Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn1 |
T |
C |
12: 80,240,446 (GRCm39) |
R214G |
probably benign |
Het |
Cacna1e |
T |
A |
1: 154,348,123 (GRCm39) |
K817N |
probably benign |
Het |
Cyp3a16 |
A |
G |
5: 145,377,244 (GRCm39) |
F448L |
probably damaging |
Het |
Dpp6 |
T |
A |
5: 27,869,760 (GRCm39) |
|
probably null |
Het |
Eif2ak3 |
C |
T |
6: 70,869,710 (GRCm39) |
T799M |
probably damaging |
Het |
Erbb4 |
A |
T |
1: 68,383,090 (GRCm39) |
S302R |
probably damaging |
Het |
Fam217a |
T |
A |
13: 35,099,632 (GRCm39) |
|
probably benign |
Het |
Flt4 |
C |
A |
11: 49,528,162 (GRCm39) |
A995D |
probably benign |
Het |
Fsd1 |
C |
T |
17: 56,303,733 (GRCm39) |
S491F |
probably damaging |
Het |
Hpcal4 |
T |
C |
4: 123,083,035 (GRCm39) |
|
probably null |
Het |
Intu |
A |
T |
3: 40,647,017 (GRCm39) |
D630V |
probably damaging |
Het |
Jak3 |
A |
G |
8: 72,136,933 (GRCm39) |
D703G |
probably damaging |
Het |
Lama4 |
A |
G |
10: 38,887,060 (GRCm39) |
I122V |
probably benign |
Het |
Mrpl11 |
A |
C |
19: 5,013,409 (GRCm39) |
K92T |
probably null |
Het |
Mtarc2 |
A |
G |
1: 184,551,413 (GRCm39) |
|
probably benign |
Het |
Mylk |
A |
G |
16: 34,791,610 (GRCm39) |
|
probably null |
Het |
Or52ab4 |
A |
T |
7: 102,987,974 (GRCm39) |
K238* |
probably null |
Het |
Parpbp |
A |
C |
10: 87,975,848 (GRCm39) |
Y88* |
probably null |
Het |
Plod2 |
G |
A |
9: 92,488,655 (GRCm39) |
R627Q |
probably damaging |
Het |
Rapsn |
G |
T |
2: 90,867,144 (GRCm39) |
A149S |
probably damaging |
Het |
Ripk3 |
T |
G |
14: 56,023,484 (GRCm39) |
Q109P |
probably damaging |
Het |
Scaf11 |
T |
C |
15: 96,318,361 (GRCm39) |
D401G |
probably damaging |
Het |
Serpine2 |
G |
A |
1: 79,779,268 (GRCm39) |
T150I |
probably damaging |
Het |
Sh2d6 |
T |
A |
6: 72,495,945 (GRCm39) |
T98S |
probably benign |
Het |
Slc28a1 |
G |
T |
7: 80,814,427 (GRCm39) |
A513S |
probably benign |
Het |
Tanc2 |
T |
C |
11: 105,777,207 (GRCm39) |
F795S |
probably damaging |
Het |
Tcim |
T |
A |
8: 24,928,705 (GRCm39) |
I70F |
probably benign |
Het |
Thbd |
G |
A |
2: 148,249,602 (GRCm39) |
Q89* |
probably null |
Het |
Tmem115 |
C |
T |
9: 107,411,859 (GRCm39) |
T61I |
probably damaging |
Het |
Tsc2 |
A |
T |
17: 24,832,259 (GRCm39) |
V650E |
probably damaging |
Het |
Tubgcp6 |
A |
T |
15: 88,992,199 (GRCm39) |
Y595* |
probably null |
Het |
Uroc1 |
C |
T |
6: 90,323,747 (GRCm39) |
A398V |
probably damaging |
Het |
Vmn1r31 |
T |
C |
6: 58,449,587 (GRCm39) |
T93A |
probably benign |
Het |
Vmn2r113 |
A |
G |
17: 23,175,024 (GRCm39) |
E545G |
possibly damaging |
Het |
Vps13a |
A |
G |
19: 16,678,516 (GRCm39) |
V1155A |
possibly damaging |
Het |
Zfp667 |
A |
G |
7: 6,307,869 (GRCm39) |
H179R |
probably benign |
Het |
|
Other mutations in Fpr-rs7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Fpr-rs7
|
APN |
17 |
20,333,480 (GRCm39) |
nonsense |
probably null |
|
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 |
|