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
39
incidental mutations are currently displayed, and affect
39
genes.
2
are Possibly Damaging.
17
are Probably Damaging.
14
are Probably Benign.
3
are Probably Null.
2
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 39 of 39]
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
279311
Ackr4
0.000
IGL02088
9
104098881
E289G
T
C
missense
Het
probably damaging
0.991
phenotype
04/16/2015
2
279338
Aldh1l1
0.000
IGL02088
6
90580590
A
T
splice site
Het
probably benign
phenotype
04/16/2015
3
279305
Ampd3
0.000
IGL02088
7
110793686
D220E
T
A
missense
Het
probably benign
0.001
phenotype
04/16/2015
4
279312
Ank3
0.837
IGL02088
10
69999373
V136A
T
C
missense
Het
probably damaging
0.996
phenotype
04/16/2015
5
279327
Atg14
0.911
IGL02088
14
47542859
K486R
T
C
missense
Het
probably benign
0.003
phenotype
04/16/2015
6
279320
Axin1
1.000
IGL02088
17
26188695
I637V
A
G
missense
Het
probably benign
0.045
phenotype
04/16/2015
7
279323
Axin2
1.000
IGL02088
11
108923616
F110Y
T
A
missense
Het
probably damaging
1.000
phenotype
04/16/2015
8
279318
Cdh12
0.296
IGL02088
15
21480339
K214*
A
T
nonsense
Het
probably null
phenotype
04/16/2015
9
279319
Cfap44
0.000
IGL02088
16
44451628
E1248A
A
C
missense
Het
possibly damaging
0.586
phenotype
04/16/2015
10
279331
Cryba4
0.067
IGL02088
5
112251009
A
G
unclassified
Het
probably benign
phenotype
04/16/2015
11
279332
Cyp2c68
0.000
IGL02088
19
39703521
A
G
splice site
Het
probably benign
04/16/2015
12
279333
Dnah5
0.802
IGL02088
15
28459118
G
T
critical splice acceptor site
Het
probably null
phenotype
04/16/2015
13
279308
Dok3
0.122
IGL02088
13
55524370
V165E
A
T
missense
Het
probably damaging
0.995
phenotype
04/16/2015
14
279313
Etl4
0.809
IGL02088
2
20806548
R1147S
A
T
missense
Het
probably damaging
1.000
phenotype
04/16/2015
15
279314
Fam212a
0.178
IGL02088
9
107984457
F220S
A
G
missense
Het
probably damaging
0.998
phenotype
04/16/2015
16
279329
Fbxl6
0.114
IGL02088
15
76535906
C502*
G
T
nonsense
Het
probably null
phenotype
04/16/2015
17
279324
Gp2
0.000
IGL02088
7
119454469
Y90N
A
T
missense
Het
probably damaging
1.000
phenotype
04/16/2015
18
279316
H1fnt
0.225
IGL02088
15
98257178
T30K
G
T
missense
Het
probably damaging
0.976
phenotype
04/16/2015
19
279315
Itfg2
0.129
IGL02088
6
128411606
V306A
A
G
missense
Het
probably benign
0.016
phenotype
04/16/2015
20
279325
Lrig2
1.000
IGL02088
3
104467108
Y219C
T
C
missense
Het
probably damaging
1.000
phenotype
04/16/2015
21
279330
Mccc1
1.000
IGL02088
3
35974202
I485N
A
T
missense
Het
probably damaging
1.000
phenotype
04/16/2015
22
279304
Mettl25
0.136
IGL02088
10
105823250
F391L
A
G
missense
Het
probably damaging
1.000
04/16/2015
23
279303
Muc19
0.144
IGL02088
15
91891168
C
T
splice site
Het
noncoding transcript
phenotype
04/16/2015
24
279326
Muc2
0.135
IGL02088
7
141751504
C182R
T
C
missense
Het
probably damaging
1.000
phenotype
04/16/2015
25
279337
Nlrp4g
0.071
IGL02088
9
124350453
T
C
unclassified
Het
noncoding transcript
04/16/2015
26
279334
Nms
0.054
IGL02088
1
38939277
A
G
utr 5 prime
Het
probably benign
phenotype
04/16/2015
27
279306
Nr3c1
1.000
IGL02088
18
39424391
N503S
T
C
missense
Het
probably damaging
0.999
phenotype
04/16/2015
28
279307
Olfr1495
0.165
IGL02088
19
13768666
F108S
T
C
missense
Het
probably damaging
1.000
phenotype
04/16/2015
29
279310
Olfr186
0.064
IGL02088
16
59027052
L285P
A
G
missense
Het
probably damaging
1.000
phenotype
04/16/2015
30
279317
Olfr828
0.140
IGL02088
9
18815923
V124I
C
T
missense
Het
probably benign
0.030
phenotype
04/16/2015
31
279301
Pcdhb5
0.112
IGL02088
18
37321959
S464N
G
A
missense
Het
probably benign
0.110
phenotype
04/16/2015
32
279309
Pcgf6
0.434
IGL02088
19
47050804
T6A
T
C
missense
Het
unknown
phenotype
04/16/2015
33
279336
Rdx
0.000
IGL02088
9
52060883
A
G
utr 5 prime
Het
probably benign
phenotype
04/16/2015
34
279322
Shmt1
0.000
IGL02088
11
60789653
T403A
T
C
missense
Het
probably damaging
1.000
phenotype
04/16/2015
35
279328
Slc35d1
1.000
IGL02088
4
103211325
F148L
A
G
missense
Het
probably benign
0.001
phenotype
04/16/2015
36
279335
Tk1
0.000
IGL02088
11
117824665
A
G
unclassified
Het
probably benign
phenotype
04/16/2015
37
279321
Tnks
0.000
IGL02088
8
34839994
I1134F
T
A
missense
Het
possibly damaging
0.503
phenotype
04/16/2015
38
279302
Ttn
1.000
IGL02088
2
76726691
V29990A
A
G
missense
Het
probably damaging
0.999
phenotype
04/16/2015
39
279339
Zcchc11
0.000
IGL02088
4
108512218
A
G
splice site
Het
probably benign
phenotype
04/16/2015
[records 1 to 39 of 39]