Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
A |
6: 128,543,236 (GRCm39) |
N595Y |
probably benign |
Het |
Abca6 |
A |
G |
11: 110,124,671 (GRCm39) |
|
probably benign |
Het |
Abo |
C |
A |
2: 26,733,609 (GRCm39) |
D199Y |
probably damaging |
Het |
Acvr1c |
A |
C |
2: 58,170,306 (GRCm39) |
V277G |
probably damaging |
Het |
Adam23 |
G |
A |
1: 63,584,731 (GRCm39) |
A380T |
probably benign |
Het |
Art2b |
A |
G |
7: 101,229,236 (GRCm39) |
V221A |
probably benign |
Het |
Bcam |
A |
G |
7: 19,500,640 (GRCm39) |
S153P |
probably damaging |
Het |
Brip1 |
T |
C |
11: 86,077,906 (GRCm39) |
H174R |
possibly damaging |
Het |
Ccdc186 |
T |
C |
19: 56,788,601 (GRCm39) |
D536G |
probably benign |
Het |
Cd109 |
A |
G |
9: 78,524,287 (GRCm39) |
N67S |
probably benign |
Het |
Cd8a |
G |
T |
6: 71,350,947 (GRCm39) |
M137I |
possibly damaging |
Het |
Ces2g |
T |
C |
8: 105,693,569 (GRCm39) |
F417L |
probably benign |
Het |
Clec2g |
A |
G |
6: 128,925,660 (GRCm39) |
N23S |
unknown |
Het |
Cntnap2 |
T |
C |
6: 46,507,567 (GRCm39) |
Y61C |
probably damaging |
Het |
Cog3 |
T |
A |
14: 75,979,784 (GRCm39) |
E182D |
probably benign |
Het |
Dbpht2 |
A |
G |
12: 74,342,624 (GRCm39) |
|
noncoding transcript |
Het |
Dock4 |
A |
T |
12: 40,686,227 (GRCm39) |
N154I |
probably damaging |
Het |
Dysf |
T |
G |
6: 84,128,906 (GRCm39) |
V1422G |
possibly damaging |
Het |
E2f3 |
T |
C |
13: 30,104,159 (GRCm39) |
D140G |
probably damaging |
Het |
Efcab3 |
A |
G |
11: 104,611,514 (GRCm39) |
K452R |
probably benign |
Het |
Epb41l2 |
T |
A |
10: 25,317,466 (GRCm39) |
|
probably null |
Het |
Epha2 |
A |
G |
4: 141,035,857 (GRCm39) |
K98E |
possibly damaging |
Het |
Esyt1 |
T |
C |
10: 128,355,487 (GRCm39) |
D444G |
probably benign |
Het |
Fam163a |
T |
C |
1: 155,955,787 (GRCm39) |
T2A |
probably damaging |
Het |
Foxp2 |
A |
T |
6: 15,379,767 (GRCm39) |
|
probably benign |
Het |
Gcm2 |
T |
C |
13: 41,259,367 (GRCm39) |
H34R |
probably benign |
Het |
Gipr |
A |
G |
7: 18,897,996 (GRCm39) |
S79P |
probably benign |
Het |
Gli3 |
T |
C |
13: 15,823,276 (GRCm39) |
S333P |
probably damaging |
Het |
Gm10717 |
T |
G |
9: 3,026,317 (GRCm39) |
F205C |
probably damaging |
Het |
Gzmk |
A |
G |
13: 113,309,427 (GRCm39) |
S208P |
probably damaging |
Het |
Htra2 |
G |
T |
6: 83,028,583 (GRCm39) |
A318D |
probably damaging |
Het |
Itpkc |
T |
C |
7: 26,907,805 (GRCm39) |
D633G |
probably damaging |
Het |
Lama1 |
G |
A |
17: 68,098,218 (GRCm39) |
R1805H |
probably benign |
Het |
Lama4 |
T |
A |
10: 38,909,121 (GRCm39) |
|
probably benign |
Het |
Lama4 |
T |
C |
10: 38,936,182 (GRCm39) |
V619A |
probably damaging |
Het |
Notch3 |
T |
C |
17: 32,362,402 (GRCm39) |
T1408A |
probably benign |
Het |
Nwd2 |
A |
G |
5: 63,962,753 (GRCm39) |
D779G |
probably benign |
Het |
Nxpe4 |
A |
G |
9: 48,304,678 (GRCm39) |
Y255C |
possibly damaging |
Het |
Obox6 |
A |
T |
7: 15,568,770 (GRCm39) |
H35Q |
possibly damaging |
Het |
Or2ab1 |
A |
G |
11: 58,489,133 (GRCm39) |
I304V |
probably damaging |
Het |
Or8b41 |
T |
A |
9: 38,055,025 (GRCm39) |
I198N |
possibly damaging |
Het |
Pkig |
T |
A |
2: 163,563,147 (GRCm39) |
I26N |
possibly damaging |
Het |
Plekhm2 |
C |
T |
4: 141,369,750 (GRCm39) |
V82M |
possibly damaging |
Het |
Plppr2 |
G |
A |
9: 21,859,220 (GRCm39) |
A446T |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,754,353 (GRCm39) |
F203L |
probably benign |
Het |
Sh3bp1 |
A |
G |
15: 78,787,880 (GRCm39) |
K137E |
probably damaging |
Het |
Shisa5 |
T |
A |
9: 108,885,108 (GRCm39) |
I126N |
probably damaging |
Het |
Slc11a1 |
T |
C |
1: 74,414,931 (GRCm39) |
L21P |
probably benign |
Het |
Slc35f1 |
C |
T |
10: 52,809,291 (GRCm39) |
P93S |
probably damaging |
Het |
Slc4a4 |
A |
G |
5: 89,194,167 (GRCm39) |
T172A |
probably damaging |
Het |
Slc9c1 |
A |
T |
16: 45,393,710 (GRCm39) |
Y551F |
probably benign |
Het |
Spata31 |
T |
C |
13: 65,069,612 (GRCm39) |
S587P |
probably benign |
Het |
Syna |
C |
A |
5: 134,588,006 (GRCm39) |
M314I |
probably benign |
Het |
Taf5l |
A |
G |
8: 124,730,152 (GRCm39) |
L144P |
probably damaging |
Het |
Tbccd1 |
T |
C |
16: 22,641,271 (GRCm39) |
T369A |
probably benign |
Het |
Tnfrsf11b |
A |
T |
15: 54,119,493 (GRCm39) |
C160* |
probably null |
Het |
Trim45 |
A |
G |
3: 100,830,283 (GRCm39) |
N19S |
probably benign |
Het |
Uba2 |
A |
G |
7: 33,850,455 (GRCm39) |
F364S |
probably damaging |
Het |
Unc50 |
T |
A |
1: 37,476,323 (GRCm39) |
L161Q |
probably damaging |
Het |
Uso1 |
A |
T |
5: 92,348,992 (GRCm39) |
|
probably null |
Het |
Usp25 |
A |
G |
16: 76,911,838 (GRCm39) |
I956V |
probably benign |
Het |
Utf1 |
C |
A |
7: 139,524,213 (GRCm39) |
L143I |
probably damaging |
Het |
Vmn1r36 |
T |
A |
6: 66,693,756 (GRCm39) |
M40L |
probably benign |
Het |
Vmn2r43 |
A |
G |
7: 8,258,055 (GRCm39) |
V386A |
possibly damaging |
Het |
Vps9d1 |
C |
A |
8: 123,973,778 (GRCm39) |
R335L |
probably damaging |
Het |
Wasf1 |
T |
A |
10: 40,802,585 (GRCm39) |
V80D |
probably damaging |
Het |
Wdr72 |
G |
A |
9: 74,183,298 (GRCm39) |
V1077I |
possibly damaging |
Het |
Wnt8a |
A |
G |
18: 34,675,422 (GRCm39) |
M1V |
probably null |
Het |
Zbtb26 |
A |
G |
2: 37,326,347 (GRCm39) |
S230P |
possibly damaging |
Het |
Zfp335 |
A |
G |
2: 164,734,525 (GRCm39) |
V1247A |
probably damaging |
Het |
Zfp429 |
T |
C |
13: 67,538,505 (GRCm39) |
N313S |
possibly damaging |
Het |
Zfp74 |
A |
T |
7: 29,634,569 (GRCm39) |
C380S |
probably damaging |
Het |
Zfyve21 |
G |
A |
12: 111,791,328 (GRCm39) |
E134K |
probably damaging |
Het |
Zmynd11 |
T |
C |
13: 9,739,616 (GRCm39) |
T474A |
possibly damaging |
Het |
|
Other mutations in Vmn1r158 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01147:Vmn1r158
|
APN |
7 |
22,490,204 (GRCm39) |
missense |
probably benign |
0.01 |
R1173:Vmn1r158
|
UTSW |
7 |
22,489,870 (GRCm39) |
missense |
probably benign |
0.19 |
R1574:Vmn1r158
|
UTSW |
7 |
22,489,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Vmn1r158
|
UTSW |
7 |
22,489,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Vmn1r158
|
UTSW |
7 |
22,490,072 (GRCm39) |
missense |
probably benign |
0.08 |
R1777:Vmn1r158
|
UTSW |
7 |
22,489,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Vmn1r158
|
UTSW |
7 |
22,490,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Vmn1r158
|
UTSW |
7 |
22,489,815 (GRCm39) |
missense |
probably benign |
0.03 |
R3749:Vmn1r158
|
UTSW |
7 |
22,489,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R4872:Vmn1r158
|
UTSW |
7 |
22,490,179 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5238:Vmn1r158
|
UTSW |
7 |
22,489,799 (GRCm39) |
missense |
probably benign |
|
R6500:Vmn1r158
|
UTSW |
7 |
22,490,078 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6511:Vmn1r158
|
UTSW |
7 |
22,490,116 (GRCm39) |
missense |
probably benign |
0.00 |
R6581:Vmn1r158
|
UTSW |
7 |
22,489,465 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6751:Vmn1r158
|
UTSW |
7 |
22,489,306 (GRCm39) |
missense |
probably damaging |
0.96 |
R7168:Vmn1r158
|
UTSW |
7 |
22,490,101 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7337:Vmn1r158
|
UTSW |
7 |
22,489,649 (GRCm39) |
missense |
probably benign |
0.00 |
R7747:Vmn1r158
|
UTSW |
7 |
22,489,725 (GRCm39) |
missense |
probably benign |
0.15 |
R7902:Vmn1r158
|
UTSW |
7 |
22,489,433 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8328:Vmn1r158
|
UTSW |
7 |
22,489,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R8400:Vmn1r158
|
UTSW |
7 |
22,489,305 (GRCm39) |
nonsense |
probably null |
|
R8809:Vmn1r158
|
UTSW |
7 |
22,489,775 (GRCm39) |
missense |
probably damaging |
0.97 |
R9227:Vmn1r158
|
UTSW |
7 |
22,489,469 (GRCm39) |
missense |
probably benign |
0.02 |
R9468:Vmn1r158
|
UTSW |
7 |
22,489,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R9702:Vmn1r158
|
UTSW |
7 |
22,490,065 (GRCm39) |
missense |
probably benign |
0.00 |
R9719:Vmn1r158
|
UTSW |
7 |
22,489,331 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Vmn1r158
|
UTSW |
7 |
22,489,883 (GRCm39) |
missense |
possibly damaging |
0.46 |
|