Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933421I07Rik |
A |
G |
7: 42,095,769 (GRCm39) |
Y160H |
probably damaging |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Adgre1 |
T |
A |
17: 57,708,912 (GRCm39) |
N34K |
possibly damaging |
Het |
Ago2 |
T |
A |
15: 73,018,260 (GRCm39) |
E59D |
probably benign |
Het |
Akap8l |
G |
T |
17: 32,553,605 (GRCm39) |
Q372K |
probably benign |
Het |
Aox1 |
A |
G |
1: 58,388,289 (GRCm39) |
|
probably null |
Het |
Apc2 |
T |
C |
10: 80,144,943 (GRCm39) |
V618A |
probably benign |
Het |
Cacna1d |
A |
T |
14: 29,764,047 (GRCm39) |
C2140S |
probably damaging |
Het |
Cadps2 |
A |
G |
6: 23,410,831 (GRCm39) |
L671P |
probably damaging |
Het |
Capn9 |
C |
T |
8: 125,335,898 (GRCm39) |
R529* |
probably null |
Het |
Ccdc180 |
T |
A |
4: 45,944,949 (GRCm39) |
N1452K |
probably damaging |
Het |
Cdh5 |
A |
T |
8: 104,869,538 (GRCm39) |
I755F |
possibly damaging |
Het |
Cdkal1 |
T |
A |
13: 29,538,741 (GRCm39) |
M473L |
probably benign |
Het |
Cfap65 |
T |
C |
1: 74,943,184 (GRCm39) |
I1614V |
probably damaging |
Het |
Champ1 |
A |
G |
8: 13,930,017 (GRCm39) |
H725R |
probably damaging |
Het |
Cntnap5a |
A |
T |
1: 116,508,369 (GRCm39) |
T1294S |
possibly damaging |
Het |
Cops8 |
A |
C |
1: 90,534,341 (GRCm39) |
N94T |
probably benign |
Het |
Cpne7 |
G |
T |
8: 123,851,177 (GRCm39) |
V155L |
probably benign |
Het |
Dhx29 |
T |
C |
13: 113,089,338 (GRCm39) |
V703A |
probably damaging |
Het |
Dhx30 |
A |
G |
9: 109,916,703 (GRCm39) |
L575P |
probably damaging |
Het |
Dmc1 |
T |
A |
15: 79,469,327 (GRCm39) |
H156L |
possibly damaging |
Het |
Dnmt3a |
A |
G |
12: 3,899,654 (GRCm39) |
|
probably benign |
Het |
Dst |
C |
G |
1: 34,209,514 (GRCm39) |
L869V |
probably damaging |
Het |
Eif3d |
A |
T |
15: 77,849,142 (GRCm39) |
M180K |
probably benign |
Het |
Erbb3 |
T |
C |
10: 128,405,740 (GRCm39) |
T1173A |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,064,364 (GRCm39) |
K4773N |
probably damaging |
Het |
Fbn2 |
G |
A |
18: 58,186,035 (GRCm39) |
P1771L |
possibly damaging |
Het |
Fer1l4 |
T |
G |
2: 155,873,684 (GRCm39) |
Y1207S |
probably damaging |
Het |
Fermt2 |
G |
A |
14: 45,713,354 (GRCm39) |
T87I |
probably benign |
Het |
Fzd2 |
A |
G |
11: 102,496,249 (GRCm39) |
E231G |
probably benign |
Het |
Ggcx |
T |
C |
6: 72,404,965 (GRCm39) |
Y458H |
probably benign |
Het |
Ggt7 |
A |
G |
2: 155,337,639 (GRCm39) |
S504P |
probably damaging |
Het |
Gm4884 |
A |
G |
7: 40,692,910 (GRCm39) |
H293R |
possibly damaging |
Het |
Gm5475 |
A |
G |
15: 100,322,094 (GRCm39) |
|
probably benign |
Het |
Gm5930 |
A |
T |
14: 44,573,993 (GRCm39) |
L115M |
probably damaging |
Het |
Itln1 |
T |
A |
1: 171,359,115 (GRCm39) |
T122S |
probably damaging |
Het |
Itpr3 |
T |
A |
17: 27,334,027 (GRCm39) |
L2033Q |
probably benign |
Het |
Lama2 |
T |
C |
10: 26,919,565 (GRCm39) |
D2222G |
probably damaging |
Het |
Lars2 |
T |
C |
9: 123,247,845 (GRCm39) |
L334P |
probably damaging |
Het |
Ly9 |
T |
C |
1: 171,425,249 (GRCm39) |
|
probably null |
Het |
Man1a |
T |
C |
10: 53,853,145 (GRCm39) |
I324M |
probably damaging |
Het |
Mast3 |
T |
C |
8: 71,233,607 (GRCm39) |
E994G |
probably damaging |
Het |
Mettl21a |
A |
T |
1: 64,655,442 (GRCm39) |
V46E |
probably damaging |
Het |
Mmp15 |
A |
G |
8: 96,096,801 (GRCm39) |
D398G |
probably benign |
Het |
Mybpc1 |
T |
A |
10: 88,391,540 (GRCm39) |
D319V |
probably damaging |
Het |
Or10ad1c |
T |
A |
15: 98,084,848 (GRCm39) |
K277* |
probably null |
Het |
Or4a47 |
A |
T |
2: 89,665,769 (GRCm39) |
D173E |
probably damaging |
Het |
Or4a78 |
A |
T |
2: 89,498,211 (GRCm39) |
N6K |
possibly damaging |
Het |
Or4c35 |
G |
A |
2: 89,808,256 (GRCm39) |
V45I |
possibly damaging |
Het |
Or4f61 |
A |
T |
2: 111,922,752 (GRCm39) |
I98N |
probably damaging |
Het |
Or5b113 |
T |
A |
19: 13,342,901 (GRCm39) |
I303N |
possibly damaging |
Het |
Or5p5 |
G |
A |
7: 107,414,429 (GRCm39) |
V213I |
probably benign |
Het |
Or9m1 |
A |
C |
2: 87,733,269 (GRCm39) |
Y250* |
probably null |
Het |
Otogl |
C |
T |
10: 107,692,838 (GRCm39) |
C882Y |
probably damaging |
Het |
Parp10 |
A |
G |
15: 76,117,783 (GRCm39) |
Y868H |
probably damaging |
Het |
Pick1 |
T |
A |
15: 79,123,899 (GRCm39) |
I90N |
probably damaging |
Het |
Piezo1 |
C |
T |
8: 123,218,227 (GRCm39) |
V1170I |
probably benign |
Het |
Pim3 |
G |
A |
15: 88,747,115 (GRCm39) |
V54I |
possibly damaging |
Het |
Pinlyp |
T |
C |
7: 24,245,433 (GRCm39) |
|
probably benign |
Het |
Pira12 |
A |
T |
7: 3,900,488 (GRCm39) |
N87K |
probably benign |
Het |
Ppfia3 |
G |
A |
7: 45,004,314 (GRCm39) |
Q473* |
probably null |
Het |
Rab3gap2 |
G |
A |
1: 185,008,113 (GRCm39) |
G1056E |
probably damaging |
Het |
Ralgapa2 |
G |
A |
2: 146,263,599 (GRCm39) |
T706I |
probably benign |
Het |
Reln |
T |
C |
5: 22,177,045 (GRCm39) |
T1874A |
possibly damaging |
Het |
Rftn1 |
C |
A |
17: 50,476,173 (GRCm39) |
M1I |
probably null |
Het |
Ros1 |
T |
A |
10: 52,042,175 (GRCm39) |
Q250L |
probably damaging |
Het |
Slc11a1 |
T |
A |
1: 74,419,824 (GRCm39) |
F166I |
probably damaging |
Het |
Slc17a9 |
A |
G |
2: 180,373,755 (GRCm39) |
T59A |
probably benign |
Het |
Slc26a5 |
T |
C |
5: 22,028,476 (GRCm39) |
K364R |
probably damaging |
Het |
Slitrk2 |
T |
C |
X: 65,698,754 (GRCm39) |
I415T |
probably damaging |
Het |
Stom |
A |
G |
2: 35,211,613 (GRCm39) |
I136T |
possibly damaging |
Het |
Strc |
G |
T |
2: 121,195,004 (GRCm39) |
P1728T |
probably damaging |
Het |
Telo2 |
C |
A |
17: 25,322,673 (GRCm39) |
V640F |
probably benign |
Het |
Tg |
T |
C |
15: 66,553,782 (GRCm39) |
V399A |
probably benign |
Het |
Tmem214 |
A |
G |
5: 31,030,975 (GRCm39) |
K383E |
possibly damaging |
Het |
Tomm40l |
A |
T |
1: 171,049,550 (GRCm39) |
L13* |
probably null |
Het |
Tonsl |
A |
T |
15: 76,518,840 (GRCm39) |
N526K |
probably damaging |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Tymp |
T |
A |
15: 89,258,965 (GRCm39) |
M240L |
probably benign |
Het |
Ubr2 |
A |
T |
17: 47,296,968 (GRCm39) |
S271T |
possibly damaging |
Het |
Uggt2 |
A |
T |
14: 119,312,749 (GRCm39) |
N353K |
probably damaging |
Het |
Ugt2b35 |
T |
A |
5: 87,151,191 (GRCm39) |
F266I |
possibly damaging |
Het |
Vmn2r103 |
C |
T |
17: 20,013,909 (GRCm39) |
R234W |
probably damaging |
Het |
Zfp109 |
C |
A |
7: 23,927,886 (GRCm39) |
D508Y |
probably damaging |
Het |
Zfp623 |
T |
C |
15: 75,819,379 (GRCm39) |
S112P |
possibly damaging |
Het |
Zfp735 |
A |
G |
11: 73,601,851 (GRCm39) |
N265S |
possibly damaging |
Het |
Zfp879 |
A |
G |
11: 50,724,094 (GRCm39) |
C321R |
probably damaging |
Het |
|
Other mutations in Fpr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01067:Fpr3
|
APN |
17 |
18,190,828 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01520:Fpr3
|
APN |
17 |
18,191,325 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02166:Fpr3
|
APN |
17 |
18,190,726 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02380:Fpr3
|
APN |
17 |
18,191,254 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02587:Fpr3
|
APN |
17 |
18,190,953 (GRCm39) |
missense |
probably benign |
0.12 |
R1521:Fpr3
|
UTSW |
17 |
18,191,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Fpr3
|
UTSW |
17 |
18,190,922 (GRCm39) |
nonsense |
probably null |
|
R1913:Fpr3
|
UTSW |
17 |
18,191,670 (GRCm39) |
missense |
probably damaging |
0.96 |
R2099:Fpr3
|
UTSW |
17 |
18,191,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Fpr3
|
UTSW |
17 |
18,190,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Fpr3
|
UTSW |
17 |
18,190,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2224:Fpr3
|
UTSW |
17 |
18,191,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R2244:Fpr3
|
UTSW |
17 |
18,191,449 (GRCm39) |
missense |
probably benign |
0.03 |
R2994:Fpr3
|
UTSW |
17 |
18,191,130 (GRCm39) |
nonsense |
probably null |
|
R5364:Fpr3
|
UTSW |
17 |
18,190,806 (GRCm39) |
missense |
probably benign |
0.00 |
R6179:Fpr3
|
UTSW |
17 |
18,190,919 (GRCm39) |
nonsense |
probably null |
|
R6781:Fpr3
|
UTSW |
17 |
18,190,978 (GRCm39) |
missense |
probably benign |
0.09 |
R6909:Fpr3
|
UTSW |
17 |
18,191,429 (GRCm39) |
missense |
probably benign |
0.00 |
R7565:Fpr3
|
UTSW |
17 |
18,191,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R8008:Fpr3
|
UTSW |
17 |
18,191,715 (GRCm39) |
missense |
probably benign |
0.03 |
R8097:Fpr3
|
UTSW |
17 |
18,191,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R8351:Fpr3
|
UTSW |
17 |
18,191,436 (GRCm39) |
missense |
probably benign |
0.27 |
R8732:Fpr3
|
UTSW |
17 |
18,191,223 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8994:Fpr3
|
UTSW |
17 |
18,191,341 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9076:Fpr3
|
UTSW |
17 |
18,191,725 (GRCm39) |
missense |
probably benign |
|
R9206:Fpr3
|
UTSW |
17 |
18,191,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Fpr3
|
UTSW |
17 |
18,191,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9327:Fpr3
|
UTSW |
17 |
18,191,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9553:Fpr3
|
UTSW |
17 |
18,191,612 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Fpr3
|
UTSW |
17 |
18,191,500 (GRCm39) |
missense |
probably benign |
0.06 |
Z1176:Fpr3
|
UTSW |
17 |
18,191,255 (GRCm39) |
missense |
possibly damaging |
0.55 |
|