Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
A |
6: 146,853,914 (GRCm39) |
N248Y |
possibly damaging |
Het |
Adamts13 |
G |
A |
2: 26,868,023 (GRCm39) |
V128M |
probably damaging |
Het |
Agl |
A |
T |
3: 116,566,175 (GRCm39) |
|
probably benign |
Het |
Arfgef1 |
A |
T |
1: 10,224,621 (GRCm39) |
M1405K |
probably damaging |
Het |
Atp6v1a |
G |
T |
16: 43,920,319 (GRCm39) |
L426M |
probably damaging |
Het |
Calhm6 |
A |
G |
10: 34,002,561 (GRCm39) |
V174A |
probably damaging |
Het |
Cdc123 |
A |
G |
2: 5,808,752 (GRCm39) |
|
probably benign |
Het |
Cept1 |
A |
G |
3: 106,438,444 (GRCm39) |
|
probably benign |
Het |
Cipc |
T |
A |
12: 87,007,047 (GRCm39) |
D60E |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,581,747 (GRCm39) |
S30P |
probably benign |
Het |
Exosc3 |
A |
G |
4: 45,319,659 (GRCm39) |
I121T |
probably benign |
Het |
Fbln5 |
A |
G |
12: 101,776,128 (GRCm39) |
Y89H |
probably damaging |
Het |
Fhod3 |
T |
C |
18: 25,030,738 (GRCm39) |
F128L |
probably damaging |
Het |
Fhod3 |
T |
A |
18: 25,037,005 (GRCm39) |
I154N |
probably damaging |
Het |
Fpgt |
T |
C |
3: 154,792,483 (GRCm39) |
T515A |
probably benign |
Het |
Gas2l2 |
G |
A |
11: 83,312,906 (GRCm39) |
T802I |
probably benign |
Het |
Gm10710 |
T |
A |
3: 83,035,156 (GRCm39) |
|
probably benign |
Het |
Hdac4 |
A |
G |
1: 91,861,417 (GRCm39) |
M1051T |
probably benign |
Het |
Heatr5b |
A |
G |
17: 79,115,909 (GRCm39) |
V849A |
probably damaging |
Het |
Helb |
T |
C |
10: 119,938,738 (GRCm39) |
I579V |
probably damaging |
Het |
Hspa1l |
A |
G |
17: 35,197,787 (GRCm39) |
I609V |
probably benign |
Het |
Itgam |
C |
A |
7: 127,670,115 (GRCm39) |
Q136K |
probably benign |
Het |
Kcnc1 |
T |
C |
7: 46,077,554 (GRCm39) |
L452P |
probably damaging |
Het |
Ltbp4 |
T |
A |
7: 27,019,071 (GRCm39) |
T1083S |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,300,686 (GRCm39) |
I1449M |
probably damaging |
Het |
Nalf1 |
A |
T |
8: 9,257,831 (GRCm39) |
V439E |
probably damaging |
Het |
P2rx5 |
T |
A |
11: 73,056,385 (GRCm39) |
V103E |
probably damaging |
Het |
Pals1 |
T |
C |
12: 78,877,681 (GRCm39) |
V531A |
possibly damaging |
Het |
Pappa |
A |
G |
4: 65,123,329 (GRCm39) |
D888G |
possibly damaging |
Het |
Pcdhb21 |
G |
T |
18: 37,647,958 (GRCm39) |
M362I |
probably benign |
Het |
Pde1a |
A |
G |
2: 79,705,628 (GRCm39) |
S333P |
probably damaging |
Het |
Ppm1j |
A |
G |
3: 104,691,408 (GRCm39) |
T299A |
probably damaging |
Het |
Pramel46 |
G |
A |
5: 95,418,510 (GRCm39) |
T162I |
probably benign |
Het |
Ptdss2 |
A |
G |
7: 140,732,749 (GRCm39) |
E168G |
probably damaging |
Het |
Rspry1 |
A |
G |
8: 95,376,444 (GRCm39) |
N322S |
probably benign |
Het |
Slc7a9 |
T |
A |
7: 35,156,485 (GRCm39) |
V309E |
probably damaging |
Het |
Slco6c1 |
A |
G |
1: 97,003,548 (GRCm39) |
|
probably benign |
Het |
Tas2r120 |
T |
A |
6: 132,634,227 (GRCm39) |
M103K |
probably damaging |
Het |
Tbxas1 |
T |
A |
6: 38,925,561 (GRCm39) |
F59I |
probably damaging |
Het |
Tfpi |
A |
G |
2: 84,274,378 (GRCm39) |
S203P |
probably benign |
Het |
Tram2 |
T |
C |
1: 21,074,083 (GRCm39) |
N285S |
possibly damaging |
Het |
Trio |
T |
A |
15: 27,846,896 (GRCm39) |
D980V |
probably damaging |
Het |
Trpv5 |
T |
A |
6: 41,637,229 (GRCm39) |
H419L |
probably damaging |
Het |
Usp28 |
C |
T |
9: 48,943,543 (GRCm39) |
R361* |
probably null |
Het |
Vmn2r12 |
A |
T |
5: 109,240,025 (GRCm39) |
N179K |
probably benign |
Het |
Vmn2r82 |
G |
T |
10: 79,214,691 (GRCm39) |
A225S |
probably benign |
Het |
Zcchc4 |
A |
G |
5: 52,965,698 (GRCm39) |
Y334C |
probably damaging |
Het |
Zfp609 |
T |
C |
9: 65,610,116 (GRCm39) |
E949G |
possibly damaging |
Het |
|
Other mutations in Vmn1r6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00905:Vmn1r6
|
APN |
6 |
56,979,789 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Vmn1r6
|
APN |
6 |
56,979,529 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01147:Vmn1r6
|
APN |
6 |
56,979,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01475:Vmn1r6
|
APN |
6 |
56,979,896 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01638:Vmn1r6
|
APN |
6 |
56,980,177 (GRCm39) |
nonsense |
probably null |
|
IGL01876:Vmn1r6
|
APN |
6 |
56,979,446 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01988:Vmn1r6
|
APN |
6 |
56,979,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R0531:Vmn1r6
|
UTSW |
6 |
56,979,583 (GRCm39) |
missense |
probably benign |
0.00 |
R1495:Vmn1r6
|
UTSW |
6 |
56,980,058 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1733:Vmn1r6
|
UTSW |
6 |
56,979,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Vmn1r6
|
UTSW |
6 |
56,980,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R3625:Vmn1r6
|
UTSW |
6 |
56,979,920 (GRCm39) |
missense |
probably damaging |
0.96 |
R4353:Vmn1r6
|
UTSW |
6 |
56,979,677 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4484:Vmn1r6
|
UTSW |
6 |
56,980,174 (GRCm39) |
missense |
probably benign |
|
R4854:Vmn1r6
|
UTSW |
6 |
56,979,683 (GRCm39) |
missense |
probably benign |
0.00 |
R5237:Vmn1r6
|
UTSW |
6 |
56,980,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R5341:Vmn1r6
|
UTSW |
6 |
56,979,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R5611:Vmn1r6
|
UTSW |
6 |
56,979,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Vmn1r6
|
UTSW |
6 |
56,979,422 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8423:Vmn1r6
|
UTSW |
6 |
56,979,495 (GRCm39) |
missense |
probably benign |
0.30 |
R9249:Vmn1r6
|
UTSW |
6 |
56,979,760 (GRCm39) |
missense |
probably benign |
|
R9582:Vmn1r6
|
UTSW |
6 |
56,979,925 (GRCm39) |
missense |
probably benign |
|
|