Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Antxrl |
T |
C |
14: 33,791,207 (GRCm39) |
F367L |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Dnah17 |
G |
A |
11: 117,933,001 (GRCm39) |
R3586W |
probably damaging |
Het |
Dpysl2 |
A |
G |
14: 67,061,850 (GRCm39) |
V252A |
probably benign |
Het |
Dus2 |
T |
C |
8: 106,771,497 (GRCm39) |
S208P |
possibly damaging |
Het |
Elk3 |
T |
C |
10: 93,101,058 (GRCm39) |
N231S |
probably benign |
Het |
Ephx1 |
A |
T |
1: 180,821,494 (GRCm39) |
M280K |
probably benign |
Het |
Fstl4 |
T |
C |
11: 52,959,373 (GRCm39) |
M138T |
probably benign |
Het |
Iqsec1 |
A |
T |
6: 90,666,659 (GRCm39) |
Y593N |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lep |
G |
T |
6: 29,071,173 (GRCm39) |
E166* |
probably null |
Het |
Limch1 |
A |
G |
5: 67,126,540 (GRCm39) |
D56G |
probably damaging |
Het |
Or4d10c |
G |
T |
19: 12,066,051 (GRCm39) |
T35K |
possibly damaging |
Het |
Pkn2 |
A |
T |
3: 142,517,286 (GRCm39) |
|
probably null |
Het |
Plxna4 |
A |
G |
6: 32,228,071 (GRCm39) |
Y512H |
probably damaging |
Het |
Tekt1 |
A |
T |
11: 72,246,039 (GRCm39) |
I161N |
probably damaging |
Het |
Trpc3 |
T |
C |
3: 36,725,497 (GRCm39) |
N160D |
probably benign |
Het |
Zfp369 |
T |
C |
13: 65,440,107 (GRCm39) |
S264P |
probably damaging |
Het |
Zfp747 |
G |
A |
7: 126,973,726 (GRCm39) |
A148V |
probably damaging |
Het |
|
Other mutations in Tex14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Tex14
|
APN |
11 |
87,426,469 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00494:Tex14
|
APN |
11 |
87,446,310 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01604:Tex14
|
APN |
11 |
87,400,524 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02690:Tex14
|
APN |
11 |
87,377,100 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02888:Tex14
|
APN |
11 |
87,418,738 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03073:Tex14
|
APN |
11 |
87,426,435 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03109:Tex14
|
APN |
11 |
87,434,191 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03047:Tex14
|
UTSW |
11 |
87,427,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R0141:Tex14
|
UTSW |
11 |
87,383,857 (GRCm39) |
splice site |
probably null |
|
R0455:Tex14
|
UTSW |
11 |
87,405,131 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0624:Tex14
|
UTSW |
11 |
87,411,525 (GRCm39) |
missense |
probably benign |
0.19 |
R0718:Tex14
|
UTSW |
11 |
87,390,439 (GRCm39) |
missense |
probably benign |
0.20 |
R1077:Tex14
|
UTSW |
11 |
87,410,571 (GRCm39) |
splice site |
probably benign |
|
R1118:Tex14
|
UTSW |
11 |
87,413,343 (GRCm39) |
missense |
probably benign |
0.07 |
R1120:Tex14
|
UTSW |
11 |
87,429,502 (GRCm39) |
splice site |
probably benign |
|
R1168:Tex14
|
UTSW |
11 |
87,427,568 (GRCm39) |
missense |
probably benign |
0.11 |
R1470:Tex14
|
UTSW |
11 |
87,440,355 (GRCm39) |
splice site |
probably benign |
|
R1563:Tex14
|
UTSW |
11 |
87,427,634 (GRCm39) |
missense |
probably damaging |
0.99 |
R1607:Tex14
|
UTSW |
11 |
87,445,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1696:Tex14
|
UTSW |
11 |
87,402,371 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1873:Tex14
|
UTSW |
11 |
87,390,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R1894:Tex14
|
UTSW |
11 |
87,365,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Tex14
|
UTSW |
11 |
87,385,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Tex14
|
UTSW |
11 |
87,400,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Tex14
|
UTSW |
11 |
87,402,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R1990:Tex14
|
UTSW |
11 |
87,440,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Tex14
|
UTSW |
11 |
87,440,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Tex14
|
UTSW |
11 |
87,427,581 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2106:Tex14
|
UTSW |
11 |
87,377,076 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2118:Tex14
|
UTSW |
11 |
87,410,569 (GRCm39) |
splice site |
probably benign |
|
R2860:Tex14
|
UTSW |
11 |
87,365,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:Tex14
|
UTSW |
11 |
87,365,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R4016:Tex14
|
UTSW |
11 |
87,429,449 (GRCm39) |
splice site |
probably null |
|
R4089:Tex14
|
UTSW |
11 |
87,403,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R4158:Tex14
|
UTSW |
11 |
87,407,595 (GRCm39) |
missense |
probably benign |
0.06 |
R4533:Tex14
|
UTSW |
11 |
87,427,655 (GRCm39) |
nonsense |
probably null |
|
R4713:Tex14
|
UTSW |
11 |
87,427,691 (GRCm39) |
missense |
probably damaging |
0.99 |
R4758:Tex14
|
UTSW |
11 |
87,405,311 (GRCm39) |
missense |
probably benign |
0.00 |
R4880:Tex14
|
UTSW |
11 |
87,377,121 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4953:Tex14
|
UTSW |
11 |
87,427,727 (GRCm39) |
critical splice donor site |
probably null |
|
R5092:Tex14
|
UTSW |
11 |
87,405,668 (GRCm39) |
missense |
probably benign |
0.03 |
R5119:Tex14
|
UTSW |
11 |
87,324,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5322:Tex14
|
UTSW |
11 |
87,402,298 (GRCm39) |
missense |
probably benign |
0.04 |
R5470:Tex14
|
UTSW |
11 |
87,442,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R5607:Tex14
|
UTSW |
11 |
87,413,404 (GRCm39) |
missense |
probably benign |
0.00 |
R5642:Tex14
|
UTSW |
11 |
87,405,046 (GRCm39) |
missense |
probably benign |
|
R5643:Tex14
|
UTSW |
11 |
87,426,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:Tex14
|
UTSW |
11 |
87,405,121 (GRCm39) |
missense |
probably damaging |
0.97 |
R6478:Tex14
|
UTSW |
11 |
87,405,199 (GRCm39) |
missense |
probably benign |
|
R6560:Tex14
|
UTSW |
11 |
87,388,688 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6661:Tex14
|
UTSW |
11 |
87,385,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:Tex14
|
UTSW |
11 |
87,388,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R7156:Tex14
|
UTSW |
11 |
87,375,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R7465:Tex14
|
UTSW |
11 |
87,405,256 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7675:Tex14
|
UTSW |
11 |
87,400,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Tex14
|
UTSW |
11 |
87,385,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Tex14
|
UTSW |
11 |
87,424,428 (GRCm39) |
critical splice donor site |
probably null |
|
R8015:Tex14
|
UTSW |
11 |
87,400,426 (GRCm39) |
missense |
probably benign |
0.13 |
R8226:Tex14
|
UTSW |
11 |
87,375,585 (GRCm39) |
missense |
probably damaging |
0.96 |
R8283:Tex14
|
UTSW |
11 |
87,365,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8292:Tex14
|
UTSW |
11 |
87,388,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Tex14
|
UTSW |
11 |
87,383,878 (GRCm39) |
missense |
probably benign |
0.22 |
R8932:Tex14
|
UTSW |
11 |
87,324,675 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9023:Tex14
|
UTSW |
11 |
87,365,239 (GRCm39) |
missense |
|
|
R9144:Tex14
|
UTSW |
11 |
87,413,423 (GRCm39) |
critical splice donor site |
probably null |
|
R9610:Tex14
|
UTSW |
11 |
87,377,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Tex14
|
UTSW |
11 |
87,377,084 (GRCm39) |
missense |
probably damaging |
1.00 |
RF018:Tex14
|
UTSW |
11 |
87,405,572 (GRCm39) |
missense |
probably benign |
0.01 |
X0017:Tex14
|
UTSW |
11 |
87,426,375 (GRCm39) |
nonsense |
probably null |
|
Z1176:Tex14
|
UTSW |
11 |
87,390,419 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Tex14
|
UTSW |
11 |
87,375,633 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Tex14
|
UTSW |
11 |
87,404,981 (GRCm39) |
missense |
probably damaging |
0.96 |
|