Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts13 |
A |
T |
2: 26,978,675 (GRCm38) |
I224F |
probably damaging |
Het |
Adamts17 |
A |
G |
7: 67,124,973 (GRCm38) |
T947A |
possibly damaging |
Het |
Ankfn1 |
T |
C |
11: 89,405,678 (GRCm38) |
E75G |
probably benign |
Het |
Arfgef1 |
G |
T |
1: 10,209,668 (GRCm38) |
H225N |
probably benign |
Het |
Arsi |
A |
G |
18: 60,917,067 (GRCm38) |
S341G |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,461,927 (GRCm38) |
|
probably benign |
Het |
Bltp1 |
A |
G |
3: 36,895,315 (GRCm38) |
E370G |
probably damaging |
Het |
Cacna1i |
C |
T |
15: 80,361,874 (GRCm38) |
R490* |
probably null |
Het |
Cd33 |
C |
T |
7: 43,528,729 (GRCm38) |
|
probably benign |
Het |
Clmn |
T |
C |
12: 104,791,853 (GRCm38) |
I135V |
probably damaging |
Het |
Crebbp |
A |
T |
16: 4,101,593 (GRCm38) |
N795K |
possibly damaging |
Het |
Dhps |
A |
G |
8: 85,073,299 (GRCm38) |
D126G |
probably damaging |
Het |
Dlg2 |
G |
T |
7: 91,940,115 (GRCm38) |
V196L |
possibly damaging |
Het |
Dsg1c |
T |
A |
18: 20,283,733 (GRCm38) |
I897N |
probably damaging |
Het |
Dzip3 |
A |
G |
16: 48,928,396 (GRCm38) |
L1059S |
probably damaging |
Het |
Epha7 |
A |
T |
4: 28,821,494 (GRCm38) |
T220S |
possibly damaging |
Het |
Fgf17 |
A |
G |
14: 70,638,528 (GRCm38) |
I88T |
probably damaging |
Het |
G3bp2 |
A |
G |
5: 92,066,524 (GRCm38) |
V137A |
possibly damaging |
Het |
Gnal |
G |
A |
18: 67,088,765 (GRCm38) |
E80K |
unknown |
Het |
Hectd1 |
T |
G |
12: 51,769,111 (GRCm38) |
S1393R |
probably damaging |
Het |
Igsf6 |
T |
C |
7: 121,068,273 (GRCm38) |
I173M |
possibly damaging |
Het |
Il2ra |
A |
C |
2: 11,683,090 (GRCm38) |
E227A |
possibly damaging |
Het |
Iqcf6 |
C |
T |
9: 106,627,280 (GRCm38) |
R48C |
probably damaging |
Het |
Kdm3a |
G |
T |
6: 71,611,586 (GRCm38) |
Q480K |
probably benign |
Het |
Larp4b |
C |
A |
13: 9,158,580 (GRCm38) |
A423E |
probably benign |
Het |
Magea6 |
T |
C |
X: 154,924,745 (GRCm38) |
D105G |
probably benign |
Het |
Nop53 |
C |
A |
7: 15,939,272 (GRCm38) |
|
probably benign |
Het |
Or14a260 |
A |
T |
7: 86,335,581 (GRCm38) |
F272I |
probably benign |
Het |
Or1j10 |
T |
C |
2: 36,377,313 (GRCm38) |
L179P |
possibly damaging |
Het |
Pgghg |
A |
G |
7: 140,944,981 (GRCm38) |
T352A |
possibly damaging |
Het |
Setd2 |
T |
C |
9: 110,553,116 (GRCm38) |
S1464P |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,484,828 (GRCm38) |
T3609N |
probably damaging |
Het |
Sulf1 |
T |
A |
1: 12,838,363 (GRCm38) |
Y533* |
probably null |
Het |
Thsd7b |
A |
G |
1: 129,613,195 (GRCm38) |
S346G |
probably benign |
Het |
Tmem161b |
T |
A |
13: 84,294,744 (GRCm38) |
L261Q |
probably damaging |
Het |
Tmem63b |
T |
A |
17: 45,665,208 (GRCm38) |
T493S |
possibly damaging |
Het |
Tmprss11d |
A |
T |
5: 86,306,305 (GRCm38) |
C214S |
probably damaging |
Het |
Trim16 |
A |
T |
11: 62,834,079 (GRCm38) |
E144V |
possibly damaging |
Het |
Unc13d |
T |
C |
11: 116,070,533 (GRCm38) |
Y356C |
probably damaging |
Het |
Urgcp |
A |
T |
11: 5,717,745 (GRCm38) |
F198I |
probably benign |
Het |
Zzz3 |
A |
T |
3: 152,427,390 (GRCm38) |
E28D |
probably damaging |
Het |
|
Other mutations in Vmn2r111 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00932:Vmn2r111
|
APN |
17 |
22,548,753 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01306:Vmn2r111
|
APN |
17 |
22,568,984 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01309:Vmn2r111
|
APN |
17 |
22,569,016 (GRCm38) |
missense |
possibly damaging |
0.51 |
IGL01457:Vmn2r111
|
APN |
17 |
22,571,985 (GRCm38) |
nonsense |
probably null |
|
IGL01465:Vmn2r111
|
APN |
17 |
22,548,737 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01505:Vmn2r111
|
APN |
17 |
22,548,572 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01571:Vmn2r111
|
APN |
17 |
22,571,392 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01715:Vmn2r111
|
APN |
17 |
22,569,073 (GRCm38) |
splice site |
probably benign |
|
IGL01962:Vmn2r111
|
APN |
17 |
22,548,284 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL02190:Vmn2r111
|
APN |
17 |
22,570,773 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02496:Vmn2r111
|
APN |
17 |
22,568,856 (GRCm38) |
missense |
probably benign |
|
IGL02616:Vmn2r111
|
APN |
17 |
22,571,050 (GRCm38) |
missense |
possibly damaging |
0.67 |
IGL02641:Vmn2r111
|
APN |
17 |
22,573,224 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL02690:Vmn2r111
|
APN |
17 |
22,559,042 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02698:Vmn2r111
|
APN |
17 |
22,571,245 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03017:Vmn2r111
|
APN |
17 |
22,570,858 (GRCm38) |
missense |
probably damaging |
1.00 |
R0046:Vmn2r111
|
UTSW |
17 |
22,548,009 (GRCm38) |
missense |
probably benign |
|
R0064:Vmn2r111
|
UTSW |
17 |
22,572,072 (GRCm38) |
missense |
probably benign |
0.00 |
R0519:Vmn2r111
|
UTSW |
17 |
22,573,121 (GRCm38) |
missense |
probably benign |
0.02 |
R1439:Vmn2r111
|
UTSW |
17 |
22,571,116 (GRCm38) |
missense |
probably benign |
0.00 |
R1467:Vmn2r111
|
UTSW |
17 |
22,571,047 (GRCm38) |
missense |
probably damaging |
0.99 |
R1467:Vmn2r111
|
UTSW |
17 |
22,571,047 (GRCm38) |
missense |
probably damaging |
0.99 |
R1636:Vmn2r111
|
UTSW |
17 |
22,571,399 (GRCm38) |
missense |
probably damaging |
1.00 |
R1647:Vmn2r111
|
UTSW |
17 |
22,569,061 (GRCm38) |
missense |
probably benign |
0.03 |
R1648:Vmn2r111
|
UTSW |
17 |
22,569,061 (GRCm38) |
missense |
probably benign |
0.03 |
R1697:Vmn2r111
|
UTSW |
17 |
22,548,060 (GRCm38) |
missense |
probably benign |
0.26 |
R1996:Vmn2r111
|
UTSW |
17 |
22,548,081 (GRCm38) |
missense |
probably benign |
0.21 |
R2040:Vmn2r111
|
UTSW |
17 |
22,548,414 (GRCm38) |
missense |
probably damaging |
1.00 |
R2075:Vmn2r111
|
UTSW |
17 |
22,559,062 (GRCm38) |
missense |
probably damaging |
1.00 |
R2134:Vmn2r111
|
UTSW |
17 |
22,573,104 (GRCm38) |
missense |
possibly damaging |
0.68 |
R2357:Vmn2r111
|
UTSW |
17 |
22,559,170 (GRCm38) |
splice site |
probably benign |
|
R3700:Vmn2r111
|
UTSW |
17 |
22,571,161 (GRCm38) |
nonsense |
probably null |
|
R3782:Vmn2r111
|
UTSW |
17 |
22,571,320 (GRCm38) |
missense |
possibly damaging |
0.89 |
R4085:Vmn2r111
|
UTSW |
17 |
22,559,115 (GRCm38) |
missense |
probably benign |
0.00 |
R4323:Vmn2r111
|
UTSW |
17 |
22,573,178 (GRCm38) |
missense |
probably benign |
0.02 |
R4900:Vmn2r111
|
UTSW |
17 |
22,548,656 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5072:Vmn2r111
|
UTSW |
17 |
22,548,041 (GRCm38) |
missense |
probably damaging |
0.99 |
R5123:Vmn2r111
|
UTSW |
17 |
22,571,143 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5181:Vmn2r111
|
UTSW |
17 |
22,571,020 (GRCm38) |
missense |
possibly damaging |
0.56 |
R5357:Vmn2r111
|
UTSW |
17 |
22,548,102 (GRCm38) |
nonsense |
probably null |
|
R5398:Vmn2r111
|
UTSW |
17 |
22,573,271 (GRCm38) |
start codon destroyed |
probably null |
0.88 |
R5434:Vmn2r111
|
UTSW |
17 |
22,548,489 (GRCm38) |
missense |
probably damaging |
0.99 |
R5462:Vmn2r111
|
UTSW |
17 |
22,548,257 (GRCm38) |
missense |
probably damaging |
1.00 |
R6149:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6149:Vmn2r111
|
UTSW |
17 |
22,548,815 (GRCm38) |
missense |
probably benign |
0.00 |
R6207:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6281:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6282:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6283:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6307:Vmn2r111
|
UTSW |
17 |
22,573,089 (GRCm38) |
missense |
probably benign |
0.00 |
R6323:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6325:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6367:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6368:Vmn2r111
|
UTSW |
17 |
22,571,908 (GRCm38) |
missense |
probably benign |
0.38 |
R6369:Vmn2r111
|
UTSW |
17 |
22,548,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R6489:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6490:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6546:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6547:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6557:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6654:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6655:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6657:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6659:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6660:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6664:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6798:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6799:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6801:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6893:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6895:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6897:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6922:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6923:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6944:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6945:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7017:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7018:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7024:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7031:Vmn2r111
|
UTSW |
17 |
22,571,245 (GRCm38) |
missense |
probably damaging |
1.00 |
R7039:Vmn2r111
|
UTSW |
17 |
22,548,184 (GRCm38) |
missense |
probably damaging |
1.00 |
R7053:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7054:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7055:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7056:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7145:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7146:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7246:Vmn2r111
|
UTSW |
17 |
22,548,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R7259:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7260:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7327:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7401:Vmn2r111
|
UTSW |
17 |
22,571,086 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7514:Vmn2r111
|
UTSW |
17 |
22,548,399 (GRCm38) |
missense |
probably benign |
0.05 |
R7651:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7781:Vmn2r111
|
UTSW |
17 |
22,570,733 (GRCm38) |
missense |
probably benign |
0.17 |
R7816:Vmn2r111
|
UTSW |
17 |
22,573,102 (GRCm38) |
missense |
probably damaging |
0.97 |
R7821:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7838:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R8078:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R8080:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R8117:Vmn2r111
|
UTSW |
17 |
22,571,488 (GRCm38) |
missense |
probably benign |
0.12 |
R8171:Vmn2r111
|
UTSW |
17 |
22,573,092 (GRCm38) |
missense |
probably benign |
0.10 |
R8195:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R8197:Vmn2r111
|
UTSW |
17 |
22,559,051 (GRCm38) |
missense |
possibly damaging |
0.50 |
R8411:Vmn2r111
|
UTSW |
17 |
22,548,581 (GRCm38) |
missense |
probably benign |
0.03 |
R8539:Vmn2r111
|
UTSW |
17 |
22,571,293 (GRCm38) |
missense |
probably benign |
0.23 |
R8540:Vmn2r111
|
UTSW |
17 |
22,559,043 (GRCm38) |
missense |
probably damaging |
1.00 |
R8540:Vmn2r111
|
UTSW |
17 |
22,559,042 (GRCm38) |
critical splice donor site |
probably null |
|
R8557:Vmn2r111
|
UTSW |
17 |
22,571,929 (GRCm38) |
nonsense |
probably null |
|
R8720:Vmn2r111
|
UTSW |
17 |
22,573,213 (GRCm38) |
missense |
possibly damaging |
0.88 |
R8729:Vmn2r111
|
UTSW |
17 |
22,548,258 (GRCm38) |
missense |
probably damaging |
1.00 |
R8843:Vmn2r111
|
UTSW |
17 |
22,548,030 (GRCm38) |
missense |
probably benign |
0.00 |
R9184:Vmn2r111
|
UTSW |
17 |
22,571,841 (GRCm38) |
missense |
probably benign |
|
R9374:Vmn2r111
|
UTSW |
17 |
22,568,878 (GRCm38) |
missense |
probably benign |
0.17 |
R9452:Vmn2r111
|
UTSW |
17 |
22,559,151 (GRCm38) |
missense |
probably damaging |
1.00 |
X0026:Vmn2r111
|
UTSW |
17 |
22,548,695 (GRCm38) |
missense |
probably damaging |
0.98 |
|