Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700022I11Rik |
T |
C |
4: 42,971,719 |
Y351H |
probably damaging |
Het |
5830411N06Rik |
A |
G |
7: 140,296,573 |
T537A |
probably benign |
Het |
Abcd3 |
A |
C |
3: 121,774,010 |
I434S |
probably benign |
Het |
Actr2 |
C |
T |
11: 20,072,514 |
R319Q |
probably damaging |
Het |
Atp13a5 |
G |
T |
16: 29,293,504 |
Y606* |
probably null |
Het |
Baiap3 |
C |
T |
17: 25,250,082 |
|
probably null |
Het |
Cers2 |
A |
G |
3: 95,320,085 |
Y8C |
probably benign |
Het |
Ces1g |
T |
A |
8: 93,317,079 |
M411L |
probably benign |
Het |
Chd6 |
A |
G |
2: 161,052,384 |
|
probably benign |
Het |
Cyp2d40 |
C |
A |
15: 82,761,521 |
K94N |
probably benign |
Het |
Ddx51 |
T |
C |
5: 110,655,621 |
V323A |
possibly damaging |
Het |
Dock1 |
G |
A |
7: 134,744,298 |
V190I |
probably benign |
Het |
Evc2 |
A |
G |
5: 37,419,157 |
T1042A |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,957,155 |
S2135T |
probably damaging |
Het |
Gpat2 |
T |
C |
2: 127,427,566 |
F46S |
probably damaging |
Het |
Klhl38 |
T |
A |
15: 58,322,455 |
K293* |
probably null |
Het |
Map4k4 |
T |
C |
1: 40,014,188 |
I916T |
probably damaging |
Het |
Nrap |
T |
A |
19: 56,345,533 |
K964M |
probably damaging |
Het |
Osbpl5 |
T |
C |
7: 143,699,334 |
|
probably null |
Het |
Perm1 |
A |
G |
4: 156,217,779 |
Q260R |
probably benign |
Het |
Ralgapb |
T |
A |
2: 158,437,394 |
N133K |
possibly damaging |
Het |
Slfn9 |
T |
C |
11: 82,981,196 |
S905G |
probably benign |
Het |
Ssh2 |
C |
T |
11: 77,453,544 |
T785I |
probably damaging |
Het |
Stk16 |
C |
A |
1: 75,213,004 |
Q69K |
probably damaging |
Het |
Stk36 |
T |
C |
1: 74,622,287 |
L491P |
probably benign |
Het |
Stxbp2 |
A |
T |
8: 3,641,971 |
I538F |
probably benign |
Het |
Tcp11 |
T |
C |
17: 28,070,516 |
N194D |
probably damaging |
Het |
Trio |
C |
A |
15: 27,830,239 |
|
probably benign |
Het |
Ugt2b1 |
A |
G |
5: 86,921,991 |
V297A |
possibly damaging |
Het |
Ugt2b5 |
T |
G |
5: 87,137,232 |
H282P |
probably damaging |
Het |
Usp53 |
A |
G |
3: 122,933,843 |
M1030T |
probably damaging |
Het |
Vmn1r234 |
T |
A |
17: 21,229,703 |
I293N |
probably damaging |
Het |
Wdr20 |
G |
T |
12: 110,794,308 |
E543* |
probably null |
Het |
Zbtb25 |
T |
A |
12: 76,349,417 |
N344Y |
probably damaging |
Het |
Zcchc2 |
T |
C |
1: 106,030,168 |
F790L |
probably damaging |
Het |
|
Other mutations in Vmn2r57 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Vmn2r57
|
APN |
7 |
41,428,785 (GRCm38) |
missense |
probably benign |
|
IGL01108:Vmn2r57
|
APN |
7 |
41,427,584 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01112:Vmn2r57
|
APN |
7 |
41,425,043 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01516:Vmn2r57
|
APN |
7 |
41,399,946 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01880:Vmn2r57
|
APN |
7 |
41,400,195 (GRCm38) |
missense |
possibly damaging |
0.73 |
IGL02117:Vmn2r57
|
APN |
7 |
41,400,450 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02500:Vmn2r57
|
APN |
7 |
41,428,226 (GRCm38) |
missense |
probably benign |
|
IGL02801:Vmn2r57
|
APN |
7 |
41,448,632 (GRCm38) |
missense |
probably benign |
0.13 |
IGL02996:Vmn2r57
|
APN |
7 |
41,399,741 (GRCm38) |
missense |
probably benign |
0.02 |
R0008:Vmn2r57
|
UTSW |
7 |
41,400,652 (GRCm38) |
missense |
probably damaging |
1.00 |
R0032:Vmn2r57
|
UTSW |
7 |
41,399,733 (GRCm38) |
splice site |
probably null |
|
R0305:Vmn2r57
|
UTSW |
7 |
41,427,543 (GRCm38) |
missense |
probably benign |
0.00 |
R0469:Vmn2r57
|
UTSW |
7 |
41,427,792 (GRCm38) |
missense |
possibly damaging |
0.58 |
R0510:Vmn2r57
|
UTSW |
7 |
41,427,792 (GRCm38) |
missense |
possibly damaging |
0.58 |
R0847:Vmn2r57
|
UTSW |
7 |
41,428,801 (GRCm38) |
missense |
probably benign |
0.00 |
R1025:Vmn2r57
|
UTSW |
7 |
41,427,804 (GRCm38) |
missense |
probably benign |
0.24 |
R1081:Vmn2r57
|
UTSW |
7 |
41,428,211 (GRCm38) |
missense |
possibly damaging |
0.47 |
R1479:Vmn2r57
|
UTSW |
7 |
41,427,830 (GRCm38) |
missense |
possibly damaging |
0.45 |
R1579:Vmn2r57
|
UTSW |
7 |
41,400,124 (GRCm38) |
missense |
probably benign |
0.38 |
R1764:Vmn2r57
|
UTSW |
7 |
41,400,643 (GRCm38) |
missense |
probably damaging |
1.00 |
R1848:Vmn2r57
|
UTSW |
7 |
41,428,107 (GRCm38) |
missense |
probably damaging |
1.00 |
R2006:Vmn2r57
|
UTSW |
7 |
41,448,577 (GRCm38) |
missense |
probably benign |
0.00 |
R2197:Vmn2r57
|
UTSW |
7 |
41,428,825 (GRCm38) |
critical splice acceptor site |
probably null |
|
R2242:Vmn2r57
|
UTSW |
7 |
41,428,074 (GRCm38) |
missense |
probably benign |
0.00 |
R2394:Vmn2r57
|
UTSW |
7 |
41,400,195 (GRCm38) |
missense |
possibly damaging |
0.73 |
R3937:Vmn2r57
|
UTSW |
7 |
41,428,130 (GRCm38) |
missense |
probably damaging |
0.97 |
R4193:Vmn2r57
|
UTSW |
7 |
41,428,239 (GRCm38) |
missense |
probably benign |
|
R4423:Vmn2r57
|
UTSW |
7 |
41,426,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R4865:Vmn2r57
|
UTSW |
7 |
41,400,468 (GRCm38) |
missense |
probably damaging |
1.00 |
R4947:Vmn2r57
|
UTSW |
7 |
41,400,495 (GRCm38) |
missense |
probably damaging |
1.00 |
R5042:Vmn2r57
|
UTSW |
7 |
41,428,662 (GRCm38) |
missense |
probably benign |
0.06 |
R5084:Vmn2r57
|
UTSW |
7 |
41,426,550 (GRCm38) |
critical splice donor site |
probably null |
|
R5177:Vmn2r57
|
UTSW |
7 |
41,400,240 (GRCm38) |
missense |
probably benign |
0.31 |
R5192:Vmn2r57
|
UTSW |
7 |
41,427,939 (GRCm38) |
missense |
probably damaging |
0.96 |
R5289:Vmn2r57
|
UTSW |
7 |
41,399,974 (GRCm38) |
missense |
probably damaging |
0.99 |
R5745:Vmn2r57
|
UTSW |
7 |
41,448,471 (GRCm38) |
missense |
possibly damaging |
0.51 |
R6051:Vmn2r57
|
UTSW |
7 |
41,448,472 (GRCm38) |
missense |
probably benign |
0.00 |
R6155:Vmn2r57
|
UTSW |
7 |
41,428,690 (GRCm38) |
missense |
probably benign |
0.14 |
R6248:Vmn2r57
|
UTSW |
7 |
41,399,860 (GRCm38) |
missense |
probably benign |
|
R6381:Vmn2r57
|
UTSW |
7 |
41,428,818 (GRCm38) |
missense |
probably benign |
0.08 |
R7019:Vmn2r57
|
UTSW |
7 |
41,428,665 (GRCm38) |
missense |
probably damaging |
1.00 |
R7126:Vmn2r57
|
UTSW |
7 |
41,399,794 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7146:Vmn2r57
|
UTSW |
7 |
41,448,471 (GRCm38) |
missense |
possibly damaging |
0.51 |
R7215:Vmn2r57
|
UTSW |
7 |
41,400,286 (GRCm38) |
missense |
probably benign |
0.00 |
R7432:Vmn2r57
|
UTSW |
7 |
41,426,724 (GRCm38) |
missense |
probably benign |
0.01 |
R7633:Vmn2r57
|
UTSW |
7 |
41,425,089 (GRCm38) |
missense |
possibly damaging |
0.76 |
R7811:Vmn2r57
|
UTSW |
7 |
41,425,015 (GRCm38) |
nonsense |
probably null |
|
R8025:Vmn2r57
|
UTSW |
7 |
41,426,759 (GRCm38) |
missense |
probably benign |
0.00 |
R8332:Vmn2r57
|
UTSW |
7 |
41,400,253 (GRCm38) |
missense |
probably benign |
0.01 |
R8345:Vmn2r57
|
UTSW |
7 |
41,427,544 (GRCm38) |
missense |
possibly damaging |
0.81 |
R8360:Vmn2r57
|
UTSW |
7 |
41,400,216 (GRCm38) |
missense |
probably damaging |
1.00 |
R8738:Vmn2r57
|
UTSW |
7 |
41,427,596 (GRCm38) |
missense |
probably benign |
0.00 |
R8758:Vmn2r57
|
UTSW |
7 |
41,428,739 (GRCm38) |
missense |
probably damaging |
1.00 |
R8955:Vmn2r57
|
UTSW |
7 |
41,400,147 (GRCm38) |
missense |
possibly damaging |
0.64 |
R8985:Vmn2r57
|
UTSW |
7 |
41,399,835 (GRCm38) |
missense |
probably benign |
|
R9108:Vmn2r57
|
UTSW |
7 |
41,428,768 (GRCm38) |
missense |
possibly damaging |
0.87 |
R9160:Vmn2r57
|
UTSW |
7 |
41,426,735 (GRCm38) |
missense |
possibly damaging |
0.48 |
R9354:Vmn2r57
|
UTSW |
7 |
41,400,239 (GRCm38) |
missense |
probably benign |
0.01 |
R9566:Vmn2r57
|
UTSW |
7 |
41,427,665 (GRCm38) |
missense |
probably benign |
0.32 |
R9633:Vmn2r57
|
UTSW |
7 |
41,426,582 (GRCm38) |
missense |
probably benign |
0.00 |
X0026:Vmn2r57
|
UTSW |
7 |
41,428,561 (GRCm38) |
missense |
possibly damaging |
0.91 |
X0026:Vmn2r57
|
UTSW |
7 |
41,428,125 (GRCm38) |
missense |
probably benign |
0.03 |
X0065:Vmn2r57
|
UTSW |
7 |
41,427,971 (GRCm38) |
missense |
probably benign |
0.09 |
Z1176:Vmn2r57
|
UTSW |
7 |
41,400,498 (GRCm38) |
missense |
probably damaging |
0.99 |
|