Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530064D06Rik |
A |
G |
17: 48,470,456 (GRCm39) |
V175A |
probably benign |
Het |
Adam19 |
G |
A |
11: 46,027,176 (GRCm39) |
R603Q |
probably benign |
Het |
Adam25 |
T |
C |
8: 41,206,760 (GRCm39) |
S9P |
probably benign |
Het |
Akr1e1 |
T |
A |
13: 4,647,477 (GRCm39) |
|
probably benign |
Het |
Ano8 |
C |
T |
8: 71,935,761 (GRCm39) |
V286I |
possibly damaging |
Het |
Baz1a |
C |
T |
12: 54,947,232 (GRCm39) |
R1139H |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,452,953 (GRCm39) |
L29H |
probably damaging |
Het |
Btaf1 |
T |
C |
19: 36,958,535 (GRCm39) |
|
probably benign |
Het |
C8b |
T |
A |
4: 104,658,525 (GRCm39) |
|
probably benign |
Het |
Cep295 |
A |
T |
9: 15,244,608 (GRCm39) |
S1283T |
probably damaging |
Het |
Cyp1a2 |
T |
C |
9: 57,584,511 (GRCm39) |
*514W |
probably null |
Het |
D2hgdh |
G |
T |
1: 93,757,558 (GRCm39) |
D158Y |
probably damaging |
Het |
Dennd1b |
G |
A |
1: 139,008,980 (GRCm39) |
V228M |
probably damaging |
Het |
Fgd6 |
T |
A |
10: 93,881,342 (GRCm39) |
L732* |
probably null |
Het |
Gm21969 |
G |
A |
4: 139,335,009 (GRCm39) |
G348S |
probably benign |
Het |
Gprc6a |
C |
T |
10: 51,502,895 (GRCm39) |
V323M |
probably damaging |
Het |
Gzme |
T |
A |
14: 56,356,166 (GRCm39) |
M111L |
probably damaging |
Het |
Iars2 |
G |
T |
1: 185,035,498 (GRCm39) |
Q581K |
probably benign |
Het |
Klra17 |
A |
T |
6: 129,845,647 (GRCm39) |
|
probably null |
Het |
Klra5 |
A |
T |
6: 129,883,577 (GRCm39) |
D93E |
possibly damaging |
Het |
Lats2 |
T |
C |
14: 57,937,805 (GRCm39) |
Y228C |
probably damaging |
Het |
Lrrn3 |
T |
C |
12: 41,502,216 (GRCm39) |
I700M |
probably damaging |
Het |
Ltb |
A |
T |
17: 35,414,348 (GRCm39) |
|
probably benign |
Het |
Myo18b |
T |
C |
5: 112,923,279 (GRCm39) |
|
probably benign |
Het |
Or10a3 |
T |
A |
7: 108,480,198 (GRCm39) |
E205V |
probably damaging |
Het |
Or11l3 |
A |
G |
11: 58,516,107 (GRCm39) |
M255T |
possibly damaging |
Het |
Or12d13 |
A |
T |
17: 37,647,600 (GRCm39) |
H174Q |
probably damaging |
Het |
Or1e35 |
G |
A |
11: 73,798,045 (GRCm39) |
T91M |
possibly damaging |
Het |
Or1j17 |
C |
T |
2: 36,578,644 (GRCm39) |
P210L |
possibly damaging |
Het |
Pgap1 |
A |
C |
1: 54,532,509 (GRCm39) |
I670S |
probably benign |
Het |
Plxna4 |
A |
T |
6: 32,493,530 (GRCm39) |
I362N |
probably damaging |
Het |
Ppef2 |
C |
T |
5: 92,383,759 (GRCm39) |
W450* |
probably null |
Het |
Prr27 |
T |
C |
5: 87,990,675 (GRCm39) |
S96P |
probably benign |
Het |
Psip1 |
T |
A |
4: 83,381,954 (GRCm39) |
|
probably benign |
Het |
Rgs3 |
T |
A |
4: 62,544,084 (GRCm39) |
H285Q |
possibly damaging |
Het |
Ror1 |
T |
C |
4: 100,191,722 (GRCm39) |
|
probably benign |
Het |
Rps6ka5 |
C |
A |
12: 100,540,258 (GRCm39) |
|
probably benign |
Het |
Sipa1l1 |
T |
A |
12: 82,404,105 (GRCm39) |
Y533N |
probably benign |
Het |
Snx6 |
T |
C |
12: 54,842,295 (GRCm39) |
|
probably benign |
Het |
Tbc1d9 |
T |
A |
8: 83,995,688 (GRCm39) |
|
probably null |
Het |
Tor2a |
T |
A |
2: 32,651,509 (GRCm39) |
H241Q |
possibly damaging |
Het |
Wnt5a |
A |
T |
14: 28,244,871 (GRCm39) |
I353F |
probably benign |
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 |
IGL00870:Tek
|
APN |
4 |
94,761,318 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|