Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
G |
T |
10: 85,224,347 (GRCm39) |
|
probably null |
Het |
Agtpbp1 |
T |
C |
13: 59,622,403 (GRCm39) |
E941G |
possibly damaging |
Het |
Akap11 |
A |
T |
14: 78,747,808 (GRCm39) |
Y1526* |
probably null |
Het |
Brd1 |
T |
C |
15: 88,572,577 (GRCm39) |
I1165V |
probably benign |
Het |
Cdan1 |
T |
C |
2: 120,558,393 (GRCm39) |
D473G |
possibly damaging |
Het |
Clstn3 |
G |
A |
6: 124,436,222 (GRCm39) |
L176F |
probably damaging |
Het |
Ctif |
T |
C |
18: 75,654,689 (GRCm39) |
N279S |
probably benign |
Het |
Dpy19l3 |
A |
G |
7: 35,452,097 (GRCm39) |
S16P |
probably benign |
Het |
Ecpas |
A |
T |
4: 58,800,288 (GRCm39) |
C1806S |
probably benign |
Het |
Fam151b |
T |
C |
13: 92,586,701 (GRCm39) |
Y244C |
probably benign |
Het |
Gbf1 |
T |
C |
19: 46,255,787 (GRCm39) |
M750T |
possibly damaging |
Het |
Gm11564 |
T |
A |
11: 99,705,879 (GRCm39) |
T184S |
unknown |
Het |
Gnptab |
A |
G |
10: 88,272,233 (GRCm39) |
K958E |
possibly damaging |
Het |
Hibch |
T |
C |
1: 52,924,310 (GRCm39) |
S162P |
possibly damaging |
Het |
Itpr1 |
T |
C |
6: 108,500,362 (GRCm39) |
S2651P |
probably benign |
Het |
LTO1 |
A |
G |
7: 144,470,197 (GRCm39) |
E42G |
probably damaging |
Het |
Lyrm1 |
A |
G |
7: 119,513,403 (GRCm39) |
D56G |
probably damaging |
Het |
Manba |
T |
C |
3: 135,256,920 (GRCm39) |
Y528H |
probably damaging |
Het |
Npas2 |
A |
C |
1: 39,352,109 (GRCm39) |
E186D |
probably damaging |
Het |
Or4f61 |
A |
T |
2: 111,922,166 (GRCm39) |
D293E |
probably benign |
Het |
Or7c19 |
A |
T |
8: 85,957,258 (GRCm39) |
I45F |
possibly damaging |
Het |
Or7d11 |
C |
A |
9: 19,966,668 (GRCm39) |
L30F |
probably benign |
Het |
Pcdhb6 |
T |
A |
18: 37,468,640 (GRCm39) |
Y520* |
probably null |
Het |
Plekhm1 |
C |
T |
11: 103,268,207 (GRCm39) |
R588H |
probably benign |
Het |
Psg23 |
A |
T |
7: 18,344,341 (GRCm39) |
H371Q |
probably benign |
Het |
Ptpn12 |
T |
C |
5: 21,207,610 (GRCm39) |
|
probably benign |
Het |
Rela |
T |
C |
19: 5,689,909 (GRCm39) |
C120R |
probably damaging |
Het |
Rps6kc1 |
T |
A |
1: 190,532,008 (GRCm39) |
I665F |
probably damaging |
Het |
Spg21 |
A |
G |
9: 65,380,990 (GRCm39) |
Q99R |
probably benign |
Het |
St14 |
A |
G |
9: 31,008,367 (GRCm39) |
|
probably null |
Het |
Sult1c2 |
A |
T |
17: 54,137,099 (GRCm39) |
N274K |
probably benign |
Het |
Syk |
T |
C |
13: 52,776,768 (GRCm39) |
V256A |
probably benign |
Het |
Tcte1 |
A |
G |
17: 45,844,222 (GRCm39) |
D66G |
probably damaging |
Het |
Tgm4 |
C |
T |
9: 122,885,580 (GRCm39) |
T374M |
probably damaging |
Het |
Tsn |
C |
T |
1: 118,232,999 (GRCm39) |
A102T |
possibly damaging |
Het |
Uvssa |
T |
A |
5: 33,549,189 (GRCm39) |
S350T |
possibly damaging |
Het |
Vmn1r3 |
T |
A |
4: 3,185,214 (GRCm39) |
Y31F |
possibly damaging |
Het |
Vmn2r114 |
A |
T |
17: 23,515,970 (GRCm39) |
|
probably benign |
Het |
Vmn2r27 |
T |
C |
6: 124,169,276 (GRCm39) |
D618G |
possibly damaging |
Het |
Vmn2r91 |
T |
A |
17: 18,330,373 (GRCm39) |
|
probably benign |
Het |
Vti1a |
T |
C |
19: 55,380,279 (GRCm39) |
Y143H |
probably damaging |
Het |
Zfand4 |
T |
A |
6: 116,250,620 (GRCm39) |
Y17N |
probably damaging |
Het |
Zfp729a |
T |
C |
13: 67,767,761 (GRCm39) |
|
probably null |
Het |
Zfp827 |
A |
G |
8: 79,787,586 (GRCm39) |
T251A |
probably damaging |
Het |
|
Other mutations in Tns4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00783:Tns4
|
APN |
11 |
98,961,221 (GRCm39) |
splice site |
probably benign |
|
IGL01940:Tns4
|
APN |
11 |
98,959,047 (GRCm39) |
missense |
probably benign |
0.43 |
IGL03376:Tns4
|
APN |
11 |
98,969,382 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4486001:Tns4
|
UTSW |
11 |
98,962,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Tns4
|
UTSW |
11 |
98,966,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Tns4
|
UTSW |
11 |
98,961,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Tns4
|
UTSW |
11 |
98,970,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Tns4
|
UTSW |
11 |
98,966,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R1998:Tns4
|
UTSW |
11 |
98,976,529 (GRCm39) |
missense |
probably benign |
|
R2126:Tns4
|
UTSW |
11 |
98,970,904 (GRCm39) |
critical splice donor site |
probably null |
|
R4468:Tns4
|
UTSW |
11 |
98,961,241 (GRCm39) |
missense |
probably benign |
0.41 |
R4973:Tns4
|
UTSW |
11 |
98,966,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R5048:Tns4
|
UTSW |
11 |
98,969,605 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5918:Tns4
|
UTSW |
11 |
98,964,497 (GRCm39) |
critical splice donor site |
probably null |
|
R6088:Tns4
|
UTSW |
11 |
98,964,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Tns4
|
UTSW |
11 |
98,966,376 (GRCm39) |
missense |
probably benign |
0.11 |
R6586:Tns4
|
UTSW |
11 |
98,971,093 (GRCm39) |
missense |
probably benign |
0.00 |
R7543:Tns4
|
UTSW |
11 |
98,963,079 (GRCm39) |
missense |
probably benign |
0.38 |
R7667:Tns4
|
UTSW |
11 |
98,962,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R7909:Tns4
|
UTSW |
11 |
98,976,849 (GRCm39) |
missense |
probably damaging |
0.99 |
R8206:Tns4
|
UTSW |
11 |
98,976,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|