Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abraxas2 |
T |
C |
7: 132,476,578 (GRCm39) |
F106S |
probably damaging |
Het |
Acsf3 |
A |
G |
8: 123,512,685 (GRCm39) |
T369A |
probably benign |
Het |
Adgrf5 |
G |
A |
17: 43,739,335 (GRCm39) |
|
probably null |
Het |
Aff1 |
T |
A |
5: 103,994,958 (GRCm39) |
I1052K |
probably benign |
Het |
Akap8 |
T |
C |
17: 32,535,549 (GRCm39) |
D155G |
possibly damaging |
Het |
Alg10b |
A |
T |
15: 90,111,653 (GRCm39) |
M166L |
probably benign |
Het |
Allc |
T |
A |
12: 28,613,408 (GRCm39) |
Q178L |
possibly damaging |
Het |
Angptl4 |
C |
A |
17: 33,996,084 (GRCm39) |
L297F |
probably damaging |
Het |
Arfgap1 |
A |
G |
2: 180,612,869 (GRCm39) |
K8E |
possibly damaging |
Het |
Bckdhb |
T |
A |
9: 83,892,379 (GRCm39) |
V270E |
possibly damaging |
Het |
Cbx3 |
T |
C |
6: 51,452,355 (GRCm39) |
|
probably null |
Het |
Cd44 |
G |
T |
2: 102,664,607 (GRCm39) |
N531K |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,246,689 (GRCm39) |
D916E |
probably damaging |
Het |
Cr2 |
A |
G |
1: 194,837,594 (GRCm39) |
V792A |
probably benign |
Het |
Cstf3 |
T |
C |
2: 104,439,301 (GRCm39) |
L38P |
probably damaging |
Het |
Cyp2a5 |
A |
G |
7: 26,536,208 (GRCm39) |
E151G |
probably benign |
Het |
Dbr1 |
T |
C |
9: 99,464,602 (GRCm39) |
F127S |
|
Het |
Ddit4 |
A |
T |
10: 59,787,317 (GRCm39) |
D6E |
probably damaging |
Het |
Disc1 |
G |
C |
8: 125,891,841 (GRCm39) |
R631S |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,235,965 (GRCm39) |
|
probably null |
Het |
Dnah9 |
T |
C |
11: 65,971,404 (GRCm39) |
K1595E |
probably damaging |
Het |
Dnmbp |
T |
C |
19: 43,889,944 (GRCm39) |
R608G |
probably damaging |
Het |
Efcab5 |
G |
C |
11: 77,028,387 (GRCm39) |
P315A |
probably benign |
Het |
Eif4a2 |
A |
G |
16: 22,932,012 (GRCm39) |
Y392C |
possibly damaging |
Het |
F5 |
G |
T |
1: 164,020,277 (GRCm39) |
K917N |
probably benign |
Het |
Fig4 |
T |
C |
10: 41,127,752 (GRCm39) |
M571V |
probably benign |
Het |
Flot2 |
T |
A |
11: 77,948,802 (GRCm39) |
I259N |
probably damaging |
Het |
Gm8122 |
C |
A |
14: 43,088,058 (GRCm39) |
|
probably null |
Het |
Gpr152 |
T |
C |
19: 4,192,963 (GRCm39) |
V168A |
possibly damaging |
Het |
H1f0 |
G |
A |
15: 78,913,103 (GRCm39) |
G61D |
probably damaging |
Het |
Ihh |
T |
A |
1: 74,987,492 (GRCm39) |
K183M |
probably damaging |
Het |
Itga2 |
A |
G |
13: 114,973,738 (GRCm39) |
L1116P |
probably damaging |
Het |
Kcnj10 |
A |
G |
1: 172,196,827 (GRCm39) |
T114A |
possibly damaging |
Het |
Kcnk3 |
T |
G |
5: 30,779,310 (GRCm39) |
L120R |
probably damaging |
Het |
Krt14 |
C |
A |
11: 100,095,926 (GRCm39) |
E211* |
probably null |
Het |
Lars2 |
T |
C |
9: 123,256,545 (GRCm39) |
L350P |
probably damaging |
Het |
Lrba |
T |
C |
3: 86,259,209 (GRCm39) |
I1408T |
probably damaging |
Het |
Lrrc27 |
A |
G |
7: 138,806,022 (GRCm39) |
E229G |
probably benign |
Het |
Lrrc8e |
G |
T |
8: 4,285,626 (GRCm39) |
R617L |
probably benign |
Het |
M1ap |
A |
G |
6: 82,958,930 (GRCm39) |
D187G |
probably benign |
Het |
Marchf1 |
A |
T |
8: 66,921,051 (GRCm39) |
K243* |
probably null |
Het |
Med16 |
C |
T |
10: 79,739,031 (GRCm39) |
V252M |
probably damaging |
Het |
Micu3 |
T |
C |
8: 40,801,999 (GRCm39) |
S189P |
probably benign |
Het |
Mindy4 |
A |
T |
6: 55,278,010 (GRCm39) |
N618I |
probably damaging |
Het |
Mmrn1 |
C |
T |
6: 60,953,320 (GRCm39) |
Q534* |
probably null |
Het |
Mroh9 |
C |
T |
1: 162,903,858 (GRCm39) |
|
probably null |
Het |
Ms4a6d |
G |
A |
19: 11,567,437 (GRCm39) |
Q155* |
probably null |
Het |
Mta3 |
T |
A |
17: 84,015,870 (GRCm39) |
I24N |
probably damaging |
Het |
Mtmr4 |
A |
T |
11: 87,491,476 (GRCm39) |
H147L |
probably damaging |
Het |
Nfam1 |
T |
C |
15: 82,894,640 (GRCm39) |
K155R |
probably benign |
Het |
Nlrp6 |
A |
T |
7: 140,501,191 (GRCm39) |
|
probably benign |
Het |
Or1q1 |
T |
A |
2: 36,886,873 (GRCm39) |
I17N |
possibly damaging |
Het |
Or5d37 |
A |
T |
2: 87,923,542 (GRCm39) |
F246Y |
probably benign |
Het |
Or5w20 |
T |
C |
2: 87,726,753 (GRCm39) |
|
probably benign |
Het |
Or6d13 |
A |
G |
6: 116,517,495 (GRCm39) |
E27G |
probably benign |
Het |
Or9g4 |
A |
G |
2: 85,505,189 (GRCm39) |
F102S |
|
Het |
P4ha1 |
A |
G |
10: 59,186,240 (GRCm39) |
R240G |
probably damaging |
Het |
Pla2r1 |
G |
T |
2: 60,288,723 (GRCm39) |
D636E |
probably benign |
Het |
Polr2a |
A |
G |
11: 69,631,886 (GRCm39) |
L1060P |
possibly damaging |
Het |
Prr35 |
A |
T |
17: 26,165,685 (GRCm39) |
V534D |
probably damaging |
Het |
Ptgdr2 |
C |
A |
19: 10,918,319 (GRCm39) |
Q279K |
probably benign |
Het |
Rab11fip2 |
T |
A |
19: 59,925,853 (GRCm39) |
R121S |
probably benign |
Het |
Rasa2 |
T |
C |
9: 96,426,408 (GRCm39) |
S813G |
probably benign |
Het |
Rassf5 |
T |
C |
1: 131,106,273 (GRCm39) |
K411E |
possibly damaging |
Het |
Reep4 |
T |
C |
14: 70,783,987 (GRCm39) |
Y35H |
probably damaging |
Het |
Ror1 |
A |
T |
4: 100,283,140 (GRCm39) |
M402L |
probably benign |
Het |
Slc32a1 |
A |
G |
2: 158,456,326 (GRCm39) |
E327G |
probably damaging |
Het |
Spen |
C |
T |
4: 141,206,696 (GRCm39) |
E644K |
unknown |
Het |
Tars3 |
C |
G |
7: 65,308,672 (GRCm39) |
Q281E |
probably damaging |
Het |
Tcl1 |
A |
G |
12: 105,184,934 (GRCm39) |
I92T |
probably damaging |
Het |
Tifab |
A |
G |
13: 56,324,120 (GRCm39) |
S108P |
probably damaging |
Het |
Traf1 |
T |
C |
2: 34,838,245 (GRCm39) |
N198D |
probably benign |
Het |
Trim35 |
T |
C |
14: 66,546,654 (GRCm39) |
Y474H |
probably damaging |
Het |
Trim54 |
T |
A |
5: 31,294,505 (GRCm39) |
D344E |
probably benign |
Het |
Ttc28 |
A |
T |
5: 111,373,903 (GRCm39) |
H1113L |
probably damaging |
Het |
Vcam1 |
T |
A |
3: 115,908,211 (GRCm39) |
D617V |
probably damaging |
Het |
Vmn2r81 |
A |
T |
10: 79,104,219 (GRCm39) |
T281S |
probably benign |
Het |
Whrn |
C |
T |
4: 63,350,196 (GRCm39) |
R507K |
possibly damaging |
Het |
Zdhhc14 |
A |
G |
17: 5,777,151 (GRCm39) |
S303G |
probably benign |
Het |
Zfp292 |
A |
T |
4: 34,806,839 (GRCm39) |
N2073K |
probably benign |
Het |
Zgpat |
T |
A |
2: 181,022,228 (GRCm39) |
V163D |
|
Het |
|
Other mutations in Mier2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01412:Mier2
|
APN |
10 |
79,377,014 (GRCm39) |
makesense |
probably null |
|
IGL01761:Mier2
|
APN |
10 |
79,384,186 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01845:Mier2
|
APN |
10 |
79,385,418 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02336:Mier2
|
APN |
10 |
79,384,184 (GRCm39) |
unclassified |
probably benign |
|
IGL02882:Mier2
|
APN |
10 |
79,383,555 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02902:Mier2
|
APN |
10 |
79,385,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Mier2
|
UTSW |
10 |
79,378,430 (GRCm39) |
critical splice donor site |
probably null |
|
R0972:Mier2
|
UTSW |
10 |
79,380,455 (GRCm39) |
unclassified |
probably benign |
|
R1326:Mier2
|
UTSW |
10 |
79,380,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1333:Mier2
|
UTSW |
10 |
79,380,991 (GRCm39) |
missense |
probably benign |
0.03 |
R1721:Mier2
|
UTSW |
10 |
79,384,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Mier2
|
UTSW |
10 |
79,384,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R1868:Mier2
|
UTSW |
10 |
79,384,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R2015:Mier2
|
UTSW |
10 |
79,377,036 (GRCm39) |
splice site |
probably null |
|
R2273:Mier2
|
UTSW |
10 |
79,380,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2274:Mier2
|
UTSW |
10 |
79,380,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3729:Mier2
|
UTSW |
10 |
79,380,876 (GRCm39) |
unclassified |
probably benign |
|
R3874:Mier2
|
UTSW |
10 |
79,377,631 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3881:Mier2
|
UTSW |
10 |
79,384,584 (GRCm39) |
splice site |
probably null |
|
R4755:Mier2
|
UTSW |
10 |
79,385,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Mier2
|
UTSW |
10 |
79,386,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Mier2
|
UTSW |
10 |
79,385,411 (GRCm39) |
missense |
probably benign |
0.03 |
R6282:Mier2
|
UTSW |
10 |
79,380,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Mier2
|
UTSW |
10 |
79,380,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Mier2
|
UTSW |
10 |
79,376,990 (GRCm39) |
start gained |
probably benign |
|
R6869:Mier2
|
UTSW |
10 |
79,378,503 (GRCm39) |
missense |
probably damaging |
0.99 |
R6897:Mier2
|
UTSW |
10 |
79,380,573 (GRCm39) |
missense |
probably damaging |
0.99 |
R6902:Mier2
|
UTSW |
10 |
79,376,673 (GRCm39) |
utr 3 prime |
probably benign |
|
R6946:Mier2
|
UTSW |
10 |
79,376,673 (GRCm39) |
utr 3 prime |
probably benign |
|
R6968:Mier2
|
UTSW |
10 |
79,376,476 (GRCm39) |
utr 3 prime |
probably benign |
|
R6971:Mier2
|
UTSW |
10 |
79,378,263 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7072:Mier2
|
UTSW |
10 |
79,376,133 (GRCm39) |
missense |
unknown |
|
R7443:Mier2
|
UTSW |
10 |
79,376,289 (GRCm39) |
missense |
unknown |
|
R7506:Mier2
|
UTSW |
10 |
79,386,176 (GRCm39) |
missense |
probably benign |
0.14 |
R7545:Mier2
|
UTSW |
10 |
79,377,028 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7625:Mier2
|
UTSW |
10 |
79,378,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R7669:Mier2
|
UTSW |
10 |
79,385,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R7895:Mier2
|
UTSW |
10 |
79,377,719 (GRCm39) |
start gained |
probably benign |
|
R8494:Mier2
|
UTSW |
10 |
79,377,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R8520:Mier2
|
UTSW |
10 |
79,378,263 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8834:Mier2
|
UTSW |
10 |
79,386,293 (GRCm39) |
missense |
unknown |
|
R8978:Mier2
|
UTSW |
10 |
79,376,790 (GRCm39) |
missense |
unknown |
|
R9005:Mier2
|
UTSW |
10 |
79,384,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R9007:Mier2
|
UTSW |
10 |
79,384,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R9008:Mier2
|
UTSW |
10 |
79,384,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R9018:Mier2
|
UTSW |
10 |
79,384,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R9051:Mier2
|
UTSW |
10 |
79,384,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R9052:Mier2
|
UTSW |
10 |
79,384,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R9108:Mier2
|
UTSW |
10 |
79,377,756 (GRCm39) |
missense |
probably benign |
0.01 |
R9111:Mier2
|
UTSW |
10 |
79,381,285 (GRCm39) |
unclassified |
probably benign |
|
R9121:Mier2
|
UTSW |
10 |
79,377,594 (GRCm39) |
missense |
|
|
R9281:Mier2
|
UTSW |
10 |
79,378,294 (GRCm39) |
missense |
probably benign |
0.06 |
R9514:Mier2
|
UTSW |
10 |
79,377,496 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Mier2
|
UTSW |
10 |
79,376,335 (GRCm39) |
missense |
unknown |
|
Z1177:Mier2
|
UTSW |
10 |
79,376,295 (GRCm39) |
missense |
unknown |
|
|