Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
A |
G |
11: 84,153,300 (GRCm39) |
T903A |
probably benign |
Het |
Acin1 |
A |
T |
14: 54,902,356 (GRCm39) |
S479T |
possibly damaging |
Het |
Actr6 |
A |
T |
10: 89,548,374 (GRCm39) |
D370E |
probably benign |
Het |
Adgrl3 |
T |
C |
5: 81,872,069 (GRCm39) |
F921S |
probably damaging |
Het |
Ankmy1 |
A |
T |
1: 92,814,546 (GRCm39) |
H320Q |
possibly damaging |
Het |
Arhgef5 |
C |
T |
6: 43,250,166 (GRCm39) |
Q306* |
probably null |
Het |
Art4 |
A |
T |
6: 136,831,547 (GRCm39) |
V198E |
probably benign |
Het |
Asph |
G |
A |
4: 9,474,917 (GRCm39) |
R686W |
probably damaging |
Het |
Atg7 |
A |
G |
6: 114,754,018 (GRCm39) |
H724R |
probably damaging |
Het |
BC034090 |
A |
G |
1: 155,117,680 (GRCm39) |
V146A |
probably damaging |
Het |
Bcl2a1d |
T |
A |
9: 88,613,639 (GRCm39) |
Q45L |
probably damaging |
Het |
Bmal1 |
T |
A |
7: 112,884,349 (GRCm39) |
M122K |
probably damaging |
Het |
Cd28 |
G |
T |
1: 60,802,332 (GRCm39) |
E84* |
probably null |
Het |
Ceacam3 |
G |
A |
7: 16,892,163 (GRCm39) |
W302* |
probably null |
Het |
Cerkl |
T |
C |
2: 79,163,934 (GRCm39) |
N462S |
probably benign |
Het |
Cisd2 |
A |
T |
3: 135,116,974 (GRCm39) |
L39H |
probably damaging |
Het |
Col11a1 |
C |
A |
3: 113,883,806 (GRCm39) |
T225K |
unknown |
Het |
Col15a1 |
A |
T |
4: 47,307,752 (GRCm39) |
Y1178F |
possibly damaging |
Het |
Cul4a |
T |
C |
8: 13,192,991 (GRCm39) |
S630P |
probably damaging |
Het |
Cyp2c38 |
T |
A |
19: 39,390,220 (GRCm39) |
I327F |
probably damaging |
Het |
Cyp3a25 |
A |
C |
5: 145,928,257 (GRCm39) |
S263A |
probably benign |
Het |
Cyp3a25 |
T |
A |
5: 145,939,868 (GRCm39) |
L46F |
probably benign |
Het |
Dmrta1 |
T |
A |
4: 89,580,408 (GRCm39) |
L456* |
probably null |
Het |
Dnah12 |
T |
C |
14: 26,536,579 (GRCm39) |
L2165P |
probably benign |
Het |
Dsg1a |
C |
A |
18: 20,461,368 (GRCm39) |
S253R |
probably damaging |
Het |
Egln2 |
A |
C |
7: 26,859,744 (GRCm39) |
I323S |
probably damaging |
Het |
Fam171b |
A |
G |
2: 83,708,574 (GRCm39) |
T359A |
probably damaging |
Het |
Fcgr2b |
G |
T |
1: 170,790,966 (GRCm39) |
Q276K |
probably benign |
Het |
Fcrl2 |
C |
T |
3: 87,159,934 (GRCm39) |
C440Y |
probably damaging |
Het |
Fmnl2 |
T |
C |
2: 52,963,666 (GRCm39) |
V266A |
unknown |
Het |
Glo1 |
A |
T |
17: 30,816,828 (GRCm39) |
D109E |
probably benign |
Het |
Grin3b |
A |
G |
10: 79,809,912 (GRCm39) |
R473G |
possibly damaging |
Het |
Ica1 |
G |
A |
6: 8,644,015 (GRCm39) |
L425F |
probably damaging |
Het |
Iho1 |
A |
T |
9: 108,281,974 (GRCm39) |
D571E |
probably damaging |
Het |
Ilrun |
A |
C |
17: 28,013,044 (GRCm39) |
|
probably null |
Het |
Kcnq5 |
T |
C |
1: 21,473,099 (GRCm39) |
E716G |
possibly damaging |
Het |
Klra17 |
A |
T |
6: 129,850,306 (GRCm39) |
I48K |
possibly damaging |
Het |
Lrrc66 |
G |
T |
5: 73,787,240 (GRCm39) |
Q37K |
probably benign |
Het |
Ly6a |
T |
A |
15: 74,868,325 (GRCm39) |
T55S |
probably benign |
Het |
Lyst |
T |
A |
13: 13,883,885 (GRCm39) |
Y2924* |
probably null |
Het |
Lyzl6 |
A |
G |
11: 103,522,177 (GRCm39) |
Y140H |
probably benign |
Het |
Mak |
T |
C |
13: 41,204,916 (GRCm39) |
I141V |
possibly damaging |
Het |
Mapk7 |
A |
G |
11: 61,379,998 (GRCm39) |
I789T |
probably benign |
Het |
Mgat4f |
A |
G |
1: 134,318,206 (GRCm39) |
D326G |
possibly damaging |
Het |
Mrpl4 |
T |
C |
9: 20,918,634 (GRCm39) |
I123T |
probably benign |
Het |
Mup18 |
G |
C |
4: 61,591,573 (GRCm39) |
|
probably null |
Het |
Myef2 |
T |
C |
2: 124,938,082 (GRCm39) |
|
probably null |
Het |
Myh7 |
T |
C |
14: 55,228,402 (GRCm39) |
T235A |
possibly damaging |
Het |
Myo18b |
C |
T |
5: 112,863,325 (GRCm39) |
C2171Y |
probably damaging |
Het |
Nat8 |
A |
T |
6: 85,807,877 (GRCm39) |
Y85* |
probably null |
Het |
Nyap1 |
A |
T |
5: 137,734,524 (GRCm39) |
S170T |
probably damaging |
Het |
Ogfr |
AGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
AGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
2: 180,236,887 (GRCm39) |
|
probably benign |
Het |
Or10ah1-ps1 |
A |
G |
5: 143,123,553 (GRCm39) |
Y157H |
probably damaging |
Het |
Or1e32 |
A |
G |
11: 73,705,167 (GRCm39) |
V247A |
probably benign |
Het |
Or51a25 |
T |
A |
7: 102,373,692 (GRCm39) |
I2F |
probably benign |
Het |
Papss1 |
T |
C |
3: 131,305,687 (GRCm39) |
L244P |
probably damaging |
Het |
Pibf1 |
A |
T |
14: 99,433,844 (GRCm39) |
D597V |
probably damaging |
Het |
Pmpcb |
T |
A |
5: 21,942,177 (GRCm39) |
M1K |
probably null |
Het |
Ppwd1 |
G |
A |
13: 104,343,680 (GRCm39) |
P575L |
probably damaging |
Het |
Pramel17 |
T |
A |
4: 101,695,338 (GRCm39) |
|
probably null |
Het |
Prc1 |
A |
G |
7: 79,960,837 (GRCm39) |
Q457R |
possibly damaging |
Het |
Prkdc |
A |
G |
16: 15,516,667 (GRCm39) |
I1014V |
probably benign |
Het |
Rab3gap2 |
A |
G |
1: 184,999,388 (GRCm39) |
Y999C |
probably damaging |
Het |
Robo3 |
G |
A |
9: 37,335,626 (GRCm39) |
Q539* |
probably null |
Het |
Rps12 |
A |
G |
10: 23,661,129 (GRCm39) |
Y127H |
probably benign |
Het |
Sar1b |
A |
G |
11: 51,679,079 (GRCm39) |
D116G |
probably benign |
Het |
Selenbp2 |
C |
T |
3: 94,609,664 (GRCm39) |
P294L |
probably benign |
Het |
Slc6a2 |
T |
C |
8: 93,722,300 (GRCm39) |
Y516H |
probably damaging |
Het |
Slit2 |
A |
G |
5: 48,394,627 (GRCm39) |
N673S |
probably null |
Het |
Snap91 |
A |
T |
9: 86,672,199 (GRCm39) |
|
probably null |
Het |
Spata31h1 |
T |
C |
10: 82,127,461 (GRCm39) |
M1850V |
probably benign |
Het |
Srpk2 |
A |
G |
5: 23,712,626 (GRCm39) |
F653L |
possibly damaging |
Het |
Supt5 |
A |
T |
7: 28,016,213 (GRCm39) |
S824T |
probably benign |
Het |
Taar7a |
A |
G |
10: 23,868,358 (GRCm39) |
V341A |
probably benign |
Het |
Tmem52 |
G |
A |
4: 155,554,778 (GRCm39) |
G134R |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,606,951 (GRCm39) |
T3949A |
probably benign |
Het |
Usp32 |
GAACAAGTCCACAACAA |
GAACAA |
11: 84,913,681 (GRCm39) |
|
probably null |
Het |
Vmn1r173 |
A |
T |
7: 23,401,583 (GRCm39) |
|
probably benign |
Het |
Vmn2r118 |
G |
A |
17: 55,915,496 (GRCm39) |
R485* |
probably null |
Het |
Vwce |
A |
G |
19: 10,615,479 (GRCm39) |
E120G |
possibly damaging |
Het |
Zfp143 |
T |
C |
7: 109,692,287 (GRCm39) |
V566A |
possibly damaging |
Het |
|
Other mutations in Prdm10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Prdm10
|
APN |
9 |
31,272,108 (GRCm39) |
splice site |
probably benign |
|
IGL00485:Prdm10
|
APN |
9 |
31,238,842 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL00757:Prdm10
|
APN |
9 |
31,229,842 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL00836:Prdm10
|
APN |
9 |
31,241,165 (GRCm39) |
splice site |
probably benign |
|
IGL01505:Prdm10
|
APN |
9 |
31,238,578 (GRCm39) |
missense |
probably benign |
|
IGL01594:Prdm10
|
APN |
9 |
31,258,149 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01894:Prdm10
|
APN |
9 |
31,227,557 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01927:Prdm10
|
APN |
9 |
31,246,694 (GRCm39) |
splice site |
probably benign |
|
IGL02053:Prdm10
|
APN |
9 |
31,272,144 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02068:Prdm10
|
APN |
9 |
31,248,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02295:Prdm10
|
APN |
9 |
31,273,664 (GRCm39) |
missense |
probably benign |
|
IGL02390:Prdm10
|
APN |
9 |
31,264,685 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02574:Prdm10
|
APN |
9 |
31,268,589 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02636:Prdm10
|
APN |
9 |
31,240,977 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02883:Prdm10
|
APN |
9 |
31,238,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03057:Prdm10
|
APN |
9 |
31,260,481 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Prdm10
|
UTSW |
9 |
31,237,063 (GRCm39) |
missense |
probably benign |
0.00 |
R0089:Prdm10
|
UTSW |
9 |
31,227,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Prdm10
|
UTSW |
9 |
31,227,455 (GRCm39) |
splice site |
probably benign |
|
R0306:Prdm10
|
UTSW |
9 |
31,227,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R0386:Prdm10
|
UTSW |
9 |
31,227,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Prdm10
|
UTSW |
9 |
31,260,564 (GRCm39) |
critical splice donor site |
probably null |
|
R1512:Prdm10
|
UTSW |
9 |
31,248,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R1528:Prdm10
|
UTSW |
9 |
31,268,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R2409:Prdm10
|
UTSW |
9 |
31,260,418 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3745:Prdm10
|
UTSW |
9 |
31,251,703 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3929:Prdm10
|
UTSW |
9 |
31,258,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R4295:Prdm10
|
UTSW |
9 |
31,227,590 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4629:Prdm10
|
UTSW |
9 |
31,248,612 (GRCm39) |
nonsense |
probably null |
|
R4660:Prdm10
|
UTSW |
9 |
31,238,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Prdm10
|
UTSW |
9 |
31,273,708 (GRCm39) |
missense |
probably benign |
0.00 |
R4793:Prdm10
|
UTSW |
9 |
31,264,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Prdm10
|
UTSW |
9 |
31,252,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Prdm10
|
UTSW |
9 |
31,241,237 (GRCm39) |
makesense |
probably null |
|
R4865:Prdm10
|
UTSW |
9 |
31,258,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Prdm10
|
UTSW |
9 |
31,270,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R5093:Prdm10
|
UTSW |
9 |
31,252,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Prdm10
|
UTSW |
9 |
31,251,714 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5656:Prdm10
|
UTSW |
9 |
31,264,713 (GRCm39) |
missense |
probably benign |
0.08 |
R5855:Prdm10
|
UTSW |
9 |
31,248,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Prdm10
|
UTSW |
9 |
31,252,548 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6396:Prdm10
|
UTSW |
9 |
31,229,842 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6970:Prdm10
|
UTSW |
9 |
31,241,119 (GRCm39) |
nonsense |
probably null |
|
R7165:Prdm10
|
UTSW |
9 |
31,227,738 (GRCm39) |
splice site |
probably null |
|
R7177:Prdm10
|
UTSW |
9 |
31,279,003 (GRCm39) |
missense |
probably benign |
|
R7313:Prdm10
|
UTSW |
9 |
31,268,456 (GRCm39) |
nonsense |
probably null |
|
R7337:Prdm10
|
UTSW |
9 |
31,227,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R7511:Prdm10
|
UTSW |
9 |
31,289,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Prdm10
|
UTSW |
9 |
31,268,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R7855:Prdm10
|
UTSW |
9 |
31,238,770 (GRCm39) |
missense |
probably benign |
0.04 |
R7965:Prdm10
|
UTSW |
9 |
31,258,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7997:Prdm10
|
UTSW |
9 |
31,264,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8168:Prdm10
|
UTSW |
9 |
31,258,263 (GRCm39) |
missense |
probably benign |
0.00 |
R8717:Prdm10
|
UTSW |
9 |
31,252,695 (GRCm39) |
missense |
probably benign |
0.31 |
R8865:Prdm10
|
UTSW |
9 |
31,238,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R8880:Prdm10
|
UTSW |
9 |
31,264,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Prdm10
|
UTSW |
9 |
31,268,424 (GRCm39) |
missense |
probably benign |
0.01 |
R9200:Prdm10
|
UTSW |
9 |
31,268,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Prdm10
|
UTSW |
9 |
31,252,674 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9607:Prdm10
|
UTSW |
9 |
31,260,486 (GRCm39) |
missense |
probably damaging |
1.00 |
RF004:Prdm10
|
UTSW |
9 |
31,270,422 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Prdm10
|
UTSW |
9 |
31,273,747 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Prdm10
|
UTSW |
9 |
31,227,589 (GRCm39) |
nonsense |
probably null |
|
Z1176:Prdm10
|
UTSW |
9 |
31,227,464 (GRCm39) |
missense |
possibly damaging |
0.95 |
|