729
Tgm6
0.000
R5397
G1
225
N
2
130141908 (GRCm38)
M329K
T
A
missense
Het
possibly damaging
0.899
phenotype
2016-09-06
46
429760
Tom1l1
0.196
R5397
G1
225
N
11
90661774 (GRCm38)
A201V
G
A
missense
Het
probably benign
0.022
2016-09-06
47
429748
Ttc13
0.000
R5397
G1
225
N
8
124675263 (GRCm38)
T662A
T
C
missense
Het
possibly damaging
0.936
2016-09-06
48
429726
Ttn
1.000
R5397
G1
225
N
2
76725255 (GRCm38)
T30469A
T
C
missense
Het
probably damaging
0.993
phenotype
2016-09-06
49
429742
Ube3a
0.626
R5397
G1
225
N
7
59286912 (GRCm38)
S645R
T
A
missense
Het
probably benign
0.264
phenotype
2016-09-06
50
429751
Vgll2
0.748
R5397
G1
225
N
10
52025166 (GRCm38)
E64G
A
G
missense
Het
probably damaging
1.000
phenotype
2016-09-06
51
429739
Vmn1r25
0.170
R5397
G1
225
N
6
57979075 (GRCm38)
C76*
A
T
nonsense
Het
probably null
2016-09-06
52
429773
Vmn2r101
0.080
R5397
G1
225
N
17
19588842 (GRCm38)
N78D
A
G
missense
Het
probably damaging
0.999
2016-09-06
53
429757
Zcchc10
0.087
R5397
G1
125
N
11
53332517 (GRCm38)
CCAGCAGCAGCAGCAGCAGCAG
CCAGCAGCAGCAGCAGCAG
unclassified
Het
probably benign
2016-09-06
54
429735
Zcchc7
0.422
R5397
G1
225
N
4
44926048 (GRCm38)
A28E
C
A
missense
Het
probably damaging
0.958
2016-09-06
[records 1 to 54 of 54]