Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,382,005 (GRCm39) |
F1320S |
possibly damaging |
Het |
Aaas |
C |
T |
15: 102,248,494 (GRCm39) |
V241I |
probably benign |
Het |
Abca17 |
A |
G |
17: 24,504,700 (GRCm39) |
I1233T |
probably benign |
Het |
Acin1 |
T |
C |
14: 54,884,156 (GRCm39) |
|
probably null |
Het |
Acly |
A |
T |
11: 100,409,977 (GRCm39) |
I185N |
probably damaging |
Het |
Adamts16 |
T |
C |
13: 70,901,386 (GRCm39) |
D897G |
probably benign |
Het |
Allc |
A |
C |
12: 28,613,482 (GRCm39) |
D153E |
probably benign |
Het |
Ankrd12 |
A |
G |
17: 66,291,879 (GRCm39) |
S1185P |
probably damaging |
Het |
Aoc1l2 |
A |
T |
6: 48,909,363 (GRCm39) |
Q536L |
probably damaging |
Het |
Ap1g2 |
T |
C |
14: 55,339,835 (GRCm39) |
E448G |
probably benign |
Het |
Atg9a |
A |
T |
1: 75,166,270 (GRCm39) |
V50D |
probably benign |
Het |
Bace2 |
A |
T |
16: 97,216,289 (GRCm39) |
D294V |
possibly damaging |
Het |
Camsap2 |
T |
C |
1: 136,199,283 (GRCm39) |
K708E |
probably damaging |
Het |
Card10 |
G |
A |
15: 78,678,175 (GRCm39) |
R358C |
probably damaging |
Het |
Ccdc81 |
A |
T |
7: 89,547,271 (GRCm39) |
V39E |
probably damaging |
Het |
Cdh20 |
A |
T |
1: 109,976,668 (GRCm39) |
D111V |
probably damaging |
Het |
Cercam |
C |
A |
2: 29,762,935 (GRCm39) |
T223K |
probably benign |
Het |
Cimip2a |
T |
G |
2: 25,110,217 (GRCm39) |
L43R |
probably damaging |
Het |
Cog5 |
A |
G |
12: 31,710,848 (GRCm39) |
H76R |
possibly damaging |
Het |
Col28a1 |
A |
T |
6: 7,999,644 (GRCm39) |
N1024K |
probably benign |
Het |
Csrnp3 |
A |
T |
2: 65,779,446 (GRCm39) |
N41Y |
probably damaging |
Het |
Cyp2t4 |
G |
A |
7: 26,857,038 (GRCm39) |
|
probably null |
Het |
Dbn1 |
T |
C |
13: 55,630,254 (GRCm39) |
H38R |
probably damaging |
Het |
Dclre1b |
A |
G |
3: 103,710,672 (GRCm39) |
V287A |
probably benign |
Het |
Dennd4c |
A |
G |
4: 86,755,634 (GRCm39) |
T1609A |
probably benign |
Het |
Depdc5 |
T |
A |
5: 33,059,250 (GRCm39) |
|
probably null |
Het |
Dhcr7 |
T |
G |
7: 143,401,167 (GRCm39) |
D446E |
probably damaging |
Het |
Dlx5 |
A |
T |
6: 6,879,680 (GRCm39) |
M129K |
possibly damaging |
Het |
Dnah11 |
C |
G |
12: 118,046,203 (GRCm39) |
G1745A |
possibly damaging |
Het |
Dnm3 |
T |
C |
1: 162,181,281 (GRCm39) |
T133A |
possibly damaging |
Het |
Eif3e |
A |
G |
15: 43,129,005 (GRCm39) |
L205P |
probably damaging |
Het |
Fam91a1 |
A |
G |
15: 58,296,044 (GRCm39) |
|
probably null |
Het |
Fank1 |
C |
T |
7: 133,463,954 (GRCm39) |
T50I |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,223,473 (GRCm39) |
T940A |
possibly damaging |
Het |
Fkbp10 |
T |
C |
11: 100,306,841 (GRCm39) |
F78L |
probably damaging |
Het |
Gabbr2 |
A |
C |
4: 46,787,502 (GRCm39) |
F387C |
probably damaging |
Het |
Ggnbp2 |
A |
T |
11: 84,751,387 (GRCm39) |
L138I |
probably damaging |
Het |
Gm2832 |
T |
A |
14: 41,002,943 (GRCm39) |
|
probably null |
Het |
Gm5084 |
T |
A |
13: 60,360,344 (GRCm39) |
|
noncoding transcript |
Het |
Gm9979 |
T |
C |
13: 40,859,228 (GRCm39) |
|
noncoding transcript |
Het |
Hepacam2 |
A |
G |
6: 3,487,241 (GRCm39) |
S39P |
probably damaging |
Het |
Hesx1 |
A |
T |
14: 26,723,340 (GRCm39) |
N57Y |
probably damaging |
Het |
Kcnh1 |
G |
A |
1: 191,959,243 (GRCm39) |
V266I |
probably damaging |
Het |
Kif24 |
T |
C |
4: 41,392,904 (GRCm39) |
T1168A |
possibly damaging |
Het |
Kng2 |
A |
T |
16: 22,843,626 (GRCm39) |
F118I |
possibly damaging |
Het |
Lig3 |
C |
T |
11: 82,678,492 (GRCm39) |
P245S |
probably benign |
Het |
Loxhd1 |
G |
T |
18: 77,383,465 (GRCm39) |
W121C |
probably damaging |
Het |
Ltn1 |
A |
G |
16: 87,178,525 (GRCm39) |
V1568A |
probably damaging |
Het |
Map3k4 |
A |
T |
17: 12,473,882 (GRCm39) |
|
probably null |
Het |
Mcm10 |
C |
T |
2: 4,998,571 (GRCm39) |
V790M |
probably damaging |
Het |
Mia3 |
A |
T |
1: 183,125,707 (GRCm39) |
F1223I |
possibly damaging |
Het |
Mlec |
C |
A |
5: 115,288,405 (GRCm39) |
K150N |
probably damaging |
Het |
Morn4 |
T |
C |
19: 42,064,977 (GRCm39) |
K70R |
possibly damaging |
Het |
Mphosph10 |
A |
C |
7: 64,037,195 (GRCm39) |
|
probably null |
Het |
Myocd |
G |
A |
11: 65,095,147 (GRCm39) |
Q47* |
probably null |
Het |
Nav2 |
T |
A |
7: 49,198,219 (GRCm39) |
S1283T |
probably benign |
Het |
Nbeal2 |
T |
C |
9: 110,461,266 (GRCm39) |
H1599R |
probably damaging |
Het |
Nek10 |
G |
T |
14: 14,827,003 (GRCm38) |
G67V |
probably benign |
Het |
Nlgn2 |
A |
C |
11: 69,718,876 (GRCm39) |
V271G |
probably damaging |
Het |
Or1o2 |
A |
G |
17: 37,542,523 (GRCm39) |
V246A |
probably damaging |
Het |
Or2l5 |
A |
C |
16: 19,333,792 (GRCm39) |
V198G |
probably damaging |
Het |
Pcolce2 |
A |
T |
9: 95,576,793 (GRCm39) |
M355L |
probably benign |
Het |
Per2 |
T |
C |
1: 91,368,581 (GRCm39) |
E264G |
probably damaging |
Het |
Phf2 |
A |
G |
13: 48,982,384 (GRCm39) |
L113P |
unknown |
Het |
Plekha6 |
G |
A |
1: 133,191,556 (GRCm39) |
A146T |
probably benign |
Het |
Plxnb2 |
C |
T |
15: 89,042,971 (GRCm39) |
V1473I |
probably benign |
Het |
Pms2 |
T |
C |
5: 143,850,518 (GRCm39) |
L111P |
probably damaging |
Het |
Polg |
A |
G |
7: 79,108,979 (GRCm39) |
L533P |
probably damaging |
Het |
Ppp1r12b |
A |
G |
1: 134,774,093 (GRCm39) |
|
probably benign |
Het |
Ppp2r1b |
T |
A |
9: 50,778,671 (GRCm39) |
M208K |
possibly damaging |
Het |
Prdm5 |
A |
G |
6: 65,913,072 (GRCm39) |
Y207C |
probably damaging |
Het |
Prkar2b |
A |
G |
12: 32,013,934 (GRCm39) |
V314A |
probably damaging |
Het |
Proser1 |
T |
A |
3: 53,386,292 (GRCm39) |
S725T |
probably benign |
Het |
Psg20 |
A |
G |
7: 18,416,535 (GRCm39) |
F194L |
probably benign |
Het |
Ptprz1 |
A |
G |
6: 23,050,496 (GRCm39) |
I2255V |
probably damaging |
Het |
Sardh |
T |
G |
2: 27,134,409 (GRCm39) |
T36P |
probably damaging |
Het |
Sec23a |
T |
A |
12: 59,048,793 (GRCm39) |
I110L |
probably benign |
Het |
Slc22a29 |
T |
A |
19: 8,195,162 (GRCm39) |
I158L |
probably benign |
Het |
Slc35c1 |
T |
C |
2: 92,284,984 (GRCm39) |
D210G |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,704,746 (GRCm39) |
N566S |
probably benign |
Het |
Tcf20 |
G |
A |
15: 82,741,431 (GRCm39) |
Q7* |
probably null |
Het |
Terb2 |
T |
A |
2: 122,035,338 (GRCm39) |
H186Q |
possibly damaging |
Het |
Tet2 |
G |
A |
3: 133,192,350 (GRCm39) |
Q695* |
probably null |
Het |
Tnfaip1 |
T |
C |
11: 78,420,973 (GRCm39) |
Y29C |
probably damaging |
Het |
Traf3 |
A |
G |
12: 111,227,095 (GRCm39) |
K328E |
probably benign |
Het |
Uaca |
A |
G |
9: 60,777,623 (GRCm39) |
E668G |
probably damaging |
Het |
Ube2o |
T |
A |
11: 116,436,163 (GRCm39) |
E326V |
probably damaging |
Het |
Ubr1 |
C |
T |
2: 120,776,754 (GRCm39) |
|
probably null |
Het |
Vmn1r19 |
T |
A |
6: 57,382,033 (GRCm39) |
S195R |
probably damaging |
Het |
Vmn1r213 |
T |
G |
13: 23,196,473 (GRCm39) |
V352G |
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,292,880 (GRCm39) |
D307E |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 102,116,812 (GRCm39) |
D76G |
probably damaging |
Het |
Zan |
A |
T |
5: 137,401,376 (GRCm39) |
C4114* |
probably null |
Het |
Zbed6 |
A |
G |
1: 133,584,451 (GRCm39) |
L962P |
probably damaging |
Het |
Zdhhc23 |
A |
T |
16: 43,799,305 (GRCm39) |
C37S |
probably damaging |
Het |
Zfp628 |
G |
T |
7: 4,921,831 (GRCm39) |
G18W |
probably damaging |
Het |
Zfp712 |
T |
A |
13: 67,190,114 (GRCm39) |
K138* |
probably null |
Het |
Zfp867 |
A |
T |
11: 59,354,417 (GRCm39) |
V304D |
probably damaging |
Het |
Zfp870 |
T |
C |
17: 33,103,027 (GRCm39) |
T102A |
possibly damaging |
Het |
Zmym5 |
G |
A |
14: 57,035,210 (GRCm39) |
S286L |
possibly damaging |
Het |
|
Other mutations in Piwil2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01474:Piwil2
|
APN |
14 |
70,635,667 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02215:Piwil2
|
APN |
14 |
70,628,822 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02427:Piwil2
|
APN |
14 |
70,635,583 (GRCm39) |
splice site |
probably benign |
|
IGL02554:Piwil2
|
APN |
14 |
70,628,935 (GRCm39) |
splice site |
probably benign |
|
R0257:Piwil2
|
UTSW |
14 |
70,660,080 (GRCm39) |
missense |
probably benign |
0.00 |
R0566:Piwil2
|
UTSW |
14 |
70,647,843 (GRCm39) |
missense |
probably damaging |
0.99 |
R0800:Piwil2
|
UTSW |
14 |
70,646,486 (GRCm39) |
unclassified |
probably benign |
|
R0828:Piwil2
|
UTSW |
14 |
70,613,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R0862:Piwil2
|
UTSW |
14 |
70,632,823 (GRCm39) |
missense |
probably benign |
0.00 |
R0864:Piwil2
|
UTSW |
14 |
70,632,823 (GRCm39) |
missense |
probably benign |
0.00 |
R0881:Piwil2
|
UTSW |
14 |
70,646,376 (GRCm39) |
missense |
probably benign |
0.34 |
R1734:Piwil2
|
UTSW |
14 |
70,663,954 (GRCm39) |
critical splice donor site |
probably null |
|
R2011:Piwil2
|
UTSW |
14 |
70,664,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R2043:Piwil2
|
UTSW |
14 |
70,628,919 (GRCm39) |
missense |
probably benign |
0.00 |
R2347:Piwil2
|
UTSW |
14 |
70,646,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R2998:Piwil2
|
UTSW |
14 |
70,648,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R4402:Piwil2
|
UTSW |
14 |
70,646,365 (GRCm39) |
missense |
probably benign |
0.01 |
R4455:Piwil2
|
UTSW |
14 |
70,628,014 (GRCm39) |
missense |
probably benign |
0.02 |
R4611:Piwil2
|
UTSW |
14 |
70,639,646 (GRCm39) |
missense |
probably benign |
0.07 |
R4763:Piwil2
|
UTSW |
14 |
70,614,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:Piwil2
|
UTSW |
14 |
70,632,811 (GRCm39) |
missense |
probably benign |
0.00 |
R5033:Piwil2
|
UTSW |
14 |
70,659,042 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5207:Piwil2
|
UTSW |
14 |
70,629,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Piwil2
|
UTSW |
14 |
70,632,846 (GRCm39) |
missense |
probably benign |
0.01 |
R5486:Piwil2
|
UTSW |
14 |
70,638,880 (GRCm39) |
missense |
probably benign |
0.01 |
R5504:Piwil2
|
UTSW |
14 |
70,627,348 (GRCm39) |
missense |
probably benign |
0.01 |
R5629:Piwil2
|
UTSW |
14 |
70,660,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R5967:Piwil2
|
UTSW |
14 |
70,628,013 (GRCm39) |
missense |
probably benign |
0.00 |
R6167:Piwil2
|
UTSW |
14 |
70,660,342 (GRCm39) |
critical splice donor site |
probably null |
|
R6168:Piwil2
|
UTSW |
14 |
70,632,800 (GRCm39) |
missense |
probably benign |
0.04 |
R6517:Piwil2
|
UTSW |
14 |
70,611,785 (GRCm39) |
missense |
probably benign |
0.44 |
R7261:Piwil2
|
UTSW |
14 |
70,611,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7727:Piwil2
|
UTSW |
14 |
70,631,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7745:Piwil2
|
UTSW |
14 |
70,631,638 (GRCm39) |
missense |
probably benign |
|
R7833:Piwil2
|
UTSW |
14 |
70,632,890 (GRCm39) |
missense |
probably benign |
0.02 |
R8044:Piwil2
|
UTSW |
14 |
70,628,887 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8066:Piwil2
|
UTSW |
14 |
70,658,168 (GRCm39) |
missense |
probably benign |
0.00 |
R8516:Piwil2
|
UTSW |
14 |
70,658,188 (GRCm39) |
missense |
probably benign |
0.19 |
R9015:Piwil2
|
UTSW |
14 |
70,627,984 (GRCm39) |
missense |
probably benign |
0.00 |
R9494:Piwil2
|
UTSW |
14 |
70,660,421 (GRCm39) |
missense |
probably benign |
0.05 |
R9695:Piwil2
|
UTSW |
14 |
70,627,349 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0023:Piwil2
|
UTSW |
14 |
70,635,648 (GRCm39) |
missense |
probably benign |
|
|