Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
A |
G |
10: 86,909,902 (GRCm39) |
|
probably benign |
Het |
Adamts5 |
G |
T |
16: 85,665,083 (GRCm39) |
S627Y |
probably damaging |
Het |
Allc |
G |
A |
12: 28,610,010 (GRCm39) |
R196C |
probably damaging |
Het |
Ccdc65 |
A |
C |
15: 98,618,568 (GRCm39) |
E241A |
probably benign |
Het |
Dclk3 |
T |
C |
9: 111,317,741 (GRCm39) |
|
probably benign |
Het |
Fzd4 |
T |
C |
7: 89,056,505 (GRCm39) |
V184A |
probably benign |
Het |
Gfap |
T |
A |
11: 102,784,083 (GRCm39) |
|
probably null |
Het |
Gpr149 |
A |
G |
3: 62,511,366 (GRCm39) |
V211A |
probably benign |
Het |
Gprc6a |
A |
G |
10: 51,491,355 (GRCm39) |
I623T |
probably damaging |
Het |
Gucy2c |
T |
C |
6: 136,696,665 (GRCm39) |
T687A |
probably benign |
Het |
Kcnc4 |
T |
G |
3: 107,355,243 (GRCm39) |
M402L |
possibly damaging |
Het |
Ktn1 |
T |
C |
14: 47,928,391 (GRCm39) |
L584S |
probably damaging |
Het |
Mrgprb2 |
C |
T |
7: 48,202,650 (GRCm39) |
S25N |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,417,875 (GRCm39) |
V3607E |
probably benign |
Het |
Or4c58 |
C |
A |
2: 89,674,913 (GRCm39) |
V135L |
probably benign |
Het |
Or6c3b |
T |
C |
10: 129,527,147 (GRCm39) |
I254M |
probably damaging |
Het |
Otx2 |
A |
G |
14: 48,898,781 (GRCm39) |
I75T |
probably damaging |
Het |
Pabpc4l |
T |
C |
3: 46,400,972 (GRCm39) |
D224G |
probably damaging |
Het |
Polq |
A |
T |
16: 36,865,156 (GRCm39) |
L669F |
probably damaging |
Het |
Prss40 |
A |
C |
1: 34,597,182 (GRCm39) |
V122G |
probably damaging |
Het |
Rims2 |
A |
G |
15: 39,326,009 (GRCm39) |
|
probably null |
Het |
Rrp12 |
A |
T |
19: 41,860,232 (GRCm39) |
M997K |
possibly damaging |
Het |
Sbno2 |
G |
A |
10: 79,902,735 (GRCm39) |
R414W |
probably damaging |
Het |
Scn1a |
T |
C |
2: 66,148,362 (GRCm39) |
D41G |
probably benign |
Het |
Serpinb1c |
A |
T |
13: 33,066,044 (GRCm39) |
D300E |
probably damaging |
Het |
Timeless |
G |
A |
10: 128,087,924 (GRCm39) |
D1165N |
probably damaging |
Het |
Tnpo1 |
T |
G |
13: 99,024,981 (GRCm39) |
K66N |
probably damaging |
Het |
Trappc11 |
A |
T |
8: 47,963,912 (GRCm39) |
N629K |
possibly damaging |
Het |
Ubr4 |
T |
A |
4: 139,179,989 (GRCm39) |
L255M |
probably damaging |
Het |
Vmn1r10 |
T |
A |
6: 57,091,042 (GRCm39) |
Y211* |
probably null |
Het |
Vmn2r76 |
T |
G |
7: 85,879,034 (GRCm39) |
N422T |
probably benign |
Het |
Xylt1 |
C |
A |
7: 117,192,940 (GRCm39) |
N415K |
probably damaging |
Het |
Zfp786 |
A |
T |
6: 47,798,458 (GRCm39) |
V160E |
possibly damaging |
Het |
|
Other mutations in Peg3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Peg3
|
APN |
7 |
6,713,273 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01410:Peg3
|
APN |
7 |
6,710,624 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01415:Peg3
|
APN |
7 |
6,714,652 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02073:Peg3
|
APN |
7 |
6,714,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02193:Peg3
|
APN |
7 |
6,714,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02212:Peg3
|
APN |
7 |
6,714,415 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02215:Peg3
|
APN |
7 |
6,712,010 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02407:Peg3
|
APN |
7 |
6,710,635 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02586:Peg3
|
APN |
7 |
6,713,068 (GRCm39) |
missense |
probably benign |
|
IGL02673:Peg3
|
APN |
7 |
6,713,413 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Peg3
|
APN |
7 |
6,714,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Peg3
|
APN |
7 |
6,714,673 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03330:Peg3
|
APN |
7 |
6,713,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Peg3
|
UTSW |
7 |
6,714,672 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0049:Peg3
|
UTSW |
7 |
6,714,672 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0518:Peg3
|
UTSW |
7 |
6,714,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Peg3
|
UTSW |
7 |
6,714,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R1477:Peg3
|
UTSW |
7 |
6,719,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Peg3
|
UTSW |
7 |
6,710,780 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1721:Peg3
|
UTSW |
7 |
6,712,900 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1732:Peg3
|
UTSW |
7 |
6,712,084 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2051:Peg3
|
UTSW |
7 |
6,715,720 (GRCm39) |
missense |
probably damaging |
0.96 |
R2288:Peg3
|
UTSW |
7 |
6,712,114 (GRCm39) |
missense |
probably damaging |
0.96 |
R3606:Peg3
|
UTSW |
7 |
6,711,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Peg3
|
UTSW |
7 |
6,711,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R5076:Peg3
|
UTSW |
7 |
6,711,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R5084:Peg3
|
UTSW |
7 |
6,710,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R5097:Peg3
|
UTSW |
7 |
6,713,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R5121:Peg3
|
UTSW |
7 |
6,713,288 (GRCm39) |
missense |
probably benign |
0.20 |
R5141:Peg3
|
UTSW |
7 |
6,712,381 (GRCm39) |
missense |
probably benign |
0.03 |
R5292:Peg3
|
UTSW |
7 |
6,711,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R5294:Peg3
|
UTSW |
7 |
6,720,848 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5342:Peg3
|
UTSW |
7 |
6,712,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5415:Peg3
|
UTSW |
7 |
6,711,628 (GRCm39) |
missense |
probably benign |
|
R5906:Peg3
|
UTSW |
7 |
6,720,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R6056:Peg3
|
UTSW |
7 |
6,712,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Peg3
|
UTSW |
7 |
6,712,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R6529:Peg3
|
UTSW |
7 |
6,711,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Peg3
|
UTSW |
7 |
6,712,069 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6855:Peg3
|
UTSW |
7 |
6,711,797 (GRCm39) |
missense |
probably benign |
0.13 |
R6861:Peg3
|
UTSW |
7 |
6,714,385 (GRCm39) |
nonsense |
probably null |
|
R6864:Peg3
|
UTSW |
7 |
6,715,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R6892:Peg3
|
UTSW |
7 |
6,711,898 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7018:Peg3
|
UTSW |
7 |
6,711,838 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7039:Peg3
|
UTSW |
7 |
6,720,858 (GRCm39) |
missense |
probably damaging |
0.99 |
R7066:Peg3
|
UTSW |
7 |
6,711,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Peg3
|
UTSW |
7 |
6,712,167 (GRCm39) |
unclassified |
probably benign |
|
R7133:Peg3
|
UTSW |
7 |
6,711,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Peg3
|
UTSW |
7 |
6,712,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Peg3
|
UTSW |
7 |
6,711,167 (GRCm39) |
missense |
probably benign |
0.00 |
R7642:Peg3
|
UTSW |
7 |
6,712,167 (GRCm39) |
unclassified |
probably benign |
|
R7646:Peg3
|
UTSW |
7 |
6,712,221 (GRCm39) |
missense |
probably benign |
|
R7658:Peg3
|
UTSW |
7 |
6,712,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Peg3
|
UTSW |
7 |
6,713,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Peg3
|
UTSW |
7 |
6,711,839 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7903:Peg3
|
UTSW |
7 |
6,712,167 (GRCm39) |
unclassified |
probably benign |
|
R7913:Peg3
|
UTSW |
7 |
6,712,167 (GRCm39) |
unclassified |
probably benign |
|
R7948:Peg3
|
UTSW |
7 |
6,711,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R8219:Peg3
|
UTSW |
7 |
6,711,364 (GRCm39) |
missense |
probably benign |
0.00 |
R8385:Peg3
|
UTSW |
7 |
6,711,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Peg3
|
UTSW |
7 |
6,711,523 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9133:Peg3
|
UTSW |
7 |
6,712,167 (GRCm39) |
unclassified |
probably benign |
|
R9209:Peg3
|
UTSW |
7 |
6,711,226 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9457:Peg3
|
UTSW |
7 |
6,710,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R9518:Peg3
|
UTSW |
7 |
6,714,280 (GRCm39) |
missense |
probably benign |
0.00 |
R9519:Peg3
|
UTSW |
7 |
6,714,394 (GRCm39) |
missense |
probably benign |
0.00 |
R9599:Peg3
|
UTSW |
7 |
6,714,723 (GRCm39) |
missense |
probably damaging |
0.97 |
RF039:Peg3
|
UTSW |
7 |
6,712,167 (GRCm39) |
unclassified |
probably benign |
|
YA93:Peg3
|
UTSW |
7 |
6,714,646 (GRCm39) |
missense |
probably damaging |
1.00 |
|