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Incidental Mutations
40
incidental mutations are currently displayed, and affect
40
genes.
12
are Possibly Damaging.
16
are Probably Damaging.
6
are Probably Benign.
6
are Probably Null.
0
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 40 of 40]
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
522531
2410131K14Rik
0.184
R6563
G1
212.01
Y
5
118258982
V92A
T
C
missense
Het
possibly damaging
0.945
0.513
06/06/2018
2
522523
Arhgap11a
0.000
R6563
G1
225.01
Y
2
113833902
C679S
A
T
missense
Het
probably benign
0.001
phenotype
06/06/2018
3
522551
Atg4d
0.000
R6563
G1
225.01
Y
9
21268460
L235F
C
T
missense
Het
possibly damaging
0.803
phenotype
06/06/2018
4
522577
Cyp2d22
0.064
R6563
G1
225.01
Y
15
82371912
W174R
A
T
missense
Het
probably damaging
1.000
0.968
06/06/2018
5
522527
Cyp4a14
0.072
R6563
G1
225.01
Y
4
115492086
H259L
T
A
missense
Het
probably benign
0.232
phenotype
06/06/2018
6
522575
Dennd3
0.145
R6563
G1
225.01
Y
15
73544380
H493L
A
T
missense
Het
probably damaging
0.984
0.414
06/06/2018
7
522517
Diexf
0.969
R6563
G1
225.01
Y
1
193118390
R374L
C
A
missense
Het
probably damaging
1.000
06/06/2018
8
522519
Dnm1
1.000
R6563
G1
196.01
N
2
32312726
D759V
T
A
missense
Het
probably damaging
1.000
phenotype
06/06/2018
9
522529
Dvl1
0.000
R6563
G1
225.01
Y
4
155856253
N443K
T
A
missense
Het
probably damaging
0.995
phenotype
06/06/2018
10
522549
Dync2h1
1.000
R6563
G1
225.01
Y
9
7120819
V2156A
A
G
missense
Het
probably benign
0.267
phenotype
06/06/2018
11
522583
Enpp5
0.000
R6563
G1
225.01
Y
17
44085264
G356S
G
A
missense
Het
probably damaging
1.000
0.917
phenotype
06/06/2018
12
522587
Ermp1
0.000
R6563
G1
225.01
Y
19
29623778
D523G
T
C
missense
Het
probably damaging
0.999
0.736
phenotype
06/06/2018
13
522525
Fam83c
0.069
R6563
G1
225.01
Y
2
155830952
V295A
A
G
missense
Het
probably damaging
0.983
06/06/2018
14
522571
Gphn
1.000
R6563
G1
225.01
Y
12
78680396
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
06/06/2018
15
522513
Irs1
0.592
R6563
G1
225.01
Y
1
82288407
N696I
T
A
missense
Het
probably damaging
0.984
0.299
phenotype
06/06/2018
16
522535
Kmt5c
0.000
R6563
G1
225.01
Y
7
4742629
Y96C
A
G
missense
Het
probably damaging
1.000
phenotype
06/06/2018
17
522579
Krt77
0.000
R6563
G1
225.01
Y
15
101862923
T315N
G
T
missense
Het
probably damaging
1.000
0.280
phenotype
06/06/2018
18
522553
L3mbtl3
1.000
R6563
G1
225.01
Y
10
26302863
A
C
splice site
Het
probably null
phenotype
06/06/2018
19
522585
Lama3
1.000
R6563
G1
225.01
Y
18
12537766
Y2409F
A
T
missense
Het
probably damaging
0.999
0.135
phenotype
06/06/2018
20
522569
Lrrc9
0.167
R6563
G1
225.01
Y
12
72486395
A
G
splice site
4 bp
Het
probably null
06/06/2018
21
522539
Ltbp4
1.000
R6563
G1
195.01
Y
7
27309063
N1273K
A
T
missense
Het
probably damaging
0.999
phenotype
06/06/2018
22
522545
Mfsd13b
0.179
R6563
G1
225.01
Y
7
120995467
A321T
G
A
missense
Het
probably damaging
0.990
0.647
06/06/2018
23
522521
Mvb12b
0.848
R6563
G1
225.01
Y
2
33825116
H167Q
A
T
missense
Het
probably benign
0.037
phenotype
06/06/2018
24
522559
Myo1g
0.000
R6563
G1
225.01
Y
11
6517146
N230Y
T
A
missense
Het
possibly damaging
0.907
0.182
phenotype
06/06/2018
25
522557
Olfr57
0.090
R6563
G1
225.01
Y
10
79035217
R140S
A
T
missense
Het
possibly damaging
0.667
phenotype
06/06/2018
26
522567
Prkar2b
0.457
R6563
G1
225.01
Y
12
31993786
G
T
splice site
Het
probably null
phenotype
06/06/2018
27
522561
Pwwp2a
0.159
R6563
G1
225.01
Y
11
43705765
A586S
G
T
missense
Het
possibly damaging
0.880
06/06/2018
28
522541
Ryr1
1.000
R6563
G1
225.01
Y
7
29095492
V1150A
A
G
missense
Het
possibly damaging
0.922
phenotype
06/06/2018
29
543445
Sh3bgr
0.106
R6563
G1
225.01
Y
16
96205943
A
G
splice site
4 bp
Het
probably null
12/21/2018
30
522589
Slk
1.000
R6563
G1
225.01
Y
19
47636469
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
06/06/2018
31
522555
Snx3
1.000
R6563
G1
225.01
Y
10
42526036
E82G
A
G
missense
Het
possibly damaging
0.540
phenotype
06/06/2018
32
522565
Srcin1
0.000
R6563
G1
112.01
Y
11
97534774
Y486N
A
T
missense
Het
possibly damaging
0.737
phenotype
06/06/2018
33
522573
Tecpr2
0.000
R6563
G1
225.01
Y
12
110929087
E336G
A
G
missense
Het
probably benign
0.002
phenotype
06/06/2018
34
522547
Terf2ip
1.000
R6563
G1
225.01
Y
8
112018202
V384F
G
T
missense
Het
probably damaging
0.999
phenotype
06/06/2018
35
522515
Tnn
0.520
R6563
G1
189.01
Y
1
160088398
S1250C
T
A
missense
Het
probably damaging
1.000
0.855
06/06/2018
36
522563
Tspoap1
0.000
R6563
G1
225.01
Y
11
87777159
E1263G
A
G
missense
Het
possibly damaging
0.865
0.074
Rimbp2
tm1.2Geno
does not exacerbate the phenotype of the latter single KO. [provided by MGI curators] (source: MGI)">phenotype
06/06/2018
37
522543
Tubgcp5
0.965
R6563
G1
225.01
Y
7
55825661
R932G
A
G
missense
Het
possibly damaging
0.903
06/06/2018
38
522537
Vmn1r175
0.076
R6563
G1
225.01
Y
7
23808605
I199T
A
G
missense
Het
possibly damaging
0.611
06/06/2018
39
522581
Vmn1r225
0.062
R6563
G1
225.01
Y
17
20502501
A68V
C
T
missense
Het
probably benign
0.034
0.183
06/06/2018
40
522533
Vmn2r24
0.071
R6563
G1
225.01
Y
6
123804178
N448Y
A
T
missense
Het
possibly damaging
0.858
06/06/2018
[records 1 to 40 of 40]