Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atosb |
C |
T |
4: 43,033,896 (GRCm39) |
R460H |
probably damaging |
Het |
Atp2a1 |
G |
T |
7: 126,049,434 (GRCm39) |
P536Q |
probably benign |
Het |
Bnip5 |
T |
A |
17: 29,123,585 (GRCm39) |
D114V |
probably damaging |
Het |
Cabyr |
T |
A |
18: 12,884,073 (GRCm39) |
S187T |
probably benign |
Het |
Camkk1 |
A |
T |
11: 72,924,696 (GRCm39) |
N303I |
probably benign |
Het |
Cdh13 |
C |
T |
8: 119,694,926 (GRCm39) |
P259S |
probably damaging |
Het |
Csnk1g3 |
A |
G |
18: 54,063,354 (GRCm39) |
D255G |
possibly damaging |
Het |
Dennd5b |
A |
C |
6: 148,915,749 (GRCm39) |
|
probably null |
Het |
Dnajc14 |
A |
G |
10: 128,650,500 (GRCm39) |
D528G |
probably benign |
Het |
Edem1 |
T |
C |
6: 108,831,318 (GRCm39) |
F593S |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,899,077 (GRCm39) |
N4343S |
probably null |
Het |
Erbb2 |
G |
A |
11: 98,326,908 (GRCm39) |
D1106N |
possibly damaging |
Het |
Ermp1 |
T |
C |
19: 29,590,321 (GRCm39) |
M794V |
possibly damaging |
Het |
Fip1l1 |
T |
A |
5: 74,707,838 (GRCm39) |
|
probably null |
Het |
Gtf2h1 |
T |
A |
7: 46,458,089 (GRCm39) |
C245S |
probably damaging |
Het |
Hdhd5 |
T |
C |
6: 120,500,515 (GRCm39) |
H61R |
probably benign |
Het |
Ighv1-71 |
A |
T |
12: 115,706,092 (GRCm39) |
V31E |
probably damaging |
Het |
Igsf9b |
T |
C |
9: 27,240,851 (GRCm39) |
F688S |
probably damaging |
Het |
Iqcd |
T |
C |
5: 120,740,443 (GRCm39) |
V258A |
probably damaging |
Het |
Kcnc2 |
G |
C |
10: 112,107,761 (GRCm39) |
G51R |
probably benign |
Het |
Lpo |
G |
T |
11: 87,708,589 (GRCm39) |
Y136* |
probably null |
Het |
Med30 |
A |
G |
15: 52,593,779 (GRCm39) |
|
probably benign |
Het |
Mertk |
T |
A |
2: 128,618,341 (GRCm39) |
V524D |
probably benign |
Het |
Ndufb11b |
A |
G |
15: 81,864,939 (GRCm39) |
D60G |
probably damaging |
Het |
Or4c126 |
T |
A |
2: 89,824,517 (GRCm39) |
F260Y |
probably benign |
Het |
Or4c52 |
T |
C |
2: 89,845,438 (GRCm39) |
Y55H |
probably damaging |
Het |
Or5l13 |
T |
C |
2: 87,780,320 (GRCm39) |
I86V |
probably benign |
Het |
Pde6b |
T |
A |
5: 108,569,367 (GRCm39) |
M358K |
possibly damaging |
Het |
Prep |
GA |
G |
10: 45,034,410 (GRCm39) |
|
probably null |
Het |
Prpf4b |
G |
A |
13: 35,080,015 (GRCm39) |
R793Q |
probably damaging |
Het |
Rela |
T |
A |
19: 5,697,366 (GRCm39) |
N524K |
probably damaging |
Het |
Relch |
T |
A |
1: 105,654,165 (GRCm39) |
F845I |
probably damaging |
Het |
Rnaset2a |
T |
C |
17: 8,360,480 (GRCm39) |
D74G |
probably damaging |
Het |
Semp2l2a |
G |
A |
8: 13,887,690 (GRCm39) |
Q134* |
probably null |
Het |
Serinc2 |
T |
A |
4: 130,152,064 (GRCm39) |
I267F |
probably damaging |
Het |
Sesn3 |
T |
C |
9: 14,232,549 (GRCm39) |
F274S |
possibly damaging |
Het |
Spag1 |
T |
C |
15: 36,195,553 (GRCm39) |
Y249H |
probably damaging |
Het |
Sstr1 |
A |
T |
12: 58,260,478 (GRCm39) |
D367V |
possibly damaging |
Het |
Tasor |
T |
G |
14: 27,151,215 (GRCm39) |
Y64D |
probably benign |
Het |
Tnnt1 |
T |
C |
7: 4,512,576 (GRCm39) |
E110G |
probably damaging |
Het |
Tpm1 |
T |
A |
9: 66,935,451 (GRCm39) |
|
probably null |
Het |
Unc93b1 |
T |
C |
19: 3,994,105 (GRCm39) |
V412A |
probably benign |
Het |
Uox |
G |
C |
3: 146,330,403 (GRCm39) |
|
probably null |
Het |
Usp44 |
T |
C |
10: 93,681,870 (GRCm39) |
Y107H |
probably benign |
Het |
|
Other mutations in Gm20730 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0323:Gm20730
|
UTSW |
6 |
43,058,449 (GRCm39) |
splice site |
probably null |
|
R3821:Gm20730
|
UTSW |
6 |
43,058,656 (GRCm39) |
missense |
probably benign |
|
R3822:Gm20730
|
UTSW |
6 |
43,058,656 (GRCm39) |
missense |
probably benign |
|
R5493:Gm20730
|
UTSW |
6 |
43,058,746 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5578:Gm20730
|
UTSW |
6 |
43,058,474 (GRCm39) |
missense |
probably benign |
0.00 |
R5796:Gm20730
|
UTSW |
6 |
43,058,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R6812:Gm20730
|
UTSW |
6 |
43,058,722 (GRCm39) |
missense |
probably benign |
0.03 |
R6836:Gm20730
|
UTSW |
6 |
43,058,767 (GRCm39) |
splice site |
probably null |
|
R7615:Gm20730
|
UTSW |
6 |
43,058,708 (GRCm39) |
missense |
probably null |
0.99 |
R7809:Gm20730
|
UTSW |
6 |
43,058,989 (GRCm39) |
missense |
probably benign |
0.00 |
R8951:Gm20730
|
UTSW |
6 |
43,058,638 (GRCm39) |
missense |
possibly damaging |
0.78 |
|