Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amt |
A |
G |
9: 108,178,418 (GRCm39) |
T342A |
probably benign |
Het |
Atosa |
G |
A |
9: 74,916,514 (GRCm39) |
R371Q |
probably damaging |
Het |
B3glct |
T |
C |
5: 149,650,299 (GRCm39) |
L134P |
probably damaging |
Het |
Bms1 |
A |
T |
6: 118,382,083 (GRCm39) |
M485K |
probably benign |
Het |
Chd6 |
T |
C |
2: 160,824,981 (GRCm39) |
N1226S |
probably null |
Het |
Cpne2 |
T |
C |
8: 95,275,000 (GRCm39) |
Y3H |
probably benign |
Het |
Dmxl2 |
A |
G |
9: 54,311,504 (GRCm39) |
V1739A |
probably damaging |
Het |
Dnah7a |
T |
A |
1: 53,669,481 (GRCm39) |
T543S |
probably benign |
Het |
Dock11 |
T |
G |
X: 35,277,603 (GRCm39) |
V1000G |
probably benign |
Het |
Ednrb |
T |
A |
14: 104,080,735 (GRCm39) |
N60Y |
probably benign |
Het |
Eif3d |
A |
G |
15: 77,843,849 (GRCm39) |
M499T |
possibly damaging |
Het |
Elmod1 |
G |
A |
9: 53,833,272 (GRCm39) |
L178F |
probably damaging |
Het |
Hrh4 |
T |
C |
18: 13,148,940 (GRCm39) |
S101P |
probably damaging |
Het |
Ift172 |
A |
G |
5: 31,424,642 (GRCm39) |
V684A |
possibly damaging |
Het |
Mtx2 |
A |
G |
2: 74,698,748 (GRCm39) |
T124A |
probably damaging |
Het |
Nat3 |
T |
A |
8: 68,000,341 (GRCm39) |
H73Q |
probably benign |
Het |
Ndst2 |
A |
G |
14: 20,780,234 (GRCm39) |
L2P |
possibly damaging |
Het |
Nipsnap3a |
G |
T |
4: 52,997,219 (GRCm39) |
A162S |
probably benign |
Het |
Or2a57 |
T |
G |
6: 43,212,876 (GRCm39) |
C111W |
probably damaging |
Het |
Or5m5 |
T |
C |
2: 85,814,517 (GRCm39) |
I111T |
probably damaging |
Het |
Prlr |
A |
G |
15: 10,328,887 (GRCm39) |
E454G |
probably benign |
Het |
Prom1 |
G |
A |
5: 44,190,313 (GRCm39) |
Q364* |
probably null |
Het |
Scgb2b7 |
A |
T |
7: 31,404,506 (GRCm39) |
C65S |
probably damaging |
Het |
Sema5b |
A |
G |
16: 35,471,682 (GRCm39) |
D425G |
probably damaging |
Het |
Slc16a7 |
A |
T |
10: 125,066,560 (GRCm39) |
C360S |
probably benign |
Het |
Slc38a7 |
T |
A |
8: 96,575,104 (GRCm39) |
I59F |
probably damaging |
Het |
Slc5a6 |
A |
G |
5: 31,195,372 (GRCm39) |
C449R |
possibly damaging |
Het |
Slc9b1 |
T |
C |
3: 135,096,269 (GRCm39) |
Y357H |
possibly damaging |
Het |
Snx17 |
A |
T |
5: 31,353,084 (GRCm39) |
|
probably benign |
Het |
Stk32b |
A |
C |
5: 37,786,320 (GRCm39) |
M48R |
probably damaging |
Het |
Tspan9 |
A |
G |
6: 127,944,038 (GRCm39) |
|
probably null |
Het |
Tst |
A |
T |
15: 78,289,521 (GRCm39) |
N171K |
probably damaging |
Het |
Vmn1r180 |
T |
A |
7: 23,652,710 (GRCm39) |
I291N |
probably damaging |
Het |
Vmn2r32 |
T |
A |
7: 7,477,251 (GRCm39) |
D380V |
probably benign |
Het |
Wdfy4 |
T |
C |
14: 32,790,861 (GRCm39) |
T2189A |
probably benign |
Het |
Zbtb20 |
A |
G |
16: 43,438,800 (GRCm39) |
N640S |
possibly damaging |
Het |
Zfp142 |
A |
G |
1: 74,610,193 (GRCm39) |
S1098P |
probably 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 |
IGL03330:Peg3
|
APN |
7 |
6,713,412 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03393:Peg3
|
APN |
7 |
6,710,648 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|