Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alox5 |
A |
G |
6: 116,404,225 (GRCm39) |
W145R |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,385,157 (GRCm39) |
V267D |
probably benign |
Het |
Bbs4 |
A |
T |
9: 59,247,096 (GRCm39) |
W135R |
probably damaging |
Het |
Cavin4 |
T |
C |
4: 48,672,593 (GRCm39) |
V346A |
probably benign |
Het |
Cdk18 |
A |
C |
1: 132,050,189 (GRCm39) |
|
probably benign |
Het |
Cyp2j11 |
C |
T |
4: 96,195,497 (GRCm39) |
|
probably null |
Het |
Dnah6 |
A |
T |
6: 73,136,118 (GRCm39) |
I1007K |
probably damaging |
Het |
Dnmt1 |
T |
C |
9: 20,852,752 (GRCm39) |
E118G |
probably benign |
Het |
Eef2 |
C |
CN |
10: 81,014,602 (GRCm39) |
|
probably null |
Het |
Eif1ad5 |
T |
A |
12: 87,946,853 (GRCm39) |
D98E |
probably benign |
Het |
Gm14496 |
T |
C |
2: 181,637,885 (GRCm39) |
F320L |
probably benign |
Het |
Gsdmc3 |
A |
T |
15: 63,732,130 (GRCm39) |
L299M |
probably damaging |
Het |
H6pd |
T |
C |
4: 150,066,971 (GRCm39) |
I472V |
probably benign |
Het |
Hao2 |
G |
T |
3: 98,790,985 (GRCm39) |
T63K |
possibly damaging |
Het |
Jag2 |
C |
T |
12: 112,879,939 (GRCm39) |
|
probably benign |
Het |
Mapre3 |
A |
G |
5: 31,022,211 (GRCm39) |
Y211C |
probably damaging |
Het |
Mycbp2 |
A |
G |
14: 103,393,334 (GRCm39) |
S2966P |
probably damaging |
Het |
Nsd3 |
T |
A |
8: 26,169,952 (GRCm39) |
V696E |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,945,723 (GRCm39) |
Y4163H |
possibly damaging |
Het |
Or11h4b |
A |
T |
14: 50,918,337 (GRCm39) |
Y251* |
probably null |
Het |
Or12e8 |
G |
A |
2: 87,188,414 (GRCm39) |
A209T |
probably benign |
Het |
Or6c3 |
G |
T |
10: 129,308,933 (GRCm39) |
C124F |
probably damaging |
Het |
Pde2a |
A |
G |
7: 101,156,409 (GRCm39) |
E607G |
probably benign |
Het |
Pinlyp |
T |
A |
7: 24,244,391 (GRCm39) |
D51V |
probably damaging |
Het |
Rcbtb2 |
T |
A |
14: 73,399,828 (GRCm39) |
I87N |
probably damaging |
Het |
Sfswap |
A |
G |
5: 129,618,442 (GRCm39) |
I459V |
probably benign |
Het |
Slitrk6 |
T |
C |
14: 110,989,297 (GRCm39) |
N137D |
possibly damaging |
Het |
Smg1 |
A |
T |
7: 117,767,434 (GRCm39) |
|
probably benign |
Het |
Sobp |
T |
A |
10: 42,898,331 (GRCm39) |
H418L |
probably damaging |
Het |
Spock1 |
A |
C |
13: 57,660,563 (GRCm39) |
D180E |
probably benign |
Het |
Upk3a |
G |
A |
15: 84,904,752 (GRCm39) |
V167I |
probably benign |
Het |
Zbtb25 |
T |
C |
12: 76,396,775 (GRCm39) |
E149G |
probably benign |
Het |
Zgrf1 |
T |
C |
3: 127,377,538 (GRCm39) |
C44R |
possibly damaging |
Het |
|
Other mutations in Vmn1r180 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00487:Vmn1r180
|
APN |
7 |
23,651,948 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01309:Vmn1r180
|
APN |
7 |
23,652,424 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01793:Vmn1r180
|
APN |
7 |
23,652,668 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02653:Vmn1r180
|
APN |
7 |
23,652,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Vmn1r180
|
APN |
7 |
23,652,710 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03352:Vmn1r180
|
APN |
7 |
23,652,077 (GRCm39) |
nonsense |
probably null |
|
R1701:Vmn1r180
|
UTSW |
7 |
23,652,395 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1702:Vmn1r180
|
UTSW |
7 |
23,652,394 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2122:Vmn1r180
|
UTSW |
7 |
23,652,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4241:Vmn1r180
|
UTSW |
7 |
23,652,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5683:Vmn1r180
|
UTSW |
7 |
23,652,635 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7241:Vmn1r180
|
UTSW |
7 |
23,651,891 (GRCm39) |
missense |
probably damaging |
0.96 |
R7522:Vmn1r180
|
UTSW |
7 |
23,652,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R8749:Vmn1r180
|
UTSW |
7 |
23,652,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R8991:Vmn1r180
|
UTSW |
7 |
23,652,076 (GRCm39) |
missense |
probably benign |
0.06 |
R9442:Vmn1r180
|
UTSW |
7 |
23,651,620 (GRCm39) |
start gained |
probably benign |
|
|