Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
A |
T |
18: 6,620,232 (GRCm39) |
K54I |
probably damaging |
Het |
Ankrd34b |
T |
A |
13: 92,575,725 (GRCm39) |
I319K |
probably benign |
Het |
Art2b |
G |
A |
7: 101,229,590 (GRCm39) |
A103V |
probably damaging |
Het |
Atmin |
T |
G |
8: 117,679,665 (GRCm39) |
F126C |
probably damaging |
Het |
Cc2d1b |
A |
T |
4: 108,482,143 (GRCm39) |
N139I |
probably benign |
Het |
Cep128 |
T |
C |
12: 91,200,987 (GRCm39) |
Y794C |
probably damaging |
Het |
Cic |
T |
A |
7: 24,988,885 (GRCm39) |
V1829D |
probably damaging |
Het |
Cnep1r1 |
G |
A |
8: 88,856,447 (GRCm39) |
R99Q |
unknown |
Het |
Cpq |
G |
C |
15: 33,213,353 (GRCm39) |
R124P |
probably damaging |
Het |
Crtc3 |
A |
T |
7: 80,327,191 (GRCm39) |
V45D |
probably damaging |
Het |
Dchs2 |
T |
G |
3: 83,036,143 (GRCm39) |
S297A |
probably benign |
Het |
Dnah9 |
A |
T |
11: 65,777,506 (GRCm39) |
S3681T |
probably damaging |
Het |
Dock8 |
T |
C |
19: 25,165,731 (GRCm39) |
Y1872H |
possibly damaging |
Het |
Fbn2 |
T |
A |
18: 58,239,395 (GRCm39) |
Q558L |
probably damaging |
Het |
Fn1 |
A |
G |
1: 71,676,491 (GRCm39) |
V580A |
probably benign |
Het |
Fscn3 |
C |
T |
6: 28,434,472 (GRCm39) |
T349I |
probably benign |
Het |
Fsip2 |
T |
C |
2: 82,815,370 (GRCm39) |
V3701A |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,496,347 (GRCm39) |
V3913A |
probably benign |
Het |
Htt |
G |
A |
5: 35,063,062 (GRCm39) |
G2898D |
probably damaging |
Het |
Ighv3-4 |
T |
G |
12: 114,217,266 (GRCm39) |
E108D |
probably benign |
Het |
Irx5 |
G |
T |
8: 93,087,135 (GRCm39) |
E356* |
probably null |
Het |
Kcnh6 |
A |
G |
11: 105,909,971 (GRCm39) |
I499V |
possibly damaging |
Het |
Kcnj10 |
T |
A |
1: 172,196,963 (GRCm39) |
I159N |
probably damaging |
Het |
Kcnmb4 |
T |
A |
10: 116,282,238 (GRCm39) |
H153L |
probably benign |
Het |
Klhl8 |
T |
C |
5: 104,018,404 (GRCm39) |
N409S |
probably benign |
Het |
Ksr1 |
A |
G |
11: 78,936,014 (GRCm39) |
S117P |
probably benign |
Het |
Lrfn3 |
A |
T |
7: 30,059,244 (GRCm39) |
V327E |
probably damaging |
Het |
Mrc2 |
C |
A |
11: 105,229,740 (GRCm39) |
H724Q |
probably benign |
Het |
Mtf2 |
T |
A |
5: 108,248,805 (GRCm39) |
F372L |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,320,997 (GRCm39) |
D2703E |
probably damaging |
Het |
Nova1 |
T |
C |
12: 46,863,800 (GRCm39) |
Y50C |
unknown |
Het |
Ofcc1 |
T |
A |
13: 40,296,277 (GRCm39) |
Y519F |
probably benign |
Het |
Or2aj5 |
T |
A |
16: 19,424,511 (GRCm39) |
K301N |
probably damaging |
Het |
Or4f54 |
T |
C |
2: 111,123,348 (GRCm39) |
I245T |
probably damaging |
Het |
Or4f61 |
A |
T |
2: 111,922,682 (GRCm39) |
D121E |
probably damaging |
Het |
Or4p19 |
A |
C |
2: 88,242,723 (GRCm39) |
M93R |
probably damaging |
Het |
Pclo |
C |
T |
5: 14,719,325 (GRCm39) |
A1154V |
unknown |
Het |
Phrf1 |
A |
G |
7: 140,823,671 (GRCm39) |
D4G |
unknown |
Het |
Ppp4r3b |
A |
T |
11: 29,123,306 (GRCm39) |
M1L |
probably damaging |
Het |
Prmt7 |
A |
G |
8: 106,943,874 (GRCm39) |
|
probably null |
Het |
Retnlg |
A |
G |
16: 48,694,038 (GRCm39) |
T65A |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 109,911,896 (GRCm39) |
N1763D |
probably benign |
Het |
Scn7a |
A |
G |
2: 66,514,588 (GRCm39) |
F1062S |
possibly damaging |
Het |
Scube3 |
A |
C |
17: 28,383,027 (GRCm39) |
K402Q |
probably damaging |
Het |
Skic2 |
T |
A |
17: 35,059,166 (GRCm39) |
D1067V |
probably damaging |
Het |
Slc25a22 |
C |
A |
7: 141,013,871 (GRCm39) |
D30Y |
probably damaging |
Het |
Smim17 |
A |
T |
7: 6,427,720 (GRCm39) |
Q2L |
possibly damaging |
Het |
Son |
G |
T |
16: 91,453,366 (GRCm39) |
M704I |
probably benign |
Het |
Son |
C |
T |
16: 91,453,608 (GRCm39) |
S785F |
possibly damaging |
Het |
Tnfrsf21 |
G |
A |
17: 43,396,299 (GRCm39) |
V528M |
probably benign |
Het |
Tnks1bp1 |
T |
C |
2: 84,894,290 (GRCm39) |
S1406P |
probably benign |
Het |
Trim21 |
A |
T |
7: 102,212,908 (GRCm39) |
V130E |
probably benign |
Het |
Try5 |
T |
A |
6: 41,289,295 (GRCm39) |
I94F |
probably benign |
Het |
Tubb4a |
C |
T |
17: 57,388,169 (GRCm39) |
V286I |
probably benign |
Het |
Vmn1r180 |
T |
A |
7: 23,652,076 (GRCm39) |
S80T |
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,234,033 (GRCm39) |
Y726* |
probably null |
Het |
Zdhhc16 |
T |
C |
19: 41,926,465 (GRCm39) |
F83L |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,979,137 (GRCm39) |
L425F |
probably damaging |
Het |
|
Other mutations in Vmn2r114 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Vmn2r114
|
APN |
17 |
23,510,639 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Vmn2r114
|
APN |
17 |
23,510,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Vmn2r114
|
APN |
17 |
23,509,957 (GRCm39) |
missense |
probably benign |
0.23 |
IGL00990:Vmn2r114
|
APN |
17 |
23,509,939 (GRCm39) |
missense |
probably benign |
|
IGL01838:Vmn2r114
|
APN |
17 |
23,515,956 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01990:Vmn2r114
|
APN |
17 |
23,529,355 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01994:Vmn2r114
|
APN |
17 |
23,529,451 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Vmn2r114
|
APN |
17 |
23,510,782 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02453:Vmn2r114
|
APN |
17 |
23,530,108 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02621:Vmn2r114
|
APN |
17 |
23,529,494 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02938:Vmn2r114
|
APN |
17 |
23,510,263 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03130:Vmn2r114
|
APN |
17 |
23,515,970 (GRCm39) |
splice site |
probably benign |
|
IGL03325:Vmn2r114
|
APN |
17 |
23,510,652 (GRCm39) |
missense |
probably damaging |
1.00 |
BB004:Vmn2r114
|
UTSW |
17 |
23,510,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Vmn2r114
|
UTSW |
17 |
23,529,549 (GRCm39) |
nonsense |
probably null |
|
R0164:Vmn2r114
|
UTSW |
17 |
23,528,800 (GRCm39) |
critical splice donor site |
probably null |
|
R0310:Vmn2r114
|
UTSW |
17 |
23,509,917 (GRCm39) |
missense |
probably benign |
0.23 |
R0583:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R0677:Vmn2r114
|
UTSW |
17 |
23,529,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R1127:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R1147:Vmn2r114
|
UTSW |
17 |
23,530,037 (GRCm39) |
missense |
probably benign |
0.00 |
R1147:Vmn2r114
|
UTSW |
17 |
23,530,037 (GRCm39) |
missense |
probably benign |
0.00 |
R1157:Vmn2r114
|
UTSW |
17 |
23,529,314 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1323:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R1347:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R1435:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R1437:Vmn2r114
|
UTSW |
17 |
23,510,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Vmn2r114
|
UTSW |
17 |
23,510,675 (GRCm39) |
missense |
probably damaging |
0.98 |
R1641:Vmn2r114
|
UTSW |
17 |
23,515,962 (GRCm39) |
missense |
probably benign |
0.00 |
R1748:Vmn2r114
|
UTSW |
17 |
23,527,035 (GRCm39) |
missense |
probably benign |
0.17 |
R1954:Vmn2r114
|
UTSW |
17 |
23,530,086 (GRCm39) |
missense |
probably benign |
0.32 |
R2081:Vmn2r114
|
UTSW |
17 |
23,510,083 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2103:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R2113:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R2134:Vmn2r114
|
UTSW |
17 |
23,510,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R2424:Vmn2r114
|
UTSW |
17 |
23,515,842 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2847:Vmn2r114
|
UTSW |
17 |
23,509,948 (GRCm39) |
missense |
probably benign |
0.00 |
R2848:Vmn2r114
|
UTSW |
17 |
23,509,948 (GRCm39) |
missense |
probably benign |
0.00 |
R2893:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R3017:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R3018:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R3019:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R3020:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R3021:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R4628:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R4668:Vmn2r114
|
UTSW |
17 |
23,529,447 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4840:Vmn2r114
|
UTSW |
17 |
23,510,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R4841:Vmn2r114
|
UTSW |
17 |
23,529,336 (GRCm39) |
missense |
probably benign |
0.04 |
R4842:Vmn2r114
|
UTSW |
17 |
23,529,336 (GRCm39) |
missense |
probably benign |
0.04 |
R4856:Vmn2r114
|
UTSW |
17 |
23,527,008 (GRCm39) |
missense |
probably benign |
0.11 |
R4886:Vmn2r114
|
UTSW |
17 |
23,527,008 (GRCm39) |
missense |
probably benign |
0.11 |
R4992:Vmn2r114
|
UTSW |
17 |
23,510,765 (GRCm39) |
missense |
probably benign |
0.03 |
R5182:Vmn2r114
|
UTSW |
17 |
23,510,632 (GRCm39) |
missense |
probably damaging |
0.96 |
R5223:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R5405:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R5449:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R5615:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
R5834:Vmn2r114
|
UTSW |
17 |
23,529,599 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6150:Vmn2r114
|
UTSW |
17 |
23,510,269 (GRCm39) |
missense |
probably benign |
0.03 |
R6277:Vmn2r114
|
UTSW |
17 |
23,509,954 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6403:Vmn2r114
|
UTSW |
17 |
23,528,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R6589:Vmn2r114
|
UTSW |
17 |
23,510,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R6613:Vmn2r114
|
UTSW |
17 |
23,529,220 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6747:Vmn2r114
|
UTSW |
17 |
23,528,850 (GRCm39) |
missense |
probably benign |
0.00 |
R6837:Vmn2r114
|
UTSW |
17 |
23,529,176 (GRCm39) |
missense |
probably benign |
0.10 |
R6911:Vmn2r114
|
UTSW |
17 |
23,510,104 (GRCm39) |
missense |
probably damaging |
0.98 |
R6950:Vmn2r114
|
UTSW |
17 |
23,529,137 (GRCm39) |
missense |
probably benign |
0.03 |
R7276:Vmn2r114
|
UTSW |
17 |
23,509,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R7482:Vmn2r114
|
UTSW |
17 |
23,510,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R7514:Vmn2r114
|
UTSW |
17 |
23,527,035 (GRCm39) |
missense |
probably null |
0.96 |
R7523:Vmn2r114
|
UTSW |
17 |
23,529,611 (GRCm39) |
missense |
probably benign |
0.01 |
R7563:Vmn2r114
|
UTSW |
17 |
23,510,000 (GRCm39) |
missense |
probably benign |
0.01 |
R7585:Vmn2r114
|
UTSW |
17 |
23,510,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Vmn2r114
|
UTSW |
17 |
23,510,817 (GRCm39) |
nonsense |
probably null |
|
R7611:Vmn2r114
|
UTSW |
17 |
23,515,944 (GRCm39) |
missense |
probably damaging |
0.97 |
R7641:Vmn2r114
|
UTSW |
17 |
23,527,177 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7651:Vmn2r114
|
UTSW |
17 |
23,509,986 (GRCm39) |
nonsense |
probably null |
|
R7970:Vmn2r114
|
UTSW |
17 |
23,530,186 (GRCm39) |
missense |
probably benign |
0.00 |
R8737:Vmn2r114
|
UTSW |
17 |
23,529,142 (GRCm39) |
missense |
probably benign |
0.36 |
R8802:Vmn2r114
|
UTSW |
17 |
23,528,836 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8847:Vmn2r114
|
UTSW |
17 |
23,528,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Vmn2r114
|
UTSW |
17 |
23,510,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R9173:Vmn2r114
|
UTSW |
17 |
23,510,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R9175:Vmn2r114
|
UTSW |
17 |
23,527,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R9657:Vmn2r114
|
UTSW |
17 |
23,510,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R9670:Vmn2r114
|
UTSW |
17 |
23,531,098 (GRCm39) |
missense |
|
|
X0065:Vmn2r114
|
UTSW |
17 |
23,529,931 (GRCm39) |
missense |
probably benign |
0.34 |
Z1088:Vmn2r114
|
UTSW |
17 |
23,509,906 (GRCm39) |
makesense |
probably null |
|
|