Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26a |
A |
T |
8: 44,022,589 (GRCm39) |
Y300* |
probably null |
Het |
Adgre1 |
T |
A |
17: 57,708,908 (GRCm39) |
V33E |
probably benign |
Het |
Atp4a |
T |
C |
7: 30,420,292 (GRCm39) |
L813P |
probably damaging |
Het |
Blmh |
A |
G |
11: 76,862,774 (GRCm39) |
N396D |
probably damaging |
Het |
Brat1 |
T |
C |
5: 140,691,750 (GRCm39) |
L9P |
probably damaging |
Het |
Ccdc171 |
T |
C |
4: 83,599,615 (GRCm39) |
I810T |
possibly damaging |
Het |
Clec2m |
C |
A |
6: 129,307,986 (GRCm39) |
V28L |
probably benign |
Het |
Cyp2a22 |
T |
C |
7: 26,634,279 (GRCm39) |
T292A |
possibly damaging |
Het |
Ecm2 |
C |
T |
13: 49,674,420 (GRCm39) |
T280I |
probably benign |
Het |
Fa2h |
C |
T |
8: 112,075,928 (GRCm39) |
V232I |
probably benign |
Het |
Fbxw24 |
T |
C |
9: 109,436,081 (GRCm39) |
D317G |
probably damaging |
Het |
Flt4 |
C |
A |
11: 49,525,620 (GRCm39) |
S722* |
probably null |
Het |
Fryl |
T |
C |
5: 73,290,649 (GRCm39) |
Q85R |
probably damaging |
Het |
Gm3239 |
A |
G |
14: 15,882,083 (GRCm39) |
R188G |
possibly damaging |
Het |
Hspa13 |
A |
T |
16: 75,554,717 (GRCm39) |
S456R |
probably damaging |
Het |
Htr1b |
T |
C |
9: 81,514,175 (GRCm39) |
Y144C |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,038,856 (GRCm39) |
H198R |
possibly damaging |
Het |
Krt78 |
A |
T |
15: 101,854,952 (GRCm39) |
M953K |
probably benign |
Het |
Lgr5 |
G |
T |
10: 115,307,893 (GRCm39) |
T255K |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,268,797 (GRCm39) |
D4162V |
probably damaging |
Het |
Map3k2 |
A |
G |
18: 32,345,201 (GRCm39) |
D342G |
probably damaging |
Het |
Miip |
A |
G |
4: 147,946,979 (GRCm39) |
V258A |
probably benign |
Het |
Muc6 |
T |
C |
7: 141,238,324 (GRCm39) |
H52R |
probably damaging |
Het |
Nfs1 |
T |
C |
2: 155,969,660 (GRCm39) |
E329G |
probably benign |
Het |
Npsr1 |
T |
C |
9: 24,009,605 (GRCm39) |
V37A |
probably benign |
Het |
Or1ak2 |
T |
C |
2: 36,827,595 (GRCm39) |
Y155H |
probably damaging |
Het |
Or1e17 |
A |
T |
11: 73,831,664 (GRCm39) |
L197F |
probably damaging |
Het |
Or5aq1b |
A |
C |
2: 86,901,904 (GRCm39) |
D191E |
probably damaging |
Het |
Pex16 |
T |
A |
2: 92,207,842 (GRCm39) |
M98K |
probably damaging |
Het |
Pla2r1 |
C |
T |
2: 60,285,517 (GRCm39) |
C699Y |
probably damaging |
Het |
Plcd4 |
A |
T |
1: 74,588,460 (GRCm39) |
D103V |
probably damaging |
Het |
Pnpla1 |
A |
G |
17: 29,095,966 (GRCm39) |
D129G |
probably damaging |
Het |
Rad23a |
T |
C |
8: 85,564,108 (GRCm39) |
E265G |
possibly damaging |
Het |
Rbm11 |
C |
T |
16: 75,397,696 (GRCm39) |
P209S |
probably benign |
Het |
Ribc2 |
T |
A |
15: 85,019,703 (GRCm39) |
W162R |
probably damaging |
Het |
Rnf4 |
A |
G |
5: 34,504,204 (GRCm39) |
E32G |
possibly damaging |
Het |
Rpe65 |
A |
T |
3: 159,320,154 (GRCm39) |
S269C |
possibly damaging |
Het |
Slc7a14 |
T |
A |
3: 31,291,558 (GRCm39) |
Y240F |
probably benign |
Het |
Sorbs2 |
C |
T |
8: 46,258,844 (GRCm39) |
P1047L |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,580,166 (GRCm39) |
I23576V |
probably damaging |
Het |
Usp24 |
T |
G |
4: 106,228,276 (GRCm39) |
Y780* |
probably null |
Het |
Wee2 |
T |
C |
6: 40,426,665 (GRCm39) |
S145P |
probably damaging |
Het |
Zcchc7 |
A |
G |
4: 44,931,188 (GRCm39) |
T126A |
probably benign |
Het |
Zpld1 |
A |
G |
16: 55,061,692 (GRCm39) |
|
probably benign |
Het |
Zup1 |
G |
A |
10: 33,804,107 (GRCm39) |
R456C |
probably benign |
Het |
|
Other mutations in AI987944 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
G1citation:AI987944
|
UTSW |
7 |
41,024,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:AI987944
|
UTSW |
7 |
41,026,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1083:AI987944
|
UTSW |
7 |
41,024,763 (GRCm39) |
missense |
probably benign |
0.09 |
R1480:AI987944
|
UTSW |
7 |
41,024,343 (GRCm39) |
missense |
probably benign |
0.00 |
R1485:AI987944
|
UTSW |
7 |
41,023,954 (GRCm39) |
nonsense |
probably null |
|
R1491:AI987944
|
UTSW |
7 |
41,023,772 (GRCm39) |
nonsense |
probably null |
|
R1662:AI987944
|
UTSW |
7 |
41,023,873 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1892:AI987944
|
UTSW |
7 |
41,024,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R1906:AI987944
|
UTSW |
7 |
41,024,550 (GRCm39) |
missense |
probably benign |
0.02 |
R2037:AI987944
|
UTSW |
7 |
41,023,815 (GRCm39) |
missense |
probably benign |
0.04 |
R2092:AI987944
|
UTSW |
7 |
41,024,041 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2202:AI987944
|
UTSW |
7 |
41,023,950 (GRCm39) |
missense |
probably damaging |
0.98 |
R5070:AI987944
|
UTSW |
7 |
41,024,748 (GRCm39) |
missense |
probably benign |
0.23 |
R5421:AI987944
|
UTSW |
7 |
41,024,200 (GRCm39) |
missense |
probably benign |
0.02 |
R5531:AI987944
|
UTSW |
7 |
41,023,814 (GRCm39) |
nonsense |
probably null |
|
R6822:AI987944
|
UTSW |
7 |
41,024,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:AI987944
|
UTSW |
7 |
41,023,880 (GRCm39) |
missense |
probably benign |
|
R8133:AI987944
|
UTSW |
7 |
41,024,489 (GRCm39) |
critical splice donor site |
probably null |
|
R8228:AI987944
|
UTSW |
7 |
41,026,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R8342:AI987944
|
UTSW |
7 |
41,024,310 (GRCm39) |
missense |
probably benign |
0.01 |
R8826:AI987944
|
UTSW |
7 |
41,024,627 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9583:AI987944
|
UTSW |
7 |
41,023,937 (GRCm39) |
missense |
probably benign |
0.02 |
|