Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
T |
C |
16: 56,488,639 (GRCm39) |
S1257P |
possibly damaging |
Het |
AC159637.1 |
C |
T |
12: 93,895,054 (GRCm39) |
|
noncoding transcript |
Het |
Agk |
T |
C |
6: 40,329,372 (GRCm39) |
|
probably benign |
Het |
Arhgef5 |
C |
A |
6: 43,250,022 (GRCm39) |
Q258K |
possibly damaging |
Het |
C1s1 |
C |
A |
6: 124,517,759 (GRCm39) |
D74Y |
probably damaging |
Het |
Cpxm2 |
A |
G |
7: 131,659,377 (GRCm39) |
S497P |
probably damaging |
Het |
Ctsj |
C |
T |
13: 61,150,357 (GRCm39) |
S214N |
probably damaging |
Het |
Dnali1 |
T |
C |
4: 124,959,340 (GRCm39) |
S18G |
possibly damaging |
Het |
Eif4g3 |
C |
T |
4: 137,893,129 (GRCm39) |
T959M |
probably damaging |
Het |
Eml6 |
A |
G |
11: 29,727,430 (GRCm39) |
F1231L |
probably benign |
Het |
Glp1r |
T |
C |
17: 31,138,406 (GRCm39) |
V160A |
probably benign |
Het |
Gm11143 |
T |
G |
6: 69,594,392 (GRCm39) |
V60G |
unknown |
Het |
Hmcn1 |
A |
T |
1: 150,555,358 (GRCm39) |
|
probably null |
Het |
Inpp5k |
T |
C |
11: 75,524,285 (GRCm39) |
|
probably benign |
Het |
Krtdap |
A |
T |
7: 30,488,975 (GRCm39) |
|
probably benign |
Het |
Ldb2 |
A |
G |
5: 44,690,016 (GRCm39) |
L201P |
probably damaging |
Het |
Loxl4 |
A |
T |
19: 42,596,994 (GRCm39) |
|
probably benign |
Het |
Odad2 |
G |
T |
18: 7,268,436 (GRCm39) |
P361Q |
probably damaging |
Het |
Otud6b |
T |
A |
4: 14,812,532 (GRCm39) |
T272S |
probably benign |
Het |
Pnpla2 |
T |
C |
7: 141,035,329 (GRCm39) |
Y44H |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Sel1l3 |
C |
T |
5: 53,289,169 (GRCm39) |
R884H |
probably damaging |
Het |
Slc43a2 |
T |
A |
11: 75,457,815 (GRCm39) |
Y363* |
probably null |
Het |
Tap2 |
C |
A |
17: 34,434,914 (GRCm39) |
D652E |
possibly damaging |
Het |
Unc80 |
T |
C |
1: 66,511,247 (GRCm39) |
V85A |
probably damaging |
Het |
Vwa3a |
T |
C |
7: 120,392,566 (GRCm39) |
Y802H |
probably damaging |
Het |
Zc3h4 |
G |
A |
7: 16,150,838 (GRCm39) |
R60Q |
possibly damaging |
Het |
Zfp385a |
A |
T |
15: 103,226,370 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Taf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00331:Taf2
|
APN |
15 |
54,934,845 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00475:Taf2
|
APN |
15 |
54,919,246 (GRCm39) |
nonsense |
probably null |
|
IGL00549:Taf2
|
APN |
15 |
54,894,511 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00839:Taf2
|
APN |
15 |
54,909,174 (GRCm39) |
nonsense |
probably null |
|
IGL01089:Taf2
|
APN |
15 |
54,879,977 (GRCm39) |
missense |
probably benign |
|
IGL01305:Taf2
|
APN |
15 |
54,911,670 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01532:Taf2
|
APN |
15 |
54,912,882 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01903:Taf2
|
APN |
15 |
54,923,412 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02324:Taf2
|
APN |
15 |
54,891,772 (GRCm39) |
missense |
probably benign |
|
IGL02328:Taf2
|
APN |
15 |
54,891,772 (GRCm39) |
missense |
probably benign |
|
IGL02405:Taf2
|
APN |
15 |
54,897,551 (GRCm39) |
splice site |
probably benign |
|
IGL02671:Taf2
|
APN |
15 |
54,897,572 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02832:Taf2
|
APN |
15 |
54,879,959 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03105:Taf2
|
APN |
15 |
54,909,195 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03118:Taf2
|
APN |
15 |
54,915,559 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU22:Taf2
|
UTSW |
15 |
54,911,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R0104:Taf2
|
UTSW |
15 |
54,901,734 (GRCm39) |
missense |
probably benign |
0.02 |
R0104:Taf2
|
UTSW |
15 |
54,901,734 (GRCm39) |
missense |
probably benign |
0.02 |
R0183:Taf2
|
UTSW |
15 |
54,919,186 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0326:Taf2
|
UTSW |
15 |
54,910,856 (GRCm39) |
missense |
probably damaging |
0.97 |
R0362:Taf2
|
UTSW |
15 |
54,909,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R0423:Taf2
|
UTSW |
15 |
54,928,078 (GRCm39) |
missense |
probably benign |
0.02 |
R0562:Taf2
|
UTSW |
15 |
54,885,584 (GRCm39) |
splice site |
probably benign |
|
R0609:Taf2
|
UTSW |
15 |
54,923,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0655:Taf2
|
UTSW |
15 |
54,901,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Taf2
|
UTSW |
15 |
54,926,461 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0743:Taf2
|
UTSW |
15 |
54,879,857 (GRCm39) |
small deletion |
probably benign |
|
R0898:Taf2
|
UTSW |
15 |
54,923,480 (GRCm39) |
missense |
probably damaging |
0.97 |
R0969:Taf2
|
UTSW |
15 |
54,894,553 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0974:Taf2
|
UTSW |
15 |
54,879,857 (GRCm39) |
small deletion |
probably benign |
|
R1145:Taf2
|
UTSW |
15 |
54,879,857 (GRCm39) |
small deletion |
probably benign |
|
R1160:Taf2
|
UTSW |
15 |
54,934,793 (GRCm39) |
missense |
probably benign |
0.01 |
R1376:Taf2
|
UTSW |
15 |
54,879,857 (GRCm39) |
small deletion |
probably benign |
|
R1388:Taf2
|
UTSW |
15 |
54,900,021 (GRCm39) |
missense |
probably benign |
0.00 |
R1416:Taf2
|
UTSW |
15 |
54,901,806 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1458:Taf2
|
UTSW |
15 |
54,923,311 (GRCm39) |
missense |
probably damaging |
0.99 |
R1477:Taf2
|
UTSW |
15 |
54,925,568 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1755:Taf2
|
UTSW |
15 |
54,879,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R1766:Taf2
|
UTSW |
15 |
54,934,793 (GRCm39) |
missense |
probably benign |
0.01 |
R2090:Taf2
|
UTSW |
15 |
54,879,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R2228:Taf2
|
UTSW |
15 |
54,928,042 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2519:Taf2
|
UTSW |
15 |
54,915,643 (GRCm39) |
missense |
probably benign |
0.03 |
R4073:Taf2
|
UTSW |
15 |
54,915,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Taf2
|
UTSW |
15 |
54,922,276 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4471:Taf2
|
UTSW |
15 |
54,922,276 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4472:Taf2
|
UTSW |
15 |
54,922,276 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4716:Taf2
|
UTSW |
15 |
54,929,364 (GRCm39) |
missense |
probably benign |
0.02 |
R4937:Taf2
|
UTSW |
15 |
54,890,619 (GRCm39) |
nonsense |
probably null |
|
R5082:Taf2
|
UTSW |
15 |
54,923,441 (GRCm39) |
missense |
probably benign |
0.41 |
R5335:Taf2
|
UTSW |
15 |
54,909,136 (GRCm39) |
missense |
probably benign |
0.14 |
R5383:Taf2
|
UTSW |
15 |
54,912,815 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5771:Taf2
|
UTSW |
15 |
54,923,335 (GRCm39) |
missense |
probably benign |
0.01 |
R5862:Taf2
|
UTSW |
15 |
54,911,719 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5873:Taf2
|
UTSW |
15 |
54,901,818 (GRCm39) |
missense |
probably benign |
0.00 |
R5908:Taf2
|
UTSW |
15 |
54,935,402 (GRCm39) |
unclassified |
probably benign |
|
R6033:Taf2
|
UTSW |
15 |
54,922,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Taf2
|
UTSW |
15 |
54,922,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6159:Taf2
|
UTSW |
15 |
54,926,440 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6568:Taf2
|
UTSW |
15 |
54,928,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R7094:Taf2
|
UTSW |
15 |
54,923,482 (GRCm39) |
missense |
probably benign |
0.27 |
R7174:Taf2
|
UTSW |
15 |
54,912,135 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7241:Taf2
|
UTSW |
15 |
54,925,537 (GRCm39) |
missense |
probably benign |
0.01 |
R7561:Taf2
|
UTSW |
15 |
54,919,229 (GRCm39) |
missense |
probably benign |
0.16 |
R7583:Taf2
|
UTSW |
15 |
54,928,072 (GRCm39) |
nonsense |
probably null |
|
R7818:Taf2
|
UTSW |
15 |
54,929,326 (GRCm39) |
missense |
probably benign |
|
R7905:Taf2
|
UTSW |
15 |
54,910,828 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8006:Taf2
|
UTSW |
15 |
54,912,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8017:Taf2
|
UTSW |
15 |
54,928,013 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8019:Taf2
|
UTSW |
15 |
54,928,013 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8119:Taf2
|
UTSW |
15 |
54,894,526 (GRCm39) |
missense |
probably benign |
0.00 |
R8127:Taf2
|
UTSW |
15 |
54,923,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R8128:Taf2
|
UTSW |
15 |
54,923,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Taf2
|
UTSW |
15 |
54,923,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R8278:Taf2
|
UTSW |
15 |
54,929,361 (GRCm39) |
nonsense |
probably null |
|
R8290:Taf2
|
UTSW |
15 |
54,926,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R8762:Taf2
|
UTSW |
15 |
54,910,849 (GRCm39) |
missense |
probably benign |
0.16 |
R8832:Taf2
|
UTSW |
15 |
54,928,001 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8916:Taf2
|
UTSW |
15 |
54,899,931 (GRCm39) |
missense |
probably benign |
0.26 |
R8937:Taf2
|
UTSW |
15 |
54,910,849 (GRCm39) |
missense |
probably benign |
0.16 |
R9006:Taf2
|
UTSW |
15 |
54,909,301 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9138:Taf2
|
UTSW |
15 |
54,879,857 (GRCm39) |
small deletion |
probably benign |
|
R9240:Taf2
|
UTSW |
15 |
54,926,464 (GRCm39) |
missense |
probably null |
1.00 |
R9257:Taf2
|
UTSW |
15 |
54,929,409 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9485:Taf2
|
UTSW |
15 |
54,911,667 (GRCm39) |
missense |
probably benign |
0.05 |
R9762:Taf2
|
UTSW |
15 |
54,894,440 (GRCm39) |
critical splice donor site |
probably null |
|
R9766:Taf2
|
UTSW |
15 |
54,910,881 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9796:Taf2
|
UTSW |
15 |
54,910,832 (GRCm39) |
missense |
probably damaging |
0.98 |
|