Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvrl1 |
G |
A |
15: 101,035,458 (GRCm39) |
R328H |
probably damaging |
Het |
Afp |
T |
C |
5: 90,652,927 (GRCm39) |
S466P |
probably damaging |
Het |
Arhgap45 |
A |
G |
10: 79,864,584 (GRCm39) |
S879G |
possibly damaging |
Het |
Asic1 |
A |
G |
15: 99,597,006 (GRCm39) |
D556G |
probably damaging |
Het |
Atp2a3 |
T |
A |
11: 72,869,633 (GRCm39) |
|
probably null |
Het |
Brinp2 |
C |
A |
1: 158,074,128 (GRCm39) |
E664D |
probably damaging |
Het |
Cap2 |
C |
A |
13: 46,768,799 (GRCm39) |
H147N |
probably damaging |
Het |
Cd209f |
G |
A |
8: 4,154,862 (GRCm39) |
Q79* |
probably null |
Het |
Chrna7 |
T |
C |
7: 62,861,890 (GRCm39) |
Y54C |
possibly damaging |
Het |
Clec1a |
T |
C |
6: 129,413,967 (GRCm39) |
D40G |
probably benign |
Het |
Col11a1 |
A |
G |
3: 113,855,184 (GRCm39) |
E148G |
unknown |
Het |
Comp |
A |
T |
8: 70,831,607 (GRCm39) |
|
probably null |
Het |
Cpz |
A |
G |
5: 35,665,460 (GRCm39) |
|
probably null |
Het |
Cyfip1 |
T |
A |
7: 55,521,646 (GRCm39) |
N13K |
probably damaging |
Het |
Cyp2c50 |
A |
T |
19: 40,079,499 (GRCm39) |
M198L |
probably benign |
Het |
Deup1 |
A |
T |
9: 15,486,487 (GRCm39) |
Y398N |
possibly damaging |
Het |
Elapor1 |
A |
G |
3: 108,377,313 (GRCm39) |
S434P |
probably benign |
Het |
Epb41l4a |
A |
G |
18: 34,054,962 (GRCm39) |
L42P |
probably damaging |
Het |
Exo1 |
T |
C |
1: 175,736,052 (GRCm39) |
I812T |
possibly damaging |
Het |
Fbxl17 |
A |
T |
17: 63,692,060 (GRCm39) |
|
probably null |
Het |
Fxn |
A |
G |
19: 24,239,377 (GRCm39) |
Y172H |
probably damaging |
Het |
Gabra6 |
A |
G |
11: 42,208,461 (GRCm39) |
S124P |
probably damaging |
Het |
Gje1 |
C |
A |
10: 14,592,551 (GRCm39) |
W77L |
possibly damaging |
Het |
Glra1 |
A |
G |
11: 55,465,225 (GRCm39) |
S23P |
probably damaging |
Het |
Gm6811 |
T |
C |
17: 21,314,529 (GRCm39) |
|
noncoding transcript |
Het |
Greb1l |
T |
A |
18: 10,501,080 (GRCm39) |
|
probably null |
Het |
Greb1l |
T |
C |
18: 10,529,708 (GRCm39) |
|
probably null |
Het |
Grm6 |
A |
T |
11: 50,750,711 (GRCm39) |
I625F |
probably damaging |
Het |
Guca1a |
A |
G |
17: 47,711,167 (GRCm39) |
F60L |
probably damaging |
Het |
Hectd1 |
T |
A |
12: 51,800,607 (GRCm39) |
E2070D |
possibly damaging |
Het |
Itga5 |
G |
A |
15: 103,256,329 (GRCm39) |
T910I |
probably benign |
Het |
Kctd10 |
A |
G |
5: 114,507,051 (GRCm39) |
V142A |
probably benign |
Het |
Kif1c |
C |
T |
11: 70,619,223 (GRCm39) |
L953F |
probably damaging |
Het |
Lmtk3 |
A |
T |
7: 45,443,588 (GRCm39) |
D757V |
probably benign |
Het |
Lpcat1 |
T |
C |
13: 73,658,242 (GRCm39) |
|
probably null |
Het |
Lrrc30 |
A |
T |
17: 67,939,200 (GRCm39) |
C127S |
probably benign |
Het |
Mc4r |
A |
G |
18: 66,992,480 (GRCm39) |
L211P |
probably damaging |
Het |
Mgat5b |
T |
A |
11: 116,874,474 (GRCm39) |
N635K |
probably benign |
Het |
Mms19 |
A |
T |
19: 41,940,995 (GRCm39) |
M443K |
possibly damaging |
Het |
Mroh5 |
T |
C |
15: 73,659,754 (GRCm39) |
N359S |
probably benign |
Het |
Nlrc4 |
G |
A |
17: 74,752,901 (GRCm39) |
T494M |
probably damaging |
Het |
Ntf3 |
T |
C |
6: 126,079,401 (GRCm39) |
D35G |
possibly damaging |
Het |
Or5g25 |
A |
T |
2: 85,478,157 (GRCm39) |
C169* |
probably null |
Het |
Osbpl5 |
T |
C |
7: 143,262,776 (GRCm39) |
H192R |
probably damaging |
Het |
Parp4 |
A |
T |
14: 56,861,620 (GRCm39) |
K984N |
possibly damaging |
Het |
Pdgfra |
G |
A |
5: 75,349,681 (GRCm39) |
G892D |
possibly damaging |
Het |
Pik3c2g |
A |
T |
6: 139,612,634 (GRCm39) |
|
probably benign |
Het |
Ppcdc |
T |
A |
9: 57,321,998 (GRCm39) |
M181L |
possibly damaging |
Het |
Pramel7 |
G |
A |
2: 87,322,747 (GRCm39) |
P6S |
probably damaging |
Het |
Prkcz |
G |
T |
4: 155,374,208 (GRCm39) |
F69L |
probably damaging |
Het |
Prkd1 |
G |
A |
12: 50,441,709 (GRCm39) |
H277Y |
probably damaging |
Het |
Ptgs2 |
A |
G |
1: 149,977,021 (GRCm39) |
Y44C |
probably damaging |
Het |
Rbck1 |
T |
A |
2: 152,158,819 (GRCm39) |
S488C |
probably damaging |
Het |
Rbl1 |
T |
C |
2: 157,001,654 (GRCm39) |
Y878C |
probably damaging |
Het |
Rbm6 |
G |
A |
9: 107,669,055 (GRCm39) |
T619I |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,420,086 (GRCm39) |
I342T |
probably damaging |
Het |
Rufy4 |
G |
A |
1: 74,186,837 (GRCm39) |
V542I |
probably benign |
Het |
Sema5b |
C |
T |
16: 35,478,852 (GRCm39) |
P559S |
probably benign |
Het |
Serpinb3d |
A |
G |
1: 107,008,481 (GRCm39) |
V128A |
probably benign |
Het |
Slc35f3 |
T |
A |
8: 127,115,960 (GRCm39) |
S296T |
probably damaging |
Het |
Slco1a8 |
T |
A |
6: 141,927,775 (GRCm39) |
|
probably null |
Het |
Smarca2 |
A |
G |
19: 26,624,434 (GRCm39) |
I365V |
possibly damaging |
Het |
Spdya |
T |
A |
17: 71,885,235 (GRCm39) |
C230S |
probably damaging |
Het |
Sv2b |
G |
A |
7: 74,856,089 (GRCm39) |
A67V |
probably benign |
Het |
Tapbpl |
A |
G |
6: 125,207,164 (GRCm39) |
V175A |
probably benign |
Het |
Tmt1a3 |
A |
G |
15: 100,233,099 (GRCm39) |
I97V |
probably benign |
Het |
Ttn |
T |
C |
2: 76,642,095 (GRCm39) |
T13373A |
probably damaging |
Het |
Tubb5 |
A |
T |
17: 36,147,530 (GRCm39) |
N52K |
probably benign |
Het |
Tyr |
T |
A |
7: 87,142,149 (GRCm39) |
Y137F |
probably damaging |
Het |
Unc45b |
T |
A |
11: 82,808,565 (GRCm39) |
I217N |
probably benign |
Het |
Vmn1r202 |
A |
T |
13: 22,685,540 (GRCm39) |
D292E |
possibly damaging |
Het |
Vmn1r22 |
A |
G |
6: 57,877,704 (GRCm39) |
M91T |
probably benign |
Het |
Washc2 |
T |
A |
6: 116,200,215 (GRCm39) |
|
probably null |
Het |
Zfp566 |
A |
T |
7: 29,777,901 (GRCm39) |
H93Q |
probably benign |
Het |
Zfp740 |
A |
G |
15: 102,116,753 (GRCm39) |
D56G |
probably damaging |
Het |
Zfp804b |
A |
C |
5: 6,821,323 (GRCm39) |
L580R |
possibly damaging |
Het |
Zmiz2 |
T |
G |
11: 6,346,836 (GRCm39) |
S148R |
probably benign |
Het |
Zmym6 |
T |
A |
4: 127,016,652 (GRCm39) |
I719N |
probably damaging |
Het |
Zyx |
T |
A |
6: 42,332,966 (GRCm39) |
V372E |
possibly damaging |
Het |
|
Other mutations in Rpn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00547:Rpn2
|
APN |
2 |
157,156,833 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01894:Rpn2
|
APN |
2 |
157,136,093 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02104:Rpn2
|
APN |
2 |
157,163,747 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02368:Rpn2
|
APN |
2 |
157,144,328 (GRCm39) |
missense |
probably benign |
|
IGL02819:Rpn2
|
APN |
2 |
157,158,130 (GRCm39) |
critical splice donor site |
probably null |
|
R0932:Rpn2
|
UTSW |
2 |
157,125,691 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1668:Rpn2
|
UTSW |
2 |
157,136,075 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1713:Rpn2
|
UTSW |
2 |
157,156,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R2276:Rpn2
|
UTSW |
2 |
157,152,208 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2279:Rpn2
|
UTSW |
2 |
157,152,208 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3409:Rpn2
|
UTSW |
2 |
157,132,572 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3411:Rpn2
|
UTSW |
2 |
157,132,572 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3777:Rpn2
|
UTSW |
2 |
157,141,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R4004:Rpn2
|
UTSW |
2 |
157,159,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Rpn2
|
UTSW |
2 |
157,137,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Rpn2
|
UTSW |
2 |
157,144,345 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4856:Rpn2
|
UTSW |
2 |
157,159,964 (GRCm39) |
critical splice donor site |
probably null |
|
R4886:Rpn2
|
UTSW |
2 |
157,159,964 (GRCm39) |
critical splice donor site |
probably null |
|
R5491:Rpn2
|
UTSW |
2 |
157,139,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R5526:Rpn2
|
UTSW |
2 |
157,165,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R5633:Rpn2
|
UTSW |
2 |
157,125,516 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5718:Rpn2
|
UTSW |
2 |
157,163,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Rpn2
|
UTSW |
2 |
157,137,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6101:Rpn2
|
UTSW |
2 |
157,152,108 (GRCm39) |
splice site |
probably null |
|
R6618:Rpn2
|
UTSW |
2 |
157,163,781 (GRCm39) |
missense |
probably benign |
|
R6698:Rpn2
|
UTSW |
2 |
157,139,330 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8882:Rpn2
|
UTSW |
2 |
157,136,102 (GRCm39) |
missense |
probably benign |
|
R8953:Rpn2
|
UTSW |
2 |
157,163,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9085:Rpn2
|
UTSW |
2 |
157,125,567 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9124:Rpn2
|
UTSW |
2 |
157,139,458 (GRCm39) |
missense |
probably benign |
|
R9368:Rpn2
|
UTSW |
2 |
157,141,500 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9638:Rpn2
|
UTSW |
2 |
157,125,566 (GRCm39) |
missense |
probably benign |
0.03 |
|