Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,243,983 (GRCm39) |
I1949V |
possibly damaging |
Het |
Anapc2 |
T |
A |
2: 25,175,108 (GRCm39) |
M742K |
probably benign |
Het |
Arhgef12 |
T |
A |
9: 42,917,200 (GRCm39) |
K380* |
probably null |
Het |
Armc1 |
G |
T |
3: 19,188,192 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
G |
A |
3: 37,098,757 (GRCm39) |
W4626* |
probably null |
Het |
Diaph3 |
A |
T |
14: 87,223,512 (GRCm39) |
L323* |
probably null |
Het |
Fbxo11 |
C |
T |
17: 88,318,711 (GRCm39) |
|
probably benign |
Het |
Flywch1 |
C |
T |
17: 23,974,676 (GRCm39) |
A655T |
probably benign |
Het |
Frmpd1 |
A |
G |
4: 45,285,160 (GRCm39) |
D1327G |
probably damaging |
Het |
Ggact |
G |
A |
14: 123,128,942 (GRCm39) |
T91I |
possibly damaging |
Het |
Gm10250 |
T |
A |
15: 5,150,412 (GRCm39) |
|
probably benign |
Het |
Gsdmc4 |
T |
C |
15: 63,765,641 (GRCm39) |
S303G |
probably damaging |
Het |
Helt |
T |
C |
8: 46,746,276 (GRCm39) |
E15G |
probably damaging |
Het |
Kcnf1 |
T |
A |
12: 17,226,144 (GRCm39) |
S26C |
probably benign |
Het |
Lilra6 |
T |
C |
7: 3,911,819 (GRCm39) |
T280A |
probably benign |
Het |
Lipo3 |
A |
T |
19: 33,559,539 (GRCm39) |
D110E |
possibly damaging |
Het |
Mepe |
C |
A |
5: 104,485,316 (GRCm39) |
T152N |
probably benign |
Het |
Nr2f1 |
C |
A |
13: 78,343,275 (GRCm39) |
|
probably benign |
Het |
Or5ak24 |
T |
C |
2: 85,260,810 (GRCm39) |
D121G |
possibly damaging |
Het |
Or6c214 |
A |
G |
10: 129,590,524 (GRCm39) |
I265T |
possibly damaging |
Het |
Peg3 |
T |
C |
7: 6,713,068 (GRCm39) |
D718G |
probably benign |
Het |
Phf2 |
A |
T |
13: 48,967,334 (GRCm39) |
|
probably benign |
Het |
Pigc |
A |
T |
1: 161,798,503 (GRCm39) |
I162F |
probably benign |
Het |
Raf1 |
A |
G |
6: 115,597,267 (GRCm39) |
L11P |
probably damaging |
Het |
Rlf |
T |
C |
4: 121,007,261 (GRCm39) |
Y573C |
probably damaging |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Rnf149 |
T |
G |
1: 39,604,296 (GRCm39) |
Q189P |
probably benign |
Het |
Slc11a1 |
T |
C |
1: 74,424,291 (GRCm39) |
|
probably benign |
Het |
Slc22a12 |
C |
T |
19: 6,590,487 (GRCm39) |
M234I |
probably benign |
Het |
Slc28a1 |
A |
T |
7: 80,814,167 (GRCm39) |
I455F |
probably benign |
Het |
Slc35f5 |
T |
G |
1: 125,512,273 (GRCm39) |
L358V |
probably damaging |
Het |
Slc47a1 |
A |
T |
11: 61,235,147 (GRCm39) |
V562D |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Ushbp1 |
T |
C |
8: 71,841,394 (GRCm39) |
|
probably benign |
Het |
Vmn2r27 |
A |
T |
6: 124,201,434 (GRCm39) |
Y174* |
probably null |
Het |
Wwox |
T |
C |
8: 115,438,947 (GRCm39) |
Y338H |
possibly damaging |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
Zup1 |
A |
T |
10: 33,811,261 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn1r88 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01828:Vmn1r88
|
APN |
7 |
12,911,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01879:Vmn1r88
|
APN |
7 |
12,912,229 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02028:Vmn1r88
|
APN |
7 |
12,911,719 (GRCm39) |
missense |
probably benign |
|
IGL03176:Vmn1r88
|
APN |
7 |
12,911,779 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4466001:Vmn1r88
|
UTSW |
7 |
12,912,403 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1163:Vmn1r88
|
UTSW |
7 |
12,912,060 (GRCm39) |
missense |
probably benign |
|
R1478:Vmn1r88
|
UTSW |
7 |
12,911,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2376:Vmn1r88
|
UTSW |
7 |
12,911,785 (GRCm39) |
missense |
probably damaging |
0.99 |
R3624:Vmn1r88
|
UTSW |
7 |
12,911,790 (GRCm39) |
missense |
probably benign |
0.08 |
R4543:Vmn1r88
|
UTSW |
7 |
12,911,907 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4593:Vmn1r88
|
UTSW |
7 |
12,911,769 (GRCm39) |
missense |
probably damaging |
0.96 |
R4721:Vmn1r88
|
UTSW |
7 |
12,912,451 (GRCm39) |
nonsense |
probably null |
|
R5927:Vmn1r88
|
UTSW |
7 |
12,912,440 (GRCm39) |
missense |
probably benign |
0.12 |
R6411:Vmn1r88
|
UTSW |
7 |
12,911,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R6535:Vmn1r88
|
UTSW |
7 |
12,912,112 (GRCm39) |
missense |
probably benign |
0.03 |
R6598:Vmn1r88
|
UTSW |
7 |
12,912,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Vmn1r88
|
UTSW |
7 |
12,912,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9389:Vmn1r88
|
UTSW |
7 |
12,912,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R9769:Vmn1r88
|
UTSW |
7 |
12,912,280 (GRCm39) |
missense |
probably damaging |
0.97 |
|