Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
A |
2: 69,117,936 (GRCm39) |
|
probably benign |
Het |
Adgrb2 |
T |
C |
4: 129,906,359 (GRCm39) |
V929A |
probably benign |
Het |
Aldh2 |
T |
C |
5: 121,710,136 (GRCm39) |
I400V |
probably benign |
Het |
Atxn2l |
T |
C |
7: 126,099,425 (GRCm39) |
D84G |
probably damaging |
Het |
Avpr1a |
T |
A |
10: 122,284,916 (GRCm39) |
N69K |
probably damaging |
Het |
BC034090 |
G |
A |
1: 155,102,085 (GRCm39) |
Q60* |
probably null |
Het |
Bltp1 |
G |
A |
3: 36,982,669 (GRCm39) |
S778N |
possibly damaging |
Het |
Bub3 |
T |
C |
7: 131,170,362 (GRCm39) |
S295P |
probably benign |
Het |
Cacna1b |
T |
C |
2: 24,499,902 (GRCm39) |
S161G |
probably damaging |
Het |
Clba1 |
C |
T |
12: 112,779,179 (GRCm39) |
T272M |
probably damaging |
Het |
Col6a4 |
T |
A |
9: 105,954,452 (GRCm39) |
S296C |
probably damaging |
Het |
Cyp4f15 |
G |
A |
17: 32,905,131 (GRCm39) |
R38H |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,122,799 (GRCm39) |
I2052M |
probably damaging |
Het |
Gm11627 |
T |
C |
11: 102,469,634 (GRCm39) |
|
probably benign |
Het |
Jmjd8 |
A |
T |
17: 26,048,212 (GRCm39) |
|
probably null |
Het |
Kmt2c |
A |
G |
5: 25,495,802 (GRCm39) |
V629A |
possibly damaging |
Het |
Kremen1 |
T |
C |
11: 5,149,667 (GRCm39) |
T335A |
probably benign |
Het |
Oosp2 |
T |
C |
19: 11,628,847 (GRCm39) |
T85A |
probably benign |
Het |
Or12d17 |
A |
G |
17: 37,777,649 (GRCm39) |
E184G |
probably damaging |
Het |
Or8s10 |
A |
G |
15: 98,335,530 (GRCm39) |
Y60C |
possibly damaging |
Het |
Pex5l |
T |
C |
3: 33,136,204 (GRCm39) |
E5G |
probably benign |
Het |
Pigk |
A |
T |
3: 152,448,156 (GRCm39) |
Q173L |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,599,407 (GRCm39) |
N174K |
possibly damaging |
Het |
Plb1 |
C |
T |
5: 32,486,429 (GRCm39) |
H893Y |
probably damaging |
Het |
Pus7 |
T |
C |
5: 23,965,302 (GRCm39) |
|
probably benign |
Het |
R3hdm1 |
G |
A |
1: 128,102,970 (GRCm39) |
|
probably null |
Het |
Samd7 |
C |
T |
3: 30,808,435 (GRCm39) |
P83S |
probably benign |
Het |
Supt5 |
T |
A |
7: 28,023,400 (GRCm39) |
Y293F |
probably damaging |
Het |
Tbc1d30 |
T |
C |
10: 121,102,956 (GRCm39) |
D692G |
probably benign |
Het |
Tmpo |
G |
A |
10: 90,999,104 (GRCm39) |
R228C |
probably benign |
Het |
Tnn |
A |
T |
1: 159,916,008 (GRCm39) |
H1236Q |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,781,914 (GRCm39) |
I667T |
probably benign |
Het |
|
Other mutations in Vmn1r183 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00987:Vmn1r183
|
APN |
7 |
23,754,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03377:Vmn1r183
|
APN |
7 |
23,754,817 (GRCm39) |
missense |
possibly damaging |
0.70 |
PIT4791001:Vmn1r183
|
UTSW |
7 |
23,754,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R0463:Vmn1r183
|
UTSW |
7 |
23,754,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Vmn1r183
|
UTSW |
7 |
23,754,250 (GRCm39) |
missense |
probably benign |
0.03 |
R0666:Vmn1r183
|
UTSW |
7 |
23,754,601 (GRCm39) |
missense |
probably benign |
|
R3928:Vmn1r183
|
UTSW |
7 |
23,754,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R4425:Vmn1r183
|
UTSW |
7 |
23,754,973 (GRCm39) |
missense |
probably benign |
0.00 |
R4767:Vmn1r183
|
UTSW |
7 |
23,754,531 (GRCm39) |
frame shift |
probably null |
|
R4835:Vmn1r183
|
UTSW |
7 |
23,754,564 (GRCm39) |
missense |
probably benign |
0.07 |
R5267:Vmn1r183
|
UTSW |
7 |
23,754,971 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5693:Vmn1r183
|
UTSW |
7 |
23,754,227 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6291:Vmn1r183
|
UTSW |
7 |
23,754,982 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6439:Vmn1r183
|
UTSW |
7 |
23,754,704 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7073:Vmn1r183
|
UTSW |
7 |
23,754,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R8732:Vmn1r183
|
UTSW |
7 |
23,754,890 (GRCm39) |
missense |
possibly damaging |
0.89 |
|