Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610010K14Rik |
G |
T |
11: 70,127,755 (GRCm39) |
R56S |
possibly damaging |
Het |
Abca14 |
T |
A |
7: 119,918,133 (GRCm39) |
I1545K |
probably damaging |
Het |
Abca3 |
A |
G |
17: 24,602,959 (GRCm39) |
Y518C |
probably damaging |
Het |
Abcd2 |
A |
G |
15: 91,058,839 (GRCm39) |
V535A |
probably benign |
Het |
Adcy9 |
T |
C |
16: 4,106,487 (GRCm39) |
T1113A |
probably damaging |
Het |
Afdn |
A |
T |
17: 14,104,062 (GRCm39) |
N1133Y |
probably benign |
Het |
Aip |
T |
A |
19: 4,166,034 (GRCm39) |
D139V |
probably damaging |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Aldh16a1 |
G |
A |
7: 44,799,115 (GRCm39) |
P56S |
probably benign |
Het |
Alpk3 |
A |
C |
7: 80,707,468 (GRCm39) |
T31P |
probably benign |
Het |
Aoc3 |
G |
T |
11: 101,232,573 (GRCm39) |
R466S |
unknown |
Het |
Atoh1 |
T |
C |
6: 64,706,641 (GRCm39) |
L112P |
probably benign |
Het |
Atp2b2 |
T |
A |
6: 113,770,772 (GRCm39) |
N424I |
probably benign |
Het |
Brms1 |
T |
C |
19: 5,091,520 (GRCm39) |
|
probably null |
Het |
Casc3 |
C |
T |
11: 98,713,607 (GRCm39) |
R280C |
probably damaging |
Het |
Cd34 |
T |
A |
1: 194,640,808 (GRCm39) |
S224R |
probably benign |
Het |
Cdh20 |
T |
A |
1: 104,898,583 (GRCm39) |
F437I |
probably benign |
Het |
Cdkal1 |
A |
T |
13: 29,510,087 (GRCm39) |
V557E |
probably benign |
Het |
Cfap276 |
A |
G |
3: 108,451,384 (GRCm39) |
H115R |
probably benign |
Het |
Chst5 |
T |
C |
8: 112,617,395 (GRCm39) |
H75R |
probably damaging |
Het |
Col5a2 |
A |
T |
1: 45,435,305 (GRCm39) |
N713K |
probably benign |
Het |
Cpne5 |
A |
T |
17: 29,407,357 (GRCm39) |
M181K |
probably benign |
Het |
Cpt1a |
T |
C |
19: 3,431,981 (GRCm39) |
F731S |
probably benign |
Het |
Cyfip1 |
A |
G |
7: 55,521,902 (GRCm39) |
M69V |
possibly damaging |
Het |
Dennd3 |
A |
G |
15: 73,442,672 (GRCm39) |
K1232E |
probably benign |
Het |
Dennd4b |
A |
T |
3: 90,181,259 (GRCm39) |
H805L |
probably benign |
Het |
Dnm1l |
C |
T |
16: 16,158,906 (GRCm39) |
R108Q |
probably damaging |
Het |
Dsc1 |
T |
A |
18: 20,222,636 (GRCm39) |
D612V |
probably benign |
Het |
Ephb2 |
C |
T |
4: 136,388,711 (GRCm39) |
G628R |
probably damaging |
Het |
Esrrb |
G |
A |
12: 86,552,595 (GRCm39) |
R195H |
probably benign |
Het |
Flg2 |
A |
T |
3: 93,107,585 (GRCm39) |
E23D |
probably damaging |
Het |
Gja8 |
A |
G |
3: 96,826,990 (GRCm39) |
L224P |
probably damaging |
Het |
Hps6 |
T |
G |
19: 45,993,867 (GRCm39) |
S601R |
possibly damaging |
Het |
Ice1 |
T |
C |
13: 70,752,495 (GRCm39) |
E1197G |
probably damaging |
Het |
Ifnar2 |
C |
A |
16: 91,200,857 (GRCm39) |
A366D |
possibly damaging |
Het |
Ighm |
A |
C |
12: 113,384,813 (GRCm39) |
S347A |
|
Het |
Immt |
C |
T |
6: 71,848,492 (GRCm39) |
R494* |
probably null |
Het |
Irs2 |
A |
G |
8: 11,056,683 (GRCm39) |
V583A |
probably damaging |
Het |
Kcnk4 |
T |
C |
19: 6,903,508 (GRCm39) |
E347G |
probably damaging |
Het |
Kif5b |
T |
A |
18: 6,213,245 (GRCm39) |
I716F |
probably benign |
Het |
Klhl1 |
T |
A |
14: 96,755,326 (GRCm39) |
D143V |
probably benign |
Het |
Lrp1b |
T |
C |
2: 40,760,272 (GRCm39) |
T2999A |
|
Het |
Map3k9 |
A |
G |
12: 81,768,970 (GRCm39) |
L1026P |
probably damaging |
Het |
Mtg1 |
T |
C |
7: 139,718,283 (GRCm39) |
V54A |
probably damaging |
Het |
Odad4 |
G |
T |
11: 100,452,731 (GRCm39) |
|
probably null |
Het |
Or10ag59 |
G |
A |
2: 87,406,083 (GRCm39) |
M218I |
probably benign |
Het |
Or56a41 |
A |
G |
7: 104,740,165 (GRCm39) |
V227A |
probably damaging |
Het |
Or5p6 |
C |
A |
7: 107,631,070 (GRCm39) |
W160L |
probably benign |
Het |
Or5p79 |
A |
G |
7: 108,221,027 (GRCm39) |
I3V |
probably benign |
Het |
Or6c65 |
T |
A |
10: 129,603,794 (GRCm39) |
V143E |
probably damaging |
Het |
Otogl |
T |
A |
10: 107,692,975 (GRCm39) |
E836D |
probably benign |
Het |
Pde6d |
A |
G |
1: 86,471,250 (GRCm39) |
S143P |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pon1 |
C |
T |
6: 5,177,327 (GRCm39) |
W194* |
probably null |
Het |
Rbm25 |
T |
A |
12: 83,711,025 (GRCm39) |
S379R |
unknown |
Het |
Rnf111 |
A |
T |
9: 70,365,223 (GRCm39) |
S415T |
probably benign |
Het |
Shoc2 |
A |
G |
19: 53,976,503 (GRCm39) |
Y131C |
probably damaging |
Het |
Slc23a1 |
T |
A |
18: 35,757,489 (GRCm39) |
M261L |
possibly damaging |
Het |
Slc34a1 |
A |
T |
13: 24,003,061 (GRCm39) |
H237L |
probably benign |
Het |
Slc35d1 |
G |
C |
4: 103,071,896 (GRCm39) |
I35M |
|
Het |
Slc8b1 |
C |
T |
5: 120,651,203 (GRCm39) |
|
probably benign |
Het |
Smr3a |
A |
C |
5: 88,152,611 (GRCm39) |
L8F |
unknown |
Het |
Snx8 |
G |
A |
5: 140,343,929 (GRCm39) |
R96C |
possibly damaging |
Het |
Srgap3 |
A |
G |
6: 112,752,509 (GRCm39) |
V325A |
possibly damaging |
Het |
Stk40 |
A |
G |
4: 126,012,127 (GRCm39) |
T10A |
probably benign |
Het |
Tmem177 |
A |
T |
1: 119,837,950 (GRCm39) |
V243D |
probably benign |
Het |
Trim6 |
G |
A |
7: 103,881,879 (GRCm39) |
V403M |
probably damaging |
Het |
Tysnd1 |
A |
G |
10: 61,531,950 (GRCm39) |
R201G |
probably benign |
Het |
Vmn2r67 |
A |
T |
7: 84,785,854 (GRCm39) |
F717Y |
probably benign |
Het |
Vmn2r72 |
A |
G |
7: 85,387,383 (GRCm39) |
V727A |
probably benign |
Het |
Wdr49 |
A |
C |
3: 75,358,997 (GRCm39) |
D43E |
probably benign |
Het |
Zbtb8b |
A |
G |
4: 129,326,424 (GRCm39) |
V247A |
probably benign |
Het |
Zfp532 |
C |
A |
18: 65,757,330 (GRCm39) |
A421E |
possibly damaging |
Het |
|
Other mutations in Mx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00553:Mx1
|
APN |
16 |
97,258,632 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01328:Mx1
|
APN |
16 |
97,256,832 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03105:Mx1
|
APN |
16 |
97,257,554 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4585001:Mx1
|
UTSW |
16 |
97,257,454 (GRCm39) |
missense |
probably benign |
0.07 |
R0003:Mx1
|
UTSW |
16 |
97,252,788 (GRCm39) |
intron |
probably benign |
|
R1597:Mx1
|
UTSW |
16 |
97,256,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Mx1
|
UTSW |
16 |
97,255,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Mx1
|
UTSW |
16 |
97,252,712 (GRCm39) |
makesense |
probably null |
|
R1826:Mx1
|
UTSW |
16 |
97,256,837 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1851:Mx1
|
UTSW |
16 |
97,249,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Mx1
|
UTSW |
16 |
97,249,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R2059:Mx1
|
UTSW |
16 |
97,255,379 (GRCm39) |
nonsense |
probably null |
|
R2223:Mx1
|
UTSW |
16 |
97,256,432 (GRCm39) |
splice site |
probably benign |
|
R3441:Mx1
|
UTSW |
16 |
97,257,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R3442:Mx1
|
UTSW |
16 |
97,257,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R3782:Mx1
|
UTSW |
16 |
97,253,195 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4460:Mx1
|
UTSW |
16 |
97,255,281 (GRCm39) |
missense |
probably damaging |
0.99 |
R4659:Mx1
|
UTSW |
16 |
97,256,439 (GRCm39) |
splice site |
probably null |
|
R5116:Mx1
|
UTSW |
16 |
97,258,679 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5186:Mx1
|
UTSW |
16 |
97,256,694 (GRCm39) |
missense |
probably benign |
0.09 |
R5215:Mx1
|
UTSW |
16 |
97,249,560 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5249:Mx1
|
UTSW |
16 |
97,258,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R5450:Mx1
|
UTSW |
16 |
97,255,347 (GRCm39) |
nonsense |
probably null |
|
R5806:Mx1
|
UTSW |
16 |
97,255,351 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5894:Mx1
|
UTSW |
16 |
97,255,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Mx1
|
UTSW |
16 |
97,252,933 (GRCm39) |
missense |
probably benign |
0.00 |
R5981:Mx1
|
UTSW |
16 |
97,255,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Mx1
|
UTSW |
16 |
97,256,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R7207:Mx1
|
UTSW |
16 |
97,253,398 (GRCm39) |
missense |
probably benign |
|
R7238:Mx1
|
UTSW |
16 |
97,249,496 (GRCm39) |
missense |
unknown |
|
R7318:Mx1
|
UTSW |
16 |
97,253,286 (GRCm39) |
missense |
probably benign |
0.06 |
R7699:Mx1
|
UTSW |
16 |
97,249,521 (GRCm39) |
missense |
unknown |
|
R7856:Mx1
|
UTSW |
16 |
97,256,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Mx1
|
UTSW |
16 |
97,258,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Mx1
|
UTSW |
16 |
97,253,987 (GRCm39) |
missense |
probably damaging |
0.99 |
R8750:Mx1
|
UTSW |
16 |
97,252,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9245:Mx1
|
UTSW |
16 |
97,252,753 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9642:Mx1
|
UTSW |
16 |
97,256,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R9645:Mx1
|
UTSW |
16 |
97,253,409 (GRCm39) |
missense |
probably benign |
0.01 |
R9797:Mx1
|
UTSW |
16 |
97,252,893 (GRCm39) |
missense |
probably benign |
0.01 |
X0028:Mx1
|
UTSW |
16 |
97,251,621 (GRCm39) |
nonsense |
probably null |
|
|