Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdhppt |
A |
G |
9: 4,309,322 (GRCm39) |
S39P |
probably damaging |
Het |
Aif1 |
G |
A |
17: 35,391,127 (GRCm39) |
P44L |
probably benign |
Het |
Anxa6 |
T |
A |
11: 54,902,561 (GRCm39) |
I58F |
probably damaging |
Het |
Ccdc30 |
T |
A |
4: 119,181,763 (GRCm39) |
K582* |
probably null |
Het |
Cebpz |
A |
G |
17: 79,227,976 (GRCm39) |
|
probably null |
Het |
Clstn3 |
T |
A |
6: 124,427,676 (GRCm39) |
D473V |
probably benign |
Het |
Cry1 |
A |
T |
10: 84,969,175 (GRCm39) |
C550S |
probably benign |
Het |
Dclk2 |
G |
A |
3: 86,827,342 (GRCm39) |
P46S |
probably damaging |
Het |
Dolk |
G |
T |
2: 30,175,497 (GRCm39) |
L183M |
probably damaging |
Het |
Dpys |
T |
C |
15: 39,691,486 (GRCm39) |
T279A |
possibly damaging |
Het |
Drd4 |
T |
C |
7: 140,873,854 (GRCm39) |
Y140H |
probably damaging |
Het |
Duox1 |
C |
A |
2: 122,164,211 (GRCm39) |
C890* |
probably null |
Het |
Epha2 |
T |
A |
4: 141,046,325 (GRCm39) |
V508E |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fahd1 |
A |
T |
17: 25,068,570 (GRCm39) |
I169N |
probably damaging |
Het |
Fgfr1 |
C |
T |
8: 26,060,909 (GRCm39) |
S527F |
probably damaging |
Het |
Flywch1 |
A |
G |
17: 23,982,000 (GRCm39) |
V68A |
probably benign |
Het |
Gm21834 |
A |
T |
17: 58,049,210 (GRCm39) |
V2E |
possibly damaging |
Het |
Gm7853 |
A |
T |
14: 35,811,621 (GRCm39) |
|
noncoding transcript |
Het |
Iqgap3 |
T |
C |
3: 88,023,338 (GRCm39) |
V543A |
probably benign |
Het |
Kcnq5 |
T |
A |
1: 21,549,595 (GRCm39) |
|
probably null |
Het |
Lsm1 |
C |
T |
8: 26,275,712 (GRCm39) |
P5S |
possibly damaging |
Het |
Marchf1 |
T |
C |
8: 66,574,442 (GRCm39) |
M1T |
probably null |
Het |
Myocd |
T |
C |
11: 65,091,633 (GRCm39) |
H103R |
probably damaging |
Het |
Myom2 |
C |
T |
8: 15,113,927 (GRCm39) |
T25I |
probably damaging |
Het |
Nck1 |
T |
C |
9: 100,380,003 (GRCm39) |
K83E |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,839,829 (GRCm39) |
D806G |
probably benign |
Het |
Onecut2 |
G |
T |
18: 64,474,268 (GRCm39) |
R254L |
probably damaging |
Het |
Or51k1 |
T |
A |
7: 103,661,436 (GRCm39) |
M158L |
probably benign |
Het |
Plxna1 |
A |
C |
6: 89,301,298 (GRCm39) |
L1534R |
probably damaging |
Het |
Polb |
C |
A |
8: 23,130,018 (GRCm39) |
A185S |
possibly damaging |
Het |
Pou3f3 |
T |
C |
1: 42,737,651 (GRCm39) |
V449A |
probably damaging |
Het |
Pskh1 |
C |
T |
8: 106,640,145 (GRCm39) |
T275I |
probably damaging |
Het |
Rab18 |
C |
A |
18: 6,788,516 (GRCm39) |
A161D |
probably damaging |
Het |
Rrp8 |
T |
C |
7: 105,384,011 (GRCm39) |
R164G |
probably benign |
Het |
Sacs |
T |
A |
14: 61,445,208 (GRCm39) |
I2418K |
probably benign |
Het |
Scrn1 |
T |
C |
6: 54,502,631 (GRCm39) |
E136G |
probably benign |
Het |
Sgk1 |
C |
T |
10: 21,872,500 (GRCm39) |
R171W |
probably damaging |
Het |
Slitrk6 |
C |
T |
14: 110,989,387 (GRCm39) |
A107T |
probably damaging |
Het |
Spata31e2 |
T |
C |
1: 26,723,783 (GRCm39) |
S466G |
probably benign |
Het |
Tktl2 |
T |
A |
8: 66,965,795 (GRCm39) |
F451Y |
probably damaging |
Het |
Tnks1bp1 |
G |
A |
2: 84,889,259 (GRCm39) |
V529M |
probably benign |
Het |
Trps1 |
T |
C |
15: 50,524,742 (GRCm39) |
K874E |
probably damaging |
Het |
Ttll9 |
T |
A |
2: 152,825,047 (GRCm39) |
D75E |
probably benign |
Het |
Ttn |
A |
G |
2: 76,596,368 (GRCm39) |
Y20182H |
probably damaging |
Het |
Ufc1 |
A |
T |
1: 171,116,821 (GRCm39) |
C116S |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Zfp809 |
A |
G |
9: 22,149,976 (GRCm39) |
K158E |
possibly damaging |
Het |
Zfp81 |
A |
G |
17: 33,553,597 (GRCm39) |
Y406H |
probably damaging |
Het |
|
Other mutations in Igf2r |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Igf2r
|
APN |
17 |
12,932,877 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00534:Igf2r
|
APN |
17 |
12,958,215 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00902:Igf2r
|
APN |
17 |
12,919,245 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00903:Igf2r
|
APN |
17 |
12,902,754 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01160:Igf2r
|
APN |
17 |
12,923,662 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01380:Igf2r
|
APN |
17 |
12,914,261 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01392:Igf2r
|
APN |
17 |
12,923,236 (GRCm39) |
missense |
probably benign |
|
IGL01557:Igf2r
|
APN |
17 |
12,923,522 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01568:Igf2r
|
APN |
17 |
12,902,872 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01611:Igf2r
|
APN |
17 |
12,944,302 (GRCm39) |
nonsense |
probably null |
|
IGL01720:Igf2r
|
APN |
17 |
12,920,200 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01756:Igf2r
|
APN |
17 |
12,902,709 (GRCm39) |
missense |
probably benign |
|
IGL01839:Igf2r
|
APN |
17 |
12,923,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01904:Igf2r
|
APN |
17 |
12,933,798 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01965:Igf2r
|
APN |
17 |
12,923,225 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02083:Igf2r
|
APN |
17 |
12,912,079 (GRCm39) |
nonsense |
probably null |
|
IGL02095:Igf2r
|
APN |
17 |
12,920,892 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02183:Igf2r
|
APN |
17 |
12,917,403 (GRCm39) |
unclassified |
probably benign |
|
IGL02576:Igf2r
|
APN |
17 |
12,967,650 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02649:Igf2r
|
APN |
17 |
12,930,974 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02807:Igf2r
|
APN |
17 |
12,938,770 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02833:Igf2r
|
APN |
17 |
12,911,610 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02885:Igf2r
|
APN |
17 |
12,913,007 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02990:Igf2r
|
APN |
17 |
12,929,633 (GRCm39) |
splice site |
probably benign |
|
IGL03080:Igf2r
|
APN |
17 |
12,945,563 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03176:Igf2r
|
APN |
17 |
12,935,559 (GRCm39) |
missense |
probably damaging |
1.00 |
blunt
|
UTSW |
17 |
12,941,062 (GRCm39) |
missense |
probably benign |
0.02 |
brusque
|
UTSW |
17 |
12,933,838 (GRCm39) |
missense |
probably damaging |
0.98 |
gruff
|
UTSW |
17 |
12,902,984 (GRCm39) |
missense |
probably damaging |
0.96 |
outlier
|
UTSW |
17 |
12,914,201 (GRCm39) |
missense |
probably benign |
0.20 |
NA:Igf2r
|
UTSW |
17 |
12,910,849 (GRCm39) |
missense |
probably benign |
|
R0165:Igf2r
|
UTSW |
17 |
12,917,414 (GRCm39) |
missense |
probably benign |
0.07 |
R0412:Igf2r
|
UTSW |
17 |
12,902,835 (GRCm39) |
missense |
probably damaging |
0.98 |
R0523:Igf2r
|
UTSW |
17 |
12,910,951 (GRCm39) |
missense |
probably benign |
0.27 |
R0631:Igf2r
|
UTSW |
17 |
12,936,161 (GRCm39) |
splice site |
probably null |
|
R0722:Igf2r
|
UTSW |
17 |
12,934,382 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0894:Igf2r
|
UTSW |
17 |
12,910,988 (GRCm39) |
missense |
probably benign |
0.02 |
R1265:Igf2r
|
UTSW |
17 |
12,913,011 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Igf2r
|
UTSW |
17 |
12,936,156 (GRCm39) |
splice site |
probably benign |
|
R1485:Igf2r
|
UTSW |
17 |
12,910,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Igf2r
|
UTSW |
17 |
12,945,196 (GRCm39) |
missense |
probably benign |
|
R1693:Igf2r
|
UTSW |
17 |
12,923,203 (GRCm39) |
missense |
probably damaging |
0.97 |
R1751:Igf2r
|
UTSW |
17 |
12,916,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1843:Igf2r
|
UTSW |
17 |
12,923,157 (GRCm39) |
critical splice donor site |
probably null |
|
R1981:Igf2r
|
UTSW |
17 |
12,952,790 (GRCm39) |
nonsense |
probably null |
|
R1994:Igf2r
|
UTSW |
17 |
12,911,625 (GRCm39) |
missense |
probably benign |
|
R2060:Igf2r
|
UTSW |
17 |
12,920,206 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2108:Igf2r
|
UTSW |
17 |
12,917,138 (GRCm39) |
missense |
probably benign |
0.02 |
R2132:Igf2r
|
UTSW |
17 |
12,941,095 (GRCm39) |
missense |
probably benign |
0.12 |
R2349:Igf2r
|
UTSW |
17 |
12,941,198 (GRCm39) |
splice site |
probably null |
|
R2696:Igf2r
|
UTSW |
17 |
12,914,231 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2864:Igf2r
|
UTSW |
17 |
12,905,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R2865:Igf2r
|
UTSW |
17 |
12,905,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R3884:Igf2r
|
UTSW |
17 |
12,928,355 (GRCm39) |
missense |
probably benign |
|
R3930:Igf2r
|
UTSW |
17 |
12,924,716 (GRCm39) |
missense |
probably benign |
0.01 |
R4021:Igf2r
|
UTSW |
17 |
12,967,638 (GRCm39) |
missense |
probably damaging |
0.97 |
R4125:Igf2r
|
UTSW |
17 |
12,921,141 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4342:Igf2r
|
UTSW |
17 |
12,928,398 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4343:Igf2r
|
UTSW |
17 |
12,928,398 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4345:Igf2r
|
UTSW |
17 |
12,928,398 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4760:Igf2r
|
UTSW |
17 |
12,922,352 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4796:Igf2r
|
UTSW |
17 |
12,903,013 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4816:Igf2r
|
UTSW |
17 |
12,902,984 (GRCm39) |
missense |
probably damaging |
0.96 |
R4826:Igf2r
|
UTSW |
17 |
12,920,240 (GRCm39) |
missense |
probably damaging |
0.98 |
R4933:Igf2r
|
UTSW |
17 |
12,910,764 (GRCm39) |
splice site |
probably null |
|
R4980:Igf2r
|
UTSW |
17 |
12,922,247 (GRCm39) |
critical splice donor site |
probably null |
|
R5389:Igf2r
|
UTSW |
17 |
12,944,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R5473:Igf2r
|
UTSW |
17 |
12,914,201 (GRCm39) |
missense |
probably benign |
0.20 |
R5494:Igf2r
|
UTSW |
17 |
12,912,032 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5619:Igf2r
|
UTSW |
17 |
12,958,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5738:Igf2r
|
UTSW |
17 |
12,936,254 (GRCm39) |
missense |
probably benign |
0.23 |
R5761:Igf2r
|
UTSW |
17 |
12,917,239 (GRCm39) |
splice site |
probably null |
|
R5794:Igf2r
|
UTSW |
17 |
12,928,332 (GRCm39) |
missense |
probably benign |
0.37 |
R6210:Igf2r
|
UTSW |
17 |
12,933,838 (GRCm39) |
missense |
probably damaging |
0.98 |
R6319:Igf2r
|
UTSW |
17 |
12,933,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R6388:Igf2r
|
UTSW |
17 |
12,902,787 (GRCm39) |
missense |
probably benign |
|
R6396:Igf2r
|
UTSW |
17 |
12,932,977 (GRCm39) |
missense |
probably benign |
0.00 |
R6584:Igf2r
|
UTSW |
17 |
12,920,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R6590:Igf2r
|
UTSW |
17 |
12,910,824 (GRCm39) |
nonsense |
probably null |
|
R6591:Igf2r
|
UTSW |
17 |
12,907,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6599:Igf2r
|
UTSW |
17 |
12,917,505 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6690:Igf2r
|
UTSW |
17 |
12,910,824 (GRCm39) |
nonsense |
probably null |
|
R6691:Igf2r
|
UTSW |
17 |
12,907,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Igf2r
|
UTSW |
17 |
12,933,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6816:Igf2r
|
UTSW |
17 |
12,932,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R6841:Igf2r
|
UTSW |
17 |
12,922,263 (GRCm39) |
missense |
probably damaging |
0.97 |
R6877:Igf2r
|
UTSW |
17 |
12,916,228 (GRCm39) |
missense |
probably damaging |
0.97 |
R6950:Igf2r
|
UTSW |
17 |
12,937,605 (GRCm39) |
missense |
probably benign |
|
R7030:Igf2r
|
UTSW |
17 |
12,952,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R7038:Igf2r
|
UTSW |
17 |
12,917,212 (GRCm39) |
missense |
probably benign |
0.23 |
R7055:Igf2r
|
UTSW |
17 |
12,923,210 (GRCm39) |
missense |
probably damaging |
0.99 |
R7074:Igf2r
|
UTSW |
17 |
12,933,003 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7348:Igf2r
|
UTSW |
17 |
12,922,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R7413:Igf2r
|
UTSW |
17 |
12,917,115 (GRCm39) |
nonsense |
probably null |
|
R7463:Igf2r
|
UTSW |
17 |
12,929,532 (GRCm39) |
missense |
probably benign |
0.16 |
R7619:Igf2r
|
UTSW |
17 |
12,917,160 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7730:Igf2r
|
UTSW |
17 |
12,954,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R7733:Igf2r
|
UTSW |
17 |
12,958,256 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7881:Igf2r
|
UTSW |
17 |
12,967,591 (GRCm39) |
missense |
probably benign |
|
R8022:Igf2r
|
UTSW |
17 |
12,937,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8138:Igf2r
|
UTSW |
17 |
12,920,125 (GRCm39) |
missense |
probably benign |
0.32 |
R8220:Igf2r
|
UTSW |
17 |
12,910,958 (GRCm39) |
missense |
probably benign |
0.22 |
R8305:Igf2r
|
UTSW |
17 |
12,952,747 (GRCm39) |
missense |
probably benign |
|
R8359:Igf2r
|
UTSW |
17 |
12,902,748 (GRCm39) |
missense |
probably benign |
|
R8500:Igf2r
|
UTSW |
17 |
12,928,328 (GRCm39) |
missense |
probably damaging |
0.99 |
R8510:Igf2r
|
UTSW |
17 |
12,923,200 (GRCm39) |
missense |
probably benign |
0.38 |
R8933:Igf2r
|
UTSW |
17 |
12,923,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Igf2r
|
UTSW |
17 |
12,920,131 (GRCm39) |
missense |
probably damaging |
0.97 |
R8976:Igf2r
|
UTSW |
17 |
12,945,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R8994:Igf2r
|
UTSW |
17 |
12,935,537 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9059:Igf2r
|
UTSW |
17 |
12,970,180 (GRCm39) |
start codon destroyed |
probably null |
|
R9097:Igf2r
|
UTSW |
17 |
12,910,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Igf2r
|
UTSW |
17 |
12,958,238 (GRCm39) |
missense |
probably damaging |
0.98 |
R9278:Igf2r
|
UTSW |
17 |
12,914,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Igf2r
|
UTSW |
17 |
12,941,062 (GRCm39) |
missense |
probably benign |
0.02 |
R9371:Igf2r
|
UTSW |
17 |
12,924,646 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9522:Igf2r
|
UTSW |
17 |
12,917,215 (GRCm39) |
missense |
probably benign |
0.26 |
R9567:Igf2r
|
UTSW |
17 |
12,905,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Igf2r
|
UTSW |
17 |
12,913,027 (GRCm39) |
missense |
probably benign |
0.17 |
R9666:Igf2r
|
UTSW |
17 |
12,945,588 (GRCm39) |
missense |
probably benign |
|
X0028:Igf2r
|
UTSW |
17 |
12,923,800 (GRCm39) |
nonsense |
probably null |
|
Z1177:Igf2r
|
UTSW |
17 |
12,916,286 (GRCm39) |
missense |
probably damaging |
0.99 |
|