Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aar2 |
T |
C |
2: 156,397,915 (GRCm39) |
I309T |
possibly damaging |
Het |
Abca12 |
A |
C |
1: 71,286,295 (GRCm39) |
L2513* |
probably null |
Het |
Abca13 |
G |
C |
11: 9,460,463 (GRCm39) |
V4158L |
probably benign |
Het |
Acaca |
A |
G |
11: 84,254,562 (GRCm39) |
T1880A |
possibly damaging |
Het |
Arhgap5 |
C |
T |
12: 52,564,783 (GRCm39) |
R585C |
probably benign |
Het |
Arsk |
A |
C |
13: 76,210,634 (GRCm39) |
I471S |
possibly damaging |
Het |
Asb7 |
T |
C |
7: 66,309,868 (GRCm39) |
D116G |
probably damaging |
Het |
Atad2 |
A |
G |
15: 57,998,322 (GRCm39) |
S17P |
probably benign |
Het |
Atf5 |
T |
C |
7: 44,464,562 (GRCm39) |
E10G |
probably damaging |
Het |
B3gntl1 |
G |
T |
11: 121,515,004 (GRCm39) |
P255T |
probably benign |
Het |
Cacna1s |
A |
G |
1: 136,014,540 (GRCm39) |
N649S |
probably damaging |
Het |
Ccnc |
A |
G |
4: 21,743,291 (GRCm39) |
Y192C |
probably damaging |
Het |
Cd28 |
A |
G |
1: 60,802,459 (GRCm39) |
N126S |
probably benign |
Het |
Cep57 |
A |
G |
9: 13,721,969 (GRCm39) |
S360P |
possibly damaging |
Het |
Ces1e |
C |
T |
8: 93,941,703 (GRCm39) |
V257I |
probably benign |
Het |
Chd1 |
A |
G |
17: 15,969,660 (GRCm39) |
K913R |
probably benign |
Het |
Cluap1 |
A |
T |
16: 3,758,657 (GRCm39) |
D373V |
probably damaging |
Het |
Cnmd |
T |
C |
14: 79,882,947 (GRCm39) |
I160V |
probably benign |
Het |
Col6a4 |
G |
A |
9: 105,897,994 (GRCm39) |
P1686S |
probably damaging |
Het |
Coro7 |
G |
T |
16: 4,486,615 (GRCm39) |
A186E |
probably benign |
Het |
Cuta |
T |
C |
17: 27,158,431 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
G |
A |
11: 69,383,631 (GRCm39) |
H1098Y |
probably benign |
Het |
Duox1 |
T |
A |
2: 122,153,711 (GRCm39) |
C345S |
probably damaging |
Het |
Ephb4 |
T |
A |
5: 137,352,687 (GRCm39) |
I90K |
possibly damaging |
Het |
Erich3 |
T |
A |
3: 154,439,198 (GRCm39) |
M280K |
probably damaging |
Het |
Fcer2a |
T |
A |
8: 3,740,335 (GRCm39) |
H4L |
probably benign |
Het |
Grk1 |
A |
T |
8: 13,455,316 (GRCm39) |
I67F |
probably damaging |
Het |
Grm8 |
A |
C |
6: 27,762,476 (GRCm39) |
S250A |
possibly damaging |
Het |
H2-Q6 |
A |
G |
17: 35,644,204 (GRCm39) |
E62G |
possibly damaging |
Het |
Inppl1 |
C |
T |
7: 101,482,144 (GRCm39) |
R144H |
probably damaging |
Het |
Itga3 |
G |
T |
11: 94,959,681 (GRCm39) |
P33Q |
probably benign |
Het |
Itgax |
G |
A |
7: 127,739,604 (GRCm39) |
S672N |
probably damaging |
Het |
Itpk1 |
A |
T |
12: 102,540,324 (GRCm39) |
V253E |
possibly damaging |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Mrps7 |
T |
C |
11: 115,495,717 (GRCm39) |
V85A |
probably benign |
Het |
Muc2 |
T |
C |
7: 141,301,863 (GRCm39) |
L427P |
|
Het |
Myef2 |
G |
T |
2: 124,952,537 (GRCm39) |
Q185K |
probably benign |
Het |
Or1e1b-ps1 |
G |
T |
11: 73,846,335 (GRCm39) |
C273F |
unknown |
Het |
Or4a76 |
T |
A |
2: 89,460,915 (GRCm39) |
D109V |
probably damaging |
Het |
Pcdh15 |
G |
A |
10: 74,289,897 (GRCm39) |
M905I |
possibly damaging |
Het |
Pgm5 |
C |
T |
19: 24,686,663 (GRCm39) |
V515M |
probably benign |
Het |
Pik3r1 |
A |
G |
13: 101,825,644 (GRCm39) |
I381T |
probably damaging |
Het |
Prmt2 |
A |
G |
10: 76,056,912 (GRCm39) |
F204L |
probably benign |
Het |
Pwwp3a |
T |
A |
10: 80,068,587 (GRCm39) |
S244T |
probably benign |
Het |
Rasa2 |
A |
G |
9: 96,493,500 (GRCm39) |
V50A |
unknown |
Het |
Scn7a |
A |
C |
2: 66,505,876 (GRCm39) |
I1671S |
probably benign |
Het |
Sco2 |
G |
A |
15: 89,255,923 (GRCm39) |
R244C |
possibly damaging |
Het |
Skic3 |
A |
T |
13: 76,296,944 (GRCm39) |
K1100N |
probably benign |
Het |
Slfn1 |
A |
G |
11: 83,011,967 (GRCm39) |
M28V |
possibly damaging |
Het |
Slfn9 |
A |
T |
11: 82,872,197 (GRCm39) |
C846* |
probably null |
Het |
Slfn9 |
A |
G |
11: 82,878,562 (GRCm39) |
I189T |
probably damaging |
Het |
Svil |
T |
A |
18: 5,056,109 (GRCm39) |
S327R |
probably benign |
Het |
Tcaf3 |
A |
T |
6: 42,573,776 (GRCm39) |
N145K |
probably benign |
Het |
Trarg1 |
G |
A |
11: 76,585,051 (GRCm39) |
R147Q |
unknown |
Het |
Trgv6 |
G |
T |
13: 19,374,814 (GRCm39) |
G40W |
possibly damaging |
Het |
Upp2 |
G |
T |
2: 58,661,586 (GRCm39) |
V130F |
possibly damaging |
Het |
Vnn3 |
G |
A |
10: 23,741,666 (GRCm39) |
A324T |
probably benign |
Het |
Wasf2 |
A |
G |
4: 132,912,412 (GRCm39) |
E88G |
unknown |
Het |
Zfp39 |
A |
T |
11: 58,780,933 (GRCm39) |
C610S |
probably damaging |
Het |
|
Other mutations in Pla2g4f |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00539:Pla2g4f
|
APN |
2 |
120,133,219 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01652:Pla2g4f
|
APN |
2 |
120,132,716 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02792:Pla2g4f
|
APN |
2 |
120,133,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R0625:Pla2g4f
|
UTSW |
2 |
120,135,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R1760:Pla2g4f
|
UTSW |
2 |
120,144,547 (GRCm39) |
unclassified |
probably benign |
|
R1799:Pla2g4f
|
UTSW |
2 |
120,141,549 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2212:Pla2g4f
|
UTSW |
2 |
120,133,587 (GRCm39) |
missense |
probably benign |
|
R2351:Pla2g4f
|
UTSW |
2 |
120,130,923 (GRCm39) |
missense |
probably benign |
0.01 |
R3412:Pla2g4f
|
UTSW |
2 |
120,133,587 (GRCm39) |
missense |
probably benign |
|
R3414:Pla2g4f
|
UTSW |
2 |
120,133,587 (GRCm39) |
missense |
probably benign |
|
R3906:Pla2g4f
|
UTSW |
2 |
120,130,980 (GRCm39) |
missense |
probably benign |
0.28 |
R4084:Pla2g4f
|
UTSW |
2 |
120,142,806 (GRCm39) |
missense |
probably benign |
0.36 |
R4477:Pla2g4f
|
UTSW |
2 |
120,134,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R4529:Pla2g4f
|
UTSW |
2 |
120,131,100 (GRCm39) |
missense |
probably damaging |
0.99 |
R4606:Pla2g4f
|
UTSW |
2 |
120,144,467 (GRCm39) |
missense |
probably benign |
0.00 |
R4685:Pla2g4f
|
UTSW |
2 |
120,135,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Pla2g4f
|
UTSW |
2 |
120,131,402 (GRCm39) |
missense |
probably benign |
0.19 |
R4782:Pla2g4f
|
UTSW |
2 |
120,133,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Pla2g4f
|
UTSW |
2 |
120,130,980 (GRCm39) |
missense |
probably benign |
0.28 |
R5781:Pla2g4f
|
UTSW |
2 |
120,135,504 (GRCm39) |
missense |
probably damaging |
0.97 |
R6158:Pla2g4f
|
UTSW |
2 |
120,131,552 (GRCm39) |
missense |
probably benign |
0.21 |
R6232:Pla2g4f
|
UTSW |
2 |
120,132,702 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6629:Pla2g4f
|
UTSW |
2 |
120,138,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Pla2g4f
|
UTSW |
2 |
120,134,077 (GRCm39) |
missense |
probably benign |
0.44 |
R6939:Pla2g4f
|
UTSW |
2 |
120,137,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Pla2g4f
|
UTSW |
2 |
120,135,035 (GRCm39) |
missense |
probably null |
0.01 |
R7221:Pla2g4f
|
UTSW |
2 |
120,131,476 (GRCm39) |
missense |
probably benign |
0.06 |
R7767:Pla2g4f
|
UTSW |
2 |
120,135,490 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8466:Pla2g4f
|
UTSW |
2 |
120,130,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R9389:Pla2g4f
|
UTSW |
2 |
120,132,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R9425:Pla2g4f
|
UTSW |
2 |
120,133,264 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9500:Pla2g4f
|
UTSW |
2 |
120,142,713 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9657:Pla2g4f
|
UTSW |
2 |
120,135,138 (GRCm39) |
missense |
probably benign |
|
R9714:Pla2g4f
|
UTSW |
2 |
120,142,900 (GRCm39) |
missense |
probably benign |
0.00 |
|