Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930544G11Rik |
T |
C |
6: 65,929,983 (GRCm39) |
S73P |
probably damaging |
Het |
5730596B20Rik |
G |
T |
6: 52,156,449 (GRCm39) |
V172F |
unknown |
Het |
Brms1 |
A |
G |
19: 5,096,229 (GRCm39) |
K69E |
probably damaging |
Het |
Calr4 |
A |
C |
4: 109,093,053 (GRCm39) |
Q44H |
possibly damaging |
Het |
Dnmt1 |
G |
A |
9: 20,823,071 (GRCm39) |
T1242I |
probably benign |
Het |
Dyrk3 |
A |
G |
1: 131,057,918 (GRCm39) |
V85A |
probably damaging |
Het |
Eif2a |
T |
C |
3: 58,452,974 (GRCm39) |
Y250H |
probably damaging |
Het |
Esco1 |
T |
C |
18: 10,572,093 (GRCm39) |
E749G |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,477,682 (GRCm39) |
I2243V |
probably damaging |
Het |
Gh |
A |
T |
11: 106,191,659 (GRCm39) |
F128I |
possibly damaging |
Het |
Gm17669 |
TAA |
TAAA |
18: 67,695,819 (GRCm39) |
|
probably null |
Het |
Gtpbp4 |
A |
G |
13: 9,041,763 (GRCm39) |
Y150H |
probably damaging |
Het |
H2ac15 |
C |
A |
13: 21,937,781 (GRCm39) |
D73Y |
probably damaging |
Het |
Itga8 |
A |
G |
2: 12,234,903 (GRCm39) |
S452P |
probably benign |
Het |
Kcnma1 |
C |
T |
14: 23,359,103 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,367,114 (GRCm39) |
E2549G |
probably benign |
Het |
Mindy1 |
C |
T |
3: 95,195,380 (GRCm39) |
A41V |
probably benign |
Het |
Mypn |
T |
A |
10: 62,955,850 (GRCm39) |
K1201M |
probably damaging |
Het |
Ncor1 |
A |
G |
11: 62,224,543 (GRCm39) |
S906P |
probably damaging |
Het |
Npy1r |
T |
C |
8: 67,156,874 (GRCm39) |
V98A |
probably benign |
Het |
Pate2 |
A |
G |
9: 35,581,889 (GRCm39) |
Y61C |
probably damaging |
Het |
Pfdn2 |
A |
G |
1: 171,173,310 (GRCm39) |
S11G |
unknown |
Het |
Prdm1 |
T |
C |
10: 44,334,504 (GRCm39) |
M1V |
probably null |
Het |
Prelp |
A |
G |
1: 133,842,903 (GRCm39) |
S81P |
possibly damaging |
Het |
Prss12 |
T |
C |
3: 123,280,764 (GRCm39) |
V483A |
probably damaging |
Het |
Ptpru |
G |
A |
4: 131,529,855 (GRCm39) |
R618* |
probably null |
Het |
Rpa1 |
A |
G |
11: 75,203,984 (GRCm39) |
S288P |
probably damaging |
Het |
Semp2l1 |
T |
C |
1: 32,585,553 (GRCm39) |
E119G |
probably damaging |
Het |
Siglec1 |
A |
G |
2: 130,920,081 (GRCm39) |
F817L |
probably damaging |
Het |
Skint6 |
T |
A |
4: 112,910,564 (GRCm39) |
S545C |
possibly damaging |
Het |
Slit1 |
A |
T |
19: 41,612,988 (GRCm39) |
V844D |
possibly damaging |
Het |
Suclg2 |
G |
T |
6: 95,563,999 (GRCm39) |
D195E |
possibly damaging |
Het |
Tln1 |
G |
T |
4: 43,539,998 (GRCm39) |
A1537D |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,472,027 (GRCm39) |
D73G |
probably damaging |
Het |
Ucp3 |
T |
C |
7: 100,129,458 (GRCm39) |
S98P |
probably benign |
Het |
Usp19 |
T |
A |
9: 108,369,931 (GRCm39) |
|
probably null |
Het |
Vmn2r112 |
T |
C |
17: 22,833,912 (GRCm39) |
F527L |
probably benign |
Het |
Vmn2r93 |
T |
C |
17: 18,533,473 (GRCm39) |
V459A |
probably benign |
Het |
|
Other mutations in Prss43 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Prss43
|
APN |
9 |
110,658,538 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01636:Prss43
|
APN |
9 |
110,656,505 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03046:Prss43
|
UTSW |
9 |
110,660,049 (GRCm39) |
missense |
probably benign |
0.01 |
R0020:Prss43
|
UTSW |
9 |
110,657,580 (GRCm39) |
unclassified |
probably benign |
|
R0278:Prss43
|
UTSW |
9 |
110,656,430 (GRCm39) |
missense |
probably benign |
0.07 |
R0883:Prss43
|
UTSW |
9 |
110,658,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Prss43
|
UTSW |
9 |
110,656,510 (GRCm39) |
missense |
probably benign |
0.10 |
R2212:Prss43
|
UTSW |
9 |
110,658,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R3412:Prss43
|
UTSW |
9 |
110,658,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R3808:Prss43
|
UTSW |
9 |
110,656,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R4202:Prss43
|
UTSW |
9 |
110,656,529 (GRCm39) |
missense |
probably benign |
0.08 |
R4530:Prss43
|
UTSW |
9 |
110,658,572 (GRCm39) |
missense |
probably benign |
0.38 |
R4752:Prss43
|
UTSW |
9 |
110,656,836 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5009:Prss43
|
UTSW |
9 |
110,656,489 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6920:Prss43
|
UTSW |
9 |
110,657,680 (GRCm39) |
missense |
probably benign |
0.04 |
R7271:Prss43
|
UTSW |
9 |
110,657,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R7406:Prss43
|
UTSW |
9 |
110,657,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7758:Prss43
|
UTSW |
9 |
110,658,459 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8257:Prss43
|
UTSW |
9 |
110,659,880 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8686:Prss43
|
UTSW |
9 |
110,658,494 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8885:Prss43
|
UTSW |
9 |
110,660,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R9217:Prss43
|
UTSW |
9 |
110,656,564 (GRCm39) |
missense |
possibly damaging |
0.75 |
|