Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adora2a |
G |
T |
10: 75,333,492 (GRCm38) |
W263C |
probably damaging |
Het |
Agtpbp1 |
G |
A |
13: 59,504,226 (GRCm38) |
H424Y |
possibly damaging |
Het |
Angpt2 |
T |
G |
8: 18,710,528 (GRCm38) |
N186T |
probably benign |
Het |
Ank2 |
A |
G |
3: 126,959,720 (GRCm38) |
V304A |
possibly damaging |
Het |
Atg3 |
T |
C |
16: 45,171,673 (GRCm38) |
M88T |
possibly damaging |
Het |
Baz1a |
G |
T |
12: 54,954,809 (GRCm38) |
P142Q |
probably damaging |
Het |
Btbd1 |
G |
T |
7: 81,794,307 (GRCm38) |
|
probably null |
Het |
Cacnb3 |
T |
C |
15: 98,639,853 (GRCm38) |
Y70H |
probably damaging |
Het |
Cd4 |
G |
A |
6: 124,879,378 (GRCm38) |
T50I |
probably benign |
Het |
Cyp7a1 |
A |
T |
4: 6,275,517 (GRCm38) |
W19R |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,531,245 (GRCm38) |
I1610F |
probably damaging |
Het |
Gm7168 |
A |
T |
17: 13,949,858 (GRCm38) |
T496S |
probably benign |
Het |
Gpc5 |
A |
G |
14: 115,399,188 (GRCm38) |
S428G |
probably benign |
Het |
Haus8 |
T |
C |
8: 71,253,113 (GRCm38) |
E309G |
probably damaging |
Het |
Ice1 |
A |
G |
13: 70,604,904 (GRCm38) |
L1021P |
possibly damaging |
Het |
Krtap14 |
A |
T |
16: 88,825,727 (GRCm38) |
H121Q |
probably benign |
Het |
Nwd1 |
T |
C |
8: 72,662,331 (GRCm38) |
V170A |
probably benign |
Het |
Or1j10 |
T |
A |
2: 36,377,448 (GRCm38) |
M224K |
probably benign |
Het |
Or6c3b |
T |
C |
10: 129,692,029 (GRCm38) |
Y4C |
probably damaging |
Het |
Or8g24 |
G |
A |
9: 39,078,724 (GRCm38) |
T7I |
possibly damaging |
Het |
Pfpl |
T |
C |
19: 12,428,673 (GRCm38) |
M96T |
possibly damaging |
Het |
Pramel5 |
A |
G |
4: 144,271,162 (GRCm38) |
|
probably benign |
Het |
Proc |
T |
C |
18: 32,123,552 (GRCm38) |
N354S |
probably benign |
Het |
Prss40 |
T |
G |
1: 34,560,766 (GRCm38) |
I47L |
probably benign |
Het |
Tmprss7 |
T |
C |
16: 45,664,175 (GRCm38) |
R541G |
probably benign |
Het |
Togaram2 |
T |
C |
17: 71,716,513 (GRCm38) |
V788A |
possibly damaging |
Het |
Trbv19 |
T |
C |
6: 41,178,904 (GRCm38) |
Y70H |
probably damaging |
Het |
Ttk |
C |
T |
9: 83,865,142 (GRCm38) |
S678L |
probably benign |
Het |
Vmn2r85 |
T |
C |
10: 130,418,821 (GRCm38) |
T665A |
probably benign |
Het |
|
Other mutations in Gm11444 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1958:Gm11444
|
UTSW |
11 |
85,848,173 (GRCm38) |
splice site |
probably benign |
|
R5199:Gm11444
|
UTSW |
11 |
85,848,019 (GRCm38) |
missense |
unknown |
|
R6283:Gm11444
|
UTSW |
11 |
85,846,791 (GRCm38) |
splice site |
probably null |
|
R7088:Gm11444
|
UTSW |
11 |
85,847,036 (GRCm38) |
missense |
|
|
R7579:Gm11444
|
UTSW |
11 |
85,850,243 (GRCm38) |
missense |
unknown |
|
R8378:Gm11444
|
UTSW |
11 |
85,850,249 (GRCm38) |
missense |
|
|
R8708:Gm11444
|
UTSW |
11 |
85,846,897 (GRCm38) |
missense |
|
|
R9803:Gm11444
|
UTSW |
11 |
85,846,873 (GRCm38) |
nonsense |
probably null |
|
|