Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,315,342 (GRCm39) |
N1860D |
probably benign |
Het |
Abca2 |
T |
A |
2: 25,336,637 (GRCm39) |
C2248S |
probably damaging |
Het |
Adamts16 |
G |
A |
13: 70,949,080 (GRCm39) |
Q194* |
probably null |
Het |
Cetn3 |
A |
T |
13: 81,932,779 (GRCm39) |
K13* |
probably null |
Het |
Cldn18 |
T |
A |
9: 99,580,901 (GRCm39) |
K116* |
probably null |
Het |
Cntn5 |
T |
A |
9: 9,831,542 (GRCm39) |
I613F |
probably damaging |
Het |
Cyp46a1 |
A |
G |
12: 108,321,745 (GRCm39) |
I324V |
probably benign |
Het |
Ddb1 |
A |
C |
19: 10,590,382 (GRCm39) |
E303A |
probably damaging |
Het |
Dnajc2 |
A |
G |
5: 21,962,361 (GRCm39) |
V539A |
probably damaging |
Het |
Dock2 |
T |
A |
11: 34,212,433 (GRCm39) |
Y1236F |
probably benign |
Het |
Dpf1 |
T |
A |
7: 29,015,926 (GRCm39) |
C383S |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,617,289 (GRCm39) |
I1052N |
possibly damaging |
Het |
Ehmt1 |
A |
G |
2: 24,681,966 (GRCm39) |
L1243P |
probably damaging |
Het |
Exoc6b |
A |
G |
6: 84,885,148 (GRCm39) |
S264P |
probably damaging |
Het |
Gbx2 |
T |
C |
1: 89,856,703 (GRCm39) |
E229G |
probably benign |
Het |
Hip1r |
T |
A |
5: 124,139,613 (GRCm39) |
|
probably null |
Het |
Lig1 |
A |
G |
7: 13,043,131 (GRCm39) |
K859E |
probably benign |
Het |
Ly6g6f |
T |
C |
17: 35,300,146 (GRCm39) |
D234G |
possibly damaging |
Het |
Mmp11 |
G |
T |
10: 75,764,304 (GRCm39) |
L54I |
probably benign |
Het |
Naip5 |
A |
T |
13: 100,358,092 (GRCm39) |
L1048Q |
probably damaging |
Het |
Or4c122 |
C |
A |
2: 89,079,566 (GRCm39) |
M157I |
probably benign |
Het |
Or6k14 |
A |
G |
1: 173,927,401 (GRCm39) |
I126V |
probably damaging |
Het |
Or7g12 |
T |
A |
9: 18,900,136 (GRCm39) |
M284K |
probably benign |
Het |
Or8g17 |
T |
C |
9: 38,930,697 (GRCm39) |
I47V |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,764,089 (GRCm39) |
D474G |
probably benign |
Het |
Plxna1 |
A |
G |
6: 89,306,628 (GRCm39) |
Y1401H |
probably damaging |
Het |
Prrg4 |
T |
A |
2: 104,663,035 (GRCm39) |
E190D |
probably damaging |
Het |
Rnf213 |
T |
C |
11: 119,333,092 (GRCm39) |
F2767S |
probably damaging |
Het |
Scgb1b2 |
T |
A |
7: 30,991,155 (GRCm39) |
|
probably benign |
Het |
Sec31a |
A |
G |
5: 100,523,065 (GRCm39) |
|
probably null |
Het |
Slc12a4 |
A |
G |
8: 106,671,033 (GRCm39) |
S1014P |
probably damaging |
Het |
Spns2 |
A |
T |
11: 72,348,130 (GRCm39) |
I279N |
possibly damaging |
Het |
Spta1 |
A |
T |
1: 174,071,746 (GRCm39) |
H2242L |
probably benign |
Het |
Tcaf3 |
T |
A |
6: 42,574,063 (GRCm39) |
I50F |
probably damaging |
Het |
Tnfaip8l1 |
G |
A |
17: 56,479,214 (GRCm39) |
S168N |
probably benign |
Het |
Trak1 |
C |
T |
9: 121,271,751 (GRCm39) |
|
probably benign |
Het |
Trpv4 |
A |
T |
5: 114,782,847 (GRCm39) |
N38K |
possibly damaging |
Het |
Ube2o |
T |
C |
11: 116,435,199 (GRCm39) |
T530A |
probably benign |
Het |
Vmn2r86 |
A |
C |
10: 130,288,858 (GRCm39) |
D214E |
probably damaging |
Het |
Wwc1 |
C |
A |
11: 35,732,751 (GRCm39) |
D986Y |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,199,754 (GRCm39) |
D1184G |
probably damaging |
Het |
|
Other mutations in Vmn2r2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00326:Vmn2r2
|
APN |
3 |
64,041,319 (GRCm39) |
splice site |
probably benign |
|
IGL00980:Vmn2r2
|
APN |
3 |
64,024,601 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01389:Vmn2r2
|
APN |
3 |
64,024,430 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02750:Vmn2r2
|
APN |
3 |
64,024,823 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02829:Vmn2r2
|
APN |
3 |
64,026,172 (GRCm39) |
splice site |
probably benign |
|
IGL03036:Vmn2r2
|
APN |
3 |
64,024,321 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03174:Vmn2r2
|
APN |
3 |
64,024,544 (GRCm39) |
nonsense |
probably null |
|
PIT4151001:Vmn2r2
|
UTSW |
3 |
64,024,334 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0029:Vmn2r2
|
UTSW |
3 |
64,024,365 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Vmn2r2
|
UTSW |
3 |
64,042,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R0357:Vmn2r2
|
UTSW |
3 |
64,041,320 (GRCm39) |
splice site |
probably null |
|
R0637:Vmn2r2
|
UTSW |
3 |
64,033,999 (GRCm39) |
missense |
probably benign |
0.00 |
R1626:Vmn2r2
|
UTSW |
3 |
64,041,921 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1662:Vmn2r2
|
UTSW |
3 |
64,024,551 (GRCm39) |
missense |
probably benign |
0.00 |
R1710:Vmn2r2
|
UTSW |
3 |
64,024,820 (GRCm39) |
missense |
probably benign |
0.19 |
R1797:Vmn2r2
|
UTSW |
3 |
64,042,128 (GRCm39) |
missense |
probably benign |
0.00 |
R1862:Vmn2r2
|
UTSW |
3 |
64,041,942 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1971:Vmn2r2
|
UTSW |
3 |
64,034,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Vmn2r2
|
UTSW |
3 |
64,024,766 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2099:Vmn2r2
|
UTSW |
3 |
64,024,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R2275:Vmn2r2
|
UTSW |
3 |
64,023,930 (GRCm39) |
missense |
probably benign |
0.00 |
R3078:Vmn2r2
|
UTSW |
3 |
64,042,053 (GRCm39) |
missense |
probably benign |
0.22 |
R3418:Vmn2r2
|
UTSW |
3 |
64,024,320 (GRCm39) |
missense |
probably benign |
0.00 |
R3419:Vmn2r2
|
UTSW |
3 |
64,024,320 (GRCm39) |
missense |
probably benign |
0.00 |
R3959:Vmn2r2
|
UTSW |
3 |
64,047,947 (GRCm39) |
missense |
probably benign |
|
R4230:Vmn2r2
|
UTSW |
3 |
64,041,912 (GRCm39) |
missense |
probably benign |
0.00 |
R4258:Vmn2r2
|
UTSW |
3 |
64,042,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Vmn2r2
|
UTSW |
3 |
64,044,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4822:Vmn2r2
|
UTSW |
3 |
64,041,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R4919:Vmn2r2
|
UTSW |
3 |
64,024,578 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4925:Vmn2r2
|
UTSW |
3 |
64,044,892 (GRCm39) |
start codon destroyed |
probably null |
0.03 |
R4954:Vmn2r2
|
UTSW |
3 |
64,047,905 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Vmn2r2
|
UTSW |
3 |
64,024,321 (GRCm39) |
missense |
probably benign |
0.01 |
R5315:Vmn2r2
|
UTSW |
3 |
64,024,377 (GRCm39) |
missense |
probably benign |
0.37 |
R5450:Vmn2r2
|
UTSW |
3 |
64,034,011 (GRCm39) |
missense |
probably benign |
|
R5577:Vmn2r2
|
UTSW |
3 |
64,024,416 (GRCm39) |
missense |
probably benign |
0.00 |
R5595:Vmn2r2
|
UTSW |
3 |
64,034,036 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5727:Vmn2r2
|
UTSW |
3 |
64,024,608 (GRCm39) |
missense |
probably benign |
0.41 |
R5810:Vmn2r2
|
UTSW |
3 |
64,024,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R5919:Vmn2r2
|
UTSW |
3 |
64,044,723 (GRCm39) |
missense |
probably benign |
0.39 |
R6052:Vmn2r2
|
UTSW |
3 |
64,024,782 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6084:Vmn2r2
|
UTSW |
3 |
64,024,467 (GRCm39) |
missense |
probably benign |
0.01 |
R6299:Vmn2r2
|
UTSW |
3 |
64,024,074 (GRCm39) |
nonsense |
probably null |
|
R6762:Vmn2r2
|
UTSW |
3 |
64,041,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Vmn2r2
|
UTSW |
3 |
64,044,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Vmn2r2
|
UTSW |
3 |
64,024,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R6990:Vmn2r2
|
UTSW |
3 |
64,024,608 (GRCm39) |
missense |
probably benign |
0.02 |
R7195:Vmn2r2
|
UTSW |
3 |
64,023,900 (GRCm39) |
missense |
probably benign |
0.01 |
R7269:Vmn2r2
|
UTSW |
3 |
64,033,998 (GRCm39) |
missense |
probably benign |
0.32 |
R7699:Vmn2r2
|
UTSW |
3 |
64,024,536 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7717:Vmn2r2
|
UTSW |
3 |
64,042,019 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7798:Vmn2r2
|
UTSW |
3 |
64,041,518 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7914:Vmn2r2
|
UTSW |
3 |
64,041,526 (GRCm39) |
missense |
probably benign |
0.20 |
R7974:Vmn2r2
|
UTSW |
3 |
64,024,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R8394:Vmn2r2
|
UTSW |
3 |
64,044,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R8478:Vmn2r2
|
UTSW |
3 |
64,024,257 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8731:Vmn2r2
|
UTSW |
3 |
64,024,404 (GRCm39) |
missense |
probably benign |
0.16 |
R9035:Vmn2r2
|
UTSW |
3 |
64,024,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R9182:Vmn2r2
|
UTSW |
3 |
64,044,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R9225:Vmn2r2
|
UTSW |
3 |
64,034,021 (GRCm39) |
missense |
probably benign |
0.00 |
R9266:Vmn2r2
|
UTSW |
3 |
64,024,057 (GRCm39) |
missense |
probably damaging |
0.98 |
R9427:Vmn2r2
|
UTSW |
3 |
64,041,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R9659:Vmn2r2
|
UTSW |
3 |
64,041,942 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9666:Vmn2r2
|
UTSW |
3 |
64,023,870 (GRCm39) |
missense |
probably benign |
0.08 |
R9771:Vmn2r2
|
UTSW |
3 |
64,042,079 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9788:Vmn2r2
|
UTSW |
3 |
64,041,942 (GRCm39) |
missense |
possibly damaging |
0.79 |
X0024:Vmn2r2
|
UTSW |
3 |
64,044,707 (GRCm39) |
nonsense |
probably null |
|
|