Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610303G11Rik |
T |
A |
9: 98,068,812 (GRCm39) |
|
noncoding transcript |
Het |
4930447C04Rik |
C |
A |
12: 72,962,208 (GRCm39) |
R52L |
probably benign |
Het |
Abca13 |
C |
T |
11: 9,632,085 (GRCm39) |
Q5002* |
probably null |
Het |
Acacb |
T |
C |
5: 114,338,573 (GRCm39) |
I761T |
probably benign |
Het |
Acap3 |
G |
T |
4: 155,983,937 (GRCm39) |
L134F |
probably benign |
Het |
Adamtsl1 |
T |
C |
4: 86,293,230 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,641,295 (GRCm39) |
V3278A |
possibly damaging |
Het |
Agxt2 |
T |
C |
15: 10,380,696 (GRCm39) |
Y196H |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,235,941 (GRCm39) |
V172A |
probably damaging |
Het |
Aqp8 |
A |
G |
7: 123,065,891 (GRCm39) |
I229V |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Brd10 |
A |
G |
19: 29,700,853 (GRCm39) |
I812T |
probably benign |
Het |
Cacng8 |
T |
C |
7: 3,463,672 (GRCm39) |
S275P |
possibly damaging |
Het |
Catsperg1 |
T |
C |
7: 28,906,289 (GRCm39) |
Y138C |
probably damaging |
Het |
Ccdc93 |
T |
G |
1: 121,418,918 (GRCm39) |
L491R |
probably damaging |
Het |
Cntnap2 |
T |
C |
6: 47,084,848 (GRCm39) |
V1103A |
probably benign |
Het |
Col12a1 |
C |
T |
9: 79,588,657 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
A |
G |
1: 90,750,138 (GRCm39) |
|
probably benign |
Het |
Csf2rb2 |
C |
T |
15: 78,182,414 (GRCm39) |
A6T |
probably damaging |
Het |
Cyp2j5 |
T |
A |
4: 96,522,522 (GRCm39) |
S351C |
probably damaging |
Het |
Cyth1 |
A |
G |
11: 118,073,172 (GRCm39) |
|
probably benign |
Het |
Dock2 |
A |
G |
11: 34,223,309 (GRCm39) |
|
probably benign |
Het |
Duoxa1 |
T |
A |
2: 122,134,468 (GRCm39) |
I262F |
possibly damaging |
Het |
Dync2h1 |
T |
C |
9: 7,125,816 (GRCm39) |
D1930G |
probably benign |
Het |
Eeig1 |
T |
C |
2: 32,455,635 (GRCm39) |
S254P |
possibly damaging |
Het |
Eno1 |
C |
T |
4: 150,332,590 (GRCm39) |
|
probably benign |
Het |
Fam98a |
T |
A |
17: 75,845,264 (GRCm39) |
H494L |
unknown |
Het |
Fcamr |
C |
A |
1: 130,732,379 (GRCm39) |
T122K |
possibly damaging |
Het |
Foxq1 |
A |
G |
13: 31,743,288 (GRCm39) |
D130G |
probably damaging |
Het |
Glb1 |
T |
A |
9: 114,249,431 (GRCm39) |
W5R |
probably damaging |
Het |
Gm17661 |
GA |
GAA |
2: 90,917,709 (GRCm38) |
|
noncoding transcript |
Het |
Gm5431 |
T |
A |
11: 48,785,842 (GRCm39) |
R178W |
possibly damaging |
Het |
Gys2 |
C |
T |
6: 142,407,009 (GRCm39) |
V116M |
probably benign |
Het |
Hif1a |
C |
T |
12: 73,989,066 (GRCm39) |
T651I |
possibly damaging |
Het |
Itgb5 |
T |
A |
16: 33,720,885 (GRCm39) |
Y3* |
probably null |
Het |
Kank3 |
A |
G |
17: 34,035,205 (GRCm39) |
N7S |
possibly damaging |
Het |
Kdm2b |
G |
T |
5: 123,018,331 (GRCm39) |
H981Q |
probably damaging |
Het |
Kdm6a |
C |
T |
X: 18,120,235 (GRCm39) |
|
probably benign |
Het |
Kif1a |
A |
T |
1: 92,983,672 (GRCm39) |
|
probably benign |
Het |
Knl1 |
T |
A |
2: 118,901,211 (GRCm39) |
S971T |
possibly damaging |
Het |
Lcn6 |
T |
C |
2: 25,567,149 (GRCm39) |
V50A |
possibly damaging |
Het |
Llgl2 |
G |
T |
11: 115,743,958 (GRCm39) |
V762F |
probably damaging |
Het |
Lpcat4 |
T |
C |
2: 112,075,021 (GRCm39) |
F342L |
probably benign |
Het |
Lrp2 |
C |
A |
2: 69,287,262 (GRCm39) |
G3725V |
probably damaging |
Het |
Map1b |
T |
C |
13: 99,569,158 (GRCm39) |
T1188A |
unknown |
Het |
Mecp2 |
G |
A |
X: 73,079,394 (GRCm39) |
P362S |
possibly damaging |
Het |
Mideas |
C |
A |
12: 84,199,705 (GRCm39) |
R1005L |
probably damaging |
Het |
Mmp13 |
T |
A |
9: 7,282,033 (GRCm39) |
F445Y |
possibly damaging |
Het |
Myo5b |
G |
T |
18: 74,777,272 (GRCm39) |
|
probably benign |
Het |
Myo7b |
A |
G |
18: 32,116,805 (GRCm39) |
|
probably benign |
Het |
Nadk2 |
C |
A |
15: 9,106,870 (GRCm39) |
L384I |
possibly damaging |
Het |
Napg |
A |
G |
18: 63,119,283 (GRCm39) |
I98V |
possibly damaging |
Het |
Ncoa1 |
G |
T |
12: 4,324,790 (GRCm39) |
N1041K |
probably benign |
Het |
Nmu |
A |
T |
5: 76,497,992 (GRCm39) |
C64* |
probably null |
Het |
Nobox |
T |
A |
6: 43,284,132 (GRCm39) |
K13M |
probably damaging |
Het |
Nos1 |
T |
C |
5: 118,091,848 (GRCm39) |
|
probably benign |
Het |
Nrg2 |
A |
G |
18: 36,329,792 (GRCm39) |
V141A |
probably damaging |
Het |
Or1b1 |
T |
G |
2: 36,994,880 (GRCm39) |
I261L |
probably benign |
Het |
Or2aj5 |
T |
C |
16: 19,424,777 (GRCm39) |
I214V |
probably damaging |
Het |
Or55b4 |
T |
A |
7: 102,133,911 (GRCm39) |
I139L |
probably benign |
Het |
Phldb2 |
C |
T |
16: 45,646,357 (GRCm39) |
E71K |
possibly damaging |
Het |
Pik3r4 |
T |
A |
9: 105,521,490 (GRCm39) |
Y19N |
probably damaging |
Het |
Pkhd1 |
A |
C |
1: 20,625,447 (GRCm39) |
|
probably benign |
Het |
Pogk |
G |
T |
1: 166,227,707 (GRCm39) |
P148Q |
possibly damaging |
Het |
Pten |
G |
T |
19: 32,775,496 (GRCm39) |
A79S |
probably benign |
Het |
Ptpdc1 |
A |
T |
13: 48,739,796 (GRCm39) |
V545E |
possibly damaging |
Het |
Qdpr |
G |
C |
5: 45,607,480 (GRCm39) |
|
probably benign |
Het |
Rhbdd3 |
T |
A |
11: 5,054,121 (GRCm39) |
H83Q |
probably damaging |
Het |
Rnf6 |
A |
G |
5: 146,148,055 (GRCm39) |
V321A |
probably benign |
Het |
Rtf1 |
T |
A |
2: 119,536,126 (GRCm39) |
|
probably null |
Het |
Serpina10 |
C |
T |
12: 103,594,500 (GRCm39) |
V240I |
probably benign |
Het |
Siah2 |
A |
G |
3: 58,598,935 (GRCm39) |
V101A |
possibly damaging |
Het |
Taok3 |
A |
G |
5: 117,344,720 (GRCm39) |
K46R |
probably damaging |
Het |
Tcaf2 |
A |
C |
6: 42,601,512 (GRCm39) |
L849R |
probably damaging |
Het |
Upf3a |
T |
C |
8: 13,842,118 (GRCm39) |
F178S |
probably damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,695,521 (GRCm39) |
V297A |
probably damaging |
Het |
Vmn2r70 |
T |
A |
7: 85,207,969 (GRCm39) |
Q836L |
probably benign |
Het |
Zfp473 |
A |
G |
7: 44,382,365 (GRCm39) |
V655A |
probably benign |
Het |
Zic5 |
A |
G |
14: 122,696,897 (GRCm39) |
S573P |
unknown |
Het |
|
Other mutations in Vmn1r218 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02014:Vmn1r218
|
APN |
13 |
23,321,001 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02670:Vmn1r218
|
APN |
13 |
23,321,174 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03085:Vmn1r218
|
APN |
13 |
23,321,481 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03334:Vmn1r218
|
APN |
13 |
23,320,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Vmn1r218
|
UTSW |
13 |
23,321,225 (GRCm39) |
nonsense |
probably null |
|
R0049:Vmn1r218
|
UTSW |
13 |
23,321,225 (GRCm39) |
nonsense |
probably null |
|
R1959:Vmn1r218
|
UTSW |
13 |
23,320,683 (GRCm39) |
missense |
probably damaging |
0.96 |
R3713:Vmn1r218
|
UTSW |
13 |
23,321,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Vmn1r218
|
UTSW |
13 |
23,321,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4038:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4039:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4432:Vmn1r218
|
UTSW |
13 |
23,321,412 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5255:Vmn1r218
|
UTSW |
13 |
23,320,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5521:Vmn1r218
|
UTSW |
13 |
23,320,743 (GRCm39) |
missense |
probably benign |
0.01 |
R7384:Vmn1r218
|
UTSW |
13 |
23,320,895 (GRCm39) |
missense |
probably benign |
0.00 |
R7565:Vmn1r218
|
UTSW |
13 |
23,320,830 (GRCm39) |
missense |
probably benign |
0.05 |
R8178:Vmn1r218
|
UTSW |
13 |
23,321,472 (GRCm39) |
missense |
probably benign |
0.08 |
R8536:Vmn1r218
|
UTSW |
13 |
23,321,535 (GRCm39) |
missense |
probably benign |
0.00 |
R9225:Vmn1r218
|
UTSW |
13 |
23,320,824 (GRCm39) |
missense |
probably benign |
0.04 |
R9609:Vmn1r218
|
UTSW |
13 |
23,320,839 (GRCm39) |
missense |
probably benign |
0.01 |
R9734:Vmn1r218
|
UTSW |
13 |
23,321,034 (GRCm39) |
missense |
probably damaging |
1.00 |
|