Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam12 |
T |
A |
7: 133,576,126 (GRCm39) |
Q228L |
probably damaging |
Het |
Arhgap45 |
A |
G |
10: 79,853,698 (GRCm39) |
T71A |
possibly damaging |
Het |
Bag6 |
T |
A |
17: 35,363,211 (GRCm39) |
S684T |
possibly damaging |
Het |
Bcam |
C |
T |
7: 19,500,806 (GRCm39) |
G123R |
probably damaging |
Het |
Cdcp3 |
T |
C |
7: 130,828,493 (GRCm39) |
L316P |
probably damaging |
Het |
Cdr2l |
C |
T |
11: 115,284,495 (GRCm39) |
A277V |
possibly damaging |
Het |
Clcn4 |
T |
A |
7: 7,302,181 (GRCm39) |
|
probably benign |
Het |
Csnk1g1 |
T |
A |
9: 65,880,794 (GRCm39) |
I72N |
probably damaging |
Het |
Cspg4b |
A |
T |
13: 113,456,743 (GRCm39) |
K930* |
probably null |
Het |
Ddx31 |
G |
A |
2: 28,764,188 (GRCm39) |
V465I |
probably benign |
Het |
Ddx54 |
C |
T |
5: 120,756,779 (GRCm39) |
Q163* |
probably null |
Het |
Dnmt3a |
A |
G |
12: 3,947,406 (GRCm39) |
E459G |
probably damaging |
Het |
Dpp8 |
T |
C |
9: 64,970,844 (GRCm39) |
S568P |
possibly damaging |
Het |
Drap1 |
G |
T |
19: 5,474,219 (GRCm39) |
T47K |
probably damaging |
Het |
Epha7 |
G |
T |
4: 28,950,528 (GRCm39) |
R777L |
possibly damaging |
Het |
Far2 |
T |
G |
6: 148,052,273 (GRCm39) |
|
probably null |
Het |
Fhdc1 |
T |
C |
3: 84,352,834 (GRCm39) |
K797R |
probably benign |
Het |
Gm10330 |
A |
T |
12: 23,830,094 (GRCm39) |
M29K |
probably damaging |
Het |
Grik3 |
A |
T |
4: 125,526,093 (GRCm39) |
I109F |
probably benign |
Het |
Il31ra |
T |
C |
13: 112,688,522 (GRCm39) |
|
probably null |
Het |
Itga1 |
T |
G |
13: 115,133,513 (GRCm39) |
I466L |
probably benign |
Het |
Itpr2 |
A |
T |
6: 146,287,371 (GRCm39) |
|
probably null |
Het |
Mical3 |
A |
C |
6: 120,935,786 (GRCm39) |
L1580R |
possibly damaging |
Het |
Or14c43 |
T |
A |
7: 86,114,835 (GRCm39) |
V72D |
probably damaging |
Het |
Or4n4 |
T |
C |
14: 50,519,644 (GRCm39) |
D22G |
probably benign |
Het |
Palb2 |
T |
A |
7: 121,726,711 (GRCm39) |
E386D |
probably damaging |
Het |
Polm |
C |
A |
11: 5,785,534 (GRCm39) |
R175L |
probably damaging |
Het |
Prpf40b |
C |
T |
15: 99,212,784 (GRCm39) |
R627W |
probably damaging |
Het |
Ptcd3 |
A |
T |
6: 71,885,627 (GRCm39) |
V33D |
probably benign |
Het |
Pwwp4c |
C |
T |
X: 73,684,021 (GRCm39) |
R355H |
probably damaging |
Homo |
Ripk4 |
C |
A |
16: 97,549,237 (GRCm39) |
R273L |
probably damaging |
Het |
Rpap2 |
A |
G |
5: 107,803,153 (GRCm39) |
T612A |
probably damaging |
Het |
Serpinb10 |
A |
G |
1: 107,474,597 (GRCm39) |
N253S |
possibly damaging |
Het |
Sgpp1 |
G |
C |
12: 75,782,243 (GRCm39) |
P32R |
probably benign |
Het |
Sim1 |
T |
C |
10: 50,784,823 (GRCm39) |
I156T |
possibly damaging |
Het |
Ski |
A |
T |
4: 155,245,289 (GRCm39) |
|
probably null |
Het |
Spaca7b |
G |
A |
8: 11,705,661 (GRCm39) |
Q39* |
probably null |
Het |
Tent2 |
G |
A |
13: 93,291,526 (GRCm39) |
A368V |
probably benign |
Het |
Tent2 |
C |
G |
13: 93,291,527 (GRCm39) |
A372P |
probably benign |
Het |
Trdn |
C |
T |
10: 33,314,811 (GRCm39) |
R512C |
probably damaging |
Het |
Trim33 |
T |
C |
3: 103,259,403 (GRCm39) |
Y1031H |
probably damaging |
Het |
Use1 |
T |
C |
8: 71,821,880 (GRCm39) |
L188P |
probably damaging |
Het |
Usp34 |
G |
A |
11: 23,362,318 (GRCm39) |
G1588D |
probably damaging |
Het |
Vmn2r33 |
C |
A |
7: 7,566,797 (GRCm39) |
R105L |
probably benign |
Het |
Vmn2r53 |
G |
A |
7: 12,335,360 (GRCm39) |
S100F |
probably damaging |
Het |
|
Other mutations in Pate8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01455:Pate8
|
APN |
9 |
36,492,659 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01693:Pate8
|
APN |
9 |
36,492,662 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02268:Pate8
|
APN |
9 |
36,493,166 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03191:Pate8
|
APN |
9 |
36,492,698 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4354001:Pate8
|
UTSW |
9 |
36,492,597 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0401:Pate8
|
UTSW |
9 |
36,493,924 (GRCm39) |
missense |
unknown |
|
R0743:Pate8
|
UTSW |
9 |
36,492,597 (GRCm39) |
missense |
probably benign |
0.03 |
R1483:Pate8
|
UTSW |
9 |
36,492,620 (GRCm39) |
missense |
probably benign |
0.00 |
R1701:Pate8
|
UTSW |
9 |
36,493,114 (GRCm39) |
critical splice donor site |
probably benign |
|
R2258:Pate8
|
UTSW |
9 |
36,493,161 (GRCm39) |
missense |
probably benign |
0.03 |
R3764:Pate8
|
UTSW |
9 |
36,493,114 (GRCm39) |
critical splice donor site |
probably null |
|
R5143:Pate8
|
UTSW |
9 |
36,493,200 (GRCm39) |
missense |
probably benign |
0.31 |
R7013:Pate8
|
UTSW |
9 |
36,493,854 (GRCm39) |
missense |
unknown |
|
R7014:Pate8
|
UTSW |
9 |
36,493,854 (GRCm39) |
missense |
unknown |
|
|