Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap35 |
A |
T |
7: 16,296,224 (GRCm39) |
I947K |
probably damaging |
Het |
B3galnt2 |
A |
T |
13: 14,170,333 (GRCm39) |
I447F |
probably damaging |
Het |
Cacna2d3 |
C |
A |
14: 29,118,522 (GRCm39) |
V134L |
probably benign |
Het |
Clcn4 |
C |
T |
7: 7,297,024 (GRCm39) |
G145S |
probably damaging |
Het |
Cndp1 |
A |
T |
18: 84,650,135 (GRCm39) |
M186K |
probably benign |
Het |
Cntn6 |
A |
G |
6: 104,627,461 (GRCm39) |
Y98C |
probably damaging |
Het |
Ctsb |
T |
C |
14: 63,375,550 (GRCm39) |
V172A |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dyrk1a |
C |
A |
16: 94,472,299 (GRCm39) |
Q230K |
probably damaging |
Het |
Ech1 |
C |
T |
7: 28,529,763 (GRCm39) |
|
probably null |
Het |
Fam81b |
T |
A |
13: 76,399,968 (GRCm39) |
R97W |
probably damaging |
Het |
Heatr1 |
A |
G |
13: 12,420,978 (GRCm39) |
E423G |
possibly damaging |
Het |
Hydin |
A |
T |
8: 111,233,521 (GRCm39) |
K1786N |
probably damaging |
Het |
Igkv10-96 |
G |
A |
6: 68,608,969 (GRCm39) |
Q109* |
probably null |
Het |
Mup6 |
T |
C |
4: 60,004,837 (GRCm39) |
I76T |
possibly damaging |
Het |
Nmt2 |
A |
G |
2: 3,315,738 (GRCm39) |
R243G |
probably benign |
Het |
Nsd1 |
G |
A |
13: 55,386,602 (GRCm39) |
G119D |
probably damaging |
Het |
Or1ad8 |
A |
G |
11: 50,898,312 (GRCm39) |
H171R |
possibly damaging |
Het |
Or4c113 |
A |
G |
2: 88,885,641 (GRCm39) |
I43T |
probably benign |
Het |
Or4c120 |
T |
G |
2: 89,001,034 (GRCm39) |
D174A |
probably damaging |
Het |
Or51ab3 |
C |
T |
7: 103,201,888 (GRCm39) |
Q299* |
probably null |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pank3 |
T |
C |
11: 35,669,516 (GRCm39) |
V250A |
probably damaging |
Het |
Pcdh10 |
A |
G |
3: 45,334,495 (GRCm39) |
I270V |
possibly damaging |
Het |
Pnp2 |
T |
A |
14: 51,200,616 (GRCm39) |
V94E |
probably damaging |
Het |
Prdm10 |
T |
C |
9: 31,229,842 (GRCm39) |
V86A |
possibly damaging |
Het |
Resf1 |
A |
G |
6: 149,229,417 (GRCm39) |
D821G |
probably damaging |
Het |
Riox1 |
G |
A |
12: 83,998,087 (GRCm39) |
D208N |
possibly damaging |
Het |
Rrp15 |
A |
G |
1: 186,469,783 (GRCm39) |
|
probably null |
Het |
Skor1 |
G |
T |
9: 63,052,232 (GRCm39) |
P579Q |
probably damaging |
Het |
Slc44a4 |
T |
A |
17: 35,147,860 (GRCm39) |
Y481* |
probably null |
Het |
Smg7 |
A |
T |
1: 152,724,351 (GRCm39) |
V610E |
probably benign |
Het |
Tlx1 |
A |
G |
19: 45,144,491 (GRCm39) |
Q71R |
probably damaging |
Het |
Vmn2r27 |
A |
T |
6: 124,201,125 (GRCm39) |
Y277* |
probably null |
Het |
Zswim2 |
T |
A |
2: 83,754,062 (GRCm39) |
R199S |
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 |
R2314:Igf2r
|
UTSW |
17 |
12,934,830 (GRCm39) |
missense |
probably benign |
0.28 |
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 |
|
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 |
|