Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
A |
T |
4: 53,143,952 (GRCm39) |
L15Q |
probably benign |
Het |
Acsf2 |
T |
C |
11: 94,450,417 (GRCm39) |
M497V |
probably benign |
Het |
Adnp2 |
T |
C |
18: 80,173,305 (GRCm39) |
N368S |
probably benign |
Het |
BC034090 |
T |
C |
1: 155,097,131 (GRCm39) |
T656A |
probably benign |
Het |
Bsph1 |
A |
G |
7: 13,192,183 (GRCm39) |
Y26C |
probably damaging |
Het |
Cct7 |
T |
C |
6: 85,443,675 (GRCm39) |
F306L |
probably benign |
Het |
Cd109 |
A |
G |
9: 78,543,885 (GRCm39) |
Q143R |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,234,477 (GRCm39) |
|
probably null |
Het |
Col3a1 |
A |
G |
1: 45,371,148 (GRCm39) |
N436D |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,721,929 (GRCm39) |
E1498G |
probably damaging |
Het |
Cyp2u1 |
T |
C |
3: 131,096,424 (GRCm39) |
D118G |
probably benign |
Het |
Dek |
A |
G |
13: 47,251,663 (GRCm39) |
S51P |
possibly damaging |
Het |
Dock6 |
C |
T |
9: 21,720,860 (GRCm39) |
G1746D |
probably damaging |
Het |
Dscam |
T |
A |
16: 96,621,988 (GRCm39) |
N488Y |
probably damaging |
Het |
Ebpl |
G |
T |
14: 61,597,693 (GRCm39) |
Y49* |
probably null |
Het |
Eefsec |
C |
T |
6: 88,423,265 (GRCm39) |
G66D |
probably benign |
Het |
Epha6 |
T |
A |
16: 60,346,825 (GRCm39) |
Y146F |
probably benign |
Het |
Fcgbpl1 |
C |
T |
7: 27,836,638 (GRCm39) |
R186C |
probably damaging |
Het |
Frmd4a |
A |
G |
2: 4,591,267 (GRCm39) |
R96G |
probably damaging |
Het |
Gm5814 |
A |
G |
17: 47,721,352 (GRCm39) |
|
probably benign |
Het |
Hspa13 |
C |
G |
16: 75,554,872 (GRCm39) |
V405L |
probably damaging |
Het |
Iqgap2 |
A |
G |
13: 95,797,565 (GRCm39) |
V1079A |
probably damaging |
Het |
Kcnj9 |
C |
A |
1: 172,153,623 (GRCm39) |
R167L |
probably damaging |
Het |
Kdm1b |
T |
A |
13: 47,227,880 (GRCm39) |
D620E |
probably benign |
Het |
Kif23 |
T |
C |
9: 61,834,436 (GRCm39) |
R442G |
possibly damaging |
Het |
Nectin1 |
C |
A |
9: 43,703,179 (GRCm39) |
P146T |
possibly damaging |
Het |
Noc4l |
A |
G |
5: 110,797,461 (GRCm39) |
I391T |
probably damaging |
Het |
Npr1 |
C |
A |
3: 90,362,452 (GRCm39) |
R956L |
possibly damaging |
Het |
Or11g7 |
T |
A |
14: 50,691,412 (GRCm39) |
M301K |
possibly damaging |
Het |
Or11j4 |
T |
A |
14: 50,631,089 (GRCm39) |
M292K |
possibly damaging |
Het |
Pcdhgb2 |
T |
C |
18: 37,825,223 (GRCm39) |
V738A |
possibly damaging |
Het |
Ptpn20 |
A |
G |
14: 33,336,461 (GRCm39) |
E100G |
probably damaging |
Het |
Rgs10 |
A |
G |
7: 127,990,797 (GRCm39) |
F97S |
probably damaging |
Het |
Shisa6 |
T |
C |
11: 66,265,982 (GRCm39) |
|
probably null |
Het |
Shld1 |
A |
T |
2: 132,592,564 (GRCm39) |
K204* |
probably null |
Het |
Sirpb1a |
T |
C |
3: 15,481,984 (GRCm39) |
T115A |
probably damaging |
Het |
Supv3l1 |
A |
G |
10: 62,277,016 (GRCm39) |
C251R |
probably damaging |
Het |
Svopl |
T |
C |
6: 37,998,543 (GRCm39) |
S244G |
probably benign |
Het |
Tes |
T |
C |
6: 17,099,862 (GRCm39) |
Y286H |
probably damaging |
Het |
Tnfrsf22 |
G |
A |
7: 143,193,641 (GRCm39) |
|
probably benign |
Het |
Vmn1r185 |
A |
G |
7: 26,311,160 (GRCm39) |
I115T |
probably damaging |
Het |
Zan |
T |
A |
5: 137,454,566 (GRCm39) |
I1413L |
unknown |
Het |
Zc3h12d |
G |
T |
10: 7,743,425 (GRCm39) |
M398I |
probably benign |
Het |
Zfp219 |
G |
A |
14: 52,244,118 (GRCm39) |
T642M |
probably benign |
Het |
Zfp646 |
G |
A |
7: 127,479,892 (GRCm39) |
E690K |
possibly damaging |
Het |
Zfr |
T |
A |
15: 12,136,541 (GRCm39) |
V66D |
unknown |
Het |
|
Other mutations in Vmn2r-ps117 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6912:Vmn2r-ps117
|
UTSW |
17 |
19,047,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R6934:Vmn2r-ps117
|
UTSW |
17 |
19,044,967 (GRCm39) |
nonsense |
probably null |
|
R6953:Vmn2r-ps117
|
UTSW |
17 |
19,045,095 (GRCm39) |
missense |
probably benign |
|
R6974:Vmn2r-ps117
|
UTSW |
17 |
19,058,495 (GRCm39) |
missense |
probably benign |
0.15 |
R7373:Vmn2r-ps117
|
UTSW |
17 |
19,044,948 (GRCm39) |
missense |
probably benign |
|
R7630:Vmn2r-ps117
|
UTSW |
17 |
19,044,909 (GRCm39) |
missense |
probably benign |
0.01 |
R7776:Vmn2r-ps117
|
UTSW |
17 |
19,043,934 (GRCm39) |
missense |
probably damaging |
0.96 |
R8060:Vmn2r-ps117
|
UTSW |
17 |
19,058,124 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8126:Vmn2r-ps117
|
UTSW |
17 |
19,042,814 (GRCm39) |
missense |
probably benign |
0.00 |
R8751:Vmn2r-ps117
|
UTSW |
17 |
19,044,021 (GRCm39) |
missense |
probably benign |
|
R8986:Vmn2r-ps117
|
UTSW |
17 |
19,044,943 (GRCm39) |
nonsense |
probably null |
|
R9324:Vmn2r-ps117
|
UTSW |
17 |
19,042,911 (GRCm39) |
missense |
probably benign |
0.20 |
R9417:Vmn2r-ps117
|
UTSW |
17 |
19,044,037 (GRCm39) |
nonsense |
probably null |
|
R9607:Vmn2r-ps117
|
UTSW |
17 |
19,043,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Vmn2r-ps117
|
UTSW |
17 |
19,058,338 (GRCm39) |
missense |
probably benign |
0.01 |
|