Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp6 |
T |
C |
3: 97,083,737 (GRCm39) |
Y404H |
possibly damaging |
Het |
Adgrv1 |
T |
A |
13: 81,620,996 (GRCm39) |
|
probably benign |
Het |
Akap13 |
A |
G |
7: 75,378,667 (GRCm39) |
K2107E |
probably damaging |
Het |
Ankrd42 |
A |
G |
7: 92,233,662 (GRCm39) |
|
probably benign |
Het |
Apba3 |
C |
T |
10: 81,108,901 (GRCm39) |
P555S |
probably damaging |
Het |
Aplnr |
A |
G |
2: 84,967,985 (GRCm39) |
S337G |
probably benign |
Het |
Arhgef40 |
A |
G |
14: 52,226,417 (GRCm39) |
N154D |
probably damaging |
Het |
Asb14 |
A |
G |
14: 26,633,998 (GRCm39) |
K401R |
probably benign |
Het |
Aspn |
C |
A |
13: 49,719,968 (GRCm39) |
T328K |
probably benign |
Het |
Barhl2 |
C |
T |
5: 106,603,365 (GRCm39) |
A265T |
possibly damaging |
Het |
Brca2 |
T |
A |
5: 150,463,363 (GRCm39) |
H1042Q |
probably benign |
Het |
C3 |
A |
G |
17: 57,533,004 (GRCm39) |
L167P |
probably benign |
Het |
Ccdc33 |
A |
G |
9: 57,977,257 (GRCm39) |
|
probably benign |
Het |
Cdk10 |
T |
A |
8: 123,957,063 (GRCm39) |
M222K |
possibly damaging |
Het |
Cfap45 |
C |
T |
1: 172,362,912 (GRCm39) |
|
probably benign |
Het |
Chil3 |
T |
A |
3: 106,056,017 (GRCm39) |
N352I |
probably damaging |
Het |
Chn2 |
G |
T |
6: 54,272,907 (GRCm39) |
|
probably null |
Het |
Cimip2b |
G |
A |
4: 43,428,158 (GRCm39) |
R100W |
possibly damaging |
Het |
Cpt1b |
T |
C |
15: 89,305,066 (GRCm39) |
E394G |
probably benign |
Het |
Fcgr2b |
T |
A |
1: 170,788,799 (GRCm39) |
N273I |
possibly damaging |
Het |
Fras1 |
T |
A |
5: 96,887,217 (GRCm39) |
N2666K |
possibly damaging |
Het |
Gfra3 |
C |
T |
18: 34,824,601 (GRCm39) |
|
probably null |
Het |
Gm4553 |
T |
C |
7: 141,718,964 (GRCm39) |
S155G |
unknown |
Het |
Gpr75 |
C |
T |
11: 30,841,590 (GRCm39) |
T165I |
probably damaging |
Het |
Gzmd |
A |
T |
14: 56,367,737 (GRCm39) |
C179S |
probably damaging |
Het |
Hand1 |
T |
G |
11: 57,722,575 (GRCm39) |
H13P |
probably damaging |
Het |
Irak3 |
C |
T |
10: 120,013,972 (GRCm39) |
|
probably null |
Het |
Isl2 |
T |
A |
9: 55,452,253 (GRCm39) |
L275Q |
possibly damaging |
Het |
Itgb2 |
T |
C |
10: 77,393,240 (GRCm39) |
V367A |
probably damaging |
Het |
Katna1 |
T |
C |
10: 7,638,758 (GRCm39) |
|
probably benign |
Het |
Myh6 |
A |
G |
14: 55,184,450 (GRCm39) |
M1627T |
probably benign |
Het |
Naprt |
A |
G |
15: 75,765,164 (GRCm39) |
Y187H |
probably damaging |
Het |
Nedd4 |
T |
A |
9: 72,642,371 (GRCm39) |
V550E |
probably damaging |
Het |
Nt5c2 |
A |
G |
19: 46,884,954 (GRCm39) |
V252A |
possibly damaging |
Het |
Or8k39 |
T |
C |
2: 86,563,579 (GRCm39) |
I126V |
possibly damaging |
Het |
Or9i16 |
C |
T |
19: 13,864,945 (GRCm39) |
V210I |
probably benign |
Het |
P2ry2 |
A |
G |
7: 100,647,393 (GRCm39) |
V304A |
probably damaging |
Het |
Pde4dip |
T |
C |
3: 97,674,593 (GRCm39) |
N108D |
probably benign |
Het |
Pdgfrl |
A |
G |
8: 41,438,660 (GRCm39) |
T199A |
probably damaging |
Het |
Plaa |
A |
G |
4: 94,470,844 (GRCm39) |
Y431H |
probably benign |
Het |
Pls1 |
A |
T |
9: 95,664,472 (GRCm39) |
I177N |
possibly damaging |
Het |
Plxna2 |
T |
C |
1: 194,472,138 (GRCm39) |
F1035L |
probably damaging |
Het |
Ppp6r3 |
A |
T |
19: 3,564,729 (GRCm39) |
|
probably null |
Het |
Prpf4b |
T |
C |
13: 35,067,890 (GRCm39) |
S240P |
probably benign |
Het |
Reg2 |
T |
A |
6: 78,383,204 (GRCm39) |
Y50* |
probably null |
Het |
Rev3l |
C |
T |
10: 39,682,965 (GRCm39) |
T361I |
probably benign |
Het |
Rps4l |
A |
G |
6: 148,256,383 (GRCm39) |
|
probably benign |
Het |
Scn11a |
A |
T |
9: 119,598,982 (GRCm39) |
F1183I |
probably damaging |
Het |
Sh2b2 |
T |
C |
5: 136,253,273 (GRCm39) |
E327G |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,965,584 (GRCm39) |
K1057R |
probably damaging |
Het |
Sim2 |
T |
A |
16: 93,915,803 (GRCm39) |
Y255* |
probably null |
Het |
Snx9 |
A |
G |
17: 5,949,636 (GRCm39) |
N112S |
probably benign |
Het |
Sphkap |
T |
A |
1: 83,258,237 (GRCm39) |
I169F |
probably damaging |
Het |
Spink5 |
A |
G |
18: 44,100,111 (GRCm39) |
T43A |
probably benign |
Het |
Stac2 |
C |
T |
11: 97,932,005 (GRCm39) |
S265N |
probably benign |
Het |
Tbx20 |
A |
G |
9: 24,670,044 (GRCm39) |
V91A |
probably damaging |
Het |
Tgfbr2 |
C |
T |
9: 115,939,257 (GRCm39) |
R190H |
probably damaging |
Het |
Ubr2 |
A |
G |
17: 47,301,916 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
C |
T |
5: 102,063,204 (GRCm39) |
|
probably null |
Het |
Wdr82 |
T |
C |
9: 106,061,449 (GRCm39) |
V166A |
probably benign |
Het |
Zfhx4 |
C |
T |
3: 5,307,401 (GRCm39) |
A209V |
probably damaging |
Het |
Zfp518b |
T |
A |
5: 38,831,109 (GRCm39) |
T299S |
possibly damaging |
Het |
|
Other mutations in Fpr-rs7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01386:Fpr-rs7
|
APN |
17 |
20,334,454 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02293:Fpr-rs7
|
APN |
17 |
20,334,232 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03303:Fpr-rs7
|
APN |
17 |
20,334,001 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0731:Fpr-rs7
|
UTSW |
17 |
20,334,116 (GRCm39) |
missense |
probably benign |
0.00 |
R0826:Fpr-rs7
|
UTSW |
17 |
20,333,888 (GRCm39) |
missense |
probably benign |
0.01 |
R1439:Fpr-rs7
|
UTSW |
17 |
20,333,869 (GRCm39) |
missense |
probably benign |
0.10 |
R1590:Fpr-rs7
|
UTSW |
17 |
20,333,678 (GRCm39) |
missense |
probably benign |
0.05 |
R1778:Fpr-rs7
|
UTSW |
17 |
20,334,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Fpr-rs7
|
UTSW |
17 |
20,333,690 (GRCm39) |
missense |
probably benign |
0.00 |
R4744:Fpr-rs7
|
UTSW |
17 |
20,334,265 (GRCm39) |
missense |
probably benign |
0.17 |
R4921:Fpr-rs7
|
UTSW |
17 |
20,334,082 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5540:Fpr-rs7
|
UTSW |
17 |
20,334,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Fpr-rs7
|
UTSW |
17 |
20,334,365 (GRCm39) |
missense |
probably benign |
|
R5959:Fpr-rs7
|
UTSW |
17 |
20,334,011 (GRCm39) |
missense |
probably benign |
0.01 |
R6042:Fpr-rs7
|
UTSW |
17 |
20,333,477 (GRCm39) |
missense |
probably benign |
0.00 |
R7921:Fpr-rs7
|
UTSW |
17 |
20,333,667 (GRCm39) |
missense |
probably benign |
0.03 |
R7984:Fpr-rs7
|
UTSW |
17 |
20,333,671 (GRCm39) |
missense |
probably benign |
0.01 |
R8137:Fpr-rs7
|
UTSW |
17 |
20,334,055 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8172:Fpr-rs7
|
UTSW |
17 |
20,334,443 (GRCm39) |
missense |
probably benign |
0.04 |
R8762:Fpr-rs7
|
UTSW |
17 |
20,333,789 (GRCm39) |
missense |
probably benign |
0.07 |
R9134:Fpr-rs7
|
UTSW |
17 |
20,334,325 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fpr-rs7
|
UTSW |
17 |
20,333,655 (GRCm39) |
missense |
probably benign |
0.02 |
|