Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
T |
C |
11: 58,312,533 (GRCm39) |
S4P |
probably benign |
Het |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Acsl6 |
A |
G |
11: 54,225,880 (GRCm39) |
N307D |
probably benign |
Het |
Atxn1 |
A |
G |
13: 45,721,433 (GRCm39) |
V154A |
probably benign |
Het |
Bltp3a |
A |
G |
17: 28,112,414 (GRCm39) |
D1201G |
probably damaging |
Het |
Cacna2d4 |
T |
C |
6: 119,213,611 (GRCm39) |
L10S |
probably benign |
Het |
Cd33 |
A |
T |
7: 43,182,150 (GRCm39) |
H98Q |
probably benign |
Het |
Cebpz |
A |
T |
17: 79,239,684 (GRCm39) |
M579K |
probably benign |
Het |
Cenpk |
T |
G |
13: 104,370,682 (GRCm39) |
C103G |
probably benign |
Het |
Cep97 |
T |
A |
16: 55,726,093 (GRCm39) |
Q670L |
probably benign |
Het |
Cfap65 |
C |
T |
1: 74,945,468 (GRCm39) |
|
probably null |
Het |
Cir1 |
A |
G |
2: 73,142,781 (GRCm39) |
S18P |
probably damaging |
Het |
Coprs |
T |
C |
8: 13,935,081 (GRCm39) |
Y158C |
probably damaging |
Het |
Creld1 |
T |
C |
6: 113,469,765 (GRCm39) |
F389S |
probably damaging |
Het |
Dimt1 |
T |
C |
13: 107,093,636 (GRCm39) |
I276T |
possibly damaging |
Het |
Dok1 |
T |
C |
6: 83,009,972 (GRCm39) |
K46E |
probably damaging |
Het |
Dsp |
T |
A |
13: 38,371,781 (GRCm39) |
C911S |
probably benign |
Het |
Egr3 |
A |
G |
14: 70,314,978 (GRCm39) |
I29V |
probably benign |
Het |
Fam186a |
A |
G |
15: 99,844,766 (GRCm39) |
S493P |
unknown |
Het |
Fam83a |
G |
A |
15: 57,849,765 (GRCm39) |
G103D |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,175,808 (GRCm39) |
Q1635L |
probably damaging |
Het |
Figla |
A |
C |
6: 85,997,689 (GRCm39) |
H139P |
probably benign |
Het |
Fryl |
T |
C |
5: 73,262,115 (GRCm39) |
K551E |
probably damaging |
Het |
Galr2 |
A |
G |
11: 116,174,452 (GRCm39) |
T361A |
probably benign |
Het |
Gart |
A |
T |
16: 91,427,596 (GRCm39) |
S467R |
probably benign |
Het |
Ggps1 |
T |
C |
13: 14,229,742 (GRCm39) |
K45R |
probably benign |
Het |
Ghsr |
G |
C |
3: 27,426,630 (GRCm39) |
V229L |
possibly damaging |
Het |
H2ac21 |
A |
G |
3: 96,127,401 (GRCm39) |
E57G |
probably damaging |
Het |
Hectd2 |
A |
T |
19: 36,582,689 (GRCm39) |
H473L |
possibly damaging |
Het |
Hic2 |
T |
C |
16: 17,076,293 (GRCm39) |
V374A |
possibly damaging |
Het |
Hivep2 |
T |
A |
10: 14,005,523 (GRCm39) |
I707N |
probably benign |
Het |
Il17rc |
T |
C |
6: 113,449,741 (GRCm39) |
S116P |
probably damaging |
Het |
Krt34 |
A |
T |
11: 99,929,226 (GRCm39) |
I328N |
probably damaging |
Het |
Krt79 |
G |
A |
15: 101,840,288 (GRCm39) |
R303C |
probably damaging |
Het |
Lama2 |
T |
C |
10: 27,100,015 (GRCm39) |
E830G |
probably benign |
Het |
Lamb2 |
C |
T |
9: 108,358,006 (GRCm39) |
T149I |
probably damaging |
Het |
Mau2 |
T |
C |
8: 70,480,153 (GRCm39) |
Y318C |
probably damaging |
Het |
Mllt10 |
A |
G |
2: 18,164,322 (GRCm39) |
D284G |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,937,366 (GRCm39) |
S748R |
probably damaging |
Het |
Ncoa6 |
A |
G |
2: 155,248,133 (GRCm39) |
S1724P |
probably benign |
Het |
Nipal4 |
T |
A |
11: 46,052,922 (GRCm39) |
|
probably null |
Het |
Nlrc4 |
G |
C |
17: 74,753,736 (GRCm39) |
L216V |
probably benign |
Het |
Ogfr |
A |
G |
2: 180,235,417 (GRCm39) |
M164V |
possibly damaging |
Het |
Or1o4 |
G |
T |
17: 37,591,386 (GRCm39) |
|
probably benign |
Het |
Or4b12 |
G |
A |
2: 90,096,709 (GRCm39) |
Q22* |
probably null |
Het |
Pcdha12 |
G |
T |
18: 37,155,526 (GRCm39) |
W748C |
probably damaging |
Het |
Pkd1l3 |
T |
C |
8: 110,395,849 (GRCm39) |
V2083A |
probably damaging |
Het |
Plin3 |
C |
A |
17: 56,587,824 (GRCm39) |
G297V |
probably benign |
Het |
Prex1 |
C |
T |
2: 166,419,896 (GRCm39) |
R1260Q |
possibly damaging |
Het |
Prpf38b |
A |
G |
3: 108,818,619 (GRCm39) |
V47A |
probably benign |
Het |
Ptch1 |
T |
C |
13: 63,675,071 (GRCm39) |
T851A |
probably benign |
Het |
Ptk7 |
T |
A |
17: 46,887,744 (GRCm39) |
I563F |
possibly damaging |
Het |
Ptprm |
A |
G |
17: 67,116,466 (GRCm39) |
Y938H |
probably damaging |
Het |
R3hcc1l |
G |
A |
19: 42,507,203 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
T |
C |
11: 54,443,684 (GRCm39) |
V89A |
probably benign |
Het |
Sh2b1 |
CTC |
CTCCGCCACGGGGACCAGTTC |
7: 126,066,770 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
AGCTCAGCCACGGGGACC |
AGCTCAGCCACGGGGACCCGCTCAGCCACGGGGACC |
7: 126,066,750 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
ACCAGCTC |
ACCAGCTCAGCCACGGGGGCCAGCTC |
7: 126,066,765 (GRCm39) |
|
probably benign |
Het |
Slain1 |
T |
A |
14: 103,932,748 (GRCm39) |
V444E |
probably damaging |
Het |
Slc10a5 |
T |
A |
3: 10,400,532 (GRCm39) |
I43F |
possibly damaging |
Het |
Smarca2 |
T |
C |
19: 26,659,452 (GRCm39) |
F914S |
possibly damaging |
Het |
Smarca5 |
A |
C |
8: 81,428,840 (GRCm39) |
L1003V |
probably damaging |
Het |
Spata18 |
A |
T |
5: 73,829,840 (GRCm39) |
I332F |
|
Het |
Spata31d1e |
A |
G |
13: 59,890,806 (GRCm39) |
V338A |
probably damaging |
Het |
Stard9 |
C |
G |
2: 120,534,564 (GRCm39) |
P3607R |
probably damaging |
Het |
Tbx19 |
A |
G |
1: 164,966,546 (GRCm39) |
S443P |
unknown |
Het |
Tktl2 |
C |
G |
8: 66,965,840 (GRCm39) |
A466G |
probably damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem129 |
A |
G |
5: 33,815,122 (GRCm39) |
V17A |
probably benign |
Het |
Tom1l2 |
T |
C |
11: 60,153,486 (GRCm39) |
T164A |
probably damaging |
Het |
Tor1aip1 |
T |
A |
1: 155,906,177 (GRCm39) |
D205V |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 44,017,648 (GRCm39) |
S751T |
probably benign |
Het |
Trim11 |
G |
T |
11: 58,878,477 (GRCm39) |
A251S |
unknown |
Het |
Trim33 |
T |
C |
3: 103,239,074 (GRCm39) |
V684A |
probably benign |
Het |
Triobp |
C |
T |
15: 78,877,378 (GRCm39) |
R1637C |
probably damaging |
Het |
Trpm3 |
A |
G |
19: 22,960,040 (GRCm39) |
N1225S |
probably benign |
Het |
Usp21 |
T |
C |
1: 171,112,503 (GRCm39) |
Y300C |
probably damaging |
Het |
Usp32 |
T |
C |
11: 84,913,560 (GRCm39) |
T924A |
probably damaging |
Het |
Vmn1r198 |
A |
T |
13: 22,539,015 (GRCm39) |
H167L |
possibly damaging |
Het |
Vmn2r23 |
A |
G |
6: 123,689,672 (GRCm39) |
T183A |
probably benign |
Het |
Zc3h8 |
T |
C |
2: 128,773,223 (GRCm39) |
Y213C |
probably damaging |
Het |
Zcchc17 |
A |
T |
4: 130,232,337 (GRCm39) |
D55E |
probably benign |
Het |
Zfp408 |
A |
T |
2: 91,478,368 (GRCm39) |
W26R |
probably damaging |
Het |
Zfp937 |
G |
T |
2: 150,080,890 (GRCm39) |
A307S |
possibly damaging |
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 |
|
R7350:Mier2
|
UTSW |
10 |
79,376,132 (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 |
Z1176:Mier2
|
UTSW |
10 |
79,376,335 (GRCm39) |
missense |
unknown |
|
Z1177:Mier2
|
UTSW |
10 |
79,376,295 (GRCm39) |
missense |
unknown |
|
|