Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts6 |
C |
A |
13: 104,613,275 (GRCm39) |
R1009S |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,261,033 (GRCm39) |
I1219K |
probably damaging |
Het |
Ap3b1 |
T |
C |
13: 94,609,439 (GRCm39) |
|
probably null |
Het |
Ap3b1 |
T |
A |
13: 94,630,239 (GRCm39) |
D831E |
unknown |
Het |
Arsa |
G |
A |
15: 89,359,995 (GRCm39) |
|
probably benign |
Het |
Clrn2 |
T |
C |
5: 45,621,254 (GRCm39) |
I216T |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,795,463 (GRCm39) |
K1066R |
probably benign |
Het |
Cul4a |
T |
C |
8: 13,155,799 (GRCm39) |
M15T |
probably benign |
Het |
Defb38 |
C |
T |
8: 19,076,558 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
T |
C |
11: 66,021,457 (GRCm39) |
D323G |
probably damaging |
Het |
Dsg1c |
T |
A |
18: 20,416,329 (GRCm39) |
D743E |
probably benign |
Het |
Eif1ad11 |
T |
C |
12: 87,993,946 (GRCm39) |
L58P |
probably damaging |
Het |
Elf1 |
T |
C |
14: 79,808,352 (GRCm39) |
L268P |
probably damaging |
Het |
Helq |
G |
T |
5: 100,918,325 (GRCm39) |
A863D |
probably benign |
Het |
Hfm1 |
T |
A |
5: 106,989,611 (GRCm39) |
R1368S |
probably benign |
Het |
Hspg2 |
G |
A |
4: 137,249,876 (GRCm39) |
G1379E |
possibly damaging |
Het |
Kcnq5 |
A |
T |
1: 21,539,692 (GRCm39) |
|
probably null |
Het |
Lrit2 |
C |
T |
14: 36,794,187 (GRCm39) |
T417I |
probably damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Macroh2a1 |
CTTACCTCCAGCT |
C |
13: 56,232,004 (GRCm39) |
|
probably null |
Het |
Mgat2 |
G |
A |
12: 69,232,497 (GRCm39) |
W357* |
probably null |
Het |
Mlkl |
A |
G |
8: 112,046,403 (GRCm39) |
L290P |
probably damaging |
Het |
Or1j11 |
T |
A |
2: 36,311,439 (GRCm39) |
S10T |
possibly damaging |
Het |
Or2k2 |
T |
C |
4: 58,785,114 (GRCm39) |
I203V |
probably benign |
Het |
Or7g32 |
A |
T |
9: 19,408,448 (GRCm39) |
I135F |
probably damaging |
Het |
Pcnx1 |
T |
C |
12: 82,022,589 (GRCm39) |
V853A |
|
Het |
Pex19 |
GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC |
GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC |
1: 171,956,150 (GRCm39) |
|
probably null |
Het |
Pik3c2a |
G |
A |
7: 116,017,004 (GRCm39) |
S251L |
probably benign |
Het |
Prkch |
T |
C |
12: 73,738,418 (GRCm39) |
M175T |
possibly damaging |
Het |
Psg22 |
A |
T |
7: 18,460,646 (GRCm39) |
Q425L |
probably damaging |
Het |
Ranbp10 |
A |
T |
8: 106,499,140 (GRCm39) |
L549M |
probably benign |
Het |
Rbbp6 |
A |
G |
7: 122,600,697 (GRCm39) |
E1568G |
unknown |
Het |
Rrh |
A |
T |
3: 129,606,903 (GRCm39) |
D173E |
probably benign |
Het |
Scart2 |
A |
T |
7: 139,877,256 (GRCm39) |
N857I |
possibly damaging |
Het |
Selplg |
A |
G |
5: 113,957,467 (GRCm39) |
S280P |
probably benign |
Het |
Septin11 |
T |
C |
5: 93,287,329 (GRCm39) |
S17P |
probably benign |
Het |
Stard9 |
T |
C |
2: 120,529,068 (GRCm39) |
V1775A |
probably damaging |
Het |
Tep1 |
A |
C |
14: 51,104,162 (GRCm39) |
V244G |
probably benign |
Het |
Tex24 |
A |
C |
8: 27,835,379 (GRCm39) |
E302D |
possibly damaging |
Het |
Trav18 |
A |
G |
14: 54,069,011 (GRCm39) |
T19A |
probably benign |
Het |
Trim56 |
T |
C |
5: 137,143,387 (GRCm39) |
D43G |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,029,056 (GRCm39) |
T1869A |
probably damaging |
Het |
Usp22 |
A |
G |
11: 61,049,201 (GRCm39) |
C383R |
probably damaging |
Het |
Zdhhc22 |
G |
A |
12: 87,035,192 (GRCm39) |
P87S |
probably benign |
Het |
|
Other mutations in Qpctl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02162:Qpctl
|
APN |
7 |
18,878,606 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5807:Qpctl
|
UTSW |
7 |
18,877,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R6223:Qpctl
|
UTSW |
7 |
18,877,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R6283:Qpctl
|
UTSW |
7 |
18,882,345 (GRCm39) |
missense |
probably benign |
0.03 |
R6453:Qpctl
|
UTSW |
7 |
18,875,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Qpctl
|
UTSW |
7 |
18,883,079 (GRCm39) |
missense |
probably benign |
|
R7042:Qpctl
|
UTSW |
7 |
18,880,943 (GRCm39) |
missense |
probably benign |
0.00 |
R7197:Qpctl
|
UTSW |
7 |
18,882,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7267:Qpctl
|
UTSW |
7 |
18,878,852 (GRCm39) |
missense |
probably benign |
0.03 |
R7295:Qpctl
|
UTSW |
7 |
18,883,055 (GRCm39) |
missense |
probably benign |
0.12 |
R8309:Qpctl
|
UTSW |
7 |
18,882,398 (GRCm39) |
missense |
probably benign |
0.00 |
R9056:Qpctl
|
UTSW |
7 |
18,880,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Qpctl
|
UTSW |
7 |
18,878,599 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9355:Qpctl
|
UTSW |
7 |
18,875,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|