Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts18 |
C |
A |
8: 114,469,749 (GRCm39) |
R651L |
probably damaging |
Het |
Amd1 |
T |
C |
10: 40,165,380 (GRCm39) |
D317G |
possibly damaging |
Het |
Artn |
A |
G |
4: 117,784,815 (GRCm39) |
|
probably benign |
Het |
Bub1b |
T |
A |
2: 118,471,604 (GRCm39) |
V988E |
probably benign |
Het |
Cyp2c65 |
G |
T |
19: 39,061,662 (GRCm39) |
C216F |
probably benign |
Het |
Cyp3a11 |
T |
C |
5: 145,805,417 (GRCm39) |
E200G |
probably benign |
Het |
Cyp3a25 |
T |
A |
5: 145,923,652 (GRCm39) |
K330N |
probably damaging |
Het |
Duox2 |
C |
A |
2: 122,115,064 (GRCm39) |
V1138L |
probably benign |
Het |
Erc2 |
A |
G |
14: 27,733,651 (GRCm39) |
D567G |
probably damaging |
Het |
Eri2 |
A |
G |
7: 119,393,139 (GRCm39) |
|
probably null |
Het |
Foxa3 |
A |
G |
7: 18,757,294 (GRCm39) |
Y17H |
probably damaging |
Het |
Fto |
T |
C |
8: 92,200,940 (GRCm39) |
S324P |
probably damaging |
Het |
Get3 |
A |
T |
8: 85,751,893 (GRCm39) |
M1K |
probably null |
Het |
Gls2 |
T |
G |
10: 128,043,180 (GRCm39) |
L457R |
probably benign |
Het |
Gstcd |
A |
T |
3: 132,692,169 (GRCm39) |
L582H |
probably damaging |
Het |
Gtf3c1 |
G |
A |
7: 125,246,786 (GRCm39) |
R1508* |
probably null |
Het |
Kif21a |
T |
C |
15: 90,853,977 (GRCm39) |
|
probably null |
Het |
Klra5 |
A |
T |
6: 129,883,577 (GRCm39) |
D93E |
possibly damaging |
Het |
Lgr5 |
T |
C |
10: 115,290,404 (GRCm39) |
D456G |
probably damaging |
Het |
Mau2 |
A |
G |
8: 70,483,305 (GRCm39) |
S186P |
probably damaging |
Het |
Msr1 |
T |
C |
8: 40,042,423 (GRCm39) |
D384G |
possibly damaging |
Het |
Ncf4 |
T |
C |
15: 78,137,503 (GRCm39) |
V93A |
probably damaging |
Het |
Oas1f |
T |
G |
5: 120,994,489 (GRCm39) |
C337G |
probably damaging |
Het |
Or10al3 |
A |
G |
17: 38,011,932 (GRCm39) |
M124V |
probably damaging |
Het |
Or5p58 |
A |
T |
7: 107,694,429 (GRCm39) |
F116Y |
probably benign |
Het |
Or6c33 |
T |
A |
10: 129,853,872 (GRCm39) |
L214H |
probably damaging |
Het |
Pwwp3a |
C |
A |
10: 80,074,713 (GRCm39) |
|
probably null |
Het |
Rasl10b |
T |
C |
11: 83,309,519 (GRCm39) |
S159P |
probably damaging |
Het |
Sephs1 |
A |
G |
2: 4,904,371 (GRCm39) |
T250A |
probably benign |
Het |
Smg8 |
C |
A |
11: 86,971,249 (GRCm39) |
D841Y |
probably damaging |
Het |
Sox7 |
T |
C |
14: 64,181,398 (GRCm39) |
V65A |
probably damaging |
Het |
Sp140 |
C |
T |
1: 85,547,772 (GRCm39) |
|
probably benign |
Het |
Srsf10 |
A |
G |
4: 135,590,501 (GRCm39) |
Y142C |
possibly damaging |
Het |
Tcam1 |
G |
A |
11: 106,174,904 (GRCm39) |
E120K |
probably benign |
Het |
Tcerg1l |
A |
G |
7: 137,878,384 (GRCm39) |
V326A |
probably benign |
Het |
Tcl1b5 |
T |
A |
12: 105,145,326 (GRCm39) |
W97R |
probably damaging |
Het |
Tmem108 |
T |
C |
9: 103,376,856 (GRCm39) |
R198G |
possibly damaging |
Het |
Ube2ql1 |
T |
A |
13: 69,887,017 (GRCm39) |
Q148L |
possibly damaging |
Het |
Wdr6 |
A |
T |
9: 108,453,063 (GRCm39) |
S273R |
probably damaging |
Het |
Ylpm1 |
C |
T |
12: 85,043,850 (GRCm39) |
|
probably benign |
Het |
Zfp90 |
G |
A |
8: 107,152,138 (GRCm39) |
R617Q |
possibly damaging |
Het |
|
Other mutations in Vmn1r5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01674:Vmn1r5
|
APN |
6 |
56,962,911 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02027:Vmn1r5
|
APN |
6 |
56,962,640 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03133:Vmn1r5
|
APN |
6 |
56,962,600 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03412:Vmn1r5
|
APN |
6 |
56,962,918 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0316:Vmn1r5
|
UTSW |
6 |
56,962,784 (GRCm39) |
missense |
probably benign |
0.27 |
R0946:Vmn1r5
|
UTSW |
6 |
56,963,150 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1511:Vmn1r5
|
UTSW |
6 |
56,962,771 (GRCm39) |
missense |
probably benign |
0.02 |
R1553:Vmn1r5
|
UTSW |
6 |
56,962,483 (GRCm39) |
missense |
probably benign |
0.00 |
R1823:Vmn1r5
|
UTSW |
6 |
56,962,580 (GRCm39) |
missense |
probably damaging |
0.98 |
R3980:Vmn1r5
|
UTSW |
6 |
56,962,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R4473:Vmn1r5
|
UTSW |
6 |
56,962,633 (GRCm39) |
missense |
probably benign |
0.01 |
R4742:Vmn1r5
|
UTSW |
6 |
56,963,236 (GRCm39) |
nonsense |
probably null |
|
R5321:Vmn1r5
|
UTSW |
6 |
56,962,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5364:Vmn1r5
|
UTSW |
6 |
56,962,583 (GRCm39) |
missense |
probably damaging |
0.98 |
R6102:Vmn1r5
|
UTSW |
6 |
56,963,099 (GRCm39) |
missense |
probably damaging |
0.96 |
R6581:Vmn1r5
|
UTSW |
6 |
56,962,366 (GRCm39) |
missense |
probably benign |
|
R6885:Vmn1r5
|
UTSW |
6 |
56,963,042 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7297:Vmn1r5
|
UTSW |
6 |
56,963,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8063:Vmn1r5
|
UTSW |
6 |
56,962,583 (GRCm39) |
missense |
probably damaging |
0.98 |
R8766:Vmn1r5
|
UTSW |
6 |
56,963,100 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8968:Vmn1r5
|
UTSW |
6 |
56,963,182 (GRCm39) |
nonsense |
probably null |
|
R9440:Vmn1r5
|
UTSW |
6 |
56,962,415 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9460:Vmn1r5
|
UTSW |
6 |
56,962,829 (GRCm39) |
missense |
|
|
Z1176:Vmn1r5
|
UTSW |
6 |
56,962,933 (GRCm39) |
missense |
possibly damaging |
0.75 |
|