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Incidental Mutations
118
incidental mutations are currently displayed, and affect
117
genes.
22
are Possibly Damaging.
41
are Probably Damaging.
38
are Probably Benign.
12
are Probably Null.
5
create premature stop codons.
5
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 100 of 118]
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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
236590
4930553M12Rik
0.080
R2144
G1
225
N
4
88868174 (GRCm38)
T69I
G
A
missense
Het
unknown
2014-10-01
2
236591
4930553M12Rik
0.080
R2144
G1
225
N
4
88868175 (GRCm38)
T69S
T
A
missense
Het
unknown
2014-10-01
3
236653
Acsl6
0.442
R2144
G1
225
N
11
54341778 (GRCm38)
Q485L
A
T
missense
Het
probably damaging
1.000
phenotype
2014-10-01
4
236639
Adam5
0.057
R2144
G1
225
N
8
24815480 (GRCm38)
V81F
C
A
missense
Het
probably benign
0.136
phenotype
2014-10-01
5
236691
Armc4
0.204
R2144
G1
225
N
18
7127229 (GRCm38)
E995K
C
T
missense
Het
probably damaging
0.961
phenotype
2014-10-01
6
236664
Atp5s
0.000
R2144
G1
225
N
12
69741054 (GRCm38)
Q88R
A
G
missense
Het
probably damaging
0.972
0.243
phenotype
2014-10-01
7
236570
Bag2
0.269
R2144
G1
225
N
1
33746831 (GRCm38)
S137P
A
G
missense
Het
possibly damaging
0.865
phenotype
2014-10-01
8
236689
Birc6
1.000
R2144
G1
225
N
17
74660413 (GRCm38)
Q4103L
A
T
missense
Het
possibly damaging
0.712
0.076
phenotype
2014-10-01
9
236655
Camta2
0.603
R2144
G1
225
N
11
70671575 (GRCm38)
F999L
A
G
missense
Het
probably benign
0.313
0.165
phenotype
2014-10-01
10
236668
Cap2
0.119
R2144
G1
225
N
13
46560502 (GRCm38)
A
T
critical splice acceptor site
Het
probably null
phenotype
2014-10-01
11
236666
Ccnk
1.000
R2144
G1
225
N
12
108189090 (GRCm38)
L102Q
T
A
missense
Het
probably null
1.000
phenotype
2014-10-01
12
236595
Cd52
R2144
G1
225
N
4
134093737 (GRCm38)
T
C
unclassified
Het
probably benign
phenotype
2014-10-01
13
236580
Cdc123
1.000
R2144
G1
223
N
2
5810806 (GRCm38)
I160K
A
T
missense
Het
probably benign
0.189
2014-10-01
14
236649
Cep85l
0.237
R2144
G1
225
N
10
53358126 (GRCm38)
N52S
T
C
missense
Het
probably benign
0.035
phenotype
2014-10-01
15
236575
Cntnap5a
0.000
R2144
G1
225
N
1
116101710 (GRCm38)
T298I
C
T
missense
Het
probably benign
0.139
phenotype
2014-10-01
16
236606
Cpsf4
0.944
R2144
G1
225
N
5
145178762 (GRCm38)
S192I
G
T
missense
Het
probably benign
0.001
phenotype
2014-10-01
17
236584
Cpxm1
0.588
R2144
G1
224
N
2
130397410 (GRCm38)
S33P
A
G
missense
Het
probably benign
0.001
phenotype
2014-10-01
18
236621
Cyp2a12
0.084
R2144
G1
225
N
7
27034769 (GRCm38)
T376S
A
T
missense
Het
possibly damaging
0.953
2014-10-01
19
236607
Cyp3a16
0.170
R2144
G1
225
N
5
145456084 (GRCm38)
F137S
A
G
missense
Het
probably damaging
1.000
2014-10-01
20
236572
Des
0.458
R2144
G1
225
N
1
75366804 (GRCm38)
T444A
A
G
missense
Het
probably benign
0.450
phenotype
2014-10-01
21
236681
Dgcr8
1.000
R2144
G1
225
N
16
18284256 (GRCm38)
G54D
C
T
missense
Het
probably damaging
1.000
phenotype
2014-10-01
22
236611
Doxl2
0.000
R2144
G1
225
N
6
48975291 (GRCm38)
H50R
A
G
missense
Het
probably benign
0.003
2014-10-01
23
236694
Dsc3
1.000
R2144
G1
225
N
18
19980686 (GRCm38)
F393S
A
G
missense
Het
possibly damaging
0.810
phenotype
2014-10-01
24
236578
Dstyk
0.193
R2144
G1
225
N
1
132463375 (GRCm38)
M838K
T
A
missense
Het
probably damaging
1.000
0.515
phenotype
2014-10-01
25
236599
Dvl1
0.000
R2144
G1
189
N
4
155847816 (GRCm38)
V28I
G
A
missense
Het
possibly damaging
0.837
0.075
phenotype
2014-10-01
26
236665
Eml5
0.264
R2144
G1
225
N
12
98810605 (GRCm38)
F1417C
A
C
missense
Het
probably damaging
1.000
2014-10-01
27
236605
Ep400
1.000
R2144
G1
225
N
5
110703518 (GRCm38)
M1366K
A
T
missense
Het
unknown
phenotype
2014-10-01
28
236699
Epg5
0.942
R2144
G1
225
N
18
77954197 (GRCm38)
C425F
G
T
missense
Het
possibly damaging
0.779
phenotype
2014-10-01
29
236683
Epha3
0.262
R2144
G1
225
N
16
63773317 (GRCm38)
R136P
C
G
missense
Het
possibly damaging
0.862
phenotype
2014-10-01
30
236596
Extl1
0.275
R2144
G1
225
N
4
134371044 (GRCm38)
E225D
C
A
missense
Het
probably benign
0.305
phenotype
2014-10-01
31
236679
Fam186b
0.000
R2144
G1
225
N
15
99280657 (GRCm38)
Y263H
A
G
missense
Het
probably benign
0.004
phenotype
2014-10-01
32
236698
Fbn2
0.929
R2144
G1
225
N
18
58052993 (GRCm38)
V1761A
A
G
missense
Het
possibly damaging
0.655
phenotype
2014-10-01
33
236674
Fer1l6
0.075
R2144
G1
225
N
15
58627534 (GRCm38)
M1251K
T
A
missense
Het
probably benign
0.000
0.090
2014-10-01
34
236685
Gart
1.000
R2144
G1
199
N
16
91630081 (GRCm38)
I555N
A
T
missense
Het
probably damaging
0.999
phenotype
2014-10-01
35
236662
Gm11596
0.082
R2144
G1
225
N
11
99792963 (GRCm38)
C110*
A
T
nonsense
Het
probably null
2014-10-01
36
236651
Gnptab
0.950
R2144
G1
225
N
10
88428506 (GRCm38)
S262L
C
T
missense
Het
possibly damaging
0.895
phenotype
2014-10-01
37
236581
Gpr21
0.103
R2144
G1
225
N
2
37518231 (GRCm38)
V263A
T
C
missense
Het
probably benign
0.017
phenotype
2014-10-01
38
236677
Gxylt1
1.000
R2144
G1
225
N
15
93254480 (GRCm38)
I224V
T
C
missense
Het
probably benign
0.313
phenotype
2014-10-01
39
236687
H2-Aa
0.129
R2144
G1
225
N
17
34283827 (GRCm38)
S122P
A
G
missense
Het
probably damaging
0.995
phenotype
2014-10-01
40
236608
Hsph1
0.477
R2144
G1
225
N
5
149630337 (GRCm38)
A
C
critical splice donor site
2 bp
Het
probably null
phenotype
2014-10-01
41
236684
Hunk
0.000
R2144
G1
225
N
16
90432532 (GRCm38)
D94N
G
A
missense
Het
probably damaging
0.994
phenotype
2014-10-01
42
236577
Ikbke
0.000
R2144
G1
225
N
1
131273474 (GRCm38)
V176L
C
A
missense
Het
probably damaging
0.978
0.265
phenotype
2014-10-01
43
236657
Inpp5k
1.000
R2144
G1
225
N
11
75647191 (GRCm38)
A
T
critical splice acceptor site
Het
probably null
0.949
phenotype
2014-10-01
44
236642
Ints10
1.000
R2144
G1
225
N
8
68796805 (GRCm38)
T96A
A
G
missense
Het
probably damaging
0.998
phenotype
2014-10-01
45
236678
Kansl2
0.955
R2144
G1
225
N
15
98526631 (GRCm38)
V306E
A
T
missense
Het
probably benign
0.005
2014-10-01
46
236696
Kif20a
1.000
R2144
G1
225
N
18
34625604 (GRCm38)
D42G
A
G
missense
Het
possibly damaging
0.545
2014-10-01
47
236602
Klhl7
0.480
R2144
G1
130
N
5
24100863 (GRCm38)
M37L
A
T
missense
Het
probably benign
0.000
phenotype
2014-10-01
48
236661
Krtap1-5
R2144
G1
225
N
11
99580818 (GRCm38)
I50V
T
C
missense
Het
probably benign
0.061
2014-10-01
49
236670
Ktn1
0.000
R2144
G1
225
N
14
47714652 (GRCm38)
E983G
A
G
missense
Het
probably damaging
1.000
phenotype
2014-10-01
50
236631
Lrrk1
1.000
R2144
G1
225
N
7
66296163 (GRCm38)
S566L
G
A
missense
Het
probably damaging
0.975
phenotype
2014-10-01
51
236615
M6pr
0.000
R2144
G1
225
N
6
122315367 (GRCm38)
M174V
A
G
missense
Het
probably benign
0.039
phenotype
2014-10-01
52
236632
Man2a2
0.150
R2144
G1
225
N
7
80363516 (GRCm38)
S510P
A
G
missense
Het
probably damaging
1.000
phenotype
2014-10-01
53
236612
Mmrn1
0.000
R2144
G1
225
N
6
60945075 (GRCm38)
S172N
G
A
missense
Het
possibly damaging
0.540
phenotype
2014-10-01
54
236603
Mpv17
0.000
R2144
G1
194
N
5
31154189 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
2014-10-01
55
236629
Mrgpra9
0.051
R2144
G1
225
N
7
47235463 (GRCm38)
E152G
T
C
missense
Het
probably benign
0.305
2014-10-01
56
236648
Mst1r
0.277
R2144
G1
225
N
9
107913168 (GRCm38)
V660A
T
C
missense
Het
probably benign
0.000
phenotype
2014-10-01
57
236702
Myof
0.000
R2144
G1
225
N
19
37981221 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
2014-10-01
58
236701
Myrf
0.792
R2144
G1
225
N
19
10228674 (GRCm38)
P126L
G
A
missense
Het
probably benign
0.054
phenotype
2014-10-01
59
236680
Nckap1l
0.916
R2144
G1
225
N
15
103475676 (GRCm38)
A567V
C
T
missense
Het
probably damaging
0.959
phenotype
2014-10-01
60
236624
Nphs1
1.000
R2144
G1
225
N
7
30460970 (GRCm38)
E169G
A
G
missense
Het
probably benign
0.131
phenotype
2014-10-01
61
236641
Npy1r
0.122
R2144
G1
225
N
8
66705184 (GRCm38)
V382D
T
A
missense
Het
probably benign
0.183
phenotype
2014-10-01
62
236671
Nrl
0.703
R2144
G1
84
N
14
55520850 (GRCm38)
M140K
A
T
missense
Het
possibly damaging
0.505
phenotype
2014-10-01
63
236583
Olfr1305
0.069
R2144
G1
225
N
2
111873423 (GRCm38)
I144T
A
G
missense
Het
probably damaging
0.959
phenotype
2014-10-01
64
236682
Olfr199
0.055
R2144
G1
225
N
16
59216026 (GRCm38)
V196M
C
T
missense
Het
probably benign
0.001
phenotype
2014-10-01
65
236634
Olfr292
0.094
R2144
G1
225
N
7
86695280 (GRCm38)
F275I
T
A
missense
Het
probably damaging
0.979
phenotype
2014-10-01
66
236636
Olfr694
0.099
R2144
G1
225
N
7
106688957 (GRCm38)
M258K
A
T
missense
Het
probably damaging
0.985
phenotype
2014-10-01
67
236646
Olfr924
0.065
R2144
G1
225
N
9
38848339 (GRCm38)
T75I
C
T
missense
Het
probably damaging
1.000
phenotype
2014-10-01
68
236601
Orc5
0.952
R2144
G1
225
N
5
22547927 (GRCm38)
L36F
T
A
missense
Het
possibly damaging
0.944
phenotype
2014-10-01
69
236693
Osbpl1a
0.146
R2144
G1
225
N
18
12871173 (GRCm38)
S396T
A
T
missense
Het
probably benign
0.060
phenotype
2014-10-01
70
236589
Pappa
0.728
R2144
G1
225
N
4
65180949 (GRCm38)
Y568*
T
A
nonsense
Het
probably null
phenotype
2014-10-01
71
236574
Pask
0.122
R2144
G1
225
N
1
93321297 (GRCm38)
A794T
C
T
missense
Het
probably benign
0.004
0.079
phenotype
2014-10-01
72
236600
Pclo
0.000
R2144
G1
225
N
5
14858752 (GRCm38)
L5025F
C
T
missense
Het
unknown
phenotype
2014-10-01
73
236617
Pde3a
0.297
R2144
G1
225
N
6
141490111 (GRCm38)
V924A
T
C
missense
Het
probably benign
0.399
phenotype
2014-10-01
74
236645
Pdpr
0.502
R2144
G1
225
N
8
111118036 (GRCm38)
N355S
A
G
missense
Het
probably damaging
0.970
phenotype
2014-10-01
75
236627
Pepd
0.000
R2144
G1
225
N
7
34921418 (GRCm38)
K36M
A
T
missense
Het
probably benign
0.085
phenotype
2014-10-01
76
236638
Pet100
0.514
R2144
G1
225
N
8
3622355 (GRCm38)
L14R
T
G
missense
Het
probably damaging
1.000
phenotype
2014-10-01
77
236576
Pfkfb2
0.000
R2144
G1
225
N
1
130698723 (GRCm38)
T438A
T
C
missense
Het
probably benign
0.005
0.090
phenotype
2014-10-01
78
236654
Pik3r6
0.065
R2144
G1
190
N
11
68543611 (GRCm38)
L546*
T
A
nonsense
Het
probably null
phenotype
2014-10-01
79
236619
Pira2
0.060
R2144
G1
225
N
7
3844345 (GRCm38)
L115Q
A
T
missense
Het
probably damaging
1.000
0.303
2014-10-01
80
236659
Plxdc1
0.117
R2144
G1
225
N
11
97934012 (GRCm38)
Y339C
T
C
missense
Het
probably damaging
1.000
2014-10-01
81
236640
Primpol
0.000
R2144
G1
225
N
8
46586343 (GRCm38)
M414K
A
T
missense
Het
probably damaging
0.991
phenotype
2014-10-01
82
236604
Prol1
0.079
R2144
G1
225
N
5
88328395 (GRCm38)
T215S
A
T
missense
Het
unknown
2014-10-01
83
236686
Prss22
0.149
R2144
G1
211
N
17
23994682 (GRCm38)
Y212H
A
G
missense
Het
probably damaging
1.000
phenotype
2014-10-01
84
236585
Ralgapa2
0.215
R2144
G1
225
N
2
146388604 (GRCm38)
V1014L
C
A
missense
Het
probably damaging
1.000
phenotype
2014-10-01
85
236656
Rap1gap2
0.202
R2144
G1
225
N
11
74425976 (GRCm38)
T245M
G
A
missense
Het
probably damaging
0.999
0.095
phenotype
2014-10-01
86
236672
Rbm26
0.686
R2144
G1
225
N
14
105115202 (GRCm38)
R1009*
T
A
nonsense
Het
probably null
2014-10-01
87
236625
Rbm42
0.935
R2144
G1
225
N
7
30641110 (GRCm38)
*450Q
A
G
makesense
Het
probably null
2014-10-01
88
236598
Rere
1.000
R2144
G1
225
N
4
150616931 (GRCm38)
V1256A
T
C
missense
Het
probably damaging
0.987
phenotype
2014-10-01
89
236669
Rmi1
0.643
R2144
G1
225
N
13
58407983 (GRCm38)
L15F
G
T
missense
Het
probably damaging
0.991
phenotype
2014-10-01
90
236663
Rnf213
0.000
R2144
G1
225
N
11
119443690 (GRCm38)
S3242P
T
C
missense
Het
probably damaging
0.993
phenotype
2014-10-01
91
236587
Rtel1
1.000
R2144
G1
225
N
2
181323706 (GRCm38)
V167E
T
A
missense
Het
probably damaging
0.967
phenotype
2014-10-01
92
236626
Scgb1b2
0.056
R2144
G1
225
N
7
31291763 (GRCm38)
G
T
intron
Het
probably benign
0.090
2014-10-01
93
236643
Sin3b
1.000
R2144
G1
225
N
8
72731265 (GRCm38)
L203P
T
C
missense
Het
probably damaging
1.000
phenotype
2014-10-01
94
236593
Skint6
0.056
R2144
G1
225
N
4
113236260 (GRCm38)
S229G
T
C
missense
Het
possibly damaging
0.841
2014-10-01
95
236618
Slco1a4
0.074
R2144
G1
225
N
6
141809378 (GRCm38)
Y566C
T
C
missense
Het
probably damaging
1.000
phenotype
2014-10-01
96
236676
Smgc
0.066
R2144
G1
225
N
15
91844421 (GRCm38)
D121E
T
G
missense
Het
possibly damaging
0.805
2014-10-01
97
236573
Sned1
0.076
R2144
G1
225
N
1
93271684 (GRCm38)
F495L
T
A
missense
Het
probably damaging
0.996
2014-10-01
98
236609
St7
0.154
R2144
G1
225
N
6
17886007 (GRCm38)
N52I
A
T
missense
Het
possibly damaging
0.577
phenotype
2014-10-01
99
236622
Sycn
0.201
R2144
G1
225
N
7
28541069 (GRCm38)
Q54K
C
A
missense
Het
probably benign
0.111
phenotype
2014-10-01
100
236628
Syngr4
0.068
R2144
G1
225
N
7
45887040 (GRCm38)
V186A
A
G
missense
Het
probably benign
0.012
0.080
phenotype
2014-10-01
[records 1 to 100 of 118]
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