Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
T |
C |
5: 36,040,756 (GRCm39) |
L663P |
probably damaging |
Het |
Atp10d |
A |
T |
5: 72,421,410 (GRCm39) |
Q682L |
probably benign |
Het |
Atp8b1 |
A |
G |
18: 64,678,268 (GRCm39) |
V876A |
probably damaging |
Het |
Bard1 |
A |
T |
1: 71,070,588 (GRCm39) |
V632E |
probably benign |
Het |
Baz1b |
A |
T |
5: 135,237,951 (GRCm39) |
E209V |
probably benign |
Het |
Bmp1 |
T |
A |
14: 70,727,534 (GRCm39) |
Y683F |
probably benign |
Het |
Cacnb1 |
A |
T |
11: 97,900,105 (GRCm39) |
|
probably null |
Het |
Capza2 |
G |
A |
6: 17,654,112 (GRCm39) |
A55T |
probably damaging |
Het |
Cc2d2a |
A |
G |
5: 43,879,804 (GRCm39) |
N1127S |
possibly damaging |
Het |
Ccdc13 |
A |
G |
9: 121,627,853 (GRCm39) |
*255R |
probably null |
Het |
Ddias |
G |
T |
7: 92,507,937 (GRCm39) |
N659K |
probably damaging |
Het |
Ddr1 |
C |
T |
17: 35,997,400 (GRCm39) |
A531T |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,740,806 (GRCm39) |
T4127A |
probably damaging |
Het |
Dnajc10 |
T |
A |
2: 80,179,712 (GRCm39) |
Y749N |
probably damaging |
Het |
Dnm1l |
A |
G |
16: 16,137,353 (GRCm39) |
L422P |
probably damaging |
Het |
Edil3 |
A |
T |
13: 89,279,931 (GRCm39) |
N203I |
probably damaging |
Het |
Egfr |
C |
T |
11: 16,861,617 (GRCm39) |
A1132V |
probably benign |
Het |
Entpd7 |
C |
T |
19: 43,679,596 (GRCm39) |
R50* |
probably null |
Het |
Fat2 |
T |
C |
11: 55,201,142 (GRCm39) |
D644G |
probably damaging |
Het |
Fhip1a |
A |
T |
3: 85,629,808 (GRCm39) |
L40Q |
probably damaging |
Het |
Galnt11 |
T |
A |
5: 25,453,856 (GRCm39) |
D27E |
probably damaging |
Het |
Gm10801 |
T |
A |
2: 98,494,396 (GRCm39) |
F158I |
probably damaging |
Het |
Gm37240 |
A |
G |
3: 84,405,102 (GRCm39) |
F234L |
probably damaging |
Het |
Gtf2ird1 |
A |
T |
5: 134,439,821 (GRCm39) |
F136L |
probably damaging |
Het |
Hspa1l |
T |
C |
17: 35,196,396 (GRCm39) |
V145A |
probably damaging |
Het |
Ice2 |
A |
G |
9: 69,335,662 (GRCm39) |
T882A |
probably benign |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kat6b |
A |
G |
14: 21,719,440 (GRCm39) |
N1264S |
probably benign |
Het |
Kcnq4 |
C |
A |
4: 120,559,608 (GRCm39) |
V531L |
probably benign |
Het |
Kif9 |
A |
T |
9: 110,353,999 (GRCm39) |
K790N |
probably damaging |
Het |
Lipe |
T |
A |
7: 25,097,833 (GRCm39) |
I37L |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,637,643 (GRCm39) |
D270G |
probably damaging |
Het |
Mrpl52 |
T |
C |
14: 54,664,686 (GRCm39) |
S49P |
probably damaging |
Het |
Or2ak5 |
G |
A |
11: 58,611,077 (GRCm39) |
H266Y |
probably damaging |
Het |
Or2h15 |
T |
A |
17: 38,442,075 (GRCm39) |
T3S |
possibly damaging |
Het |
Or5k14 |
A |
G |
16: 58,692,847 (GRCm39) |
L222P |
probably damaging |
Het |
Or5p56 |
A |
T |
7: 107,589,592 (GRCm39) |
T7S |
probably benign |
Het |
Pcbp2 |
C |
T |
15: 102,395,524 (GRCm39) |
A141V |
probably damaging |
Het |
Pcsk9 |
T |
A |
4: 106,316,113 (GRCm39) |
Y110F |
probably damaging |
Het |
Plxna4 |
A |
G |
6: 32,494,551 (GRCm39) |
S22P |
possibly damaging |
Het |
Polq |
T |
A |
16: 36,860,896 (GRCm39) |
L506Q |
probably damaging |
Het |
Prkn |
C |
T |
17: 11,456,536 (GRCm39) |
A119V |
probably damaging |
Het |
Prx |
C |
T |
7: 27,217,029 (GRCm39) |
P510L |
probably damaging |
Het |
Ptpre |
T |
C |
7: 135,255,672 (GRCm39) |
F54L |
probably damaging |
Het |
Rspry1 |
T |
G |
8: 95,363,239 (GRCm39) |
|
probably null |
Het |
Tnfrsf11b |
A |
T |
15: 54,123,262 (GRCm39) |
L113Q |
probably damaging |
Het |
Tnk1 |
C |
T |
11: 69,744,411 (GRCm39) |
G411S |
probably damaging |
Het |
Tor3a |
A |
G |
1: 156,484,080 (GRCm39) |
L290S |
probably damaging |
Het |
Tril |
T |
C |
6: 53,794,970 (GRCm39) |
T751A |
probably benign |
Het |
Tubgcp6 |
C |
T |
15: 88,992,815 (GRCm39) |
V547I |
possibly damaging |
Het |
Txnrd3 |
T |
C |
6: 89,631,067 (GRCm39) |
L121P |
probably benign |
Het |
Vmn1r210 |
T |
A |
13: 23,011,378 (GRCm39) |
R303* |
probably null |
Het |
Vmn2r38 |
T |
C |
7: 9,100,764 (GRCm39) |
M1V |
probably null |
Het |
|
Other mutations in Mon2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00497:Mon2
|
APN |
10 |
122,862,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01072:Mon2
|
APN |
10 |
122,846,444 (GRCm39) |
nonsense |
probably null |
|
IGL02080:Mon2
|
APN |
10 |
122,888,095 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02157:Mon2
|
APN |
10 |
122,849,377 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02419:Mon2
|
APN |
10 |
122,852,352 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02498:Mon2
|
APN |
10 |
122,870,235 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02638:Mon2
|
APN |
10 |
122,859,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Mon2
|
APN |
10 |
122,845,401 (GRCm39) |
splice site |
probably benign |
|
IGL02690:Mon2
|
APN |
10 |
122,845,532 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02878:Mon2
|
APN |
10 |
122,842,896 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03092:Mon2
|
APN |
10 |
122,854,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03103:Mon2
|
APN |
10 |
122,866,008 (GRCm39) |
splice site |
probably benign |
|
IGL03208:Mon2
|
APN |
10 |
122,853,974 (GRCm39) |
splice site |
probably benign |
|
R0010:Mon2
|
UTSW |
10 |
122,868,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Mon2
|
UTSW |
10 |
122,871,451 (GRCm39) |
missense |
probably damaging |
0.96 |
R0016:Mon2
|
UTSW |
10 |
122,871,451 (GRCm39) |
missense |
probably damaging |
0.96 |
R0027:Mon2
|
UTSW |
10 |
122,871,953 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0027:Mon2
|
UTSW |
10 |
122,871,953 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0145:Mon2
|
UTSW |
10 |
122,849,417 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0390:Mon2
|
UTSW |
10 |
122,842,926 (GRCm39) |
missense |
probably null |
0.05 |
R0481:Mon2
|
UTSW |
10 |
122,849,301 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0513:Mon2
|
UTSW |
10 |
122,874,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Mon2
|
UTSW |
10 |
122,861,970 (GRCm39) |
splice site |
probably benign |
|
R1226:Mon2
|
UTSW |
10 |
122,838,724 (GRCm39) |
missense |
probably benign |
0.17 |
R1548:Mon2
|
UTSW |
10 |
122,871,912 (GRCm39) |
splice site |
probably benign |
|
R1598:Mon2
|
UTSW |
10 |
122,852,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Mon2
|
UTSW |
10 |
122,831,682 (GRCm39) |
missense |
probably benign |
0.45 |
R1687:Mon2
|
UTSW |
10 |
122,862,029 (GRCm39) |
missense |
probably damaging |
0.98 |
R1721:Mon2
|
UTSW |
10 |
122,867,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R1768:Mon2
|
UTSW |
10 |
122,849,668 (GRCm39) |
missense |
probably benign |
0.00 |
R1827:Mon2
|
UTSW |
10 |
122,882,216 (GRCm39) |
missense |
probably damaging |
0.97 |
R1879:Mon2
|
UTSW |
10 |
122,838,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Mon2
|
UTSW |
10 |
122,874,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Mon2
|
UTSW |
10 |
122,874,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Mon2
|
UTSW |
10 |
122,845,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Mon2
|
UTSW |
10 |
122,831,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R2160:Mon2
|
UTSW |
10 |
122,911,834 (GRCm39) |
nonsense |
probably null |
|
R2165:Mon2
|
UTSW |
10 |
122,878,269 (GRCm39) |
splice site |
probably null |
|
R3737:Mon2
|
UTSW |
10 |
122,849,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R3814:Mon2
|
UTSW |
10 |
122,849,470 (GRCm39) |
missense |
probably damaging |
0.98 |
R4058:Mon2
|
UTSW |
10 |
122,838,724 (GRCm39) |
missense |
probably benign |
0.17 |
R4091:Mon2
|
UTSW |
10 |
122,874,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Mon2
|
UTSW |
10 |
122,852,397 (GRCm39) |
missense |
probably benign |
0.03 |
R4354:Mon2
|
UTSW |
10 |
122,862,888 (GRCm39) |
missense |
probably benign |
0.02 |
R4422:Mon2
|
UTSW |
10 |
122,878,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R4505:Mon2
|
UTSW |
10 |
122,845,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R4791:Mon2
|
UTSW |
10 |
122,841,962 (GRCm39) |
missense |
probably benign |
0.01 |
R4797:Mon2
|
UTSW |
10 |
122,852,422 (GRCm39) |
missense |
probably benign |
0.45 |
R4944:Mon2
|
UTSW |
10 |
122,874,364 (GRCm39) |
critical splice donor site |
probably null |
|
R4982:Mon2
|
UTSW |
10 |
122,831,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R5298:Mon2
|
UTSW |
10 |
122,846,511 (GRCm39) |
missense |
probably benign |
|
R5503:Mon2
|
UTSW |
10 |
122,868,550 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5687:Mon2
|
UTSW |
10 |
122,844,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R5838:Mon2
|
UTSW |
10 |
122,846,397 (GRCm39) |
critical splice donor site |
probably null |
|
R6108:Mon2
|
UTSW |
10 |
122,868,600 (GRCm39) |
missense |
probably benign |
0.00 |
R6182:Mon2
|
UTSW |
10 |
122,874,564 (GRCm39) |
splice site |
probably null |
|
R6355:Mon2
|
UTSW |
10 |
122,858,825 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6358:Mon2
|
UTSW |
10 |
122,849,409 (GRCm39) |
missense |
probably damaging |
0.98 |
R6548:Mon2
|
UTSW |
10 |
122,871,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R6557:Mon2
|
UTSW |
10 |
122,852,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R6649:Mon2
|
UTSW |
10 |
122,874,385 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7140:Mon2
|
UTSW |
10 |
122,871,358 (GRCm39) |
missense |
probably benign |
0.00 |
R7303:Mon2
|
UTSW |
10 |
122,874,364 (GRCm39) |
critical splice donor site |
probably null |
|
R7317:Mon2
|
UTSW |
10 |
122,849,851 (GRCm39) |
missense |
probably damaging |
0.97 |
R7355:Mon2
|
UTSW |
10 |
122,845,421 (GRCm39) |
missense |
probably benign |
|
R7508:Mon2
|
UTSW |
10 |
122,859,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R7509:Mon2
|
UTSW |
10 |
122,868,457 (GRCm39) |
missense |
probably benign |
|
R7647:Mon2
|
UTSW |
10 |
122,841,931 (GRCm39) |
missense |
probably benign |
|
R7720:Mon2
|
UTSW |
10 |
122,868,493 (GRCm39) |
missense |
probably benign |
0.00 |
R7799:Mon2
|
UTSW |
10 |
122,878,236 (GRCm39) |
missense |
probably benign |
0.41 |
R7801:Mon2
|
UTSW |
10 |
122,895,091 (GRCm39) |
critical splice donor site |
probably null |
|
R7823:Mon2
|
UTSW |
10 |
122,868,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R7985:Mon2
|
UTSW |
10 |
122,852,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8310:Mon2
|
UTSW |
10 |
122,838,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Mon2
|
UTSW |
10 |
122,845,516 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8825:Mon2
|
UTSW |
10 |
122,849,776 (GRCm39) |
missense |
probably benign |
0.00 |
R8937:Mon2
|
UTSW |
10 |
122,895,110 (GRCm39) |
missense |
probably benign |
|
R8978:Mon2
|
UTSW |
10 |
122,871,469 (GRCm39) |
nonsense |
probably null |
|
R9011:Mon2
|
UTSW |
10 |
122,862,213 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9213:Mon2
|
UTSW |
10 |
122,872,016 (GRCm39) |
nonsense |
probably null |
|
R9358:Mon2
|
UTSW |
10 |
122,868,452 (GRCm39) |
missense |
probably benign |
0.00 |
R9630:Mon2
|
UTSW |
10 |
122,874,415 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Mon2
|
UTSW |
10 |
122,842,007 (GRCm39) |
missense |
probably benign |
0.07 |
|