Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030469F06Rik |
T |
C |
12: 31,235,042 (GRCm39) |
|
noncoding transcript |
Het |
Cops3 |
A |
G |
11: 59,712,217 (GRCm39) |
|
probably benign |
Het |
Cyth2 |
A |
T |
7: 45,457,805 (GRCm39) |
Y304N |
probably benign |
Het |
Evpl |
A |
G |
11: 116,114,048 (GRCm39) |
L1214P |
probably damaging |
Het |
Gm94 |
A |
G |
18: 43,917,746 (GRCm39) |
S40P |
probably damaging |
Het |
Gpm6a |
A |
T |
8: 55,503,212 (GRCm39) |
M154L |
probably benign |
Het |
Ipo13 |
A |
G |
4: 117,761,078 (GRCm39) |
S547P |
probably damaging |
Het |
Mfsd14b |
A |
C |
13: 65,234,907 (GRCm39) |
V90G |
possibly damaging |
Het |
Mfsd4b4 |
A |
T |
10: 39,768,025 (GRCm39) |
M356K |
probably damaging |
Het |
Msh6 |
T |
G |
17: 88,292,519 (GRCm39) |
F425V |
possibly damaging |
Het |
Or4k15c |
T |
C |
14: 50,321,737 (GRCm39) |
T134A |
probably benign |
Het |
Or52m2 |
A |
T |
7: 102,263,546 (GRCm39) |
L217I |
probably damaging |
Het |
Or6c215 |
A |
G |
10: 129,638,119 (GRCm39) |
Y92H |
probably damaging |
Het |
Ptk2 |
T |
C |
15: 73,114,322 (GRCm39) |
I679V |
probably benign |
Het |
Rtel1 |
T |
C |
2: 180,991,106 (GRCm39) |
|
probably benign |
Het |
Sema3d |
T |
A |
5: 12,613,282 (GRCm39) |
V453E |
probably damaging |
Het |
Spata31e2 |
C |
T |
1: 26,724,340 (GRCm39) |
C280Y |
probably damaging |
Het |
Syk |
C |
A |
13: 52,785,776 (GRCm39) |
D327E |
probably benign |
Het |
Triobp |
G |
A |
15: 78,856,847 (GRCm39) |
|
probably null |
Het |
Tubgcp5 |
G |
A |
7: 55,468,505 (GRCm39) |
E667K |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r76 |
G |
T |
7: 85,877,925 (GRCm39) |
H491N |
probably benign |
Het |
|
Other mutations in Dhx8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01922:Dhx8
|
APN |
11 |
101,630,633 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02039:Dhx8
|
APN |
11 |
101,654,853 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02115:Dhx8
|
APN |
11 |
101,643,214 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Dhx8
|
APN |
11 |
101,648,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02691:Dhx8
|
APN |
11 |
101,642,830 (GRCm39) |
splice site |
probably benign |
|
IGL02697:Dhx8
|
APN |
11 |
101,645,607 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Dhx8
|
UTSW |
11 |
101,629,014 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Dhx8
|
UTSW |
11 |
101,629,032 (GRCm39) |
frame shift |
probably null |
|
FR4449:Dhx8
|
UTSW |
11 |
101,629,020 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Dhx8
|
UTSW |
11 |
101,629,032 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Dhx8
|
UTSW |
11 |
101,629,033 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Dhx8
|
UTSW |
11 |
101,629,010 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Dhx8
|
UTSW |
11 |
101,629,016 (GRCm39) |
small deletion |
probably benign |
|
FR4589:Dhx8
|
UTSW |
11 |
101,629,014 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Dhx8
|
UTSW |
11 |
101,629,015 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Dhx8
|
UTSW |
11 |
101,629,005 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Dhx8
|
UTSW |
11 |
101,629,008 (GRCm39) |
small insertion |
probably benign |
|
R0402:Dhx8
|
UTSW |
11 |
101,643,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Dhx8
|
UTSW |
11 |
101,654,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R0969:Dhx8
|
UTSW |
11 |
101,630,526 (GRCm39) |
splice site |
probably benign |
|
R1497:Dhx8
|
UTSW |
11 |
101,626,213 (GRCm39) |
intron |
probably benign |
|
R1576:Dhx8
|
UTSW |
11 |
101,643,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1758:Dhx8
|
UTSW |
11 |
101,657,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R1773:Dhx8
|
UTSW |
11 |
101,643,189 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1941:Dhx8
|
UTSW |
11 |
101,643,024 (GRCm39) |
critical splice donor site |
probably null |
|
R1954:Dhx8
|
UTSW |
11 |
101,644,105 (GRCm39) |
missense |
probably damaging |
0.98 |
R2124:Dhx8
|
UTSW |
11 |
101,653,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R2128:Dhx8
|
UTSW |
11 |
101,629,235 (GRCm39) |
missense |
probably benign |
0.06 |
R2148:Dhx8
|
UTSW |
11 |
101,629,203 (GRCm39) |
nonsense |
probably null |
|
R2206:Dhx8
|
UTSW |
11 |
101,641,797 (GRCm39) |
missense |
probably benign |
0.03 |
R2207:Dhx8
|
UTSW |
11 |
101,641,797 (GRCm39) |
missense |
probably benign |
0.03 |
R4667:Dhx8
|
UTSW |
11 |
101,628,987 (GRCm39) |
missense |
unknown |
|
R4678:Dhx8
|
UTSW |
11 |
101,630,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Dhx8
|
UTSW |
11 |
101,628,996 (GRCm39) |
nonsense |
probably null |
|
R4943:Dhx8
|
UTSW |
11 |
101,628,526 (GRCm39) |
nonsense |
probably null |
|
R5341:Dhx8
|
UTSW |
11 |
101,629,016 (GRCm39) |
small deletion |
probably benign |
|
R5586:Dhx8
|
UTSW |
11 |
101,623,862 (GRCm39) |
unclassified |
probably benign |
|
R5662:Dhx8
|
UTSW |
11 |
101,657,584 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5664:Dhx8
|
UTSW |
11 |
101,631,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R6082:Dhx8
|
UTSW |
11 |
101,655,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R6085:Dhx8
|
UTSW |
11 |
101,655,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R6415:Dhx8
|
UTSW |
11 |
101,628,513 (GRCm39) |
missense |
unknown |
|
R6658:Dhx8
|
UTSW |
11 |
101,655,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6841:Dhx8
|
UTSW |
11 |
101,655,618 (GRCm39) |
missense |
probably damaging |
0.98 |
R6918:Dhx8
|
UTSW |
11 |
101,629,247 (GRCm39) |
nonsense |
probably null |
|
R7011:Dhx8
|
UTSW |
11 |
101,632,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Dhx8
|
UTSW |
11 |
101,628,594 (GRCm39) |
critical splice donor site |
probably null |
|
R7153:Dhx8
|
UTSW |
11 |
101,631,001 (GRCm39) |
splice site |
probably null |
|
R7284:Dhx8
|
UTSW |
11 |
101,645,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R7604:Dhx8
|
UTSW |
11 |
101,655,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R8135:Dhx8
|
UTSW |
11 |
101,629,090 (GRCm39) |
missense |
unknown |
|
R8137:Dhx8
|
UTSW |
11 |
101,654,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R8256:Dhx8
|
UTSW |
11 |
101,631,588 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8284:Dhx8
|
UTSW |
11 |
101,648,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R8289:Dhx8
|
UTSW |
11 |
101,631,571 (GRCm39) |
missense |
probably benign |
0.01 |
R8696:Dhx8
|
UTSW |
11 |
101,623,958 (GRCm39) |
missense |
unknown |
|
R9061:Dhx8
|
UTSW |
11 |
101,632,406 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9076:Dhx8
|
UTSW |
11 |
101,629,021 (GRCm39) |
missense |
|
|
R9443:Dhx8
|
UTSW |
11 |
101,655,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R9492:Dhx8
|
UTSW |
11 |
101,654,808 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9554:Dhx8
|
UTSW |
11 |
101,645,614 (GRCm39) |
nonsense |
probably null |
|
R9700:Dhx8
|
UTSW |
11 |
101,624,015 (GRCm39) |
critical splice donor site |
probably null |
|
R9780:Dhx8
|
UTSW |
11 |
101,632,403 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Dhx8
|
UTSW |
11 |
101,648,486 (GRCm39) |
missense |
probably damaging |
1.00 |
|