Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh8a1 |
G |
A |
10: 21,271,470 (GRCm39) |
V399I |
probably benign |
Het |
Apold1 |
A |
G |
6: 134,960,869 (GRCm39) |
I108V |
probably benign |
Het |
Arpc5 |
G |
A |
1: 152,644,607 (GRCm39) |
|
probably benign |
Het |
Capn11 |
T |
A |
17: 45,964,682 (GRCm39) |
D45V |
probably damaging |
Het |
Dctpp1 |
G |
A |
7: 126,856,285 (GRCm39) |
R146C |
probably damaging |
Het |
Dlat |
C |
T |
9: 50,560,931 (GRCm39) |
|
probably null |
Het |
Dock10 |
T |
A |
1: 80,584,286 (GRCm39) |
D140V |
probably damaging |
Het |
Dtx3 |
A |
G |
10: 127,027,040 (GRCm39) |
V378A |
probably benign |
Het |
Ezh2 |
A |
G |
6: 47,521,516 (GRCm39) |
I414T |
probably benign |
Het |
Gm1979 |
C |
T |
5: 26,209,604 (GRCm39) |
W41* |
probably null |
Het |
Igf2bp2 |
T |
C |
16: 21,882,426 (GRCm39) |
N425S |
probably damaging |
Het |
Kdm5a |
T |
A |
6: 120,371,067 (GRCm39) |
Y504N |
probably damaging |
Het |
Map3k21 |
T |
A |
8: 126,637,924 (GRCm39) |
I170N |
probably damaging |
Het |
Mrgpra6 |
C |
A |
7: 46,838,463 (GRCm39) |
C245F |
possibly damaging |
Het |
Nipal2 |
T |
G |
15: 34,600,207 (GRCm39) |
K203N |
possibly damaging |
Het |
Nlrp1b |
A |
G |
11: 71,063,911 (GRCm39) |
F621S |
probably damaging |
Het |
Nos3 |
G |
A |
5: 24,576,714 (GRCm39) |
V448M |
probably damaging |
Het |
Ntrk3 |
G |
T |
7: 78,112,695 (GRCm39) |
|
probably benign |
Het |
Or5b118 |
A |
T |
19: 13,448,561 (GRCm39) |
T76S |
possibly damaging |
Het |
P2rx1 |
T |
C |
11: 72,900,799 (GRCm39) |
C190R |
probably damaging |
Het |
Pdzrn4 |
T |
A |
15: 92,297,630 (GRCm39) |
D198E |
probably benign |
Het |
Ptar1 |
A |
G |
19: 23,664,824 (GRCm39) |
M1V |
probably null |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Purg |
T |
A |
8: 33,877,019 (GRCm39) |
L219* |
probably null |
Het |
Rbp3 |
G |
T |
14: 33,677,347 (GRCm39) |
V432L |
possibly damaging |
Het |
Scnn1b |
G |
T |
7: 121,513,555 (GRCm39) |
|
probably null |
Het |
Sgms1 |
A |
G |
19: 32,120,192 (GRCm39) |
V238A |
possibly damaging |
Het |
Slc16a14 |
G |
T |
1: 84,890,228 (GRCm39) |
S359* |
probably null |
Het |
Smarca2 |
G |
A |
19: 26,661,327 (GRCm39) |
|
probably null |
Het |
Spatc1l |
A |
G |
10: 76,398,323 (GRCm39) |
S42G |
probably benign |
Het |
Stra6 |
T |
A |
9: 58,042,473 (GRCm39) |
V34E |
probably damaging |
Het |
Tox4 |
T |
C |
14: 52,523,361 (GRCm39) |
|
probably null |
Het |
Tyr |
A |
G |
7: 87,087,148 (GRCm39) |
S455P |
probably benign |
Het |
Uggt2 |
T |
C |
14: 119,263,845 (GRCm39) |
N1062D |
possibly damaging |
Het |
Umod |
A |
C |
7: 119,075,913 (GRCm39) |
N284K |
possibly damaging |
Het |
Unc93b1 |
T |
C |
19: 3,993,572 (GRCm39) |
I338T |
probably damaging |
Het |
Vmn2r99 |
C |
T |
17: 19,598,832 (GRCm39) |
T172I |
possibly damaging |
Het |
Whrn |
G |
A |
4: 63,333,876 (GRCm39) |
Q415* |
probably null |
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 |
R1190:Tex14
|
UTSW |
11 |
87,385,934 (GRCm39) |
splice site |
probably null |
|
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 |
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 |
|