Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
G |
T |
10: 79,841,881 (GRCm39) |
V1005L |
possibly damaging |
Het |
Abcc9 |
A |
G |
6: 142,643,516 (GRCm39) |
S11P |
possibly damaging |
Het |
Acsl1 |
A |
T |
8: 46,945,873 (GRCm39) |
E2V |
possibly damaging |
Het |
Aox3 |
G |
A |
1: 58,205,055 (GRCm39) |
V757I |
probably benign |
Het |
Aqp4 |
T |
C |
18: 15,530,632 (GRCm39) |
|
probably null |
Het |
Arhgef7 |
A |
G |
8: 11,831,245 (GRCm39) |
|
probably benign |
Het |
Armc9 |
T |
A |
1: 86,172,293 (GRCm39) |
D2E |
probably damaging |
Het |
Celsr2 |
G |
A |
3: 108,321,429 (GRCm39) |
P461L |
probably benign |
Het |
Cep170 |
T |
C |
1: 176,570,080 (GRCm39) |
D1339G |
probably damaging |
Het |
Clk1 |
T |
A |
1: 58,453,635 (GRCm39) |
N317I |
probably damaging |
Het |
Comp |
G |
A |
8: 70,829,337 (GRCm39) |
G305S |
possibly damaging |
Het |
Depdc5 |
G |
A |
5: 33,050,712 (GRCm39) |
|
probably benign |
Het |
Dse |
T |
C |
10: 34,059,712 (GRCm39) |
E131G |
probably damaging |
Het |
Ecpas |
T |
A |
4: 58,864,343 (GRCm39) |
|
probably benign |
Het |
Emilin3 |
G |
A |
2: 160,750,649 (GRCm39) |
Q320* |
probably null |
Het |
Epha2 |
A |
G |
4: 141,046,230 (GRCm39) |
|
probably benign |
Het |
Fam243 |
A |
G |
16: 92,117,616 (GRCm39) |
I224T |
probably damaging |
Het |
Fmnl1 |
A |
G |
11: 103,087,592 (GRCm39) |
|
probably benign |
Het |
Gbp9 |
T |
C |
5: 105,231,624 (GRCm39) |
N321D |
probably damaging |
Het |
Gm5884 |
A |
G |
6: 128,622,738 (GRCm39) |
|
noncoding transcript |
Het |
Gp2 |
A |
T |
7: 119,051,452 (GRCm39) |
N254K |
probably benign |
Het |
Hgh1 |
T |
A |
15: 76,253,754 (GRCm39) |
|
probably null |
Het |
Inpp5f |
A |
G |
7: 128,284,030 (GRCm39) |
N543S |
probably damaging |
Het |
Ints7 |
T |
C |
1: 191,351,853 (GRCm39) |
V854A |
probably damaging |
Het |
Itgb1bp1 |
T |
G |
12: 21,320,879 (GRCm39) |
|
probably benign |
Het |
Lrrtm4 |
A |
T |
6: 79,998,947 (GRCm39) |
N120Y |
probably damaging |
Het |
Map3k5 |
T |
C |
10: 19,900,782 (GRCm39) |
S319P |
probably damaging |
Het |
Mc4r |
A |
G |
18: 66,992,318 (GRCm39) |
L265S |
probably damaging |
Het |
Morc1 |
T |
C |
16: 48,378,869 (GRCm39) |
|
probably benign |
Het |
Mre11a |
T |
A |
9: 14,701,966 (GRCm39) |
|
probably null |
Het |
Msh4 |
T |
C |
3: 153,607,037 (GRCm39) |
|
probably benign |
Het |
Mterf4 |
A |
G |
1: 93,232,455 (GRCm39) |
L132P |
probably damaging |
Het |
Myo15a |
A |
T |
11: 60,368,005 (GRCm39) |
E255V |
probably benign |
Het |
Myot |
T |
C |
18: 44,479,127 (GRCm39) |
V288A |
probably damaging |
Het |
Nipa2 |
T |
C |
7: 55,592,766 (GRCm39) |
Y53C |
probably damaging |
Het |
Npas1 |
T |
A |
7: 16,190,041 (GRCm39) |
I502F |
probably damaging |
Het |
Or12j5 |
C |
T |
7: 140,083,533 (GRCm39) |
V280M |
probably damaging |
Het |
Or2y1d |
T |
A |
11: 49,321,749 (GRCm39) |
W149R |
probably damaging |
Het |
Osbp2 |
A |
G |
11: 3,664,637 (GRCm39) |
V565A |
probably benign |
Het |
Otof |
A |
G |
5: 30,531,426 (GRCm39) |
S1666P |
probably benign |
Het |
Per3 |
A |
C |
4: 151,108,927 (GRCm39) |
S476A |
probably damaging |
Het |
Pja2 |
T |
C |
17: 64,604,789 (GRCm39) |
N465D |
probably damaging |
Het |
Plcd4 |
T |
A |
1: 74,596,967 (GRCm39) |
L403Q |
probably damaging |
Het |
Psg26 |
T |
C |
7: 18,209,080 (GRCm39) |
T443A |
probably benign |
Het |
Snapc4 |
T |
A |
2: 26,259,384 (GRCm39) |
T589S |
probably benign |
Het |
Spag8 |
G |
A |
4: 43,651,755 (GRCm39) |
R404W |
probably damaging |
Het |
Tdrd7 |
A |
G |
4: 45,994,406 (GRCm39) |
D268G |
probably benign |
Het |
Tfap2d |
A |
G |
1: 19,213,151 (GRCm39) |
H325R |
possibly damaging |
Het |
Vmn1r59 |
C |
T |
7: 5,457,176 (GRCm39) |
V195I |
probably damaging |
Het |
Vmn1r67 |
G |
A |
7: 10,180,945 (GRCm39) |
E70K |
probably benign |
Het |
Wdr18 |
T |
A |
10: 79,796,898 (GRCm39) |
N91K |
possibly damaging |
Het |
Zbtb7b |
T |
C |
3: 89,287,081 (GRCm39) |
T463A |
probably damaging |
Het |
|
Other mutations in Pla2g4c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00953:Pla2g4c
|
APN |
7 |
13,077,951 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00972:Pla2g4c
|
APN |
7 |
13,074,583 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01759:Pla2g4c
|
APN |
7 |
13,082,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Pla2g4c
|
APN |
7 |
13,079,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02629:Pla2g4c
|
APN |
7 |
13,069,302 (GRCm39) |
nonsense |
probably null |
|
IGL02719:Pla2g4c
|
APN |
7 |
13,064,019 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Pla2g4c
|
UTSW |
7 |
13,077,316 (GRCm39) |
missense |
probably benign |
|
R0184:Pla2g4c
|
UTSW |
7 |
13,090,145 (GRCm39) |
missense |
probably benign |
0.16 |
R1052:Pla2g4c
|
UTSW |
7 |
13,077,334 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1747:Pla2g4c
|
UTSW |
7 |
13,071,655 (GRCm39) |
splice site |
probably benign |
|
R4381:Pla2g4c
|
UTSW |
7 |
13,079,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R4486:Pla2g4c
|
UTSW |
7 |
13,071,676 (GRCm39) |
missense |
probably benign |
0.09 |
R4674:Pla2g4c
|
UTSW |
7 |
13,077,439 (GRCm39) |
missense |
probably null |
0.24 |
R4811:Pla2g4c
|
UTSW |
7 |
13,071,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Pla2g4c
|
UTSW |
7 |
13,063,889 (GRCm39) |
splice site |
probably null |
|
R5791:Pla2g4c
|
UTSW |
7 |
13,073,617 (GRCm39) |
missense |
probably benign |
0.32 |
R5814:Pla2g4c
|
UTSW |
7 |
13,074,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R6381:Pla2g4c
|
UTSW |
7 |
13,077,933 (GRCm39) |
missense |
probably benign |
0.05 |
R6395:Pla2g4c
|
UTSW |
7 |
13,077,933 (GRCm39) |
missense |
probably benign |
0.05 |
R6974:Pla2g4c
|
UTSW |
7 |
13,078,459 (GRCm39) |
critical splice donor site |
probably null |
|
R7257:Pla2g4c
|
UTSW |
7 |
13,059,669 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7823:Pla2g4c
|
UTSW |
7 |
13,063,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R8385:Pla2g4c
|
UTSW |
7 |
13,063,589 (GRCm39) |
missense |
probably benign |
0.00 |
R8737:Pla2g4c
|
UTSW |
7 |
13,069,154 (GRCm39) |
missense |
probably benign |
0.15 |
R8933:Pla2g4c
|
UTSW |
7 |
13,073,627 (GRCm39) |
missense |
probably benign |
0.25 |
R9086:Pla2g4c
|
UTSW |
7 |
13,071,692 (GRCm39) |
missense |
probably benign |
0.13 |
R9121:Pla2g4c
|
UTSW |
7 |
13,091,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R9226:Pla2g4c
|
UTSW |
7 |
13,059,671 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9456:Pla2g4c
|
UTSW |
7 |
13,077,900 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Pla2g4c
|
UTSW |
7 |
13,063,678 (GRCm39) |
missense |
probably benign |
0.13 |
Z1177:Pla2g4c
|
UTSW |
7 |
13,082,252 (GRCm39) |
missense |
possibly damaging |
0.91 |
|