Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf3 |
A |
G |
5: 30,401,992 (GRCm39) |
S679P |
probably damaging |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cryl1 |
T |
C |
14: 57,513,375 (GRCm39) |
E282G |
probably benign |
Het |
Dbn1 |
A |
G |
13: 55,630,234 (GRCm39) |
F45L |
probably damaging |
Het |
Dclre1b |
T |
C |
3: 103,715,430 (GRCm39) |
M105V |
probably damaging |
Het |
Defb12 |
T |
C |
8: 19,164,830 (GRCm39) |
N3D |
probably benign |
Het |
Eprs1 |
G |
A |
1: 185,111,939 (GRCm39) |
|
probably null |
Het |
Fa2h |
T |
C |
8: 112,120,281 (GRCm39) |
D35G |
probably damaging |
Het |
Fdxacb1 |
C |
T |
9: 50,679,699 (GRCm39) |
A39V |
probably benign |
Het |
Fras1 |
G |
A |
5: 96,881,774 (GRCm39) |
R2502K |
probably benign |
Het |
Grm1 |
A |
G |
10: 10,955,601 (GRCm39) |
S228P |
probably benign |
Het |
Il27ra |
T |
A |
8: 84,758,242 (GRCm39) |
|
probably benign |
Het |
Lrrtm1 |
A |
T |
6: 77,221,962 (GRCm39) |
Q473L |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,369,704 (GRCm39) |
I121F |
probably damaging |
Het |
Mael |
A |
T |
1: 166,054,179 (GRCm39) |
F188I |
probably damaging |
Het |
Mapk4 |
C |
T |
18: 74,068,236 (GRCm39) |
A232T |
probably benign |
Het |
Mrpl9 |
C |
A |
3: 94,351,108 (GRCm39) |
T96K |
probably damaging |
Het |
Musk |
C |
A |
4: 58,366,938 (GRCm39) |
L511I |
probably damaging |
Het |
Mutyh |
G |
A |
4: 116,672,826 (GRCm39) |
D60N |
probably damaging |
Het |
Nckap5 |
A |
T |
1: 125,954,274 (GRCm39) |
|
probably null |
Het |
Nktr |
T |
C |
9: 121,578,670 (GRCm39) |
|
probably benign |
Het |
Otud7b |
C |
A |
3: 96,063,272 (GRCm39) |
A837E |
probably benign |
Het |
Pigb |
A |
T |
9: 72,947,060 (GRCm39) |
|
probably null |
Het |
Pip4k2b |
G |
T |
11: 97,613,260 (GRCm39) |
N245K |
probably benign |
Het |
Ptprd |
T |
A |
4: 75,865,338 (GRCm39) |
D1464V |
probably damaging |
Het |
Rab22a |
A |
G |
2: 173,537,074 (GRCm39) |
N98S |
probably benign |
Het |
Rictor |
G |
T |
15: 6,799,476 (GRCm39) |
|
probably null |
Het |
Rims1 |
T |
C |
1: 22,844,711 (GRCm39) |
E32G |
probably damaging |
Het |
Slx4ip |
A |
G |
2: 136,909,511 (GRCm39) |
|
probably null |
Het |
Snx19 |
G |
A |
9: 30,344,828 (GRCm39) |
|
probably benign |
Het |
Snx29 |
C |
T |
16: 11,265,317 (GRCm39) |
R516W |
probably damaging |
Het |
Tcof1 |
T |
C |
18: 60,949,156 (GRCm39) |
D1253G |
possibly damaging |
Het |
Tmod1 |
A |
T |
4: 46,092,259 (GRCm39) |
N203I |
probably damaging |
Het |
Tmprss15 |
T |
C |
16: 78,759,078 (GRCm39) |
N880S |
probably benign |
Het |
Ttn |
A |
T |
2: 76,599,979 (GRCm39) |
I19065N |
probably damaging |
Het |
Txk |
T |
C |
5: 72,881,794 (GRCm39) |
N154S |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,590,337 (GRCm39) |
|
probably null |
Het |
Yes1 |
T |
C |
5: 32,797,926 (GRCm39) |
S82P |
probably benign |
Het |
|
Other mutations in Vmn1r65 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01636:Vmn1r65
|
APN |
7 |
6,011,720 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02821:Vmn1r65
|
APN |
7 |
6,011,893 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0991:Vmn1r65
|
UTSW |
7 |
6,012,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R1457:Vmn1r65
|
UTSW |
7 |
6,012,156 (GRCm39) |
missense |
probably benign |
0.10 |
R1507:Vmn1r65
|
UTSW |
7 |
6,012,108 (GRCm39) |
missense |
probably benign |
0.13 |
R1856:Vmn1r65
|
UTSW |
7 |
6,011,265 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5147:Vmn1r65
|
UTSW |
7 |
6,011,818 (GRCm39) |
missense |
probably benign |
0.01 |
R5279:Vmn1r65
|
UTSW |
7 |
6,011,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Vmn1r65
|
UTSW |
7 |
6,011,809 (GRCm39) |
nonsense |
probably null |
|
R5409:Vmn1r65
|
UTSW |
7 |
6,012,012 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5646:Vmn1r65
|
UTSW |
7 |
6,012,223 (GRCm39) |
missense |
probably benign |
0.01 |
R5963:Vmn1r65
|
UTSW |
7 |
6,011,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Vmn1r65
|
UTSW |
7 |
6,011,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Vmn1r65
|
UTSW |
7 |
6,011,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6327:Vmn1r65
|
UTSW |
7 |
6,011,651 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7958:Vmn1r65
|
UTSW |
7 |
6,011,254 (GRCm39) |
missense |
probably benign |
0.01 |
R8121:Vmn1r65
|
UTSW |
7 |
6,011,464 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8345:Vmn1r65
|
UTSW |
7 |
6,011,256 (GRCm39) |
missense |
probably benign |
|
R8725:Vmn1r65
|
UTSW |
7 |
6,011,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Vmn1r65
|
UTSW |
7 |
6,011,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Vmn1r65
|
UTSW |
7 |
6,011,769 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9279:Vmn1r65
|
UTSW |
7 |
6,011,988 (GRCm39) |
missense |
probably benign |
0.06 |
R9778:Vmn1r65
|
UTSW |
7 |
6,011,387 (GRCm39) |
nonsense |
probably null |
|
|