Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
G |
1: 71,323,256 (GRCm39) |
K1609Q |
probably damaging |
Het |
Arl5a |
A |
G |
2: 52,314,614 (GRCm39) |
F12L |
probably benign |
Het |
Armc9 |
C |
T |
1: 86,202,125 (GRCm39) |
T761I |
probably benign |
Het |
Bmp1 |
A |
G |
14: 70,727,573 (GRCm39) |
F670S |
possibly damaging |
Het |
Cd34 |
T |
C |
1: 194,621,281 (GRCm39) |
V3A |
probably benign |
Het |
Cdkn2a |
A |
T |
4: 89,212,759 (GRCm39) |
M1K |
probably null |
Het |
Cep135 |
C |
A |
5: 76,786,054 (GRCm39) |
H1052Q |
probably benign |
Het |
Cfap100 |
T |
C |
6: 90,390,721 (GRCm39) |
|
probably benign |
Het |
Cib4 |
A |
T |
5: 30,703,075 (GRCm39) |
Y17N |
probably damaging |
Het |
Col3a1 |
T |
G |
1: 45,385,116 (GRCm39) |
S78A |
probably benign |
Het |
Crebzf |
A |
G |
7: 90,092,706 (GRCm39) |
M162V |
probably benign |
Het |
Dbx2 |
T |
A |
15: 95,552,454 (GRCm39) |
M64L |
possibly damaging |
Het |
Epb41l2 |
A |
T |
10: 25,380,128 (GRCm39) |
T884S |
probably damaging |
Het |
Erich3 |
T |
A |
3: 154,401,461 (GRCm39) |
S37T |
|
Het |
Eya1 |
G |
T |
1: 14,254,899 (GRCm39) |
Q383K |
possibly damaging |
Het |
Gm15130 |
A |
T |
2: 110,983,230 (GRCm39) |
|
probably null |
Het |
Ido1 |
A |
T |
8: 25,086,954 (GRCm39) |
M1K |
probably null |
Het |
Loxhd1 |
C |
T |
18: 77,529,162 (GRCm39) |
T1069M |
possibly damaging |
Het |
Lrrtm2 |
T |
G |
18: 35,346,451 (GRCm39) |
|
probably null |
Het |
Map1a |
C |
T |
2: 121,135,045 (GRCm39) |
H1716Y |
possibly damaging |
Het |
Mycbp2 |
T |
A |
14: 103,446,267 (GRCm39) |
T1854S |
probably benign |
Het |
Myh13 |
T |
C |
11: 67,255,351 (GRCm39) |
S1574P |
probably damaging |
Het |
Neu1 |
G |
A |
17: 35,150,982 (GRCm39) |
A78T |
probably benign |
Het |
Nfam1 |
T |
C |
15: 82,907,238 (GRCm39) |
|
probably benign |
Het |
Or1e27-ps1 |
T |
A |
11: 73,555,675 (GRCm39) |
L80Q |
probably damaging |
Het |
Or4c10b |
A |
C |
2: 89,711,511 (GRCm39) |
T114P |
probably damaging |
Het |
Or8k33 |
A |
T |
2: 86,384,027 (GRCm39) |
M147K |
probably benign |
Het |
Pdgfra |
T |
C |
5: 75,331,329 (GRCm39) |
|
probably null |
Het |
Ptgfrn |
A |
T |
3: 100,963,686 (GRCm39) |
M642K |
probably damaging |
Het |
R3hdm1 |
T |
A |
1: 128,162,864 (GRCm39) |
H980Q |
probably benign |
Het |
Rfc2 |
C |
A |
5: 134,611,698 (GRCm39) |
S19* |
probably null |
Het |
Rhbdf1 |
C |
A |
11: 32,160,162 (GRCm39) |
S738I |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,001,011 (GRCm39) |
N1488K |
probably damaging |
Het |
Rnf31 |
G |
A |
14: 55,833,566 (GRCm39) |
V525I |
probably damaging |
Het |
Rps27a |
T |
C |
11: 29,496,719 (GRCm39) |
D58G |
probably benign |
Het |
Serpinc1 |
T |
G |
1: 160,817,028 (GRCm39) |
C41G |
probably damaging |
Het |
Siglece |
A |
T |
7: 43,309,486 (GRCm39) |
V24D |
probably benign |
Het |
Sparcl1 |
T |
A |
5: 104,233,574 (GRCm39) |
R592W |
probably null |
Het |
Stard13 |
A |
G |
5: 150,987,090 (GRCm39) |
S104P |
probably damaging |
Het |
Ston2 |
A |
G |
12: 91,614,905 (GRCm39) |
V501A |
possibly damaging |
Het |
Sv2b |
C |
A |
7: 74,855,833 (GRCm39) |
|
probably null |
Het |
Tiam1 |
T |
C |
16: 89,681,932 (GRCm39) |
R349G |
probably damaging |
Het |
Tmprss11g |
A |
G |
5: 86,639,976 (GRCm39) |
|
probably null |
Het |
Tnik |
G |
T |
3: 28,650,321 (GRCm39) |
R507L |
probably damaging |
Het |
Trabd2b |
G |
T |
4: 114,460,113 (GRCm39) |
S417I |
probably damaging |
Het |
Ube2q1 |
T |
A |
3: 89,681,308 (GRCm39) |
V97E |
probably benign |
Het |
Vim |
A |
T |
2: 13,584,265 (GRCm39) |
N306Y |
probably damaging |
Het |
Vmn1r216 |
G |
T |
13: 23,283,979 (GRCm39) |
A221S |
possibly damaging |
Het |
Vmn2r66 |
A |
G |
7: 84,654,794 (GRCm39) |
|
probably null |
Het |
Vps45 |
T |
C |
3: 95,948,661 (GRCm39) |
S365G |
probably benign |
Het |
Zzz3 |
T |
A |
3: 152,134,290 (GRCm39) |
C449* |
probably null |
Het |
|
Other mutations in Vmn2r113 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01318:Vmn2r113
|
APN |
17 |
23,177,309 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01386:Vmn2r113
|
APN |
17 |
23,175,024 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01743:Vmn2r113
|
APN |
17 |
23,177,285 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02224:Vmn2r113
|
APN |
17 |
23,174,960 (GRCm39) |
nonsense |
probably null |
|
IGL02498:Vmn2r113
|
APN |
17 |
23,177,349 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02969:Vmn2r113
|
APN |
17 |
23,177,591 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03010:Vmn2r113
|
APN |
17 |
23,175,038 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03240:Vmn2r113
|
APN |
17 |
23,174,931 (GRCm39) |
missense |
probably benign |
0.19 |
R1853:Vmn2r113
|
UTSW |
17 |
23,164,501 (GRCm39) |
missense |
probably benign |
|
R2058:Vmn2r113
|
UTSW |
17 |
23,177,223 (GRCm39) |
nonsense |
probably null |
|
R3010:Vmn2r113
|
UTSW |
17 |
23,177,105 (GRCm39) |
missense |
probably damaging |
0.97 |
R4942:Vmn2r113
|
UTSW |
17 |
23,177,321 (GRCm39) |
missense |
probably damaging |
0.97 |
R5072:Vmn2r113
|
UTSW |
17 |
23,177,329 (GRCm39) |
nonsense |
probably null |
|
R5755:Vmn2r113
|
UTSW |
17 |
23,176,955 (GRCm39) |
missense |
probably benign |
0.00 |
R6513:Vmn2r113
|
UTSW |
17 |
23,177,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R7164:Vmn2r113
|
UTSW |
17 |
23,167,137 (GRCm39) |
missense |
probably benign |
|
R7936:Vmn2r113
|
UTSW |
17 |
23,176,917 (GRCm39) |
missense |
probably benign |
0.05 |
R8087:Vmn2r113
|
UTSW |
17 |
23,177,711 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8193:Vmn2r113
|
UTSW |
17 |
23,164,501 (GRCm39) |
missense |
probably benign |
0.06 |
R8196:Vmn2r113
|
UTSW |
17 |
23,176,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R8414:Vmn2r113
|
UTSW |
17 |
23,177,753 (GRCm39) |
nonsense |
probably null |
|
|