Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
A |
G |
1: 58,348,183 (GRCm39) |
I634V |
possibly damaging |
Het |
Atp13a4 |
T |
G |
16: 29,234,595 (GRCm39) |
|
probably benign |
Het |
BC049715 |
A |
T |
6: 136,817,489 (GRCm39) |
Q243L |
probably benign |
Het |
C2cd6 |
G |
A |
1: 59,036,604 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
C |
T |
17: 43,137,251 (GRCm39) |
|
probably null |
Het |
Cd2ap |
T |
A |
17: 43,137,252 (GRCm39) |
|
probably null |
Het |
Cd86 |
G |
A |
16: 36,427,481 (GRCm39) |
R283W |
probably benign |
Het |
CK137956 |
T |
A |
4: 127,840,442 (GRCm39) |
K421N |
probably damaging |
Het |
Coro2b |
G |
A |
9: 62,338,639 (GRCm39) |
T193I |
possibly damaging |
Het |
Dido1 |
G |
A |
2: 180,325,824 (GRCm39) |
|
probably benign |
Het |
Fas |
A |
G |
19: 34,296,003 (GRCm39) |
T149A |
probably benign |
Het |
Gbp4 |
T |
A |
5: 105,273,468 (GRCm39) |
I121F |
probably damaging |
Het |
Hes3 |
C |
T |
4: 152,371,557 (GRCm39) |
A106T |
probably damaging |
Het |
Hyal2 |
T |
C |
9: 107,448,105 (GRCm39) |
Y253H |
probably damaging |
Het |
Kcnt1 |
T |
C |
2: 25,802,731 (GRCm39) |
|
probably null |
Het |
Klhl12 |
C |
A |
1: 134,417,158 (GRCm39) |
R557S |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,600,453 (GRCm39) |
T315A |
probably benign |
Het |
Mchr1 |
A |
G |
15: 81,122,066 (GRCm39) |
Y272C |
probably damaging |
Het |
Mroh7 |
T |
C |
4: 106,538,071 (GRCm39) |
I1202V |
probably benign |
Het |
Mrpl38 |
T |
A |
11: 116,026,140 (GRCm39) |
K87* |
probably null |
Het |
Msh6 |
A |
G |
17: 88,293,140 (GRCm39) |
T632A |
probably damaging |
Het |
Myo9b |
T |
C |
8: 71,808,962 (GRCm39) |
I1767T |
probably damaging |
Het |
Myo9b |
C |
A |
8: 71,807,901 (GRCm39) |
H1630Q |
possibly damaging |
Het |
Naprt |
A |
G |
15: 75,765,648 (GRCm39) |
F92S |
probably damaging |
Het |
Nsd3 |
T |
A |
8: 26,130,668 (GRCm39) |
I11N |
probably damaging |
Het |
Or5ae1 |
A |
G |
7: 84,565,860 (GRCm39) |
Y291C |
probably damaging |
Het |
Otof |
T |
C |
5: 30,556,564 (GRCm39) |
T306A |
probably damaging |
Het |
Pcdh18 |
A |
G |
3: 49,711,279 (GRCm39) |
F12S |
probably benign |
Het |
Pcdhb12 |
A |
T |
18: 37,570,692 (GRCm39) |
N613Y |
probably damaging |
Het |
Polr1a |
T |
C |
6: 71,925,446 (GRCm39) |
I731T |
probably benign |
Het |
Ptprd |
G |
A |
4: 76,046,832 (GRCm39) |
T465I |
probably damaging |
Het |
Rabgap1 |
A |
G |
2: 37,454,773 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,610,311 (GRCm39) |
I607L |
possibly damaging |
Het |
Slc39a9 |
G |
A |
12: 80,720,073 (GRCm39) |
|
probably benign |
Het |
Srek1 |
C |
A |
13: 103,885,293 (GRCm39) |
|
probably benign |
Het |
Ssb |
A |
G |
2: 69,701,147 (GRCm39) |
T377A |
possibly damaging |
Het |
Sympk |
G |
T |
7: 18,777,360 (GRCm39) |
A537S |
probably benign |
Het |
Tcf20 |
A |
G |
15: 82,739,898 (GRCm39) |
S518P |
probably damaging |
Het |
Ttc39d |
A |
G |
17: 80,523,475 (GRCm39) |
K45E |
probably benign |
Het |
Vmn2r69 |
A |
G |
7: 85,061,576 (GRCm39) |
Y133H |
probably damaging |
Het |
Vmn2r79 |
A |
T |
7: 86,686,354 (GRCm39) |
E578D |
probably benign |
Het |
Vwf |
G |
A |
6: 125,567,133 (GRCm39) |
|
probably benign |
Het |
Zbtb11 |
A |
G |
16: 55,811,371 (GRCm39) |
N510D |
probably benign |
Het |
|
Other mutations in Vmn1r40 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01099:Vmn1r40
|
APN |
6 |
89,691,578 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01432:Vmn1r40
|
APN |
6 |
89,691,201 (GRCm39) |
missense |
probably benign |
|
IGL01777:Vmn1r40
|
APN |
6 |
89,691,204 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01908:Vmn1r40
|
APN |
6 |
89,691,285 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01908:Vmn1r40
|
APN |
6 |
89,691,291 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01999:Vmn1r40
|
APN |
6 |
89,691,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02728:Vmn1r40
|
APN |
6 |
89,691,998 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03169:Vmn1r40
|
APN |
6 |
89,692,005 (GRCm39) |
missense |
probably damaging |
0.97 |
R0448:Vmn1r40
|
UTSW |
6 |
89,691,642 (GRCm39) |
missense |
probably benign |
0.23 |
R0971:Vmn1r40
|
UTSW |
6 |
89,691,272 (GRCm39) |
missense |
probably benign |
0.00 |
R1208:Vmn1r40
|
UTSW |
6 |
89,691,326 (GRCm39) |
missense |
probably benign |
0.13 |
R1208:Vmn1r40
|
UTSW |
6 |
89,691,326 (GRCm39) |
missense |
probably benign |
0.13 |
R1448:Vmn1r40
|
UTSW |
6 |
89,691,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Vmn1r40
|
UTSW |
6 |
89,691,297 (GRCm39) |
missense |
probably benign |
0.00 |
R2170:Vmn1r40
|
UTSW |
6 |
89,691,957 (GRCm39) |
missense |
probably benign |
0.11 |
R3151:Vmn1r40
|
UTSW |
6 |
89,691,548 (GRCm39) |
missense |
probably benign |
0.01 |
R3804:Vmn1r40
|
UTSW |
6 |
89,691,991 (GRCm39) |
missense |
probably benign |
0.29 |
R5098:Vmn1r40
|
UTSW |
6 |
89,691,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R6015:Vmn1r40
|
UTSW |
6 |
89,691,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R7216:Vmn1r40
|
UTSW |
6 |
89,691,606 (GRCm39) |
missense |
not run |
|
R7555:Vmn1r40
|
UTSW |
6 |
89,692,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R7591:Vmn1r40
|
UTSW |
6 |
89,691,755 (GRCm39) |
missense |
probably benign |
0.00 |
R9056:Vmn1r40
|
UTSW |
6 |
89,691,198 (GRCm39) |
missense |
probably benign |
0.14 |
R9286:Vmn1r40
|
UTSW |
6 |
89,692,079 (GRCm39) |
missense |
probably benign |
0.03 |
R9344:Vmn1r40
|
UTSW |
6 |
89,691,235 (GRCm39) |
missense |
probably benign |
0.00 |
R9449:Vmn1r40
|
UTSW |
6 |
89,691,854 (GRCm39) |
missense |
probably benign |
0.39 |
|