Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
T |
A |
19: 8,991,062 (GRCm39) |
D4115E |
probably damaging |
Het |
Asb5 |
T |
C |
8: 55,036,695 (GRCm39) |
|
probably null |
Het |
Cpeb3 |
A |
T |
19: 37,031,695 (GRCm39) |
I569N |
probably damaging |
Het |
Cpsf7 |
T |
C |
19: 10,517,014 (GRCm39) |
|
probably null |
Het |
Dlat |
A |
G |
9: 50,562,169 (GRCm39) |
L285P |
probably damaging |
Het |
Dytn |
T |
C |
1: 63,716,272 (GRCm39) |
|
probably benign |
Het |
Ears2 |
A |
T |
7: 121,654,899 (GRCm39) |
L123Q |
probably damaging |
Het |
Gad2 |
T |
C |
2: 22,519,983 (GRCm39) |
V212A |
probably benign |
Het |
Gon4l |
T |
C |
3: 88,764,492 (GRCm39) |
Y358H |
probably damaging |
Het |
Gys1 |
T |
C |
7: 45,097,437 (GRCm39) |
|
probably null |
Het |
Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
Krtap20-2 |
G |
A |
16: 89,002,875 (GRCm39) |
G25D |
unknown |
Het |
Lrif1 |
T |
C |
3: 106,641,957 (GRCm39) |
|
probably null |
Het |
Naip2 |
A |
G |
13: 100,288,568 (GRCm39) |
|
probably benign |
Het |
Or8b37 |
A |
T |
9: 37,959,036 (GRCm39) |
I173F |
probably damaging |
Het |
Oxct1 |
T |
A |
15: 4,131,300 (GRCm39) |
L396Q |
probably damaging |
Het |
Pclo |
A |
T |
5: 14,589,997 (GRCm39) |
R766W |
unknown |
Het |
Pkhd1 |
T |
A |
1: 20,641,614 (GRCm39) |
I275F |
probably damaging |
Het |
Rxfp3 |
A |
G |
15: 11,036,301 (GRCm39) |
F357S |
probably damaging |
Het |
Rxfp3 |
A |
G |
15: 11,036,391 (GRCm39) |
V327A |
probably damaging |
Het |
Serpinb2 |
A |
G |
1: 107,450,800 (GRCm39) |
I181V |
probably damaging |
Het |
Smad5 |
A |
G |
13: 56,871,480 (GRCm39) |
D25G |
probably benign |
Het |
Strada |
A |
G |
11: 106,062,083 (GRCm39) |
L82P |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,870,167 (GRCm39) |
T209A |
probably benign |
Het |
Tnks1bp1 |
C |
T |
2: 84,892,580 (GRCm39) |
Q836* |
probably null |
Het |
Toporsl |
T |
C |
4: 52,610,172 (GRCm39) |
S22P |
probably benign |
Het |
Ttc17 |
T |
C |
2: 94,202,078 (GRCm39) |
|
probably null |
Het |
Ttc39a |
A |
G |
4: 109,299,542 (GRCm39) |
|
probably benign |
Het |
Vangl1 |
T |
C |
3: 102,096,756 (GRCm39) |
D60G |
probably damaging |
Het |
Vmn1r13 |
A |
T |
6: 57,187,098 (GRCm39) |
M86L |
probably benign |
Het |
Vmn1r220 |
C |
T |
13: 23,368,647 (GRCm39) |
M16I |
probably null |
Het |
|
Other mutations in Tek |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00654:Tek
|
APN |
4 |
94,715,538 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00805:Tek
|
APN |
4 |
94,686,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00806:Tek
|
APN |
4 |
94,686,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00807:Tek
|
APN |
4 |
94,686,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01348:Tek
|
APN |
4 |
94,747,895 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01398:Tek
|
APN |
4 |
94,738,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01683:Tek
|
APN |
4 |
94,747,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01827:Tek
|
APN |
4 |
94,627,882 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02063:Tek
|
APN |
4 |
94,627,882 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02218:Tek
|
APN |
4 |
94,743,574 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02502:Tek
|
APN |
4 |
94,741,818 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02852:Tek
|
APN |
4 |
94,743,561 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02995:Tek
|
APN |
4 |
94,627,877 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03182:Tek
|
APN |
4 |
94,740,002 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03247:Tek
|
APN |
4 |
94,753,680 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03014:Tek
|
UTSW |
4 |
94,715,500 (GRCm39) |
missense |
probably benign |
0.05 |
R0022:Tek
|
UTSW |
4 |
94,725,509 (GRCm39) |
missense |
probably damaging |
0.98 |
R0373:Tek
|
UTSW |
4 |
94,692,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0479:Tek
|
UTSW |
4 |
94,692,549 (GRCm39) |
missense |
probably benign |
0.01 |
R1178:Tek
|
UTSW |
4 |
94,692,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1289:Tek
|
UTSW |
4 |
94,693,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1331:Tek
|
UTSW |
4 |
94,627,943 (GRCm39) |
splice site |
probably benign |
|
R1502:Tek
|
UTSW |
4 |
94,669,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1606:Tek
|
UTSW |
4 |
94,738,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R2073:Tek
|
UTSW |
4 |
94,715,966 (GRCm39) |
missense |
probably benign |
0.01 |
R2075:Tek
|
UTSW |
4 |
94,715,966 (GRCm39) |
missense |
probably benign |
0.01 |
R2230:Tek
|
UTSW |
4 |
94,699,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2851:Tek
|
UTSW |
4 |
94,708,461 (GRCm39) |
missense |
probably benign |
0.30 |
R2852:Tek
|
UTSW |
4 |
94,708,461 (GRCm39) |
missense |
probably benign |
0.30 |
R3775:Tek
|
UTSW |
4 |
94,692,549 (GRCm39) |
missense |
probably benign |
0.01 |
R3845:Tek
|
UTSW |
4 |
94,693,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4114:Tek
|
UTSW |
4 |
94,737,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R4115:Tek
|
UTSW |
4 |
94,737,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R4273:Tek
|
UTSW |
4 |
94,718,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4425:Tek
|
UTSW |
4 |
94,751,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R4488:Tek
|
UTSW |
4 |
94,737,993 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4579:Tek
|
UTSW |
4 |
94,751,903 (GRCm39) |
nonsense |
probably null |
|
R4623:Tek
|
UTSW |
4 |
94,751,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Tek
|
UTSW |
4 |
94,669,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Tek
|
UTSW |
4 |
94,669,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4723:Tek
|
UTSW |
4 |
94,687,397 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5059:Tek
|
UTSW |
4 |
94,692,551 (GRCm39) |
missense |
probably benign |
0.10 |
R5652:Tek
|
UTSW |
4 |
94,743,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R5793:Tek
|
UTSW |
4 |
94,708,333 (GRCm39) |
missense |
probably benign |
0.01 |
R5855:Tek
|
UTSW |
4 |
94,741,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Tek
|
UTSW |
4 |
94,686,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R6537:Tek
|
UTSW |
4 |
94,725,561 (GRCm39) |
missense |
probably benign |
0.19 |
R6727:Tek
|
UTSW |
4 |
94,741,732 (GRCm39) |
nonsense |
probably null |
|
R6835:Tek
|
UTSW |
4 |
94,741,671 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6883:Tek
|
UTSW |
4 |
94,725,426 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6887:Tek
|
UTSW |
4 |
94,693,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R7027:Tek
|
UTSW |
4 |
94,753,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7108:Tek
|
UTSW |
4 |
94,741,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Tek
|
UTSW |
4 |
94,699,647 (GRCm39) |
missense |
probably benign |
0.19 |
R7220:Tek
|
UTSW |
4 |
94,692,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Tek
|
UTSW |
4 |
94,715,533 (GRCm39) |
missense |
probably benign |
|
R7417:Tek
|
UTSW |
4 |
94,699,582 (GRCm39) |
missense |
probably benign |
|
R7465:Tek
|
UTSW |
4 |
94,716,063 (GRCm39) |
critical splice donor site |
probably null |
|
R7818:Tek
|
UTSW |
4 |
94,715,953 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7917:Tek
|
UTSW |
4 |
94,708,372 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7942:Tek
|
UTSW |
4 |
94,740,111 (GRCm39) |
splice site |
probably null |
|
R7956:Tek
|
UTSW |
4 |
94,687,580 (GRCm39) |
splice site |
probably null |
|
R8098:Tek
|
UTSW |
4 |
94,715,907 (GRCm39) |
missense |
probably benign |
0.19 |
R8442:Tek
|
UTSW |
4 |
94,715,922 (GRCm39) |
missense |
probably benign |
0.04 |
R8523:Tek
|
UTSW |
4 |
94,687,403 (GRCm39) |
missense |
probably benign |
0.12 |
R8676:Tek
|
UTSW |
4 |
94,738,074 (GRCm39) |
missense |
probably benign |
|
R8787:Tek
|
UTSW |
4 |
94,738,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Tek
|
UTSW |
4 |
94,708,339 (GRCm39) |
missense |
probably benign |
0.40 |
R9172:Tek
|
UTSW |
4 |
94,692,583 (GRCm39) |
missense |
probably benign |
0.02 |
R9429:Tek
|
UTSW |
4 |
94,715,515 (GRCm39) |
missense |
probably benign |
|
R9564:Tek
|
UTSW |
4 |
94,762,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R9602:Tek
|
UTSW |
4 |
94,715,968 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9643:Tek
|
UTSW |
4 |
94,692,523 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9721:Tek
|
UTSW |
4 |
94,692,539 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9722:Tek
|
UTSW |
4 |
94,692,539 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9723:Tek
|
UTSW |
4 |
94,692,539 (GRCm39) |
missense |
possibly damaging |
0.94 |
|