Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930455H04Rik |
T |
A |
3: 116,777,124 (GRCm39) |
*59R |
probably null |
Het |
Adam10 |
G |
T |
9: 70,647,458 (GRCm39) |
|
probably null |
Het |
Adam2 |
A |
T |
14: 66,275,025 (GRCm39) |
N569K |
possibly damaging |
Het |
Adam20 |
T |
C |
8: 41,249,696 (GRCm39) |
V602A |
probably benign |
Het |
Adgrb3 |
T |
C |
1: 25,133,375 (GRCm39) |
Y1237C |
probably damaging |
Het |
Ago3 |
T |
C |
4: 126,265,338 (GRCm39) |
T318A |
probably null |
Het |
Aknad1 |
G |
A |
3: 108,659,655 (GRCm39) |
G223D |
possibly damaging |
Het |
Camkv |
T |
C |
9: 107,825,516 (GRCm39) |
S478P |
possibly damaging |
Het |
Ccl27a |
T |
A |
4: 41,773,342 (GRCm39) |
H39L |
probably damaging |
Het |
Ccser2 |
C |
A |
14: 36,601,043 (GRCm39) |
S447I |
probably damaging |
Het |
Clvs2 |
A |
G |
10: 33,404,517 (GRCm39) |
L233P |
probably damaging |
Het |
Csn1s2b |
T |
A |
5: 87,970,127 (GRCm39) |
H124Q |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,353,082 (GRCm39) |
L2745P |
probably benign |
Het |
Dync1i2 |
T |
A |
2: 71,077,484 (GRCm39) |
F219L |
probably benign |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Ephb6 |
C |
T |
6: 41,594,308 (GRCm39) |
Q613* |
probably null |
Het |
Erc2 |
A |
C |
14: 27,620,524 (GRCm39) |
D50A |
possibly damaging |
Het |
Fam149a |
T |
A |
8: 45,834,211 (GRCm39) |
D196V |
probably damaging |
Het |
Ficd |
T |
C |
5: 113,876,773 (GRCm39) |
V316A |
probably damaging |
Het |
Gstm6 |
T |
A |
3: 107,850,041 (GRCm39) |
K18* |
probably null |
Het |
Ighv1-62-1 |
A |
T |
12: 115,350,512 (GRCm39) |
W52R |
probably benign |
Het |
Klhl18 |
C |
T |
9: 110,257,979 (GRCm39) |
C417Y |
probably damaging |
Het |
Ly9 |
T |
A |
1: 171,432,737 (GRCm39) |
Y92F |
probably benign |
Het |
Mettl18 |
C |
T |
1: 163,824,750 (GRCm39) |
T357I |
probably damaging |
Het |
Myoz2 |
C |
A |
3: 122,810,276 (GRCm39) |
G100C |
probably damaging |
Het |
Or10a49 |
A |
T |
7: 108,467,780 (GRCm39) |
F194I |
probably benign |
Het |
Or4k47 |
A |
G |
2: 111,452,080 (GRCm39) |
V113A |
probably damaging |
Het |
Or7h8 |
T |
C |
9: 20,123,798 (GRCm39) |
I51T |
probably benign |
Het |
Pars2 |
C |
T |
4: 106,510,628 (GRCm39) |
L128F |
probably damaging |
Het |
Pcsk6 |
G |
T |
7: 65,629,996 (GRCm39) |
R374L |
probably damaging |
Het |
Ptpn3 |
T |
C |
4: 57,270,088 (GRCm39) |
T25A |
probably benign |
Het |
Rab11fip1 |
G |
A |
8: 27,633,257 (GRCm39) |
P1150S |
probably damaging |
Het |
Rabep1 |
A |
G |
11: 70,831,212 (GRCm39) |
Q831R |
possibly damaging |
Het |
Rad17 |
T |
C |
13: 100,786,253 (GRCm39) |
|
probably benign |
Het |
Rxfp1 |
T |
A |
3: 79,557,898 (GRCm39) |
R527* |
probably null |
Het |
Scnn1b |
C |
T |
7: 121,502,100 (GRCm39) |
P253S |
probably damaging |
Het |
Skic2 |
G |
A |
17: 35,064,166 (GRCm39) |
R507* |
probably null |
Het |
Slc2a7 |
T |
C |
4: 150,242,605 (GRCm39) |
F231S |
probably damaging |
Het |
Svil |
A |
G |
18: 5,049,311 (GRCm39) |
N196S |
probably benign |
Het |
Tent5c |
T |
A |
3: 100,380,273 (GRCm39) |
N161I |
probably benign |
Het |
Urb1 |
T |
C |
16: 90,575,971 (GRCm39) |
S862G |
possibly damaging |
Het |
Usp30 |
T |
C |
5: 114,241,770 (GRCm39) |
S87P |
probably damaging |
Het |
Vmn2r106 |
T |
A |
17: 20,499,096 (GRCm39) |
I272L |
possibly damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,832,012 (GRCm39) |
D259V |
probably benign |
Het |
|
Other mutations in Vmn1r177 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01456:Vmn1r177
|
APN |
7 |
23,565,753 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01504:Vmn1r177
|
APN |
7 |
23,565,835 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01535:Vmn1r177
|
APN |
7 |
23,565,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01551:Vmn1r177
|
APN |
7 |
23,565,688 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01647:Vmn1r177
|
APN |
7 |
23,565,600 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU74:Vmn1r177
|
UTSW |
7 |
23,565,645 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0396:Vmn1r177
|
UTSW |
7 |
23,565,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R0894:Vmn1r177
|
UTSW |
7 |
23,565,475 (GRCm39) |
missense |
probably benign |
0.09 |
R1446:Vmn1r177
|
UTSW |
7 |
23,565,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Vmn1r177
|
UTSW |
7 |
23,565,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Vmn1r177
|
UTSW |
7 |
23,565,573 (GRCm39) |
missense |
probably benign |
0.02 |
R1995:Vmn1r177
|
UTSW |
7 |
23,565,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Vmn1r177
|
UTSW |
7 |
23,565,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R3889:Vmn1r177
|
UTSW |
7 |
23,565,289 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4458:Vmn1r177
|
UTSW |
7 |
23,565,645 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4579:Vmn1r177
|
UTSW |
7 |
23,565,772 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5290:Vmn1r177
|
UTSW |
7 |
23,565,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R6128:Vmn1r177
|
UTSW |
7 |
23,565,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R6128:Vmn1r177
|
UTSW |
7 |
23,565,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R6785:Vmn1r177
|
UTSW |
7 |
23,565,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R7100:Vmn1r177
|
UTSW |
7 |
23,565,535 (GRCm39) |
missense |
probably benign |
0.15 |
R7738:Vmn1r177
|
UTSW |
7 |
23,565,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Vmn1r177
|
UTSW |
7 |
23,565,736 (GRCm39) |
nonsense |
probably null |
|
R8980:Vmn1r177
|
UTSW |
7 |
23,565,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9723:Vmn1r177
|
UTSW |
7 |
23,565,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R9771:Vmn1r177
|
UTSW |
7 |
23,565,657 (GRCm39) |
missense |
probably damaging |
0.98 |
X0020:Vmn1r177
|
UTSW |
7 |
23,565,718 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn1r177
|
UTSW |
7 |
23,565,360 (GRCm39) |
missense |
probably damaging |
0.99 |
|