Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
C |
T |
4: 62,450,578 (GRCm39) |
R51W |
probably damaging |
Het |
Abcb1a |
T |
A |
5: 8,752,920 (GRCm39) |
L557Q |
probably damaging |
Het |
Abcb4 |
T |
C |
5: 8,968,662 (GRCm39) |
F334L |
possibly damaging |
Het |
Adamts14 |
T |
A |
10: 61,034,583 (GRCm39) |
T1102S |
probably benign |
Het |
Adamtsl1 |
T |
C |
4: 86,344,102 (GRCm39) |
Y1719H |
probably damaging |
Het |
Adcyap1 |
T |
C |
17: 93,507,550 (GRCm39) |
|
probably null |
Het |
Ankrd13c |
T |
A |
3: 157,677,947 (GRCm39) |
L219Q |
probably damaging |
Het |
Ano3 |
C |
A |
2: 110,711,174 (GRCm39) |
A97S |
probably benign |
Het |
Apaf1 |
T |
C |
10: 90,898,022 (GRCm39) |
N245S |
probably benign |
Het |
Apob |
A |
G |
12: 8,056,047 (GRCm39) |
T1510A |
probably benign |
Het |
Apob |
A |
G |
12: 8,061,937 (GRCm39) |
D3473G |
possibly damaging |
Het |
Arfgap3 |
G |
A |
15: 83,191,138 (GRCm39) |
T12I |
probably benign |
Het |
Bend4 |
A |
G |
5: 67,557,418 (GRCm39) |
V466A |
probably damaging |
Het |
Bend7 |
G |
A |
2: 4,749,239 (GRCm39) |
E119K |
probably damaging |
Het |
Capn5 |
G |
T |
7: 97,781,049 (GRCm39) |
R243S |
possibly damaging |
Het |
Cd84 |
A |
G |
1: 171,679,510 (GRCm39) |
I63V |
probably benign |
Het |
Cd86 |
T |
A |
16: 36,449,350 (GRCm39) |
T16S |
probably benign |
Het |
Cdc42bpb |
A |
G |
12: 111,262,734 (GRCm39) |
|
probably benign |
Het |
Cep20 |
G |
A |
16: 14,122,380 (GRCm39) |
T128I |
possibly damaging |
Het |
Cep95 |
C |
T |
11: 106,708,781 (GRCm39) |
S26L |
probably damaging |
Het |
Cldn19 |
C |
T |
4: 119,112,810 (GRCm39) |
A14V |
probably damaging |
Het |
Cluap1 |
T |
A |
16: 3,755,453 (GRCm39) |
M356K |
probably damaging |
Het |
Coq7 |
C |
T |
7: 118,109,260 (GRCm39) |
G263S |
unknown |
Het |
Ctnnd2 |
A |
C |
15: 30,847,445 (GRCm39) |
T679P |
probably damaging |
Het |
Dnah10 |
A |
G |
5: 124,820,750 (GRCm39) |
D528G |
possibly damaging |
Het |
Dvl1 |
T |
A |
4: 155,938,476 (GRCm39) |
N133K |
probably damaging |
Het |
Efcab7 |
T |
G |
4: 99,769,744 (GRCm39) |
H550Q |
probably null |
Het |
Fastkd5 |
C |
T |
2: 130,456,717 (GRCm39) |
M624I |
probably damaging |
Het |
Fbxo42 |
T |
C |
4: 140,895,073 (GRCm39) |
V12A |
probably benign |
Het |
Gabarapl1 |
T |
A |
6: 129,515,635 (GRCm39) |
M91K |
possibly damaging |
Het |
Gas7 |
A |
G |
11: 67,552,902 (GRCm39) |
N154S |
probably damaging |
Het |
Gm21814 |
T |
A |
6: 149,483,650 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
G |
A |
14: 30,739,803 (GRCm39) |
R12C |
probably damaging |
Het |
Golga2 |
T |
G |
2: 32,187,807 (GRCm39) |
|
probably null |
Het |
Grk3 |
T |
A |
5: 113,062,878 (GRCm39) |
R656S |
probably benign |
Het |
Gsap |
T |
A |
5: 21,412,236 (GRCm39) |
|
probably benign |
Het |
H60c |
T |
C |
10: 3,210,240 (GRCm39) |
Q103R |
probably benign |
Het |
Hnrnpr |
T |
A |
4: 136,056,755 (GRCm39) |
S252T |
probably damaging |
Het |
Itgb4 |
A |
T |
11: 115,869,937 (GRCm39) |
T40S |
probably benign |
Het |
Krtap27-1 |
T |
C |
16: 88,468,302 (GRCm39) |
N81D |
probably benign |
Het |
Lilrb4a |
T |
A |
10: 51,367,683 (GRCm39) |
L75Q |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,290,821 (GRCm39) |
E3546D |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,313,738 (GRCm39) |
D2331V |
probably damaging |
Het |
Lzts2 |
T |
A |
19: 45,009,893 (GRCm39) |
V9E |
probably damaging |
Het |
Matr3 |
T |
A |
18: 35,717,709 (GRCm39) |
D302E |
probably benign |
Het |
Mcoln2 |
A |
G |
3: 145,897,979 (GRCm39) |
|
probably null |
Het |
Metap2 |
T |
C |
10: 93,704,811 (GRCm39) |
D272G |
probably damaging |
Het |
Mitf |
A |
G |
6: 97,987,428 (GRCm39) |
D337G |
probably damaging |
Het |
Mrtfb |
T |
C |
16: 13,219,433 (GRCm39) |
V693A |
possibly damaging |
Het |
Msh2 |
A |
G |
17: 87,985,771 (GRCm39) |
E116G |
probably benign |
Het |
Nlrp10 |
T |
A |
7: 108,523,555 (GRCm39) |
M642L |
probably benign |
Het |
Noxa1 |
G |
T |
2: 24,982,558 (GRCm39) |
Q86K |
probably benign |
Het |
Nrap |
T |
C |
19: 56,372,562 (GRCm39) |
T48A |
probably benign |
Het |
Nup160 |
T |
A |
2: 90,520,494 (GRCm39) |
H308Q |
probably damaging |
Het |
Osbpl11 |
T |
C |
16: 33,056,699 (GRCm39) |
L711P |
probably damaging |
Het |
Osbpl6 |
A |
G |
2: 76,385,409 (GRCm39) |
N281S |
probably benign |
Het |
Pcnp |
C |
T |
16: 55,844,703 (GRCm39) |
E66K |
possibly damaging |
Het |
Phf11 |
T |
A |
14: 59,482,227 (GRCm39) |
E175D |
probably damaging |
Het |
Pik3cg |
A |
G |
12: 32,254,983 (GRCm39) |
Y335H |
probably damaging |
Het |
Plekhg4 |
T |
C |
8: 106,108,431 (GRCm39) |
L1053S |
probably damaging |
Het |
Plekhh2 |
G |
T |
17: 84,918,203 (GRCm39) |
E1271* |
probably null |
Het |
Ppp2r2b |
T |
A |
18: 42,871,055 (GRCm39) |
Y82F |
probably damaging |
Het |
Prkd3 |
T |
C |
17: 79,278,796 (GRCm39) |
D430G |
probably damaging |
Het |
Prl7d1 |
C |
T |
13: 27,893,240 (GRCm39) |
D224N |
possibly damaging |
Het |
Ptpdc1 |
A |
T |
13: 48,740,173 (GRCm39) |
N419K |
possibly damaging |
Het |
Serinc5 |
T |
A |
13: 92,797,695 (GRCm39) |
|
probably null |
Het |
Sipa1 |
A |
G |
19: 5,701,692 (GRCm39) |
L981P |
probably damaging |
Het |
Slc16a7 |
A |
T |
10: 125,066,489 (GRCm39) |
C383* |
probably null |
Het |
Slc19a1 |
C |
G |
10: 76,878,369 (GRCm39) |
Y301* |
probably null |
Het |
Slc22a14 |
A |
T |
9: 119,052,827 (GRCm39) |
V14E |
possibly damaging |
Het |
Slpi |
C |
A |
2: 164,196,837 (GRCm39) |
C95F |
probably damaging |
Het |
Smurf2 |
G |
A |
11: 106,743,333 (GRCm39) |
H225Y |
possibly damaging |
Het |
Son |
T |
C |
16: 91,452,230 (GRCm39) |
S326P |
possibly damaging |
Het |
Sptb |
T |
A |
12: 76,658,657 (GRCm39) |
K1262M |
probably benign |
Het |
Sugp2 |
T |
A |
8: 70,696,714 (GRCm39) |
|
probably benign |
Het |
Tatdn2 |
T |
A |
6: 113,687,031 (GRCm39) |
H747Q |
probably damaging |
Het |
Tcn2 |
C |
A |
11: 3,877,516 (GRCm39) |
R44L |
probably benign |
Het |
Tenm3 |
G |
A |
8: 48,689,006 (GRCm39) |
R2194C |
probably damaging |
Het |
Tnks2 |
T |
A |
19: 36,822,931 (GRCm39) |
|
probably benign |
Het |
Top3a |
A |
T |
11: 60,650,188 (GRCm39) |
I120N |
probably damaging |
Het |
Umodl1 |
T |
A |
17: 31,201,232 (GRCm39) |
|
probably benign |
Het |
Umodl1 |
T |
C |
17: 31,205,478 (GRCm39) |
V662A |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,595,048 (GRCm39) |
S3827P |
probably benign |
Het |
Vasn |
T |
A |
16: 4,466,473 (GRCm39) |
|
probably null |
Het |
Vmn2r79 |
C |
A |
7: 86,687,002 (GRCm39) |
H794Q |
probably benign |
Het |
|
Other mutations in Vmn2r69 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01019:Vmn2r69
|
APN |
7 |
85,055,739 (GRCm39) |
missense |
probably benign |
|
IGL01457:Vmn2r69
|
APN |
7 |
85,055,836 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01760:Vmn2r69
|
APN |
7 |
85,056,072 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01834:Vmn2r69
|
APN |
7 |
85,061,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02001:Vmn2r69
|
APN |
7 |
85,056,434 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02057:Vmn2r69
|
APN |
7 |
85,060,990 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02289:Vmn2r69
|
APN |
7 |
85,056,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02472:Vmn2r69
|
APN |
7 |
85,058,960 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02478:Vmn2r69
|
APN |
7 |
85,055,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02554:Vmn2r69
|
APN |
7 |
85,059,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02723:Vmn2r69
|
APN |
7 |
85,059,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Vmn2r69
|
UTSW |
7 |
85,060,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R0560:Vmn2r69
|
UTSW |
7 |
85,058,922 (GRCm39) |
critical splice donor site |
probably null |
|
R0909:Vmn2r69
|
UTSW |
7 |
85,055,873 (GRCm39) |
missense |
probably benign |
0.00 |
R0976:Vmn2r69
|
UTSW |
7 |
85,056,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1158:Vmn2r69
|
UTSW |
7 |
85,059,058 (GRCm39) |
splice site |
probably benign |
|
R1482:Vmn2r69
|
UTSW |
7 |
85,056,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Vmn2r69
|
UTSW |
7 |
85,060,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R2016:Vmn2r69
|
UTSW |
7 |
85,056,493 (GRCm39) |
missense |
probably damaging |
0.98 |
R2108:Vmn2r69
|
UTSW |
7 |
85,059,404 (GRCm39) |
missense |
probably benign |
|
R2571:Vmn2r69
|
UTSW |
7 |
85,064,764 (GRCm39) |
missense |
probably benign |
|
R2910:Vmn2r69
|
UTSW |
7 |
85,055,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2920:Vmn2r69
|
UTSW |
7 |
85,060,973 (GRCm39) |
missense |
probably benign |
0.08 |
R3708:Vmn2r69
|
UTSW |
7 |
85,061,029 (GRCm39) |
missense |
probably damaging |
0.98 |
R3710:Vmn2r69
|
UTSW |
7 |
85,055,601 (GRCm39) |
missense |
probably benign |
|
R4757:Vmn2r69
|
UTSW |
7 |
85,061,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R4823:Vmn2r69
|
UTSW |
7 |
85,060,508 (GRCm39) |
missense |
probably benign |
0.21 |
R4870:Vmn2r69
|
UTSW |
7 |
85,060,793 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4918:Vmn2r69
|
UTSW |
7 |
85,055,967 (GRCm39) |
missense |
probably benign |
0.06 |
R5022:Vmn2r69
|
UTSW |
7 |
85,060,367 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5174:Vmn2r69
|
UTSW |
7 |
85,064,739 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5200:Vmn2r69
|
UTSW |
7 |
85,055,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R5278:Vmn2r69
|
UTSW |
7 |
85,060,991 (GRCm39) |
missense |
probably benign |
0.02 |
R5643:Vmn2r69
|
UTSW |
7 |
85,056,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R5996:Vmn2r69
|
UTSW |
7 |
85,061,117 (GRCm39) |
splice site |
probably null |
|
R6083:Vmn2r69
|
UTSW |
7 |
85,055,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R6140:Vmn2r69
|
UTSW |
7 |
85,060,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R6306:Vmn2r69
|
UTSW |
7 |
85,064,799 (GRCm39) |
missense |
probably benign |
0.04 |
R6330:Vmn2r69
|
UTSW |
7 |
85,060,835 (GRCm39) |
missense |
probably benign |
|
R6380:Vmn2r69
|
UTSW |
7 |
85,061,067 (GRCm39) |
missense |
probably benign |
|
R6466:Vmn2r69
|
UTSW |
7 |
85,056,378 (GRCm39) |
missense |
probably benign |
0.01 |
R6542:Vmn2r69
|
UTSW |
7 |
85,060,413 (GRCm39) |
nonsense |
probably null |
|
R6583:Vmn2r69
|
UTSW |
7 |
85,059,017 (GRCm39) |
missense |
probably benign |
|
R6623:Vmn2r69
|
UTSW |
7 |
85,056,309 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6709:Vmn2r69
|
UTSW |
7 |
85,061,069 (GRCm39) |
missense |
probably benign |
0.03 |
R6732:Vmn2r69
|
UTSW |
7 |
85,060,351 (GRCm39) |
missense |
probably benign |
0.00 |
R6741:Vmn2r69
|
UTSW |
7 |
85,061,724 (GRCm39) |
missense |
probably benign |
0.01 |
R7070:Vmn2r69
|
UTSW |
7 |
85,060,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R7234:Vmn2r69
|
UTSW |
7 |
85,056,315 (GRCm39) |
missense |
probably benign |
0.22 |
R7323:Vmn2r69
|
UTSW |
7 |
85,060,972 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7427:Vmn2r69
|
UTSW |
7 |
85,060,467 (GRCm39) |
missense |
probably benign |
0.28 |
R7428:Vmn2r69
|
UTSW |
7 |
85,060,467 (GRCm39) |
missense |
probably benign |
0.28 |
R7453:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
frame shift |
probably null |
|
R7532:Vmn2r69
|
UTSW |
7 |
85,059,622 (GRCm39) |
missense |
probably benign |
0.36 |
R7556:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
frame shift |
probably null |
|
R7562:Vmn2r69
|
UTSW |
7 |
85,056,420 (GRCm39) |
missense |
probably benign |
|
R7592:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
frame shift |
probably null |
|
R7708:Vmn2r69
|
UTSW |
7 |
85,061,755 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7803:Vmn2r69
|
UTSW |
7 |
85,056,324 (GRCm39) |
missense |
probably benign |
0.00 |
R7960:Vmn2r69
|
UTSW |
7 |
85,055,973 (GRCm39) |
missense |
probably benign |
|
R7966:Vmn2r69
|
UTSW |
7 |
85,060,762 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8071:Vmn2r69
|
UTSW |
7 |
85,055,713 (GRCm39) |
nonsense |
probably null |
|
R8237:Vmn2r69
|
UTSW |
7 |
85,060,340 (GRCm39) |
missense |
probably benign |
0.02 |
R8347:Vmn2r69
|
UTSW |
7 |
85,064,838 (GRCm39) |
missense |
probably benign |
0.00 |
R8737:Vmn2r69
|
UTSW |
7 |
85,055,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Vmn2r69
|
UTSW |
7 |
85,064,883 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R8831:Vmn2r69
|
UTSW |
7 |
85,059,018 (GRCm39) |
nonsense |
probably null |
|
R8856:Vmn2r69
|
UTSW |
7 |
85,061,663 (GRCm39) |
missense |
probably benign |
0.00 |
R8998:Vmn2r69
|
UTSW |
7 |
85,060,307 (GRCm39) |
missense |
probably benign |
0.33 |
R8999:Vmn2r69
|
UTSW |
7 |
85,060,307 (GRCm39) |
missense |
probably benign |
0.33 |
R9161:Vmn2r69
|
UTSW |
7 |
85,056,177 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9228:Vmn2r69
|
UTSW |
7 |
85,064,697 (GRCm39) |
missense |
probably benign |
0.01 |
R9494:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R9494:Vmn2r69
|
UTSW |
7 |
85,056,084 (GRCm39) |
missense |
probably benign |
0.08 |
R9541:Vmn2r69
|
UTSW |
7 |
85,056,209 (GRCm39) |
missense |
probably benign |
|
R9620:Vmn2r69
|
UTSW |
7 |
85,061,504 (GRCm39) |
missense |
probably benign |
0.10 |
Z1176:Vmn2r69
|
UTSW |
7 |
85,055,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|