Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl3 |
A |
C |
5: 81,942,606 (GRCm39) |
D1412A |
probably benign |
Het |
Arhgap26 |
A |
G |
18: 39,032,916 (GRCm39) |
|
probably benign |
Het |
Card14 |
A |
G |
11: 119,224,814 (GRCm39) |
M614V |
probably benign |
Het |
Cbx2 |
A |
G |
11: 118,919,961 (GRCm39) |
T509A |
probably damaging |
Het |
Cep135 |
A |
G |
5: 76,788,815 (GRCm39) |
D1136G |
probably benign |
Het |
Cep170 |
T |
A |
1: 176,583,898 (GRCm39) |
Q827L |
probably damaging |
Het |
Clock |
A |
T |
5: 76,389,801 (GRCm39) |
I349K |
probably damaging |
Het |
Cnppd1 |
A |
T |
1: 75,113,539 (GRCm39) |
V243E |
probably damaging |
Het |
Cops3 |
A |
G |
11: 59,723,960 (GRCm39) |
F93L |
probably damaging |
Het |
Cplane1 |
C |
A |
15: 8,273,706 (GRCm39) |
A2563D |
probably damaging |
Het |
Cxxc5 |
T |
G |
18: 35,992,372 (GRCm39) |
C258G |
possibly damaging |
Het |
Cycs |
G |
A |
6: 50,543,443 (GRCm39) |
|
probably benign |
Het |
Cyp2c40 |
A |
T |
19: 39,790,990 (GRCm39) |
H280Q |
probably damaging |
Het |
Cyp4f14 |
C |
T |
17: 33,133,619 (GRCm39) |
R79H |
probably benign |
Het |
Dnajc27 |
A |
G |
12: 4,153,114 (GRCm39) |
S197G |
probably benign |
Het |
Dscam |
C |
T |
16: 96,446,273 (GRCm39) |
G1456E |
probably benign |
Het |
Dst |
G |
A |
1: 34,218,332 (GRCm39) |
V1591I |
probably benign |
Het |
Epha5 |
A |
G |
5: 84,385,387 (GRCm39) |
S315P |
possibly damaging |
Het |
Frmd4a |
A |
G |
2: 4,610,873 (GRCm39) |
T1012A |
probably benign |
Het |
Fxr2 |
G |
A |
11: 69,532,416 (GRCm39) |
|
probably null |
Het |
Hcn4 |
T |
A |
9: 58,765,010 (GRCm39) |
V534E |
unknown |
Het |
Hrh4 |
A |
G |
18: 13,155,454 (GRCm39) |
Y331C |
probably damaging |
Het |
Insyn1 |
A |
G |
9: 58,406,533 (GRCm39) |
I148V |
probably benign |
Het |
Kif16b |
T |
A |
2: 142,554,362 (GRCm39) |
H812L |
probably benign |
Het |
Krt14 |
T |
A |
11: 100,094,786 (GRCm39) |
R451S |
probably benign |
Het |
Man2b1 |
A |
G |
8: 85,811,108 (GRCm39) |
T80A |
probably damaging |
Het |
Nedd4l |
A |
G |
18: 65,307,305 (GRCm39) |
T383A |
probably damaging |
Het |
Pcdha9 |
T |
A |
18: 37,131,707 (GRCm39) |
L259M |
possibly damaging |
Het |
Pdgfd |
T |
C |
9: 6,293,818 (GRCm39) |
C131R |
probably damaging |
Het |
Prrc2a |
C |
G |
17: 35,374,396 (GRCm39) |
R1418P |
probably damaging |
Het |
Ptpra |
G |
T |
2: 30,327,589 (GRCm39) |
E114D |
probably damaging |
Het |
Ptprt |
A |
T |
2: 161,395,760 (GRCm39) |
C1157S |
probably damaging |
Het |
Rnf126 |
A |
T |
10: 79,597,397 (GRCm39) |
|
probably null |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Sel1l3 |
A |
G |
5: 53,297,202 (GRCm39) |
V748A |
probably damaging |
Het |
Serinc5 |
T |
A |
13: 92,825,194 (GRCm39) |
S208T |
probably benign |
Het |
Sftpb |
A |
G |
6: 72,282,639 (GRCm39) |
I74V |
possibly damaging |
Het |
Slc22a14 |
A |
C |
9: 118,999,643 (GRCm39) |
I516S |
possibly damaging |
Het |
Slco2a1 |
G |
A |
9: 102,951,704 (GRCm39) |
C411Y |
possibly damaging |
Het |
Spata31f1e |
T |
A |
4: 42,793,111 (GRCm39) |
L340F |
probably damaging |
Het |
Tent5a |
G |
T |
9: 85,208,509 (GRCm39) |
R105S |
probably damaging |
Het |
Tet3 |
G |
A |
6: 83,380,426 (GRCm39) |
P581S |
probably benign |
Het |
Tmem231 |
T |
C |
8: 112,645,563 (GRCm39) |
D112G |
probably damaging |
Het |
Tnrc6b |
T |
A |
15: 80,763,385 (GRCm39) |
W296R |
probably damaging |
Het |
Trpm1 |
T |
A |
7: 63,890,343 (GRCm39) |
L982H |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,550,862 (GRCm39) |
R23183I |
possibly damaging |
Het |
Tuft1 |
T |
A |
3: 94,542,726 (GRCm39) |
Y46F |
probably damaging |
Het |
Zfp808 |
A |
G |
13: 62,319,646 (GRCm39) |
R292G |
possibly damaging |
Het |
Zp2 |
T |
C |
7: 119,731,748 (GRCm39) |
E669G |
probably benign |
Het |
Zp2 |
C |
T |
7: 119,741,136 (GRCm39) |
M129I |
probably benign |
Het |
|
Other mutations in Vmn1r167 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02137:Vmn1r167
|
APN |
7 |
23,204,864 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02261:Vmn1r167
|
APN |
7 |
23,204,261 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02963:Vmn1r167
|
APN |
7 |
23,204,975 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0054:Vmn1r167
|
UTSW |
7 |
23,204,334 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0555:Vmn1r167
|
UTSW |
7 |
23,204,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Vmn1r167
|
UTSW |
7 |
23,204,548 (GRCm39) |
missense |
probably benign |
0.01 |
R1312:Vmn1r167
|
UTSW |
7 |
23,204,548 (GRCm39) |
missense |
probably benign |
0.01 |
R1464:Vmn1r167
|
UTSW |
7 |
23,204,681 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1464:Vmn1r167
|
UTSW |
7 |
23,204,681 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1532:Vmn1r167
|
UTSW |
7 |
23,204,204 (GRCm39) |
missense |
probably benign |
0.01 |
R1937:Vmn1r167
|
UTSW |
7 |
23,204,452 (GRCm39) |
missense |
probably benign |
0.25 |
R2162:Vmn1r167
|
UTSW |
7 |
23,204,224 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4639:Vmn1r167
|
UTSW |
7 |
23,205,011 (GRCm39) |
missense |
probably benign |
0.00 |
R4661:Vmn1r167
|
UTSW |
7 |
23,204,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R4845:Vmn1r167
|
UTSW |
7 |
23,204,158 (GRCm39) |
missense |
probably benign |
0.01 |
R4868:Vmn1r167
|
UTSW |
7 |
23,204,161 (GRCm39) |
missense |
probably benign |
|
R4993:Vmn1r167
|
UTSW |
7 |
23,204,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Vmn1r167
|
UTSW |
7 |
23,204,646 (GRCm39) |
nonsense |
probably null |
|
R7800:Vmn1r167
|
UTSW |
7 |
23,204,069 (GRCm39) |
makesense |
probably null |
|
R8297:Vmn1r167
|
UTSW |
7 |
23,204,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8365:Vmn1r167
|
UTSW |
7 |
23,204,200 (GRCm39) |
missense |
probably benign |
0.03 |
R8411:Vmn1r167
|
UTSW |
7 |
23,204,981 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9667:Vmn1r167
|
UTSW |
7 |
23,204,990 (GRCm39) |
missense |
probably benign |
0.06 |
|