Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
T |
C |
14: 118,767,317 (GRCm39) |
E920G |
probably damaging |
Het |
Acss2 |
A |
C |
2: 155,399,066 (GRCm39) |
N443H |
probably damaging |
Het |
Adam3 |
C |
A |
8: 25,167,279 (GRCm39) |
A71S |
unknown |
Het |
Agpat3 |
A |
G |
10: 78,123,746 (GRCm39) |
L38P |
probably damaging |
Het |
Akap9 |
C |
G |
5: 4,018,745 (GRCm39) |
H1109D |
probably benign |
Het |
Amtn |
C |
A |
5: 88,526,711 (GRCm39) |
|
probably null |
Het |
App |
T |
G |
16: 84,775,146 (GRCm39) |
Y497S |
possibly damaging |
Het |
Bphl |
T |
A |
13: 34,244,473 (GRCm39) |
Y197N |
probably damaging |
Het |
Btrc |
T |
A |
19: 45,491,525 (GRCm39) |
M160K |
possibly damaging |
Het |
Ccdc181 |
A |
C |
1: 164,107,527 (GRCm39) |
N70T |
probably benign |
Het |
Cd55b |
T |
C |
1: 130,347,473 (GRCm39) |
N113D |
possibly damaging |
Het |
Ctrb1 |
T |
A |
8: 112,413,783 (GRCm39) |
I194F |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,391,622 (GRCm39) |
H691R |
probably damaging |
Het |
Dst |
T |
A |
1: 34,333,603 (GRCm39) |
F5030I |
probably damaging |
Het |
Eppk1 |
G |
A |
15: 76,004,308 (GRCm39) |
|
probably benign |
Het |
Fbxw4 |
T |
C |
19: 45,648,449 (GRCm39) |
E7G |
unknown |
Het |
Fos |
T |
A |
12: 85,522,432 (GRCm39) |
C154S |
probably damaging |
Het |
Foxh1 |
A |
G |
15: 76,553,511 (GRCm39) |
V97A |
probably benign |
Het |
Gmeb1 |
G |
A |
4: 131,959,361 (GRCm39) |
T231I |
possibly damaging |
Het |
Golga3 |
T |
A |
5: 110,360,098 (GRCm39) |
V1112E |
probably damaging |
Het |
Gprin3 |
T |
C |
6: 59,331,017 (GRCm39) |
D430G |
possibly damaging |
Het |
Hpse2 |
T |
C |
19: 42,801,463 (GRCm39) |
D441G |
probably damaging |
Het |
Hydin |
G |
A |
8: 111,107,204 (GRCm39) |
W460* |
probably null |
Het |
Ifi204 |
T |
C |
1: 173,579,406 (GRCm39) |
I480V |
probably benign |
Het |
Impg2 |
T |
C |
16: 56,080,743 (GRCm39) |
V849A |
possibly damaging |
Het |
Kars1 |
T |
C |
8: 112,737,866 (GRCm39) |
D12G |
probably benign |
Het |
Klhdc7a |
A |
T |
4: 139,694,828 (GRCm39) |
Y40N |
probably damaging |
Het |
Krtap5-3 |
T |
C |
7: 141,755,219 (GRCm39) |
C19R |
unknown |
Het |
Macf1 |
G |
A |
4: 123,325,852 (GRCm39) |
A5217V |
possibly damaging |
Het |
Mlc1 |
A |
T |
15: 88,858,710 (GRCm39) |
I146N |
possibly damaging |
Het |
Myo3a |
A |
T |
2: 22,270,925 (GRCm39) |
R129* |
probably null |
Het |
Nsun4 |
G |
T |
4: 115,891,391 (GRCm39) |
Y329* |
probably null |
Het |
Or4k1 |
A |
G |
14: 50,377,277 (GRCm39) |
V273A |
possibly damaging |
Het |
Or56a3b |
T |
C |
7: 104,771,071 (GRCm39) |
Y136H |
probably damaging |
Het |
Pard3 |
G |
A |
8: 128,329,646 (GRCm39) |
R1214H |
probably damaging |
Het |
Phf20 |
T |
A |
2: 156,144,928 (GRCm39) |
Y845* |
probably null |
Het |
Pik3c2a |
A |
G |
7: 115,993,474 (GRCm39) |
I431T |
probably damaging |
Het |
Plxna2 |
A |
G |
1: 194,494,464 (GRCm39) |
S1894G |
probably damaging |
Het |
Ppp1r7 |
C |
T |
1: 93,282,123 (GRCm39) |
Q225* |
probably null |
Het |
Ppp4r1 |
C |
A |
17: 66,120,493 (GRCm39) |
T209K |
probably damaging |
Het |
Prc1 |
T |
C |
7: 79,950,183 (GRCm39) |
|
probably null |
Het |
Prex2 |
T |
G |
1: 11,274,316 (GRCm39) |
D1329E |
probably damaging |
Het |
Ptch1 |
C |
T |
13: 63,659,528 (GRCm39) |
R1375H |
probably benign |
Het |
Rab24 |
A |
T |
13: 55,468,921 (GRCm39) |
C87S |
probably damaging |
Het |
Rnf43 |
A |
T |
11: 87,622,954 (GRCm39) |
Y558F |
probably benign |
Het |
Serpinb6e |
T |
C |
13: 34,016,474 (GRCm39) |
I420V |
possibly damaging |
Het |
Slain2 |
C |
A |
5: 73,072,143 (GRCm39) |
S59* |
probably null |
Het |
Slfn3 |
A |
G |
11: 83,105,731 (GRCm39) |
D576G |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,141,960 (GRCm39) |
M11T |
probably benign |
Het |
Tdh |
T |
C |
14: 63,731,460 (GRCm39) |
D238G |
probably damaging |
Het |
Top2b |
T |
A |
14: 16,395,427 (GRCm38) |
Y337* |
probably null |
Het |
Trav15-2-dv6-2 |
A |
C |
14: 53,887,308 (GRCm39) |
Y76S |
probably benign |
Het |
Vmn1r172 |
G |
T |
7: 23,359,189 (GRCm39) |
G25C |
probably damaging |
Het |
Vmn2r60 |
AG |
A |
7: 41,845,158 (GRCm39) |
|
probably null |
Het |
Vps13d |
T |
C |
4: 144,818,492 (GRCm39) |
E3125G |
|
Het |
Xkr6 |
G |
T |
14: 64,056,610 (GRCm39) |
V430F |
probably benign |
Het |
Zfp142 |
T |
C |
1: 74,610,061 (GRCm39) |
T1245A |
probably benign |
Het |
Zfp960 |
C |
T |
17: 17,307,825 (GRCm39) |
H180Y |
possibly damaging |
Het |
|
Other mutations in Dnajc13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Dnajc13
|
APN |
9 |
104,039,979 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00754:Dnajc13
|
APN |
9 |
104,051,697 (GRCm39) |
nonsense |
probably null |
|
IGL00914:Dnajc13
|
APN |
9 |
104,090,081 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01014:Dnajc13
|
APN |
9 |
104,080,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01077:Dnajc13
|
APN |
9 |
104,108,220 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01137:Dnajc13
|
APN |
9 |
104,037,689 (GRCm39) |
missense |
probably benign |
|
IGL01305:Dnajc13
|
APN |
9 |
104,107,836 (GRCm39) |
splice site |
probably null |
|
IGL01707:Dnajc13
|
APN |
9 |
104,106,178 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01868:Dnajc13
|
APN |
9 |
104,039,944 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01950:Dnajc13
|
APN |
9 |
104,067,631 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02102:Dnajc13
|
APN |
9 |
104,106,208 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02350:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02357:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02470:Dnajc13
|
APN |
9 |
104,052,946 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02888:Dnajc13
|
APN |
9 |
104,057,261 (GRCm39) |
splice site |
probably benign |
|
IGL03079:Dnajc13
|
APN |
9 |
104,090,068 (GRCm39) |
nonsense |
probably null |
|
IGL03179:Dnajc13
|
APN |
9 |
104,044,634 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03293:Dnajc13
|
APN |
9 |
104,051,625 (GRCm39) |
missense |
possibly damaging |
0.64 |
impressario
|
UTSW |
9 |
104,091,085 (GRCm39) |
missense |
probably benign |
0.12 |
Kaiser
|
UTSW |
9 |
104,091,387 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
BB018:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4142001:Dnajc13
|
UTSW |
9 |
104,115,672 (GRCm39) |
missense |
probably damaging |
0.96 |
R0323:Dnajc13
|
UTSW |
9 |
104,034,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R0361:Dnajc13
|
UTSW |
9 |
104,044,258 (GRCm39) |
missense |
probably benign |
0.18 |
R0480:Dnajc13
|
UTSW |
9 |
104,077,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R0558:Dnajc13
|
UTSW |
9 |
104,079,151 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0707:Dnajc13
|
UTSW |
9 |
104,049,781 (GRCm39) |
missense |
probably benign |
0.12 |
R0831:Dnajc13
|
UTSW |
9 |
104,049,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1234:Dnajc13
|
UTSW |
9 |
104,091,356 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1433:Dnajc13
|
UTSW |
9 |
104,057,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Dnajc13
|
UTSW |
9 |
104,056,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Dnajc13
|
UTSW |
9 |
104,091,366 (GRCm39) |
missense |
probably benign |
0.10 |
R1464:Dnajc13
|
UTSW |
9 |
104,091,366 (GRCm39) |
missense |
probably benign |
0.10 |
R1489:Dnajc13
|
UTSW |
9 |
104,108,234 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1575:Dnajc13
|
UTSW |
9 |
104,034,037 (GRCm39) |
missense |
probably benign |
0.29 |
R1750:Dnajc13
|
UTSW |
9 |
104,098,676 (GRCm39) |
missense |
probably damaging |
0.98 |
R1903:Dnajc13
|
UTSW |
9 |
104,106,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R2066:Dnajc13
|
UTSW |
9 |
104,098,640 (GRCm39) |
missense |
probably benign |
0.01 |
R2206:Dnajc13
|
UTSW |
9 |
104,080,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Dnajc13
|
UTSW |
9 |
104,097,097 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3162:Dnajc13
|
UTSW |
9 |
104,097,097 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4158:Dnajc13
|
UTSW |
9 |
104,067,641 (GRCm39) |
missense |
probably damaging |
0.96 |
R4460:Dnajc13
|
UTSW |
9 |
104,058,262 (GRCm39) |
missense |
probably damaging |
0.96 |
R4537:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4538:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4631:Dnajc13
|
UTSW |
9 |
104,067,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Dnajc13
|
UTSW |
9 |
104,084,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Dnajc13
|
UTSW |
9 |
104,091,017 (GRCm39) |
missense |
probably benign |
|
R4731:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4732:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4758:Dnajc13
|
UTSW |
9 |
104,049,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Dnajc13
|
UTSW |
9 |
104,052,926 (GRCm39) |
missense |
probably benign |
0.16 |
R4802:Dnajc13
|
UTSW |
9 |
104,052,926 (GRCm39) |
missense |
probably benign |
0.16 |
R4928:Dnajc13
|
UTSW |
9 |
104,110,837 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4944:Dnajc13
|
UTSW |
9 |
104,044,586 (GRCm39) |
unclassified |
probably benign |
|
R4979:Dnajc13
|
UTSW |
9 |
104,063,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5177:Dnajc13
|
UTSW |
9 |
104,108,185 (GRCm39) |
missense |
probably benign |
0.39 |
R5190:Dnajc13
|
UTSW |
9 |
104,051,724 (GRCm39) |
missense |
probably benign |
0.00 |
R5256:Dnajc13
|
UTSW |
9 |
104,080,528 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5452:Dnajc13
|
UTSW |
9 |
104,069,313 (GRCm39) |
missense |
probably benign |
0.01 |
R5657:Dnajc13
|
UTSW |
9 |
104,105,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R5752:Dnajc13
|
UTSW |
9 |
104,069,973 (GRCm39) |
splice site |
probably null |
|
R5789:Dnajc13
|
UTSW |
9 |
104,091,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R5837:Dnajc13
|
UTSW |
9 |
104,053,865 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5846:Dnajc13
|
UTSW |
9 |
104,067,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R5982:Dnajc13
|
UTSW |
9 |
104,061,814 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6189:Dnajc13
|
UTSW |
9 |
104,091,085 (GRCm39) |
missense |
probably benign |
0.12 |
R6355:Dnajc13
|
UTSW |
9 |
104,080,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R6483:Dnajc13
|
UTSW |
9 |
104,085,003 (GRCm39) |
missense |
probably damaging |
0.96 |
R6613:Dnajc13
|
UTSW |
9 |
104,091,076 (GRCm39) |
missense |
probably benign |
0.07 |
R6962:Dnajc13
|
UTSW |
9 |
104,058,208 (GRCm39) |
missense |
probably benign |
0.02 |
R7048:Dnajc13
|
UTSW |
9 |
104,080,613 (GRCm39) |
critical splice donor site |
probably null |
|
R7101:Dnajc13
|
UTSW |
9 |
104,042,221 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7304:Dnajc13
|
UTSW |
9 |
104,115,713 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Dnajc13
|
UTSW |
9 |
104,107,230 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7366:Dnajc13
|
UTSW |
9 |
104,061,905 (GRCm39) |
missense |
probably benign |
0.43 |
R7635:Dnajc13
|
UTSW |
9 |
104,039,566 (GRCm39) |
missense |
probably benign |
|
R7673:Dnajc13
|
UTSW |
9 |
104,110,891 (GRCm39) |
missense |
probably benign |
0.09 |
R7856:Dnajc13
|
UTSW |
9 |
104,044,684 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7931:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
R7995:Dnajc13
|
UTSW |
9 |
104,051,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8319:Dnajc13
|
UTSW |
9 |
104,067,590 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Dnajc13
|
UTSW |
9 |
104,094,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Dnajc13
|
UTSW |
9 |
104,057,338 (GRCm39) |
missense |
probably benign |
|
R8686:Dnajc13
|
UTSW |
9 |
104,048,004 (GRCm39) |
missense |
probably benign |
0.00 |
R8707:Dnajc13
|
UTSW |
9 |
104,069,847 (GRCm39) |
missense |
probably damaging |
0.96 |
R8847:Dnajc13
|
UTSW |
9 |
104,057,360 (GRCm39) |
nonsense |
probably null |
|
R8868:Dnajc13
|
UTSW |
9 |
104,042,987 (GRCm39) |
missense |
probably benign |
0.13 |
R8986:Dnajc13
|
UTSW |
9 |
104,057,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Dnajc13
|
UTSW |
9 |
104,085,039 (GRCm39) |
missense |
probably benign |
0.02 |
R9334:Dnajc13
|
UTSW |
9 |
104,051,659 (GRCm39) |
missense |
probably benign |
0.00 |
R9353:Dnajc13
|
UTSW |
9 |
104,067,571 (GRCm39) |
missense |
probably benign |
0.31 |
R9470:Dnajc13
|
UTSW |
9 |
104,107,919 (GRCm39) |
missense |
probably benign |
0.01 |
R9528:Dnajc13
|
UTSW |
9 |
104,114,904 (GRCm39) |
missense |
probably benign |
|
R9578:Dnajc13
|
UTSW |
9 |
104,115,726 (GRCm39) |
missense |
probably benign |
0.04 |
R9658:Dnajc13
|
UTSW |
9 |
104,115,728 (GRCm39) |
missense |
probably benign |
0.11 |
R9691:Dnajc13
|
UTSW |
9 |
104,042,211 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Dnajc13
|
UTSW |
9 |
104,115,677 (GRCm39) |
missense |
possibly damaging |
0.90 |
X0028:Dnajc13
|
UTSW |
9 |
104,042,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|