Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
T |
6: 128,524,268 (GRCm39) |
N1121K |
probably null |
Het |
Actr10 |
A |
G |
12: 71,006,795 (GRCm39) |
N351D |
probably damaging |
Het |
Adcy7 |
G |
A |
8: 89,044,606 (GRCm39) |
A500T |
probably damaging |
Het |
Ankrd35 |
T |
C |
3: 96,586,564 (GRCm39) |
I80T |
possibly damaging |
Het |
Arap2 |
G |
A |
5: 62,864,028 (GRCm39) |
T532I |
probably damaging |
Het |
Bag3 |
AAAGG |
AAAGGAAGG |
7: 128,147,493 (GRCm39) |
|
probably null |
Het |
Cc2d2a |
T |
C |
5: 43,841,375 (GRCm39) |
|
probably benign |
Het |
Cep85l |
A |
T |
10: 53,224,827 (GRCm39) |
M254K |
probably benign |
Het |
Clic4 |
A |
G |
4: 134,950,850 (GRCm39) |
S114P |
probably damaging |
Het |
Ctsj |
T |
C |
13: 61,150,363 (GRCm39) |
Y213C |
probably damaging |
Het |
Ddx28 |
A |
G |
8: 106,737,206 (GRCm39) |
V284A |
probably damaging |
Het |
Dnase2b |
T |
A |
3: 146,290,443 (GRCm39) |
D176V |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,729,111 (GRCm39) |
N663K |
probably damaging |
Het |
Dst |
T |
A |
1: 34,235,002 (GRCm39) |
S3694T |
possibly damaging |
Het |
Emilin1 |
T |
C |
5: 31,073,036 (GRCm39) |
S158P |
probably benign |
Het |
Eng |
T |
C |
2: 32,563,752 (GRCm39) |
|
probably benign |
Het |
Entrep2 |
T |
A |
7: 64,409,141 (GRCm39) |
M418L |
probably benign |
Het |
Fdxr |
C |
A |
11: 115,161,208 (GRCm39) |
V223L |
probably benign |
Het |
Fhip1b |
T |
C |
7: 105,037,398 (GRCm39) |
N395S |
probably damaging |
Het |
Frem2 |
T |
A |
3: 53,423,994 (GRCm39) |
M3148L |
probably benign |
Het |
Hip1 |
A |
T |
5: 135,460,584 (GRCm39) |
D114E |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,706,183 (GRCm39) |
|
probably benign |
Het |
Kcnt2 |
T |
A |
1: 140,437,179 (GRCm39) |
N487K |
probably damaging |
Het |
Krt6a |
A |
G |
15: 101,601,606 (GRCm39) |
F172L |
probably benign |
Het |
Megf8 |
C |
T |
7: 25,040,170 (GRCm39) |
R1034W |
probably damaging |
Het |
Muc6 |
C |
T |
7: 141,236,075 (GRCm39) |
D451N |
probably damaging |
Het |
Myo5a |
A |
G |
9: 75,125,225 (GRCm39) |
T1838A |
possibly damaging |
Het |
N4bp2l2 |
A |
T |
5: 150,585,073 (GRCm39) |
D302E |
probably damaging |
Het |
Nbeal2 |
T |
A |
9: 110,459,318 (GRCm39) |
I1930F |
probably benign |
Het |
Nhsl3 |
A |
G |
4: 129,116,432 (GRCm39) |
V732A |
probably benign |
Het |
Npas4 |
A |
T |
19: 5,037,392 (GRCm39) |
Y301N |
probably benign |
Het |
Nt5m |
A |
G |
11: 59,766,741 (GRCm39) |
K211E |
probably benign |
Het |
Pfn4 |
A |
G |
12: 4,824,382 (GRCm39) |
|
probably null |
Het |
Pfpl |
A |
C |
19: 12,407,843 (GRCm39) |
D698A |
probably benign |
Het |
Pias1 |
G |
T |
9: 62,859,137 (GRCm39) |
H124N |
possibly damaging |
Het |
Pja2 |
A |
T |
17: 64,618,162 (GRCm39) |
|
probably benign |
Het |
Polr3e |
T |
C |
7: 120,531,465 (GRCm39) |
Y185H |
probably benign |
Het |
Pomc |
T |
C |
12: 4,010,275 (GRCm39) |
L172S |
probably benign |
Het |
Rapgef4 |
A |
G |
2: 71,875,533 (GRCm39) |
T129A |
probably damaging |
Het |
Reep1 |
T |
C |
6: 71,750,278 (GRCm39) |
S97P |
probably damaging |
Het |
Rttn |
T |
A |
18: 89,029,067 (GRCm39) |
I595N |
possibly damaging |
Het |
Sap30 |
T |
C |
8: 57,938,506 (GRCm39) |
|
probably null |
Het |
Slc1a7 |
T |
C |
4: 107,850,203 (GRCm39) |
Y105H |
probably damaging |
Het |
Slc5a5 |
C |
T |
8: 71,345,102 (GRCm39) |
M68I |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,776,503 (GRCm39) |
Y791F |
probably benign |
Het |
Tdrd1 |
C |
A |
19: 56,847,094 (GRCm39) |
H912N |
probably benign |
Het |
Tdrd1 |
C |
A |
19: 56,847,093 (GRCm39) |
S911R |
probably benign |
Het |
Tgm7 |
A |
T |
2: 120,929,062 (GRCm39) |
F278Y |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,283,039 (GRCm39) |
T310A |
probably damaging |
Het |
Tmem256 |
T |
C |
11: 69,730,271 (GRCm39) |
I93T |
probably benign |
Het |
Trpm2 |
G |
A |
10: 77,756,305 (GRCm39) |
Q1172* |
probably null |
Het |
Ttll8 |
A |
G |
15: 88,818,156 (GRCm39) |
V173A |
possibly damaging |
Het |
Ubr5 |
T |
C |
15: 38,002,543 (GRCm39) |
S1497G |
possibly damaging |
Het |
Ubr7 |
G |
A |
12: 102,727,764 (GRCm39) |
|
probably null |
Het |
Vmn1r37 |
T |
A |
6: 66,708,878 (GRCm39) |
M1K |
probably null |
Het |
Vmn2r14 |
A |
G |
5: 109,366,698 (GRCm39) |
|
probably null |
Het |
Vps8 |
A |
G |
16: 21,395,507 (GRCm39) |
R1266G |
probably damaging |
Het |
Wdr87-ps |
T |
A |
7: 29,235,950 (GRCm39) |
|
noncoding transcript |
Het |
Zfhx4 |
A |
G |
3: 5,307,349 (GRCm39) |
N192D |
probably damaging |
Het |
Zfp638 |
G |
C |
6: 83,906,500 (GRCm39) |
D222H |
probably damaging |
Het |
Zscan29 |
A |
C |
2: 120,999,883 (GRCm39) |
V106G |
probably damaging |
Het |
|
Other mutations in Vmn2r72 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00931:Vmn2r72
|
APN |
7 |
85,398,854 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01019:Vmn2r72
|
APN |
7 |
85,387,542 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01445:Vmn2r72
|
APN |
7 |
85,398,854 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02076:Vmn2r72
|
APN |
7 |
85,387,575 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02082:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02086:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02089:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02125:Vmn2r72
|
APN |
7 |
85,399,919 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02146:Vmn2r72
|
APN |
7 |
85,387,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Vmn2r72
|
APN |
7 |
85,399,901 (GRCm39) |
missense |
probably benign |
|
IGL02514:Vmn2r72
|
APN |
7 |
85,387,907 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02662:Vmn2r72
|
APN |
7 |
85,387,391 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02697:Vmn2r72
|
APN |
7 |
85,387,879 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02733:Vmn2r72
|
APN |
7 |
85,401,021 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03070:Vmn2r72
|
APN |
7 |
85,401,249 (GRCm39) |
splice site |
probably benign |
|
IGL03150:Vmn2r72
|
APN |
7 |
85,400,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03159:Vmn2r72
|
APN |
7 |
85,404,162 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03333:Vmn2r72
|
APN |
7 |
85,400,075 (GRCm39) |
missense |
probably benign |
0.10 |
R0081:Vmn2r72
|
UTSW |
7 |
85,401,044 (GRCm39) |
missense |
probably benign |
0.01 |
R0090:Vmn2r72
|
UTSW |
7 |
85,404,084 (GRCm39) |
missense |
probably benign |
|
R0655:Vmn2r72
|
UTSW |
7 |
85,387,319 (GRCm39) |
nonsense |
probably null |
|
R0778:Vmn2r72
|
UTSW |
7 |
85,398,947 (GRCm39) |
missense |
probably benign |
0.00 |
R1169:Vmn2r72
|
UTSW |
7 |
85,400,517 (GRCm39) |
missense |
probably benign |
0.01 |
R1172:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1173:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1175:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1248:Vmn2r72
|
UTSW |
7 |
85,398,396 (GRCm39) |
missense |
probably benign |
0.02 |
R1302:Vmn2r72
|
UTSW |
7 |
85,387,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R1506:Vmn2r72
|
UTSW |
7 |
85,398,419 (GRCm39) |
missense |
probably benign |
|
R1632:Vmn2r72
|
UTSW |
7 |
85,401,000 (GRCm39) |
missense |
probably benign |
0.13 |
R1775:Vmn2r72
|
UTSW |
7 |
85,387,378 (GRCm39) |
missense |
probably benign |
0.01 |
R1962:Vmn2r72
|
UTSW |
7 |
85,398,369 (GRCm39) |
missense |
probably benign |
0.00 |
R2290:Vmn2r72
|
UTSW |
7 |
85,387,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R2327:Vmn2r72
|
UTSW |
7 |
85,387,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Vmn2r72
|
UTSW |
7 |
85,400,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2655:Vmn2r72
|
UTSW |
7 |
85,400,477 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2860:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
R2861:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
R2862:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
R3009:Vmn2r72
|
UTSW |
7 |
85,398,850 (GRCm39) |
missense |
probably benign |
0.00 |
R3797:Vmn2r72
|
UTSW |
7 |
85,387,285 (GRCm39) |
missense |
probably benign |
0.44 |
R3798:Vmn2r72
|
UTSW |
7 |
85,387,285 (GRCm39) |
missense |
probably benign |
0.44 |
R3902:Vmn2r72
|
UTSW |
7 |
85,398,943 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3959:Vmn2r72
|
UTSW |
7 |
85,400,339 (GRCm39) |
missense |
probably benign |
0.36 |
R3974:Vmn2r72
|
UTSW |
7 |
85,399,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R4399:Vmn2r72
|
UTSW |
7 |
85,387,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4421:Vmn2r72
|
UTSW |
7 |
85,387,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4426:Vmn2r72
|
UTSW |
7 |
85,387,036 (GRCm39) |
nonsense |
probably null |
|
R4522:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
R4523:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
R4533:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
R4691:Vmn2r72
|
UTSW |
7 |
85,387,119 (GRCm39) |
nonsense |
probably null |
|
R4781:Vmn2r72
|
UTSW |
7 |
85,387,069 (GRCm39) |
missense |
probably benign |
0.14 |
R4863:Vmn2r72
|
UTSW |
7 |
85,399,806 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4952:Vmn2r72
|
UTSW |
7 |
85,400,317 (GRCm39) |
missense |
probably benign |
|
R4991:Vmn2r72
|
UTSW |
7 |
85,400,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R4995:Vmn2r72
|
UTSW |
7 |
85,387,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5095:Vmn2r72
|
UTSW |
7 |
85,387,061 (GRCm39) |
missense |
probably damaging |
0.98 |
R5174:Vmn2r72
|
UTSW |
7 |
85,387,048 (GRCm39) |
missense |
probably benign |
0.00 |
R5276:Vmn2r72
|
UTSW |
7 |
85,387,462 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5395:Vmn2r72
|
UTSW |
7 |
85,400,105 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5560:Vmn2r72
|
UTSW |
7 |
85,401,150 (GRCm39) |
missense |
probably damaging |
0.96 |
R5933:Vmn2r72
|
UTSW |
7 |
85,387,058 (GRCm39) |
missense |
probably benign |
0.05 |
R6033:Vmn2r72
|
UTSW |
7 |
85,387,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Vmn2r72
|
UTSW |
7 |
85,387,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Vmn2r72
|
UTSW |
7 |
85,399,747 (GRCm39) |
critical splice donor site |
probably null |
|
R6362:Vmn2r72
|
UTSW |
7 |
85,400,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6594:Vmn2r72
|
UTSW |
7 |
85,398,892 (GRCm39) |
missense |
probably benign |
0.32 |
R6794:Vmn2r72
|
UTSW |
7 |
85,387,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R7113:Vmn2r72
|
UTSW |
7 |
85,399,011 (GRCm39) |
splice site |
probably null |
|
R7189:Vmn2r72
|
UTSW |
7 |
85,404,125 (GRCm39) |
missense |
probably benign |
0.36 |
R7266:Vmn2r72
|
UTSW |
7 |
85,387,482 (GRCm39) |
nonsense |
probably null |
|
R7323:Vmn2r72
|
UTSW |
7 |
85,399,771 (GRCm39) |
missense |
probably benign |
|
R7426:Vmn2r72
|
UTSW |
7 |
85,400,348 (GRCm39) |
missense |
probably benign |
|
R7606:Vmn2r72
|
UTSW |
7 |
85,400,362 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7651:Vmn2r72
|
UTSW |
7 |
85,401,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R7688:Vmn2r72
|
UTSW |
7 |
85,404,098 (GRCm39) |
missense |
probably benign |
0.32 |
R7753:Vmn2r72
|
UTSW |
7 |
85,399,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Vmn2r72
|
UTSW |
7 |
85,398,838 (GRCm39) |
missense |
probably benign |
0.01 |
R8157:Vmn2r72
|
UTSW |
7 |
85,400,441 (GRCm39) |
missense |
probably benign |
0.09 |
R8254:Vmn2r72
|
UTSW |
7 |
85,400,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R8389:Vmn2r72
|
UTSW |
7 |
85,401,168 (GRCm39) |
missense |
probably damaging |
0.99 |
R8444:Vmn2r72
|
UTSW |
7 |
85,387,383 (GRCm39) |
missense |
probably benign |
|
R8989:Vmn2r72
|
UTSW |
7 |
85,404,134 (GRCm39) |
missense |
probably benign |
0.10 |
R9015:Vmn2r72
|
UTSW |
7 |
85,398,388 (GRCm39) |
missense |
probably benign |
0.01 |
R9080:Vmn2r72
|
UTSW |
7 |
85,387,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R9269:Vmn2r72
|
UTSW |
7 |
85,400,411 (GRCm39) |
missense |
probably benign |
0.03 |
R9317:Vmn2r72
|
UTSW |
7 |
85,404,022 (GRCm39) |
missense |
probably benign |
0.04 |
R9509:Vmn2r72
|
UTSW |
7 |
85,404,075 (GRCm39) |
missense |
probably benign |
|
Z1176:Vmn2r72
|
UTSW |
7 |
85,398,399 (GRCm39) |
missense |
probably damaging |
0.99 |
|