Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl4 |
T |
A |
3: 151,203,511 (GRCm39) |
C124S |
probably damaging |
Het |
Aldh1a7 |
T |
C |
19: 20,704,368 (GRCm39) |
N42S |
probably damaging |
Het |
Arhgef1 |
T |
C |
7: 24,623,240 (GRCm39) |
L667P |
probably damaging |
Het |
C1qb |
C |
A |
4: 136,607,811 (GRCm39) |
R184L |
possibly damaging |
Het |
Cacna1s |
A |
G |
1: 136,002,914 (GRCm39) |
|
probably benign |
Het |
Cdk20 |
A |
G |
13: 64,585,734 (GRCm39) |
E244G |
probably benign |
Het |
Copg2 |
C |
A |
6: 30,840,469 (GRCm39) |
|
probably null |
Het |
Cyp2d40 |
A |
T |
15: 82,645,149 (GRCm39) |
|
probably benign |
Het |
Cyp2j6 |
A |
G |
4: 96,414,170 (GRCm39) |
I365T |
probably damaging |
Het |
Dhx29 |
A |
G |
13: 113,064,342 (GRCm39) |
K6E |
probably damaging |
Het |
Dpp10 |
T |
A |
1: 123,295,531 (GRCm39) |
T539S |
probably benign |
Het |
Ehbp1 |
A |
T |
11: 22,046,048 (GRCm39) |
I542K |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,493,593 (GRCm39) |
Y3913C |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,536,822 (GRCm39) |
T1264I |
probably benign |
Het |
Fmnl1 |
A |
G |
11: 103,070,364 (GRCm39) |
D51G |
probably damaging |
Het |
Gm17093 |
A |
G |
14: 44,755,807 (GRCm39) |
T25A |
unknown |
Het |
Gpatch2 |
A |
G |
1: 186,957,936 (GRCm39) |
E97G |
probably damaging |
Het |
Hcn1 |
T |
C |
13: 118,039,422 (GRCm39) |
L446P |
unknown |
Het |
Hpse2 |
A |
T |
19: 42,920,038 (GRCm39) |
L354I |
probably damaging |
Het |
Hspa4 |
A |
G |
11: 53,190,885 (GRCm39) |
|
probably null |
Het |
Krtap16-1 |
C |
T |
11: 99,877,129 (GRCm39) |
V92M |
probably damaging |
Het |
Med23 |
A |
T |
10: 24,773,239 (GRCm39) |
Q281L |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,039,873 (GRCm39) |
S963P |
probably benign |
Het |
Mical1 |
G |
A |
10: 41,362,660 (GRCm39) |
E932K |
possibly damaging |
Het |
Mycbp2 |
A |
G |
14: 103,479,643 (GRCm39) |
S1217P |
probably damaging |
Het |
Myocd |
C |
A |
11: 65,069,484 (GRCm39) |
L785F |
probably benign |
Het |
Nell2 |
T |
C |
15: 95,126,982 (GRCm39) |
T798A |
probably damaging |
Het |
Nfat5 |
T |
C |
8: 108,092,808 (GRCm39) |
|
probably benign |
Het |
Olfm5 |
T |
C |
7: 103,803,302 (GRCm39) |
|
probably null |
Het |
Or1e26 |
A |
G |
11: 73,480,081 (GRCm39) |
V161A |
probably benign |
Het |
P2ry1 |
A |
T |
3: 60,911,199 (GRCm39) |
N113Y |
possibly damaging |
Het |
Pan3 |
A |
G |
5: 147,466,933 (GRCm39) |
|
probably null |
Het |
Pappa |
A |
G |
4: 65,115,045 (GRCm39) |
R714G |
probably damaging |
Het |
Plcd1 |
A |
G |
9: 118,901,710 (GRCm39) |
F579L |
probably damaging |
Het |
Ptprb |
T |
C |
10: 116,155,238 (GRCm39) |
V664A |
probably benign |
Het |
Slc27a5 |
T |
A |
7: 12,731,487 (GRCm39) |
Q168L |
probably benign |
Het |
Spag8 |
T |
C |
4: 43,651,781 (GRCm39) |
E395G |
probably damaging |
Het |
Stfa2l1 |
T |
C |
16: 35,982,138 (GRCm39) |
Y70H |
probably damaging |
Het |
Tnfrsf25 |
C |
A |
4: 152,203,779 (GRCm39) |
Q296K |
probably damaging |
Het |
Trpm3 |
T |
A |
19: 22,676,143 (GRCm39) |
I103N |
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 |
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 |
|
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 |
|