Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl1 |
A |
C |
4: 86,306,762 (GRCm39) |
D1392A |
probably benign |
Het |
Afdn |
T |
C |
17: 14,103,999 (GRCm39) |
|
probably benign |
Het |
Aph1b |
A |
T |
9: 66,691,921 (GRCm39) |
M121K |
probably damaging |
Het |
Aspg |
G |
A |
12: 112,080,868 (GRCm39) |
A120T |
probably damaging |
Het |
Bicd1 |
A |
G |
6: 149,418,503 (GRCm39) |
T725A |
probably damaging |
Het |
Cd1d2 |
A |
T |
3: 86,895,847 (GRCm39) |
I292F |
probably damaging |
Het |
Cdcp3 |
A |
T |
7: 130,849,186 (GRCm39) |
|
probably null |
Het |
Cdk13 |
A |
G |
13: 17,894,120 (GRCm39) |
V495A |
probably damaging |
Het |
Cfd |
A |
T |
10: 79,728,039 (GRCm39) |
|
probably null |
Het |
Col9a2 |
C |
G |
4: 120,911,455 (GRCm39) |
R599G |
probably damaging |
Het |
Cradd |
A |
C |
10: 95,011,735 (GRCm39) |
V135G |
probably benign |
Het |
Cry1 |
A |
G |
10: 84,979,617 (GRCm39) |
C460R |
probably damaging |
Het |
Ctu2 |
A |
G |
8: 123,207,649 (GRCm39) |
E375G |
probably damaging |
Het |
Dym |
T |
G |
18: 75,363,236 (GRCm39) |
I580S |
probably damaging |
Het |
Eif3e |
A |
G |
15: 43,114,943 (GRCm39) |
L411P |
possibly damaging |
Het |
Emsy |
T |
C |
7: 98,239,982 (GRCm39) |
E1091G |
possibly damaging |
Het |
Enkur |
A |
G |
2: 21,194,130 (GRCm39) |
|
probably benign |
Het |
Fam184a |
G |
A |
10: 53,531,175 (GRCm39) |
T733M |
probably damaging |
Het |
Frem2 |
G |
A |
3: 53,424,278 (GRCm39) |
A3053V |
probably benign |
Het |
Gbgt1 |
T |
C |
2: 28,388,435 (GRCm39) |
L40P |
probably damaging |
Het |
Gm5174 |
T |
A |
10: 86,492,372 (GRCm39) |
|
noncoding transcript |
Het |
Gys2 |
G |
T |
6: 142,402,148 (GRCm39) |
D230E |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,818,766 (GRCm39) |
|
probably null |
Het |
Hps3 |
A |
T |
3: 20,056,527 (GRCm39) |
S815R |
probably benign |
Het |
Igf1r |
C |
A |
7: 67,851,710 (GRCm39) |
S983R |
probably damaging |
Het |
Itsn1 |
T |
A |
16: 91,650,656 (GRCm39) |
|
probably benign |
Het |
Kcnc2 |
A |
G |
10: 112,292,431 (GRCm39) |
N91D |
probably damaging |
Het |
Kif28 |
C |
A |
1: 179,560,676 (GRCm39) |
A210S |
possibly damaging |
Het |
Klri2 |
T |
A |
6: 129,717,272 (GRCm39) |
Q37L |
probably damaging |
Het |
Lrrc38 |
T |
A |
4: 143,096,419 (GRCm39) |
C243* |
probably null |
Het |
Map3k5 |
T |
C |
10: 19,943,666 (GRCm39) |
V590A |
possibly damaging |
Het |
Mdn1 |
C |
A |
4: 32,763,306 (GRCm39) |
F5135L |
probably benign |
Het |
Megf11 |
G |
A |
9: 64,567,713 (GRCm39) |
G401S |
possibly damaging |
Het |
Mst1r |
T |
C |
9: 107,785,547 (GRCm39) |
F402L |
probably damaging |
Het |
Ntrk3 |
T |
C |
7: 77,848,600 (GRCm39) |
I759V |
probably damaging |
Het |
Nup188 |
T |
C |
2: 30,226,936 (GRCm39) |
|
probably benign |
Het |
Or4a71 |
C |
T |
2: 89,358,281 (GRCm39) |
V158I |
probably benign |
Het |
Or8b12i |
T |
C |
9: 20,082,388 (GRCm39) |
S160G |
possibly damaging |
Het |
Prdm2 |
T |
C |
4: 142,861,469 (GRCm39) |
N607S |
possibly damaging |
Het |
Prl2a1 |
T |
A |
13: 27,990,369 (GRCm39) |
|
probably null |
Het |
Serpina9 |
T |
A |
12: 103,964,523 (GRCm39) |
I305F |
probably damaging |
Het |
Setx |
GTGGCT |
GT |
2: 29,044,073 (GRCm39) |
1814 |
probably null |
Het |
Slc19a1 |
C |
T |
10: 76,878,320 (GRCm39) |
T285I |
probably benign |
Het |
Snap91 |
T |
C |
9: 86,674,580 (GRCm39) |
T544A |
possibly damaging |
Het |
Srgap3 |
A |
G |
6: 112,923,454 (GRCm39) |
S2P |
probably damaging |
Het |
Tcof1 |
A |
G |
18: 60,970,973 (GRCm39) |
V210A |
possibly damaging |
Het |
Tex261 |
A |
G |
6: 83,748,497 (GRCm39) |
I136T |
probably benign |
Het |
Trpa1 |
A |
T |
1: 14,973,480 (GRCm39) |
F279L |
probably null |
Het |
Ttc39b |
T |
C |
4: 83,150,999 (GRCm39) |
N532S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,572,438 (GRCm39) |
T26152A |
probably damaging |
Het |
Ube2w |
A |
G |
1: 16,668,183 (GRCm39) |
S97P |
possibly damaging |
Het |
Vmn1r64 |
T |
C |
7: 5,887,448 (GRCm39) |
I32V |
probably benign |
Het |
Vmn2r112 |
T |
G |
17: 22,820,214 (GRCm39) |
M29R |
possibly damaging |
Het |
Vmn2r71 |
T |
A |
7: 85,273,301 (GRCm39) |
M705K |
probably benign |
Het |
Vps13b |
G |
A |
15: 35,884,743 (GRCm39) |
V3139I |
probably benign |
Het |
Zfp628 |
T |
C |
7: 4,923,830 (GRCm39) |
V684A |
probably benign |
Het |
|
Other mutations in Vmn1r25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01867:Vmn1r25
|
APN |
6 |
57,956,196 (GRCm39) |
missense |
probably damaging |
0.99 |
R0299:Vmn1r25
|
UTSW |
6 |
57,955,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Vmn1r25
|
UTSW |
6 |
57,955,696 (GRCm39) |
missense |
probably benign |
0.01 |
R0499:Vmn1r25
|
UTSW |
6 |
57,955,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1294:Vmn1r25
|
UTSW |
6 |
57,955,464 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1562:Vmn1r25
|
UTSW |
6 |
57,955,786 (GRCm39) |
missense |
probably benign |
0.03 |
R1661:Vmn1r25
|
UTSW |
6 |
57,955,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1665:Vmn1r25
|
UTSW |
6 |
57,955,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1879:Vmn1r25
|
UTSW |
6 |
57,955,912 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2223:Vmn1r25
|
UTSW |
6 |
57,956,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2374:Vmn1r25
|
UTSW |
6 |
57,955,543 (GRCm39) |
missense |
probably benign |
0.10 |
R4073:Vmn1r25
|
UTSW |
6 |
57,955,572 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4398:Vmn1r25
|
UTSW |
6 |
57,955,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Vmn1r25
|
UTSW |
6 |
57,955,480 (GRCm39) |
missense |
probably benign |
0.02 |
R4779:Vmn1r25
|
UTSW |
6 |
57,956,011 (GRCm39) |
missense |
probably damaging |
0.98 |
R5397:Vmn1r25
|
UTSW |
6 |
57,956,060 (GRCm39) |
nonsense |
probably null |
|
R6113:Vmn1r25
|
UTSW |
6 |
57,955,557 (GRCm39) |
missense |
probably benign |
0.00 |
R6858:Vmn1r25
|
UTSW |
6 |
57,955,996 (GRCm39) |
missense |
probably benign |
0.22 |
R7407:Vmn1r25
|
UTSW |
6 |
57,956,044 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7748:Vmn1r25
|
UTSW |
6 |
57,955,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8001:Vmn1r25
|
UTSW |
6 |
57,956,065 (GRCm39) |
nonsense |
probably null |
|
R8472:Vmn1r25
|
UTSW |
6 |
57,955,531 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9235:Vmn1r25
|
UTSW |
6 |
57,955,488 (GRCm39) |
missense |
probably damaging |
0.96 |
R9651:Vmn1r25
|
UTSW |
6 |
57,956,306 (GRCm39) |
unclassified |
probably benign |
|
|