Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
T |
G |
13: 81,709,593 (GRCm39) |
E1133D |
probably damaging |
Het |
Ankrd13b |
A |
T |
11: 77,363,335 (GRCm39) |
D505E |
probably benign |
Het |
Ano1 |
C |
T |
7: 144,192,289 (GRCm39) |
E361K |
probably damaging |
Het |
Arap3 |
T |
A |
18: 38,107,495 (GRCm39) |
K1341* |
probably null |
Het |
Arhgef17 |
A |
C |
7: 100,579,198 (GRCm39) |
Y583* |
probably null |
Het |
Ash1l |
G |
A |
3: 88,892,647 (GRCm39) |
E1509K |
probably damaging |
Het |
B430305J03Rik |
T |
G |
3: 61,271,681 (GRCm39) |
R21S |
unknown |
Het |
Bbof1 |
A |
G |
12: 84,473,609 (GRCm39) |
E313G |
probably damaging |
Het |
Catsperb |
C |
T |
12: 101,475,497 (GRCm39) |
T347I |
probably benign |
Het |
Ccdc24 |
G |
T |
4: 117,729,201 (GRCm39) |
A92D |
probably damaging |
Het |
Ccdc63 |
T |
C |
5: 122,249,073 (GRCm39) |
T419A |
probably benign |
Het |
Ccdc7a |
C |
T |
8: 129,618,866 (GRCm39) |
V893I |
possibly damaging |
Het |
Ccdc88b |
G |
T |
19: 6,831,330 (GRCm39) |
D537E |
probably benign |
Het |
Cd276 |
T |
C |
9: 58,444,615 (GRCm39) |
S119G |
probably damaging |
Het |
Cdkn3 |
T |
C |
14: 47,004,647 (GRCm39) |
Y70H |
possibly damaging |
Het |
Cdo1 |
G |
A |
18: 46,861,266 (GRCm39) |
|
probably benign |
Het |
Cdr2 |
A |
T |
7: 120,581,247 (GRCm39) |
F10Y |
probably damaging |
Het |
Cep290 |
A |
T |
10: 100,374,865 (GRCm39) |
K1370N |
possibly damaging |
Het |
Crb1 |
T |
A |
1: 139,176,049 (GRCm39) |
I645F |
probably damaging |
Het |
Cul7 |
T |
C |
17: 46,969,657 (GRCm39) |
W975R |
probably damaging |
Het |
Ddx39b |
A |
C |
17: 35,471,826 (GRCm39) |
E324A |
probably benign |
Het |
Diaph1 |
T |
G |
18: 38,022,867 (GRCm39) |
|
probably null |
Het |
Dnah2 |
G |
A |
11: 69,321,318 (GRCm39) |
R3917* |
probably null |
Het |
Dnph1 |
T |
A |
17: 46,807,815 (GRCm39) |
L27Q |
probably damaging |
Het |
Duox2 |
A |
G |
2: 122,119,788 (GRCm39) |
F880S |
probably damaging |
Het |
Ell2 |
C |
A |
13: 75,910,006 (GRCm39) |
L119M |
probably damaging |
Het |
Enpep |
A |
T |
3: 129,106,319 (GRCm39) |
Y302* |
probably null |
Het |
Ergic2 |
G |
T |
6: 148,096,707 (GRCm39) |
H186Q |
probably damaging |
Het |
Fam83b |
T |
C |
9: 76,453,031 (GRCm39) |
D12G |
probably benign |
Het |
Fbxw16 |
A |
T |
9: 109,270,123 (GRCm39) |
V206D |
probably damaging |
Het |
Fhod1 |
A |
T |
8: 106,063,771 (GRCm39) |
V278D |
unknown |
Het |
Gba2 |
G |
C |
4: 43,573,753 (GRCm39) |
Q180E |
probably damaging |
Het |
Grhl3 |
G |
A |
4: 135,300,723 (GRCm39) |
L5F |
probably benign |
Het |
H2-T15 |
A |
T |
17: 36,369,235 (GRCm39) |
C7S |
unknown |
Het |
Ifit1bl1 |
C |
T |
19: 34,576,667 (GRCm39) |
|
probably null |
Het |
Ift57 |
A |
G |
16: 49,584,230 (GRCm39) |
T413A |
probably benign |
Het |
Itga2 |
A |
G |
13: 114,996,149 (GRCm39) |
F714S |
probably damaging |
Het |
Jmy |
A |
G |
13: 93,577,841 (GRCm39) |
S776P |
probably benign |
Het |
Kbtbd8 |
G |
A |
6: 95,098,814 (GRCm39) |
A108T |
probably damaging |
Het |
Kpna6 |
G |
A |
4: 129,548,139 (GRCm39) |
A230V |
probably damaging |
Het |
Lrfn1 |
C |
T |
7: 28,159,397 (GRCm39) |
L439F |
possibly damaging |
Het |
Lrrc1 |
T |
A |
9: 77,375,847 (GRCm39) |
I147F |
probably benign |
Het |
Lrrc7 |
C |
T |
3: 157,832,884 (GRCm39) |
G1425R |
probably damaging |
Het |
Madd |
T |
A |
2: 90,992,854 (GRCm39) |
I1022F |
probably damaging |
Het |
Map2k2 |
A |
T |
10: 80,942,017 (GRCm39) |
T13S |
probably benign |
Het |
Mdc1 |
G |
A |
17: 36,164,960 (GRCm39) |
V1459I |
probably benign |
Het |
Mdh1b |
G |
A |
1: 63,760,719 (GRCm39) |
T114M |
probably damaging |
Het |
Mfsd2a |
T |
C |
4: 122,845,088 (GRCm39) |
I208V |
possibly damaging |
Het |
Mmrn1 |
T |
A |
6: 60,965,411 (GRCm39) |
D1147E |
probably damaging |
Het |
Nbeal2 |
T |
A |
9: 110,455,177 (GRCm39) |
I2574F |
probably damaging |
Het |
Nr1d1 |
T |
G |
11: 98,662,892 (GRCm39) |
S34R |
probably damaging |
Het |
Nr3c1 |
A |
T |
18: 39,619,449 (GRCm39) |
D279E |
probably benign |
Het |
Nrde2 |
T |
C |
12: 100,098,747 (GRCm39) |
D640G |
probably benign |
Het |
Odf4 |
A |
G |
11: 68,817,514 (GRCm39) |
L58P |
probably damaging |
Het |
Or4k41 |
A |
T |
2: 111,279,631 (GRCm39) |
I49F |
probably benign |
Het |
Or4p22 |
A |
T |
2: 88,317,651 (GRCm39) |
I192F |
probably benign |
Het |
Otud6b |
A |
C |
4: 14,811,743 (GRCm39) |
M300R |
probably damaging |
Het |
Pamr1 |
T |
A |
2: 102,471,280 (GRCm39) |
D534E |
probably benign |
Het |
Pcdh7 |
T |
A |
5: 57,878,299 (GRCm39) |
V618E |
probably benign |
Het |
Pcgf6 |
A |
C |
19: 47,031,226 (GRCm39) |
N266K |
possibly damaging |
Het |
Plcz1 |
A |
T |
6: 139,968,849 (GRCm39) |
Y196* |
probably null |
Het |
Plxna1 |
A |
T |
6: 89,334,311 (GRCm39) |
L106Q |
probably damaging |
Het |
Qrich2 |
G |
A |
11: 116,337,701 (GRCm39) |
A184V |
probably damaging |
Het |
Rimkla |
A |
G |
4: 119,325,275 (GRCm39) |
L378S |
probably benign |
Het |
Rufy1 |
G |
T |
11: 50,295,290 (GRCm39) |
H472Q |
probably benign |
Het |
Samd7 |
T |
A |
3: 30,810,631 (GRCm39) |
M216K |
probably benign |
Het |
Samd9l |
A |
T |
6: 3,375,856 (GRCm39) |
Y468* |
probably null |
Het |
Scn2a |
T |
G |
2: 65,558,787 (GRCm39) |
L1194R |
probably benign |
Het |
Sgo2a |
T |
A |
1: 58,056,944 (GRCm39) |
S1043T |
possibly damaging |
Het |
Slc6a17 |
G |
T |
3: 107,378,755 (GRCm39) |
H642Q |
probably benign |
Het |
Smox |
C |
T |
2: 131,364,031 (GRCm39) |
A45V |
possibly damaging |
Het |
St6galnac3 |
T |
A |
3: 153,117,274 (GRCm39) |
T150S |
possibly damaging |
Het |
Strip2 |
T |
A |
6: 29,941,911 (GRCm39) |
I627N |
possibly damaging |
Het |
Sv2c |
A |
T |
13: 96,224,758 (GRCm39) |
C184S |
probably damaging |
Het |
Tm7sf2 |
A |
T |
19: 6,116,527 (GRCm39) |
|
probably null |
Het |
Ttc28 |
T |
C |
5: 111,371,282 (GRCm39) |
I608T |
possibly damaging |
Het |
Vmn1r183 |
T |
G |
7: 23,754,926 (GRCm39) |
L243R |
probably damaging |
Het |
Vmn1r68 |
T |
C |
7: 10,261,778 (GRCm39) |
T107A |
probably benign |
Het |
Zfp516 |
T |
A |
18: 83,006,325 (GRCm39) |
|
probably null |
Het |
Zpbp2 |
A |
G |
11: 98,443,335 (GRCm39) |
D56G |
probably damaging |
Het |
|
Other mutations in Vnn3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00675:Vnn3
|
APN |
10 |
23,743,066 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01300:Vnn3
|
APN |
10 |
23,740,263 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01349:Vnn3
|
APN |
10 |
23,727,814 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02491:Vnn3
|
APN |
10 |
23,741,816 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03256:Vnn3
|
APN |
10 |
23,727,698 (GRCm39) |
splice site |
probably benign |
|
IGL03289:Vnn3
|
APN |
10 |
23,741,735 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02799:Vnn3
|
UTSW |
10 |
23,727,869 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0599:Vnn3
|
UTSW |
10 |
23,741,603 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1703:Vnn3
|
UTSW |
10 |
23,741,828 (GRCm39) |
missense |
probably benign |
|
R1753:Vnn3
|
UTSW |
10 |
23,741,718 (GRCm39) |
missense |
probably benign |
0.27 |
R2119:Vnn3
|
UTSW |
10 |
23,740,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R2288:Vnn3
|
UTSW |
10 |
23,740,354 (GRCm39) |
missense |
probably benign |
0.03 |
R4255:Vnn3
|
UTSW |
10 |
23,741,720 (GRCm39) |
missense |
probably benign |
0.18 |
R4458:Vnn3
|
UTSW |
10 |
23,741,567 (GRCm39) |
missense |
probably benign |
0.23 |
R4518:Vnn3
|
UTSW |
10 |
23,743,124 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4545:Vnn3
|
UTSW |
10 |
23,732,224 (GRCm39) |
missense |
probably benign |
0.00 |
R4723:Vnn3
|
UTSW |
10 |
23,727,589 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4791:Vnn3
|
UTSW |
10 |
23,740,519 (GRCm39) |
missense |
probably benign |
|
R4921:Vnn3
|
UTSW |
10 |
23,740,473 (GRCm39) |
missense |
probably benign |
0.01 |
R5152:Vnn3
|
UTSW |
10 |
23,740,237 (GRCm39) |
missense |
probably benign |
0.01 |
R5390:Vnn3
|
UTSW |
10 |
23,727,483 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R5545:Vnn3
|
UTSW |
10 |
23,742,992 (GRCm39) |
missense |
probably benign |
0.00 |
R6197:Vnn3
|
UTSW |
10 |
23,732,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Vnn3
|
UTSW |
10 |
23,745,523 (GRCm39) |
missense |
probably benign |
0.00 |
R6846:Vnn3
|
UTSW |
10 |
23,727,620 (GRCm39) |
missense |
probably benign |
|
R6917:Vnn3
|
UTSW |
10 |
23,741,832 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7100:Vnn3
|
UTSW |
10 |
23,741,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R7152:Vnn3
|
UTSW |
10 |
23,727,513 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7336:Vnn3
|
UTSW |
10 |
23,727,806 (GRCm39) |
missense |
probably benign |
0.42 |
R7421:Vnn3
|
UTSW |
10 |
23,741,666 (GRCm39) |
missense |
probably benign |
0.06 |
R7875:Vnn3
|
UTSW |
10 |
23,743,146 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8353:Vnn3
|
UTSW |
10 |
23,745,443 (GRCm39) |
missense |
probably benign |
0.01 |
R8453:Vnn3
|
UTSW |
10 |
23,745,443 (GRCm39) |
missense |
probably benign |
0.01 |
R8465:Vnn3
|
UTSW |
10 |
23,741,780 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9105:Vnn3
|
UTSW |
10 |
23,740,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Vnn3
|
UTSW |
10 |
23,741,607 (GRCm39) |
missense |
probably damaging |
0.97 |
R9441:Vnn3
|
UTSW |
10 |
23,740,498 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9718:Vnn3
|
UTSW |
10 |
23,745,454 (GRCm39) |
nonsense |
probably null |
|
R9737:Vnn3
|
UTSW |
10 |
23,741,813 (GRCm39) |
missense |
probably benign |
0.02 |
|