Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
C |
T |
17: 46,623,333 (GRCm39) |
V860M |
probably benign |
Het |
Accs |
A |
T |
2: 93,666,392 (GRCm39) |
L432M |
probably damaging |
Het |
Actrt3 |
T |
A |
3: 30,652,813 (GRCm39) |
N94Y |
possibly damaging |
Het |
Adamts18 |
T |
C |
8: 114,504,380 (GRCm39) |
Q80R |
probably benign |
Het |
Ccr8 |
G |
T |
9: 119,923,772 (GRCm39) |
V296F |
probably damaging |
Het |
Cep170 |
T |
A |
1: 176,583,985 (GRCm39) |
E798V |
probably damaging |
Het |
Cttnbp2 |
T |
A |
6: 18,448,439 (GRCm39) |
E73D |
probably damaging |
Het |
Cyp2a4 |
A |
T |
7: 26,010,129 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
A |
T |
9: 7,117,466 (GRCm39) |
Y41* |
probably null |
Het |
Enc1 |
G |
A |
13: 97,382,887 (GRCm39) |
D466N |
probably benign |
Het |
Enpp1 |
C |
A |
10: 24,551,966 (GRCm39) |
E138* |
probably null |
Het |
Entrep1 |
A |
G |
19: 23,963,834 (GRCm39) |
V245A |
probably damaging |
Het |
Ezh2 |
T |
C |
6: 47,554,516 (GRCm39) |
R27G |
possibly damaging |
Het |
Fut10 |
A |
G |
8: 31,691,485 (GRCm39) |
N110S |
possibly damaging |
Het |
Glt1d1 |
A |
T |
5: 127,721,534 (GRCm39) |
|
probably null |
Het |
Gm14393 |
G |
A |
2: 174,903,689 (GRCm39) |
Q73* |
probably null |
Het |
Gpr156 |
C |
T |
16: 37,825,264 (GRCm39) |
P494S |
probably benign |
Het |
Has2 |
T |
A |
15: 56,531,192 (GRCm39) |
K508* |
probably null |
Het |
Hook2 |
C |
T |
8: 85,721,409 (GRCm39) |
|
probably null |
Het |
Klhdc7b |
A |
C |
15: 89,271,634 (GRCm39) |
I839L |
probably benign |
Het |
Kndc1 |
T |
C |
7: 139,516,792 (GRCm39) |
L1584P |
probably damaging |
Het |
Lamp1 |
T |
C |
8: 13,223,941 (GRCm39) |
F358L |
probably damaging |
Het |
Man2a1 |
A |
G |
17: 64,932,375 (GRCm39) |
K154R |
probably benign |
Het |
Mga |
A |
G |
2: 119,777,440 (GRCm39) |
I1871V |
probably benign |
Het |
Mgmt |
T |
A |
7: 136,723,219 (GRCm39) |
D96E |
probably benign |
Het |
Morc2a |
C |
A |
11: 3,629,936 (GRCm39) |
T424K |
probably damaging |
Het |
Myo1g |
A |
G |
11: 6,464,888 (GRCm39) |
L462P |
probably damaging |
Het |
Ncaph |
C |
A |
2: 126,958,608 (GRCm39) |
|
probably null |
Het |
Nlrc3 |
A |
T |
16: 3,767,293 (GRCm39) |
D969E |
probably damaging |
Het |
Nt5c3 |
A |
T |
6: 56,874,839 (GRCm39) |
|
probably null |
Het |
Or4c12b |
G |
T |
2: 89,646,684 (GRCm39) |
E5* |
probably null |
Het |
Or5ac15 |
A |
T |
16: 58,940,039 (GRCm39) |
Y131* |
probably null |
Het |
Or5d41 |
A |
C |
2: 88,054,916 (GRCm39) |
I153M |
probably benign |
Het |
Or8h8 |
T |
C |
2: 86,753,750 (GRCm39) |
N42S |
probably damaging |
Het |
Parp14 |
C |
A |
16: 35,659,737 (GRCm39) |
M1628I |
probably damaging |
Het |
Parp8 |
G |
T |
13: 117,005,969 (GRCm39) |
P693Q |
probably benign |
Het |
Parp9 |
A |
G |
16: 35,792,259 (GRCm39) |
D485G |
possibly damaging |
Het |
Pcdha1 |
T |
A |
18: 37,063,444 (GRCm39) |
V36D |
probably damaging |
Het |
Pcdhb5 |
C |
T |
18: 37,453,838 (GRCm39) |
Q73* |
probably null |
Het |
Pecam1 |
G |
T |
11: 106,552,809 (GRCm39) |
|
probably benign |
Het |
Pex1 |
A |
G |
5: 3,660,277 (GRCm39) |
I527V |
probably benign |
Het |
Phf11 |
G |
A |
14: 59,497,593 (GRCm39) |
P13S |
probably benign |
Het |
Ppp4r4 |
T |
A |
12: 103,553,706 (GRCm39) |
V388D |
possibly damaging |
Het |
Psmc4 |
C |
T |
7: 27,746,480 (GRCm39) |
V202I |
probably damaging |
Het |
Ptx3 |
T |
G |
3: 66,127,484 (GRCm39) |
M1R |
probably null |
Het |
Rimbp3 |
A |
G |
16: 17,029,752 (GRCm39) |
T1059A |
probably benign |
Het |
Rmdn3 |
G |
A |
2: 118,978,058 (GRCm39) |
A181V |
probably damaging |
Het |
Rnase10 |
A |
T |
14: 51,246,735 (GRCm39) |
M38L |
probably benign |
Het |
Sec16b |
T |
A |
1: 157,358,920 (GRCm39) |
Y118N |
probably damaging |
Het |
Sigmar1 |
T |
C |
4: 41,741,159 (GRCm39) |
T32A |
probably benign |
Het |
Srcap |
A |
G |
7: 127,137,180 (GRCm39) |
D954G |
probably damaging |
Het |
Tfrc |
A |
G |
16: 32,445,533 (GRCm39) |
N618S |
possibly damaging |
Het |
Tnrc6a |
A |
G |
7: 122,785,888 (GRCm39) |
D1028G |
probably damaging |
Het |
Tns3 |
A |
T |
11: 8,385,860 (GRCm39) |
D1379E |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,580,505 (GRCm39) |
C23463S |
possibly damaging |
Het |
Ufl1 |
T |
C |
4: 25,250,619 (GRCm39) |
T745A |
probably benign |
Het |
Vmn1r231 |
T |
A |
17: 21,110,417 (GRCm39) |
Y166F |
possibly damaging |
Het |
Wbp1l |
C |
A |
19: 46,642,869 (GRCm39) |
T290K |
probably damaging |
Het |
Wdr25 |
A |
G |
12: 108,864,392 (GRCm39) |
N179S |
probably benign |
Het |
Wdr62 |
G |
A |
7: 29,942,504 (GRCm39) |
Q1035* |
probably null |
Het |
Yif1a |
C |
T |
19: 5,141,669 (GRCm39) |
R196C |
probably damaging |
Het |
Zfp352 |
A |
T |
4: 90,113,307 (GRCm39) |
K482N |
probably damaging |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
|
Other mutations in Hc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00694:Hc
|
APN |
2 |
34,881,641 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00922:Hc
|
APN |
2 |
34,881,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Hc
|
APN |
2 |
34,929,250 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01746:Hc
|
APN |
2 |
34,947,338 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01793:Hc
|
APN |
2 |
34,918,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01972:Hc
|
APN |
2 |
34,873,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Hc
|
APN |
2 |
34,903,531 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02048:Hc
|
APN |
2 |
34,886,039 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02227:Hc
|
APN |
2 |
34,899,923 (GRCm39) |
intron |
probably benign |
|
IGL02230:Hc
|
APN |
2 |
34,903,682 (GRCm39) |
missense |
probably benign |
|
IGL02254:Hc
|
APN |
2 |
34,874,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02363:Hc
|
APN |
2 |
34,890,847 (GRCm39) |
missense |
probably benign |
|
IGL02650:Hc
|
APN |
2 |
34,890,886 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03053:Hc
|
APN |
2 |
34,914,210 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03168:Hc
|
APN |
2 |
34,914,210 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03341:Hc
|
APN |
2 |
34,893,389 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4142001:Hc
|
UTSW |
2 |
34,921,833 (GRCm39) |
splice site |
probably benign |
|
PIT4378001:Hc
|
UTSW |
2 |
34,921,876 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4508001:Hc
|
UTSW |
2 |
34,874,816 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4812001:Hc
|
UTSW |
2 |
34,919,464 (GRCm39) |
missense |
probably benign |
0.16 |
R0025:Hc
|
UTSW |
2 |
34,876,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Hc
|
UTSW |
2 |
34,947,287 (GRCm39) |
missense |
probably benign |
0.32 |
R0197:Hc
|
UTSW |
2 |
34,874,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0218:Hc
|
UTSW |
2 |
34,918,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Hc
|
UTSW |
2 |
34,926,166 (GRCm39) |
splice site |
probably benign |
|
R0496:Hc
|
UTSW |
2 |
34,903,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Hc
|
UTSW |
2 |
34,893,536 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1468:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R1468:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R1574:Hc
|
UTSW |
2 |
34,890,777 (GRCm39) |
intron |
probably benign |
|
R1610:Hc
|
UTSW |
2 |
34,896,173 (GRCm39) |
missense |
probably benign |
0.44 |
R1640:Hc
|
UTSW |
2 |
34,947,336 (GRCm39) |
nonsense |
probably null |
|
R1887:Hc
|
UTSW |
2 |
34,924,623 (GRCm39) |
missense |
probably benign |
|
R1920:Hc
|
UTSW |
2 |
34,919,407 (GRCm39) |
splice site |
probably benign |
|
R2018:Hc
|
UTSW |
2 |
34,903,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Hc
|
UTSW |
2 |
34,903,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Hc
|
UTSW |
2 |
34,881,115 (GRCm39) |
intron |
probably benign |
|
R2366:Hc
|
UTSW |
2 |
34,903,648 (GRCm39) |
missense |
probably benign |
|
R4093:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R4288:Hc
|
UTSW |
2 |
34,920,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R4501:Hc
|
UTSW |
2 |
34,887,488 (GRCm39) |
splice site |
probably null |
|
R4502:Hc
|
UTSW |
2 |
34,896,264 (GRCm39) |
missense |
probably benign |
0.00 |
R4508:Hc
|
UTSW |
2 |
34,903,077 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4583:Hc
|
UTSW |
2 |
34,918,189 (GRCm39) |
missense |
probably benign |
0.00 |
R4686:Hc
|
UTSW |
2 |
34,929,260 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4776:Hc
|
UTSW |
2 |
34,929,746 (GRCm39) |
missense |
probably benign |
0.12 |
R4846:Hc
|
UTSW |
2 |
34,909,682 (GRCm39) |
missense |
probably benign |
0.00 |
R5032:Hc
|
UTSW |
2 |
34,903,544 (GRCm39) |
missense |
probably benign |
0.07 |
R5089:Hc
|
UTSW |
2 |
34,914,902 (GRCm39) |
missense |
probably benign |
0.01 |
R5289:Hc
|
UTSW |
2 |
34,886,026 (GRCm39) |
critical splice donor site |
probably null |
|
R5347:Hc
|
UTSW |
2 |
34,927,636 (GRCm39) |
missense |
probably benign |
0.04 |
R5356:Hc
|
UTSW |
2 |
34,885,007 (GRCm39) |
missense |
probably benign |
0.00 |
R5379:Hc
|
UTSW |
2 |
34,881,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5403:Hc
|
UTSW |
2 |
34,947,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R5418:Hc
|
UTSW |
2 |
34,898,195 (GRCm39) |
critical splice donor site |
probably null |
|
R5450:Hc
|
UTSW |
2 |
34,903,050 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5494:Hc
|
UTSW |
2 |
34,893,551 (GRCm39) |
splice site |
probably null |
|
R5713:Hc
|
UTSW |
2 |
34,903,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R5898:Hc
|
UTSW |
2 |
34,887,449 (GRCm39) |
missense |
probably benign |
0.06 |
R5925:Hc
|
UTSW |
2 |
34,920,462 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5991:Hc
|
UTSW |
2 |
34,896,117 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6036:Hc
|
UTSW |
2 |
34,929,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6036:Hc
|
UTSW |
2 |
34,929,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6115:Hc
|
UTSW |
2 |
34,903,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R6234:Hc
|
UTSW |
2 |
34,918,058 (GRCm39) |
missense |
probably benign |
|
R6264:Hc
|
UTSW |
2 |
34,896,285 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6313:Hc
|
UTSW |
2 |
34,879,851 (GRCm39) |
splice site |
probably null |
|
R6525:Hc
|
UTSW |
2 |
34,881,236 (GRCm39) |
missense |
probably benign |
0.06 |
R6577:Hc
|
UTSW |
2 |
34,922,138 (GRCm39) |
missense |
probably benign |
0.00 |
R6601:Hc
|
UTSW |
2 |
34,935,906 (GRCm39) |
missense |
probably benign |
0.03 |
R6916:Hc
|
UTSW |
2 |
34,900,044 (GRCm39) |
nonsense |
probably null |
|
R7108:Hc
|
UTSW |
2 |
34,929,706 (GRCm39) |
missense |
probably benign |
0.03 |
R7143:Hc
|
UTSW |
2 |
34,940,450 (GRCm39) |
missense |
probably benign |
0.00 |
R7388:Hc
|
UTSW |
2 |
34,874,859 (GRCm39) |
splice site |
probably null |
|
R7468:Hc
|
UTSW |
2 |
34,918,063 (GRCm39) |
missense |
probably benign |
0.00 |
R7504:Hc
|
UTSW |
2 |
34,951,331 (GRCm39) |
missense |
not run |
|
R7521:Hc
|
UTSW |
2 |
34,935,344 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7582:Hc
|
UTSW |
2 |
34,881,278 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7596:Hc
|
UTSW |
2 |
34,890,859 (GRCm39) |
missense |
probably damaging |
0.96 |
R7599:Hc
|
UTSW |
2 |
34,940,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R7692:Hc
|
UTSW |
2 |
34,914,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Hc
|
UTSW |
2 |
34,900,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Hc
|
UTSW |
2 |
34,887,411 (GRCm39) |
nonsense |
probably null |
|
R8329:Hc
|
UTSW |
2 |
34,902,910 (GRCm39) |
splice site |
probably null |
|
R8375:Hc
|
UTSW |
2 |
34,873,731 (GRCm39) |
missense |
probably benign |
0.32 |
R8477:Hc
|
UTSW |
2 |
34,879,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Hc
|
UTSW |
2 |
34,909,535 (GRCm39) |
missense |
probably benign |
0.06 |
R8888:Hc
|
UTSW |
2 |
34,890,861 (GRCm39) |
missense |
probably benign |
0.00 |
R8895:Hc
|
UTSW |
2 |
34,890,861 (GRCm39) |
missense |
probably benign |
0.00 |
R8968:Hc
|
UTSW |
2 |
34,922,317 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8969:Hc
|
UTSW |
2 |
34,909,475 (GRCm39) |
critical splice donor site |
probably null |
|
R9146:Hc
|
UTSW |
2 |
34,924,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R9218:Hc
|
UTSW |
2 |
34,922,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9340:Hc
|
UTSW |
2 |
34,876,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R9396:Hc
|
UTSW |
2 |
34,927,615 (GRCm39) |
nonsense |
probably null |
|
R9569:Hc
|
UTSW |
2 |
34,926,359 (GRCm39) |
missense |
probably benign |
0.00 |
R9576:Hc
|
UTSW |
2 |
34,873,767 (GRCm39) |
missense |
probably benign |
0.01 |
R9706:Hc
|
UTSW |
2 |
34,914,196 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Hc
|
UTSW |
2 |
34,873,723 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Hc
|
UTSW |
2 |
34,919,482 (GRCm39) |
missense |
probably benign |
0.02 |
Z1088:Hc
|
UTSW |
2 |
34,898,261 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Hc
|
UTSW |
2 |
34,896,285 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Hc
|
UTSW |
2 |
34,903,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|