Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
G |
16: 14,290,797 (GRCm39) |
I1469S |
possibly damaging |
Het |
Aff1 |
A |
T |
5: 103,994,931 (GRCm39) |
D1043V |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,991,607 (GRCm39) |
I4297N |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,981,533 (GRCm39) |
N939S |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,922,634 (GRCm39) |
N465S |
possibly damaging |
Het |
Carns1 |
A |
G |
19: 4,216,548 (GRCm39) |
S545P |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,432,561 (GRCm39) |
Q121L |
probably benign |
Het |
Cfap221 |
G |
T |
1: 119,862,352 (GRCm39) |
Q577K |
probably benign |
Het |
Dlg1 |
T |
G |
16: 31,665,683 (GRCm39) |
L680R |
probably benign |
Het |
Fahd2a |
T |
C |
2: 127,278,304 (GRCm39) |
E301G |
probably benign |
Het |
Fn3k |
T |
A |
11: 121,341,191 (GRCm39) |
L282H |
probably damaging |
Het |
Fubp1 |
T |
A |
3: 151,927,823 (GRCm39) |
I424N |
probably damaging |
Het |
Gkn1 |
A |
G |
6: 87,323,289 (GRCm39) |
S175P |
probably damaging |
Het |
Gm12695 |
A |
G |
4: 96,616,466 (GRCm39) |
S456P |
probably damaging |
Het |
Kcna5 |
T |
C |
6: 126,511,844 (GRCm39) |
T95A |
probably benign |
Het |
Kcnj13 |
G |
T |
1: 87,314,737 (GRCm39) |
T83K |
probably benign |
Het |
Kif19b |
G |
A |
5: 140,460,651 (GRCm39) |
R439H |
probably benign |
Het |
Klra10 |
C |
T |
6: 130,252,849 (GRCm39) |
G142R |
probably benign |
Het |
Krt14 |
T |
C |
11: 100,097,902 (GRCm39) |
N127S |
probably damaging |
Het |
Layn |
T |
C |
9: 50,968,775 (GRCm39) |
M323V |
probably benign |
Het |
Lrrd1 |
A |
G |
5: 3,901,147 (GRCm39) |
D484G |
probably benign |
Het |
Lrrtm2 |
A |
G |
18: 35,345,788 (GRCm39) |
C505R |
probably damaging |
Het |
Ms4a14 |
A |
T |
19: 11,280,729 (GRCm39) |
S610T |
probably benign |
Het |
Myo5b |
A |
G |
18: 74,856,841 (GRCm39) |
N1282S |
probably benign |
Het |
Naip5 |
A |
T |
13: 100,358,784 (GRCm39) |
D817E |
possibly damaging |
Het |
Ndufs2 |
A |
G |
1: 171,074,629 (GRCm39) |
L10P |
possibly damaging |
Het |
Nxn |
T |
C |
11: 76,169,362 (GRCm39) |
D139G |
probably damaging |
Het |
Or3a1b |
A |
G |
11: 74,012,612 (GRCm39) |
T166A |
probably benign |
Het |
Or5b105 |
G |
A |
19: 13,080,272 (GRCm39) |
T132I |
possibly damaging |
Het |
Or6aa1 |
A |
C |
7: 86,043,973 (GRCm39) |
H244Q |
probably damaging |
Het |
Pcdhb22 |
G |
T |
18: 37,652,794 (GRCm39) |
V164F |
probably damaging |
Het |
Plch2 |
T |
C |
4: 155,084,992 (GRCm39) |
T417A |
probably damaging |
Het |
Prcp |
G |
T |
7: 92,567,035 (GRCm39) |
|
probably null |
Het |
Rasgrp2 |
A |
G |
19: 6,454,694 (GRCm39) |
Y178C |
probably damaging |
Het |
Rasgrp2 |
A |
G |
19: 6,463,907 (GRCm39) |
N535S |
probably benign |
Het |
Rgs20 |
G |
T |
1: 4,980,793 (GRCm39) |
Y208* |
probably null |
Het |
Slc39a10 |
A |
G |
1: 46,849,223 (GRCm39) |
C798R |
probably damaging |
Het |
Slco2b1 |
A |
G |
7: 99,335,265 (GRCm39) |
S172P |
probably benign |
Het |
Styk1 |
GTCTCTTCATGATT |
GT |
6: 131,278,610 (GRCm39) |
|
probably benign |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Tmc2 |
T |
A |
2: 130,089,881 (GRCm39) |
I622N |
probably damaging |
Het |
Trav16n |
A |
G |
14: 53,588,559 (GRCm39) |
S5G |
probably benign |
Het |
Tti1 |
C |
T |
2: 157,849,304 (GRCm39) |
R645H |
probably benign |
Het |
Ttll3 |
A |
G |
6: 113,386,114 (GRCm39) |
D649G |
probably damaging |
Het |
Vcam1 |
C |
T |
3: 115,922,287 (GRCm39) |
V79I |
possibly damaging |
Het |
Vmn1r211 |
T |
C |
13: 23,036,506 (GRCm39) |
I54V |
probably benign |
Het |
Vps33a |
A |
T |
5: 123,669,135 (GRCm39) |
W589R |
possibly damaging |
Het |
Zic1 |
A |
G |
9: 91,246,875 (GRCm39) |
S66P |
probably damaging |
Het |
|
Other mutations in Vmn1r238 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Vmn1r238
|
APN |
18 |
3,123,243 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01385:Vmn1r238
|
APN |
18 |
3,122,770 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02716:Vmn1r238
|
APN |
18 |
3,123,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R1219:Vmn1r238
|
UTSW |
18 |
3,123,135 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1568:Vmn1r238
|
UTSW |
18 |
3,123,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1864:Vmn1r238
|
UTSW |
18 |
3,123,040 (GRCm39) |
nonsense |
probably null |
|
R3024:Vmn1r238
|
UTSW |
18 |
3,123,305 (GRCm39) |
missense |
probably benign |
0.13 |
R4291:Vmn1r238
|
UTSW |
18 |
3,123,214 (GRCm39) |
nonsense |
probably null |
|
R4304:Vmn1r238
|
UTSW |
18 |
3,123,040 (GRCm39) |
nonsense |
probably null |
|
R4586:Vmn1r238
|
UTSW |
18 |
3,123,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Vmn1r238
|
UTSW |
18 |
3,123,300 (GRCm39) |
missense |
probably damaging |
0.99 |
R5123:Vmn1r238
|
UTSW |
18 |
3,123,243 (GRCm39) |
missense |
probably benign |
|
R5430:Vmn1r238
|
UTSW |
18 |
3,122,521 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5834:Vmn1r238
|
UTSW |
18 |
3,123,168 (GRCm39) |
missense |
probably benign |
|
R7186:Vmn1r238
|
UTSW |
18 |
3,122,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R7206:Vmn1r238
|
UTSW |
18 |
3,122,623 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7308:Vmn1r238
|
UTSW |
18 |
3,122,875 (GRCm39) |
missense |
probably benign |
0.09 |
R7346:Vmn1r238
|
UTSW |
18 |
3,123,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Vmn1r238
|
UTSW |
18 |
3,123,393 (GRCm39) |
missense |
probably benign |
0.10 |
R7571:Vmn1r238
|
UTSW |
18 |
3,122,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Vmn1r238
|
UTSW |
18 |
3,123,033 (GRCm39) |
missense |
probably benign |
0.03 |
R8085:Vmn1r238
|
UTSW |
18 |
3,123,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R8086:Vmn1r238
|
UTSW |
18 |
3,123,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8325:Vmn1r238
|
UTSW |
18 |
3,122,529 (GRCm39) |
missense |
probably benign |
0.00 |
R8423:Vmn1r238
|
UTSW |
18 |
3,123,365 (GRCm39) |
nonsense |
probably null |
|
R8747:Vmn1r238
|
UTSW |
18 |
3,123,232 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8930:Vmn1r238
|
UTSW |
18 |
3,123,127 (GRCm39) |
missense |
probably benign |
0.03 |
R8932:Vmn1r238
|
UTSW |
18 |
3,123,127 (GRCm39) |
missense |
probably benign |
0.03 |
R9279:Vmn1r238
|
UTSW |
18 |
3,122,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R9382:Vmn1r238
|
UTSW |
18 |
3,122,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R9644:Vmn1r238
|
UTSW |
18 |
3,122,635 (GRCm39) |
missense |
probably benign |
0.10 |
Z1177:Vmn1r238
|
UTSW |
18 |
3,122,505 (GRCm39) |
missense |
probably benign |
0.00 |
|