Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130230L23Rik |
A |
T |
5: 66,157,560 (GRCm39) |
M1K |
probably null |
Het |
Abca4 |
T |
A |
3: 121,899,010 (GRCm39) |
I664N |
probably damaging |
Het |
Acin1 |
T |
C |
14: 54,881,718 (GRCm39) |
D335G |
probably damaging |
Het |
Acoxl |
A |
G |
2: 127,719,707 (GRCm39) |
Y156C |
probably damaging |
Het |
Adamts20 |
A |
G |
15: 94,236,340 (GRCm39) |
F844L |
probably benign |
Het |
Ago1 |
A |
G |
4: 126,335,029 (GRCm39) |
Y398H |
probably damaging |
Het |
Aldob |
A |
G |
4: 49,543,835 (GRCm39) |
V49A |
possibly damaging |
Het |
Arhgap18 |
A |
G |
10: 26,722,026 (GRCm39) |
E71G |
probably damaging |
Het |
Asb12 |
G |
T |
X: 94,513,950 (GRCm39) |
H307N |
probably damaging |
Het |
Atp2b1 |
T |
C |
10: 98,832,750 (GRCm39) |
V417A |
probably damaging |
Het |
AY358078 |
T |
C |
14: 52,037,504 (GRCm39) |
M1T |
probably null |
Het |
Bcl2l15 |
A |
G |
3: 103,745,914 (GRCm39) |
|
probably null |
Het |
Brpf3 |
A |
G |
17: 29,026,342 (GRCm39) |
M472V |
probably benign |
Het |
Bsn |
A |
G |
9: 107,983,918 (GRCm39) |
S3379P |
unknown |
Het |
Cap2 |
T |
C |
13: 46,793,555 (GRCm39) |
V333A |
probably damaging |
Het |
Cd207 |
T |
A |
6: 83,652,635 (GRCm39) |
D165V |
probably damaging |
Het |
Cfap210 |
A |
T |
2: 69,612,181 (GRCm39) |
|
probably null |
Het |
Cmtr1 |
A |
G |
17: 29,893,148 (GRCm39) |
T496A |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,310,858 (GRCm39) |
|
probably benign |
Het |
Cstb |
A |
G |
10: 78,263,273 (GRCm39) |
*99W |
probably null |
Het |
Cstdc6 |
T |
G |
16: 36,142,148 (GRCm39) |
D76A |
possibly damaging |
Het |
Ddx11 |
G |
A |
17: 66,442,934 (GRCm39) |
|
probably null |
Het |
Dip2c |
T |
C |
13: 9,671,985 (GRCm39) |
M990T |
possibly damaging |
Het |
Epc2 |
A |
G |
2: 49,422,117 (GRCm39) |
Y337C |
probably damaging |
Het |
Fmn1 |
A |
G |
2: 113,539,783 (GRCm39) |
E1326G |
probably damaging |
Het |
Focad |
A |
T |
4: 88,096,326 (GRCm39) |
D236V |
probably damaging |
Het |
Fsd1 |
G |
A |
17: 56,298,254 (GRCm39) |
S193N |
probably benign |
Het |
Gm4922 |
T |
A |
10: 18,660,211 (GRCm39) |
R170S |
possibly damaging |
Het |
Gm5129 |
T |
C |
5: 29,940,654 (GRCm39) |
|
probably benign |
Het |
Gucy2d |
T |
A |
7: 98,103,268 (GRCm39) |
L504H |
probably damaging |
Het |
Hspbap1 |
A |
T |
16: 35,621,934 (GRCm39) |
Y93F |
possibly damaging |
Het |
Iars2 |
A |
T |
1: 185,050,765 (GRCm39) |
D441E |
probably benign |
Het |
Il1rap |
A |
T |
16: 26,541,676 (GRCm39) |
H639L |
probably damaging |
Het |
Inhbc |
A |
T |
10: 127,193,416 (GRCm39) |
V200E |
probably benign |
Het |
Ints8 |
C |
A |
4: 11,241,684 (GRCm39) |
C253F |
probably damaging |
Het |
Intu |
G |
T |
3: 40,618,765 (GRCm39) |
G257V |
probably damaging |
Het |
Kif23 |
C |
A |
9: 61,826,243 (GRCm39) |
A929S |
possibly damaging |
Het |
Kmt2b |
A |
T |
7: 30,274,083 (GRCm39) |
V2207E |
possibly damaging |
Het |
Ksr2 |
A |
C |
5: 117,643,594 (GRCm39) |
E121A |
probably benign |
Het |
Lce1b |
A |
G |
3: 92,563,318 (GRCm39) |
S72P |
unknown |
Het |
Lpl |
TGG |
TG |
8: 69,349,254 (GRCm39) |
|
probably null |
Het |
Mcmdc2 |
T |
C |
1: 10,001,030 (GRCm39) |
V435A |
probably damaging |
Het |
Mecom |
A |
G |
3: 30,563,577 (GRCm39) |
|
probably null |
Het |
Mmp16 |
A |
T |
4: 18,116,013 (GRCm39) |
D539V |
probably benign |
Het |
Mpp1 |
A |
G |
X: 74,168,975 (GRCm39) |
|
probably null |
Het |
Mpp2 |
C |
T |
11: 101,955,493 (GRCm39) |
E86K |
probably benign |
Het |
Mtor |
T |
A |
4: 148,539,089 (GRCm39) |
F195L |
probably damaging |
Het |
Myo3a |
T |
C |
2: 22,404,657 (GRCm39) |
I663T |
probably benign |
Het |
Nlrp5 |
G |
A |
7: 23,123,407 (GRCm39) |
G756E |
possibly damaging |
Het |
Nudt18 |
T |
C |
14: 70,817,335 (GRCm39) |
L255P |
probably damaging |
Het |
Nup62 |
T |
A |
7: 44,478,472 (GRCm39) |
S162R |
possibly damaging |
Het |
Oosp2 |
C |
T |
19: 11,626,959 (GRCm39) |
|
probably null |
Het |
Or52n20 |
T |
A |
7: 104,320,524 (GRCm39) |
I205N |
possibly damaging |
Het |
Or6c66 |
A |
T |
10: 129,461,621 (GRCm39) |
I103K |
probably damaging |
Het |
Or7g20 |
G |
A |
9: 18,946,562 (GRCm39) |
A48T |
probably benign |
Het |
Or8h7 |
A |
G |
2: 86,720,956 (GRCm39) |
S188P |
probably damaging |
Het |
Pan2 |
A |
G |
10: 128,149,050 (GRCm39) |
D506G |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 94,125,471 (GRCm39) |
S233L |
probably damaging |
Het |
Pcdhgc5 |
T |
G |
18: 37,954,471 (GRCm39) |
S582A |
possibly damaging |
Het |
Pdik1l |
T |
C |
4: 134,006,222 (GRCm39) |
D70G |
probably damaging |
Het |
Peg12 |
T |
C |
7: 62,113,416 (GRCm39) |
H227R |
probably benign |
Het |
Pms1 |
C |
T |
1: 53,228,546 (GRCm39) |
V901I |
probably benign |
Het |
Pnisr |
C |
T |
4: 21,874,086 (GRCm39) |
|
probably benign |
Het |
Pole |
A |
G |
5: 110,482,063 (GRCm39) |
E135G |
probably benign |
Het |
Ppp6r2 |
C |
A |
15: 89,166,141 (GRCm39) |
A715E |
probably benign |
Het |
Prickle4 |
T |
G |
17: 48,001,044 (GRCm39) |
H174P |
possibly damaging |
Het |
Prl2a1 |
T |
C |
13: 27,988,923 (GRCm39) |
L16P |
probably damaging |
Het |
Prss32 |
C |
T |
17: 24,072,868 (GRCm39) |
T33M |
probably benign |
Het |
Psmd13 |
C |
T |
7: 140,463,430 (GRCm39) |
T38I |
probably damaging |
Het |
Rai14 |
C |
A |
15: 10,633,314 (GRCm39) |
Q25H |
probably damaging |
Het |
Rbbp6 |
T |
C |
7: 122,596,252 (GRCm39) |
V598A |
probably damaging |
Het |
Rbm34 |
C |
A |
8: 127,697,631 (GRCm39) |
A27S |
probably benign |
Het |
Rbm4b |
A |
G |
19: 4,812,331 (GRCm39) |
T247A |
probably benign |
Het |
Riiad1 |
G |
A |
3: 94,380,176 (GRCm39) |
P40S |
possibly damaging |
Het |
Sema4f |
T |
C |
6: 82,894,824 (GRCm39) |
D457G |
possibly damaging |
Het |
Sema6c |
A |
T |
3: 95,078,099 (GRCm39) |
I492F |
probably damaging |
Het |
Serpina3a |
A |
T |
12: 104,084,886 (GRCm39) |
I94L |
probably benign |
Het |
Skida1 |
TTGCTGCTGCTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTGCTG |
2: 18,051,155 (GRCm39) |
|
probably benign |
Het |
Slc38a1 |
G |
A |
15: 96,485,016 (GRCm39) |
T221M |
probably damaging |
Het |
Slc6a17 |
T |
A |
3: 107,379,492 (GRCm39) |
M559L |
probably damaging |
Het |
Sntg2 |
T |
C |
12: 30,286,650 (GRCm39) |
N315D |
probably benign |
Het |
Snx10 |
T |
A |
6: 51,552,890 (GRCm39) |
V11E |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,047,405 (GRCm39) |
E1683G |
probably benign |
Het |
Ssc5d |
A |
T |
7: 4,931,506 (GRCm39) |
R238W |
probably damaging |
Het |
Ssh1 |
A |
T |
5: 114,081,512 (GRCm39) |
F617L |
probably damaging |
Het |
Taf1 |
T |
G |
X: 100,606,563 (GRCm39) |
M1254R |
probably damaging |
Het |
Tcirg1 |
A |
G |
19: 3,948,835 (GRCm39) |
L450P |
probably damaging |
Het |
Ticam1 |
C |
A |
17: 56,578,718 (GRCm39) |
A126S |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,890,821 (GRCm39) |
V388E |
probably damaging |
Het |
Tomm5 |
A |
G |
4: 45,107,939 (GRCm39) |
L32P |
probably damaging |
Het |
Ubr5 |
A |
T |
15: 38,042,090 (GRCm39) |
S169T |
probably benign |
Het |
Usp28 |
T |
G |
9: 48,920,494 (GRCm39) |
D240E |
probably benign |
Het |
Usp34 |
T |
C |
11: 23,311,593 (GRCm39) |
Y462H |
possibly damaging |
Het |
Utp14b |
C |
A |
1: 78,643,148 (GRCm39) |
Q349K |
probably damaging |
Het |
Utp20 |
G |
T |
10: 88,585,305 (GRCm39) |
D2586E |
probably benign |
Het |
Vmn1r173 |
A |
G |
7: 23,402,660 (GRCm39) |
I298M |
unknown |
Het |
Vmn1r37 |
T |
A |
6: 66,708,461 (GRCm39) |
I29K |
probably benign |
Het |
Vmn2r23 |
G |
A |
6: 123,679,874 (GRCm39) |
G32D |
probably damaging |
Het |
Xpo7 |
A |
T |
14: 70,931,431 (GRCm39) |
F296I |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,477,774 (GRCm39) |
E3463G |
probably damaging |
Het |
Zfp455 |
G |
T |
13: 67,355,509 (GRCm39) |
R194L |
probably benign |
Het |
Zfp663 |
T |
C |
2: 165,194,651 (GRCm39) |
T523A |
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 |
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 |
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 |
|
|