Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
C |
A |
12: 118,838,422 (GRCm39) |
V1047L |
probably damaging |
Het |
Akap6 |
G |
A |
12: 53,188,318 (GRCm39) |
A1911T |
probably benign |
Het |
Ank2 |
T |
A |
3: 126,726,838 (GRCm39) |
K819* |
probably null |
Het |
Apc2 |
A |
G |
10: 80,147,183 (GRCm39) |
R746G |
possibly damaging |
Het |
Baz1a |
A |
G |
12: 54,988,345 (GRCm39) |
I268T |
probably benign |
Het |
Bysl |
A |
G |
17: 47,914,865 (GRCm39) |
I206T |
probably benign |
Het |
Ccdc70 |
A |
C |
8: 22,463,357 (GRCm39) |
E49A |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,955,976 (GRCm39) |
H525L |
probably damaging |
Het |
Col4a4 |
T |
C |
1: 82,496,670 (GRCm39) |
E442G |
unknown |
Het |
Cpd |
G |
A |
11: 76,693,133 (GRCm39) |
P718S |
probably benign |
Het |
Dip2b |
T |
A |
15: 100,107,461 (GRCm39) |
I1391N |
probably damaging |
Het |
Dpp9 |
T |
C |
17: 56,501,946 (GRCm39) |
T541A |
probably damaging |
Het |
Dst |
C |
T |
1: 34,218,947 (GRCm39) |
Q1796* |
probably null |
Het |
Gm10267 |
T |
C |
18: 44,291,397 (GRCm39) |
I25V |
probably benign |
Het |
Gm32742 |
C |
T |
9: 51,061,441 (GRCm39) |
R744Q |
probably benign |
Het |
Gm37240 |
T |
C |
3: 84,422,952 (GRCm39) |
Y139C |
probably damaging |
Het |
Gm39115 |
A |
G |
7: 141,689,255 (GRCm39) |
C173R |
unknown |
Het |
Grm6 |
T |
G |
11: 50,750,877 (GRCm39) |
V680G |
probably damaging |
Het |
Grxcr2 |
C |
T |
18: 42,131,956 (GRCm39) |
D38N |
probably damaging |
Het |
Iah1 |
G |
A |
12: 21,366,587 (GRCm39) |
R52H |
probably damaging |
Het |
Ift43 |
A |
G |
12: 86,131,920 (GRCm39) |
Y36C |
possibly damaging |
Het |
Igfn1 |
T |
A |
1: 135,897,692 (GRCm39) |
Q958L |
possibly damaging |
Het |
Il4i1 |
G |
A |
7: 44,489,263 (GRCm39) |
A343T |
possibly damaging |
Het |
Ints1 |
T |
C |
5: 139,748,217 (GRCm39) |
I1128V |
probably benign |
Het |
Irx1 |
C |
A |
13: 72,111,588 (GRCm39) |
G7V |
probably damaging |
Het |
Krr1 |
A |
G |
10: 111,818,896 (GRCm39) |
R312G |
possibly damaging |
Het |
Lmna |
CAGCACGGTGCGTGAGC |
CAGC |
3: 88,389,857 (GRCm39) |
|
probably null |
Het |
Lpin2 |
A |
T |
17: 71,529,065 (GRCm39) |
N108Y |
probably damaging |
Het |
Man2a1 |
A |
T |
17: 64,943,557 (GRCm39) |
E204V |
possibly damaging |
Het |
Megf8 |
A |
G |
7: 25,030,166 (GRCm39) |
T434A |
possibly damaging |
Het |
Minar1 |
A |
T |
9: 89,484,072 (GRCm39) |
S442T |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,567,285 (GRCm39) |
T1745A |
unknown |
Het |
Mycbp2 |
G |
T |
14: 103,371,474 (GRCm39) |
P4135T |
probably damaging |
Het |
Nuggc |
T |
C |
14: 65,857,045 (GRCm39) |
V398A |
possibly damaging |
Het |
Or1e22 |
A |
G |
11: 73,376,885 (GRCm39) |
I255T |
probably damaging |
Het |
Or1e29 |
A |
T |
11: 73,667,976 (GRCm39) |
M59K |
probably damaging |
Het |
Or5w11 |
C |
T |
2: 87,459,152 (GRCm39) |
A115V |
possibly damaging |
Het |
Or6a2 |
A |
T |
7: 106,600,099 (GRCm39) |
S323T |
probably benign |
Het |
Or6e1 |
G |
T |
14: 54,520,342 (GRCm39) |
N3K |
probably damaging |
Het |
Or6f1 |
A |
G |
7: 85,970,444 (GRCm39) |
S239P |
probably damaging |
Het |
Parg |
A |
G |
14: 31,964,294 (GRCm39) |
N653S |
probably damaging |
Het |
Plek |
A |
G |
11: 16,945,346 (GRCm39) |
F18L |
probably benign |
Het |
Pnoc |
A |
G |
14: 65,639,247 (GRCm39) |
I206T |
possibly damaging |
Het |
Ppp4r3a |
T |
C |
12: 101,049,129 (GRCm39) |
M1V |
probably null |
Het |
Pramel21 |
A |
G |
4: 143,341,699 (GRCm39) |
T43A |
probably benign |
Het |
Psg22 |
T |
C |
7: 18,458,248 (GRCm39) |
V313A |
probably benign |
Het |
Ptk2b |
G |
T |
14: 66,409,546 (GRCm39) |
P497T |
probably damaging |
Het |
Rer1 |
A |
G |
4: 155,160,044 (GRCm39) |
|
probably null |
Het |
Rnf130 |
A |
G |
11: 49,986,618 (GRCm39) |
T321A |
probably benign |
Het |
Rnf207 |
A |
T |
4: 152,397,717 (GRCm39) |
F346I |
probably damaging |
Het |
Rraga |
T |
A |
4: 86,494,574 (GRCm39) |
I140N |
possibly damaging |
Het |
Rusc2 |
A |
T |
4: 43,416,262 (GRCm39) |
M523L |
probably benign |
Het |
Sh3bp1 |
T |
A |
15: 78,792,622 (GRCm39) |
V495D |
probably benign |
Het |
Slc44a5 |
T |
C |
3: 153,945,926 (GRCm39) |
L153P |
probably benign |
Het |
Spag16 |
T |
C |
1: 70,764,072 (GRCm39) |
S631P |
probably damaging |
Het |
Syne1 |
A |
C |
10: 4,984,937 (GRCm39) |
L747R |
probably damaging |
Het |
Tac1 |
A |
G |
6: 7,555,675 (GRCm39) |
E21G |
probably benign |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tln1 |
T |
C |
4: 43,542,957 (GRCm39) |
D1344G |
probably damaging |
Het |
Tnc |
C |
T |
4: 63,926,045 (GRCm39) |
E912K |
probably damaging |
Het |
Trav16d-dv11 |
A |
G |
14: 53,285,037 (GRCm39) |
T38A |
probably benign |
Het |
Trbv15 |
T |
A |
6: 41,118,364 (GRCm39) |
L40Q |
probably damaging |
Het |
Trpa1 |
T |
C |
1: 14,973,455 (GRCm39) |
I288V |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,604,941 (GRCm39) |
I18331N |
probably damaging |
Het |
Tubgcp2 |
A |
T |
7: 139,587,836 (GRCm39) |
I263N |
probably damaging |
Het |
Ugt8a |
T |
C |
3: 125,708,957 (GRCm39) |
H51R |
probably benign |
Het |
Vmn2r2 |
T |
C |
3: 64,023,870 (GRCm39) |
T904A |
probably benign |
Het |
Zfp575 |
G |
A |
7: 24,285,323 (GRCm39) |
T106M |
probably damaging |
Het |
Zfp617 |
A |
G |
8: 72,686,539 (GRCm39) |
T290A |
probably benign |
Het |
Zfp809 |
T |
C |
9: 22,149,863 (GRCm39) |
V120A |
probably benign |
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 |
|
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 |
X0028:Igf2r
|
UTSW |
17 |
12,923,800 (GRCm39) |
nonsense |
probably null |
|
Z1177:Igf2r
|
UTSW |
17 |
12,916,286 (GRCm39) |
missense |
probably damaging |
0.99 |
|