Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810408A11Rik |
G |
T |
11: 69,791,198 (GRCm39) |
T127K |
possibly damaging |
Het |
A2m |
T |
G |
6: 121,653,918 (GRCm39) |
I1417S |
probably damaging |
Het |
Acad10 |
A |
G |
5: 121,787,523 (GRCm39) |
I142T |
possibly damaging |
Het |
Adprm |
T |
A |
11: 66,932,678 (GRCm39) |
D77V |
probably damaging |
Het |
Apob |
C |
T |
12: 8,062,240 (GRCm39) |
T3574I |
probably damaging |
Het |
Bahcc1 |
A |
G |
11: 120,178,908 (GRCm39) |
K2489R |
probably damaging |
Het |
Bub1b |
A |
G |
2: 118,452,676 (GRCm39) |
E443G |
possibly damaging |
Het |
Cd9 |
A |
T |
6: 125,440,734 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
G |
A |
9: 71,538,160 (GRCm39) |
T1194M |
probably damaging |
Het |
Clec9a |
T |
C |
6: 129,387,274 (GRCm39) |
V43A |
probably benign |
Het |
Col11a1 |
C |
T |
3: 113,951,791 (GRCm39) |
R1074C |
probably damaging |
Het |
Dpep3 |
A |
G |
8: 106,701,346 (GRCm39) |
V401A |
probably damaging |
Het |
Duox2 |
G |
T |
2: 122,111,448 (GRCm39) |
H1417N |
probably damaging |
Het |
Efhb |
C |
T |
17: 53,733,937 (GRCm39) |
|
probably null |
Het |
F2r |
T |
C |
13: 95,741,418 (GRCm39) |
N39S |
probably benign |
Het |
Fcamr |
T |
C |
1: 130,739,335 (GRCm39) |
F212L |
probably damaging |
Het |
Galt |
G |
A |
4: 41,758,162 (GRCm39) |
R309Q |
probably damaging |
Het |
Gas2l2 |
C |
A |
11: 83,318,209 (GRCm39) |
A167S |
probably benign |
Het |
Hecw1 |
A |
T |
13: 14,438,672 (GRCm39) |
F904I |
possibly damaging |
Het |
Herc2 |
C |
A |
7: 55,862,713 (GRCm39) |
H4127Q |
possibly damaging |
Het |
Hipk1 |
T |
C |
3: 103,657,670 (GRCm39) |
T805A |
probably benign |
Het |
Hivep1 |
A |
G |
13: 42,337,226 (GRCm39) |
E2435G |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,015,273 (GRCm39) |
C1813* |
probably null |
Het |
Hyal4 |
C |
T |
6: 24,755,749 (GRCm39) |
|
probably benign |
Het |
Inpp4b |
A |
G |
8: 82,678,903 (GRCm39) |
Y311C |
probably damaging |
Het |
Itih4 |
A |
G |
14: 30,614,280 (GRCm39) |
Y410C |
possibly damaging |
Het |
Lama2 |
A |
T |
10: 27,080,837 (GRCm39) |
C995* |
probably null |
Het |
Lingo4 |
C |
A |
3: 94,309,552 (GRCm39) |
D163E |
probably damaging |
Het |
Malt1 |
A |
G |
18: 65,606,218 (GRCm39) |
D642G |
probably damaging |
Het |
Mbd4 |
T |
A |
6: 115,825,918 (GRCm39) |
M358L |
probably benign |
Het |
Mbd5 |
T |
A |
2: 49,169,323 (GRCm39) |
F1498Y |
possibly damaging |
Het |
Me1 |
T |
C |
9: 86,495,607 (GRCm39) |
Q280R |
probably damaging |
Het |
Megf9 |
T |
C |
4: 70,367,004 (GRCm39) |
H326R |
probably damaging |
Het |
Nid2 |
G |
A |
14: 19,828,111 (GRCm39) |
G516S |
probably benign |
Het |
Or13p10 |
T |
C |
4: 118,523,301 (GRCm39) |
S196P |
probably damaging |
Het |
Or1e1 |
T |
C |
11: 73,245,247 (GRCm39) |
S223P |
possibly damaging |
Het |
Or4k1 |
T |
A |
14: 50,377,580 (GRCm39) |
N172I |
probably damaging |
Het |
Or5h18 |
C |
T |
16: 58,848,232 (GRCm39) |
V13I |
probably benign |
Het |
Or8b1c |
A |
G |
9: 38,384,223 (GRCm39) |
Y60C |
probably damaging |
Het |
Polr2j |
T |
C |
5: 136,145,625 (GRCm39) |
F7L |
probably damaging |
Het |
Ppp1r16a |
T |
A |
15: 76,577,796 (GRCm39) |
D303E |
probably damaging |
Het |
Prickle2 |
T |
C |
6: 92,353,345 (GRCm39) |
E763G |
probably damaging |
Het |
Rdh11 |
T |
C |
12: 79,229,556 (GRCm39) |
Y239C |
possibly damaging |
Het |
Sdhaf3 |
A |
G |
6: 6,956,048 (GRCm39) |
R8G |
probably benign |
Het |
Sgk2 |
T |
C |
2: 162,854,890 (GRCm39) |
S305P |
probably damaging |
Het |
Sptbn2 |
A |
G |
19: 4,788,587 (GRCm39) |
S1189G |
probably benign |
Het |
Stab2 |
A |
G |
10: 86,790,023 (GRCm39) |
L581P |
probably damaging |
Het |
Tifab |
T |
C |
13: 56,324,110 (GRCm39) |
Q111R |
probably damaging |
Het |
Usp17lb |
T |
A |
7: 104,489,622 (GRCm39) |
Q434L |
possibly damaging |
Het |
Wdr46 |
G |
T |
17: 34,160,425 (GRCm39) |
E135* |
probably null |
Het |
Zfp318 |
T |
A |
17: 46,720,590 (GRCm39) |
|
probably null |
Het |
Zfp874a |
T |
A |
13: 67,590,967 (GRCm39) |
H239L |
probably damaging |
Het |
Zscan29 |
A |
T |
2: 121,000,427 (GRCm39) |
L60* |
probably null |
Het |
|
Other mutations in Ubr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Ubr3
|
APN |
2 |
69,819,154 (GRCm39) |
missense |
probably benign |
0.40 |
IGL00985:Ubr3
|
APN |
2 |
69,833,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01061:Ubr3
|
APN |
2 |
69,813,569 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01325:Ubr3
|
APN |
2 |
69,747,441 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01398:Ubr3
|
APN |
2 |
69,789,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01484:Ubr3
|
APN |
2 |
69,851,888 (GRCm39) |
nonsense |
probably null |
|
IGL01599:Ubr3
|
APN |
2 |
69,768,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01616:Ubr3
|
APN |
2 |
69,850,828 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01634:Ubr3
|
APN |
2 |
69,803,916 (GRCm39) |
missense |
probably benign |
|
IGL01684:Ubr3
|
APN |
2 |
69,846,502 (GRCm39) |
nonsense |
probably null |
|
IGL01810:Ubr3
|
APN |
2 |
69,833,809 (GRCm39) |
splice site |
probably null |
|
IGL01813:Ubr3
|
APN |
2 |
69,781,914 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01994:Ubr3
|
APN |
2 |
69,851,520 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02188:Ubr3
|
APN |
2 |
69,789,955 (GRCm39) |
nonsense |
probably null |
|
IGL02318:Ubr3
|
APN |
2 |
69,809,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02379:Ubr3
|
APN |
2 |
69,778,832 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02635:Ubr3
|
APN |
2 |
69,850,827 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02858:Ubr3
|
APN |
2 |
69,783,203 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03140:Ubr3
|
APN |
2 |
69,800,533 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03343:Ubr3
|
APN |
2 |
69,803,490 (GRCm39) |
splice site |
probably benign |
|
Hyrax
|
UTSW |
2 |
69,783,212 (GRCm39) |
missense |
probably benign |
0.32 |
manatee
|
UTSW |
2 |
69,809,730 (GRCm39) |
nonsense |
probably null |
|
sea_cow
|
UTSW |
2 |
69,790,013 (GRCm39) |
splice site |
probably null |
|
R0094:Ubr3
|
UTSW |
2 |
69,781,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Ubr3
|
UTSW |
2 |
69,781,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R0122:Ubr3
|
UTSW |
2 |
69,809,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Ubr3
|
UTSW |
2 |
69,781,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R0710:Ubr3
|
UTSW |
2 |
69,783,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R0787:Ubr3
|
UTSW |
2 |
69,781,765 (GRCm39) |
splice site |
probably benign |
|
R1137:Ubr3
|
UTSW |
2 |
69,768,659 (GRCm39) |
splice site |
probably benign |
|
R1191:Ubr3
|
UTSW |
2 |
69,851,525 (GRCm39) |
nonsense |
probably null |
|
R1416:Ubr3
|
UTSW |
2 |
69,775,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Ubr3
|
UTSW |
2 |
69,808,067 (GRCm39) |
nonsense |
probably null |
|
R1735:Ubr3
|
UTSW |
2 |
69,839,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Ubr3
|
UTSW |
2 |
69,846,711 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1793:Ubr3
|
UTSW |
2 |
69,830,895 (GRCm39) |
splice site |
probably benign |
|
R1932:Ubr3
|
UTSW |
2 |
69,783,820 (GRCm39) |
splice site |
probably null |
|
R2042:Ubr3
|
UTSW |
2 |
69,808,118 (GRCm39) |
nonsense |
probably null |
|
R2090:Ubr3
|
UTSW |
2 |
69,766,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Ubr3
|
UTSW |
2 |
69,808,136 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2173:Ubr3
|
UTSW |
2 |
69,727,743 (GRCm39) |
missense |
probably benign |
|
R2215:Ubr3
|
UTSW |
2 |
69,809,661 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2273:Ubr3
|
UTSW |
2 |
69,846,685 (GRCm39) |
missense |
probably benign |
0.11 |
R2274:Ubr3
|
UTSW |
2 |
69,846,685 (GRCm39) |
missense |
probably benign |
0.11 |
R2275:Ubr3
|
UTSW |
2 |
69,846,685 (GRCm39) |
missense |
probably benign |
0.11 |
R2292:Ubr3
|
UTSW |
2 |
69,727,604 (GRCm39) |
unclassified |
probably benign |
|
R2447:Ubr3
|
UTSW |
2 |
69,833,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Ubr3
|
UTSW |
2 |
69,768,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R2517:Ubr3
|
UTSW |
2 |
69,766,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R2901:Ubr3
|
UTSW |
2 |
69,846,536 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3109:Ubr3
|
UTSW |
2 |
69,819,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R3737:Ubr3
|
UTSW |
2 |
69,801,578 (GRCm39) |
critical splice donor site |
probably null |
|
R3793:Ubr3
|
UTSW |
2 |
69,747,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3821:Ubr3
|
UTSW |
2 |
69,824,157 (GRCm39) |
critical splice donor site |
probably null |
|
R3918:Ubr3
|
UTSW |
2 |
69,846,474 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4157:Ubr3
|
UTSW |
2 |
69,790,013 (GRCm39) |
splice site |
probably null |
|
R4235:Ubr3
|
UTSW |
2 |
69,846,729 (GRCm39) |
nonsense |
probably null |
|
R4276:Ubr3
|
UTSW |
2 |
69,768,731 (GRCm39) |
nonsense |
probably null |
|
R4544:Ubr3
|
UTSW |
2 |
69,786,437 (GRCm39) |
missense |
probably benign |
0.18 |
R4678:Ubr3
|
UTSW |
2 |
69,766,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Ubr3
|
UTSW |
2 |
69,768,714 (GRCm39) |
intron |
probably benign |
|
R4785:Ubr3
|
UTSW |
2 |
69,789,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4872:Ubr3
|
UTSW |
2 |
69,800,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Ubr3
|
UTSW |
2 |
69,843,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R4920:Ubr3
|
UTSW |
2 |
69,783,212 (GRCm39) |
missense |
probably benign |
0.32 |
R4989:Ubr3
|
UTSW |
2 |
69,850,790 (GRCm39) |
splice site |
probably benign |
|
R5104:Ubr3
|
UTSW |
2 |
69,768,600 (GRCm39) |
missense |
probably damaging |
0.98 |
R5134:Ubr3
|
UTSW |
2 |
69,850,790 (GRCm39) |
splice site |
probably benign |
|
R5137:Ubr3
|
UTSW |
2 |
69,803,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Ubr3
|
UTSW |
2 |
69,839,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5195:Ubr3
|
UTSW |
2 |
69,786,378 (GRCm39) |
missense |
probably benign |
0.00 |
R5437:Ubr3
|
UTSW |
2 |
69,774,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5539:Ubr3
|
UTSW |
2 |
69,850,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R5781:Ubr3
|
UTSW |
2 |
69,846,588 (GRCm39) |
splice site |
probably null |
|
R5809:Ubr3
|
UTSW |
2 |
69,795,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5913:Ubr3
|
UTSW |
2 |
69,851,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R5969:Ubr3
|
UTSW |
2 |
69,809,730 (GRCm39) |
nonsense |
probably null |
|
R6136:Ubr3
|
UTSW |
2 |
69,824,107 (GRCm39) |
missense |
probably benign |
0.26 |
R6140:Ubr3
|
UTSW |
2 |
69,803,673 (GRCm39) |
missense |
probably benign |
0.09 |
R6185:Ubr3
|
UTSW |
2 |
69,768,621 (GRCm39) |
missense |
probably damaging |
0.98 |
R6220:Ubr3
|
UTSW |
2 |
69,850,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Ubr3
|
UTSW |
2 |
69,813,208 (GRCm39) |
splice site |
probably null |
|
R6319:Ubr3
|
UTSW |
2 |
69,803,758 (GRCm39) |
missense |
probably benign |
0.00 |
R6322:Ubr3
|
UTSW |
2 |
69,786,429 (GRCm39) |
nonsense |
probably null |
|
R6470:Ubr3
|
UTSW |
2 |
69,795,804 (GRCm39) |
missense |
probably benign |
0.02 |
R6477:Ubr3
|
UTSW |
2 |
69,809,773 (GRCm39) |
nonsense |
probably null |
|
R6702:Ubr3
|
UTSW |
2 |
69,786,393 (GRCm39) |
missense |
probably benign |
0.23 |
R6709:Ubr3
|
UTSW |
2 |
69,843,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R6803:Ubr3
|
UTSW |
2 |
69,766,368 (GRCm39) |
critical splice donor site |
probably null |
|
R6806:Ubr3
|
UTSW |
2 |
69,786,308 (GRCm39) |
splice site |
probably benign |
|
R6834:Ubr3
|
UTSW |
2 |
69,830,825 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6841:Ubr3
|
UTSW |
2 |
69,850,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R6847:Ubr3
|
UTSW |
2 |
69,813,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Ubr3
|
UTSW |
2 |
69,774,644 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7065:Ubr3
|
UTSW |
2 |
69,784,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Ubr3
|
UTSW |
2 |
69,728,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R7156:Ubr3
|
UTSW |
2 |
69,851,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R7209:Ubr3
|
UTSW |
2 |
69,846,478 (GRCm39) |
missense |
probably benign |
0.01 |
R7273:Ubr3
|
UTSW |
2 |
69,809,677 (GRCm39) |
missense |
probably damaging |
0.97 |
R7314:Ubr3
|
UTSW |
2 |
69,821,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Ubr3
|
UTSW |
2 |
69,783,886 (GRCm39) |
critical splice donor site |
probably null |
|
R7584:Ubr3
|
UTSW |
2 |
69,821,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7588:Ubr3
|
UTSW |
2 |
69,801,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Ubr3
|
UTSW |
2 |
69,803,812 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7697:Ubr3
|
UTSW |
2 |
69,728,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R7737:Ubr3
|
UTSW |
2 |
69,821,910 (GRCm39) |
missense |
probably benign |
0.07 |
R7743:Ubr3
|
UTSW |
2 |
69,774,793 (GRCm39) |
missense |
probably benign |
0.28 |
R7946:Ubr3
|
UTSW |
2 |
69,781,739 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7991:Ubr3
|
UTSW |
2 |
69,783,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Ubr3
|
UTSW |
2 |
69,819,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R8136:Ubr3
|
UTSW |
2 |
69,851,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Ubr3
|
UTSW |
2 |
69,784,706 (GRCm39) |
missense |
probably null |
1.00 |
R8313:Ubr3
|
UTSW |
2 |
69,775,478 (GRCm39) |
missense |
probably damaging |
0.99 |
R8675:Ubr3
|
UTSW |
2 |
69,850,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R8834:Ubr3
|
UTSW |
2 |
69,833,785 (GRCm39) |
missense |
probably benign |
|
R8975:Ubr3
|
UTSW |
2 |
69,752,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R9060:Ubr3
|
UTSW |
2 |
69,839,489 (GRCm39) |
nonsense |
probably null |
|
R9153:Ubr3
|
UTSW |
2 |
69,795,822 (GRCm39) |
missense |
|
|
R9234:Ubr3
|
UTSW |
2 |
69,727,990 (GRCm39) |
missense |
probably benign |
|
R9293:Ubr3
|
UTSW |
2 |
69,727,769 (GRCm39) |
missense |
probably benign |
0.02 |
R9312:Ubr3
|
UTSW |
2 |
69,784,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Ubr3
|
UTSW |
2 |
69,727,957 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9762:Ubr3
|
UTSW |
2 |
69,839,497 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Ubr3
|
UTSW |
2 |
69,752,711 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Ubr3
|
UTSW |
2 |
69,803,550 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ubr3
|
UTSW |
2 |
69,728,010 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ubr3
|
UTSW |
2 |
69,727,805 (GRCm39) |
missense |
probably benign |
0.17 |
|