Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
C |
A |
9: 55,990,132 (GRCm38) |
E272D |
possibly damaging |
Het |
Abi2 |
A |
G |
1: 60,453,651 (GRCm38) |
T158A |
possibly damaging |
Het |
Acacb |
T |
C |
5: 114,216,823 (GRCm38) |
S1221P |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,419,830 (GRCm38) |
D370G |
probably benign |
Het |
Apeh |
A |
G |
9: 108,087,243 (GRCm38) |
I487T |
probably damaging |
Het |
Arid1b |
C |
A |
17: 5,332,533 (GRCm38) |
N1297K |
possibly damaging |
Het |
Ascc3 |
G |
A |
10: 50,699,985 (GRCm38) |
G779S |
probably damaging |
Het |
Atp7b |
A |
C |
8: 22,020,755 (GRCm38) |
|
probably null |
Het |
Bsn |
C |
T |
9: 108,111,314 (GRCm38) |
|
probably benign |
Het |
Caps2 |
C |
T |
10: 112,194,968 (GRCm38) |
Q268* |
probably null |
Het |
Cnfn |
C |
T |
7: 25,367,961 (GRCm38) |
|
probably null |
Het |
Cr2 |
A |
G |
1: 195,168,472 (GRCm38) |
S229P |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,430,995 (GRCm38) |
Y1050C |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,476,123 (GRCm38) |
E307G |
probably damaging |
Het |
Cyb5r3 |
A |
C |
15: 83,160,124 (GRCm38) |
Y182D |
possibly damaging |
Het |
Dclre1a |
A |
T |
19: 56,546,791 (GRCm38) |
H120Q |
probably benign |
Het |
Ddx6 |
T |
C |
9: 44,635,776 (GRCm38) |
I457T |
probably damaging |
Het |
E2f1 |
A |
T |
2: 154,564,476 (GRCm38) |
H93Q |
possibly damaging |
Het |
Fam186a |
T |
C |
15: 99,943,317 (GRCm38) |
K1682R |
possibly damaging |
Het |
Farsb |
A |
G |
1: 78,466,965 (GRCm38) |
|
probably null |
Het |
Flii |
A |
T |
11: 60,721,136 (GRCm38) |
L347Q |
probably damaging |
Het |
Galntl6 |
T |
G |
8: 58,911,441 (GRCm38) |
T12P |
probably damaging |
Het |
Gm11595 |
G |
A |
11: 99,772,555 (GRCm38) |
R100C |
unknown |
Het |
Gm21680 |
T |
C |
5: 25,969,036 (GRCm38) |
N190S |
probably damaging |
Het |
Ifit1bl2 |
T |
C |
19: 34,619,125 (GRCm38) |
S364G |
probably benign |
Het |
Kdm2a |
A |
G |
19: 4,350,317 (GRCm38) |
I234T |
probably damaging |
Het |
Kdm5b |
T |
C |
1: 134,599,207 (GRCm38) |
C356R |
probably damaging |
Het |
Kel |
A |
T |
6: 41,688,851 (GRCm38) |
C174* |
probably null |
Het |
Krt16 |
T |
A |
11: 100,246,676 (GRCm38) |
D401V |
probably damaging |
Het |
Ltb4r1 |
A |
C |
14: 55,767,743 (GRCm38) |
I168L |
probably benign |
Het |
Luzp1 |
T |
A |
4: 136,541,780 (GRCm38) |
M438K |
probably benign |
Het |
Mtf1 |
C |
T |
4: 124,824,352 (GRCm38) |
T281M |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,924,948 (GRCm38) |
S2587T |
probably benign |
Het |
Olfr1311 |
A |
T |
2: 112,021,551 (GRCm38) |
I101N |
probably damaging |
Het |
Olfr1377 |
T |
A |
11: 50,984,786 (GRCm38) |
F28L |
probably benign |
Het |
Olfr532 |
G |
T |
7: 140,419,667 (GRCm38) |
Y35* |
probably null |
Het |
Olfr860 |
T |
C |
9: 19,846,409 (GRCm38) |
D70G |
probably damaging |
Het |
Pcm1 |
T |
A |
8: 41,293,544 (GRCm38) |
F1221Y |
probably benign |
Het |
Pnldc1 |
A |
T |
17: 12,905,864 (GRCm38) |
N90K |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,420,237 (GRCm38) |
L169Q |
probably damaging |
Het |
Ralgps2 |
A |
T |
1: 156,884,574 (GRCm38) |
L147I |
probably damaging |
Het |
Rfx3 |
A |
T |
19: 27,768,609 (GRCm38) |
L674Q |
possibly damaging |
Het |
Rpl3 |
C |
A |
15: 80,082,544 (GRCm38) |
L14F |
probably damaging |
Het |
Rrbp1 |
C |
T |
2: 143,989,555 (GRCm38) |
G231R |
probably damaging |
Het |
Sema3d |
C |
T |
5: 12,571,013 (GRCm38) |
L529F |
probably damaging |
Het |
Slain1 |
A |
T |
14: 103,656,955 (GRCm38) |
T193S |
probably benign |
Het |
Slc2a6 |
G |
T |
2: 27,024,587 (GRCm38) |
Q256K |
possibly damaging |
Het |
Slk |
A |
G |
19: 47,620,183 (GRCm38) |
E525G |
possibly damaging |
Het |
Spsb4 |
G |
T |
9: 96,944,645 (GRCm38) |
Q252K |
probably benign |
Het |
Taf1b |
A |
G |
12: 24,558,257 (GRCm38) |
T552A |
possibly damaging |
Het |
Tmprss15 |
T |
C |
16: 79,006,057 (GRCm38) |
|
probably null |
Het |
Tph2 |
T |
C |
10: 115,179,326 (GRCm38) |
H177R |
probably damaging |
Het |
Ttll1 |
A |
G |
15: 83,489,617 (GRCm38) |
S332P |
probably damaging |
Het |
Twf2 |
T |
G |
9: 106,212,833 (GRCm38) |
N128K |
probably benign |
Het |
Vegfc |
T |
A |
8: 54,181,230 (GRCm38) |
C315S |
probably damaging |
Het |
Wnk2 |
T |
C |
13: 49,061,338 (GRCm38) |
E496G |
probably damaging |
Het |
Zfp148 |
C |
A |
16: 33,497,198 (GRCm38) |
Q705K |
probably damaging |
Het |
Zw10 |
C |
T |
9: 49,073,235 (GRCm38) |
A539V |
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 |
|
IGL02519:Vmn2r111
|
APN |
17 |
22,548,339 (GRCm38) |
missense |
possibly damaging |
0.80 |
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 |
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 |
|