Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
T |
A |
4: 62,457,164 (GRCm39) |
V161E |
possibly damaging |
Het |
Arhgap40 |
T |
C |
2: 158,388,629 (GRCm39) |
V521A |
possibly damaging |
Het |
Atrn |
T |
C |
2: 130,841,050 (GRCm39) |
|
probably benign |
Het |
Casp12 |
T |
C |
9: 5,352,923 (GRCm39) |
|
probably benign |
Het |
Cenpf |
G |
A |
1: 189,411,230 (GRCm39) |
T318M |
probably damaging |
Het |
Cfap119 |
C |
T |
7: 127,184,663 (GRCm39) |
R172H |
probably benign |
Het |
Clcn2 |
T |
C |
16: 20,527,892 (GRCm39) |
K525E |
probably damaging |
Het |
Cntln |
A |
G |
4: 84,889,419 (GRCm39) |
T301A |
probably benign |
Het |
Crat |
T |
C |
2: 30,305,378 (GRCm39) |
|
probably benign |
Het |
Cul5 |
A |
G |
9: 53,545,027 (GRCm39) |
|
probably benign |
Het |
Cxcl14 |
A |
T |
13: 56,443,708 (GRCm39) |
I34N |
probably damaging |
Het |
Cyp2b19 |
A |
G |
7: 26,470,819 (GRCm39) |
I487V |
probably benign |
Het |
Cyp4a10 |
T |
A |
4: 115,386,690 (GRCm39) |
F446I |
probably damaging |
Het |
D430041D05Rik |
T |
A |
2: 104,063,824 (GRCm39) |
M659L |
possibly damaging |
Het |
Dclk3 |
T |
C |
9: 111,296,963 (GRCm39) |
F169S |
probably damaging |
Het |
Ddx52 |
T |
C |
11: 83,848,306 (GRCm39) |
I532T |
probably damaging |
Het |
Dnm1 |
T |
C |
2: 32,226,023 (GRCm39) |
D352G |
probably damaging |
Het |
Eif4g2 |
T |
C |
7: 110,677,509 (GRCm39) |
E174G |
probably damaging |
Het |
Enpp6 |
G |
T |
8: 47,546,067 (GRCm39) |
V386L |
probably damaging |
Het |
Entr1 |
C |
A |
2: 26,278,909 (GRCm39) |
|
probably benign |
Het |
Eps15l1 |
T |
C |
8: 73,095,238 (GRCm39) |
D904G |
probably damaging |
Het |
Esrrb |
A |
G |
12: 86,565,604 (GRCm39) |
Y356C |
probably damaging |
Het |
Flt3 |
A |
T |
5: 147,291,509 (GRCm39) |
S619T |
possibly damaging |
Het |
Fndc7 |
A |
T |
3: 108,766,218 (GRCm39) |
C716S |
probably damaging |
Het |
Gm26996 |
T |
A |
6: 130,556,448 (GRCm39) |
|
noncoding transcript |
Het |
Grik2 |
A |
T |
10: 49,298,711 (GRCm39) |
F50I |
possibly damaging |
Het |
Guf1 |
T |
C |
5: 69,723,786 (GRCm39) |
V367A |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Ifnar2 |
T |
C |
16: 91,188,684 (GRCm39) |
V55A |
probably benign |
Het |
Impg1 |
T |
A |
9: 80,322,907 (GRCm39) |
I33F |
probably benign |
Het |
Ltbp4 |
A |
C |
7: 27,024,608 (GRCm39) |
V674G |
probably damaging |
Het |
Negr1 |
T |
C |
3: 156,914,023 (GRCm39) |
|
probably benign |
Het |
Neurog3 |
A |
G |
10: 61,969,599 (GRCm39) |
T25A |
probably damaging |
Het |
Or10v1 |
T |
C |
19: 11,874,126 (GRCm39) |
V247A |
probably benign |
Het |
Or4a69 |
T |
A |
2: 89,313,100 (GRCm39) |
K126N |
probably damaging |
Het |
Or51h1 |
A |
C |
7: 102,308,685 (GRCm39) |
Y219S |
probably damaging |
Het |
Or5k17 |
T |
C |
16: 58,746,455 (GRCm39) |
T160A |
probably benign |
Het |
Pax8 |
T |
A |
2: 24,333,201 (GRCm39) |
|
probably benign |
Het |
Pcsk6 |
A |
C |
7: 65,581,480 (GRCm39) |
I254L |
possibly damaging |
Het |
Pde3a |
A |
G |
6: 141,404,942 (GRCm39) |
K389R |
probably benign |
Het |
Rab3gap1 |
C |
A |
1: 127,852,996 (GRCm39) |
|
probably benign |
Het |
Rbck1 |
G |
A |
2: 152,160,653 (GRCm39) |
Q428* |
probably null |
Het |
Rptor |
A |
G |
11: 119,689,666 (GRCm39) |
D321G |
probably null |
Het |
Sall2 |
C |
A |
14: 52,551,260 (GRCm39) |
R643L |
probably damaging |
Het |
Skp1 |
T |
C |
11: 52,134,446 (GRCm39) |
I59T |
possibly damaging |
Het |
Slc23a3 |
T |
G |
1: 75,105,200 (GRCm39) |
N456T |
probably damaging |
Het |
Slc4a7 |
G |
A |
14: 14,778,850 (GRCm38) |
G920S |
probably damaging |
Het |
Smarcd3 |
T |
C |
5: 24,797,802 (GRCm39) |
I467V |
probably benign |
Het |
Spata31d1c |
C |
T |
13: 65,183,874 (GRCm39) |
A472V |
probably damaging |
Het |
Spmap1 |
A |
G |
11: 97,662,441 (GRCm39) |
S144P |
probably damaging |
Het |
Srsf6 |
T |
C |
2: 162,773,643 (GRCm39) |
I18T |
probably damaging |
Het |
Stom |
C |
T |
2: 35,213,758 (GRCm39) |
G80D |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,084,028 (GRCm39) |
Y1915N |
possibly damaging |
Het |
Tmf1 |
C |
T |
6: 97,150,361 (GRCm39) |
V449I |
probably benign |
Het |
Triobp |
C |
T |
15: 78,851,295 (GRCm39) |
A483V |
probably benign |
Het |
Vdac1 |
G |
A |
11: 52,265,799 (GRCm39) |
|
probably null |
Het |
Vmn2r75 |
T |
G |
7: 85,815,494 (GRCm39) |
E123D |
probably benign |
Het |
Vmn2r79 |
T |
A |
7: 86,653,319 (GRCm39) |
V528D |
possibly damaging |
Het |
Zdbf2 |
T |
G |
1: 63,345,750 (GRCm39) |
N1376K |
possibly damaging |
Het |
Zeb1os1 |
T |
C |
18: 5,525,375 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Mroh2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Mroh2b
|
APN |
15 |
4,928,679 (GRCm39) |
missense |
probably benign |
|
IGL00507:Mroh2b
|
APN |
15 |
4,991,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00548:Mroh2b
|
APN |
15 |
4,960,798 (GRCm39) |
missense |
probably benign |
0.35 |
IGL00902:Mroh2b
|
APN |
15 |
4,944,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00944:Mroh2b
|
APN |
15 |
4,980,609 (GRCm39) |
splice site |
probably benign |
|
IGL00954:Mroh2b
|
APN |
15 |
4,932,536 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01015:Mroh2b
|
APN |
15 |
4,971,024 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:Mroh2b
|
APN |
15 |
4,944,634 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01337:Mroh2b
|
APN |
15 |
4,934,506 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01780:Mroh2b
|
APN |
15 |
4,941,482 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01919:Mroh2b
|
APN |
15 |
4,953,170 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02069:Mroh2b
|
APN |
15 |
4,933,806 (GRCm39) |
splice site |
probably benign |
|
IGL02146:Mroh2b
|
APN |
15 |
4,980,776 (GRCm39) |
splice site |
probably null |
|
IGL02221:Mroh2b
|
APN |
15 |
4,953,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02281:Mroh2b
|
APN |
15 |
4,981,745 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02350:Mroh2b
|
APN |
15 |
4,941,482 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02357:Mroh2b
|
APN |
15 |
4,941,482 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02401:Mroh2b
|
APN |
15 |
4,929,983 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02427:Mroh2b
|
APN |
15 |
4,981,042 (GRCm39) |
splice site |
probably benign |
|
IGL02432:Mroh2b
|
APN |
15 |
4,943,668 (GRCm39) |
missense |
probably benign |
|
IGL02582:Mroh2b
|
APN |
15 |
4,937,997 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02632:Mroh2b
|
APN |
15 |
4,960,583 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02741:Mroh2b
|
APN |
15 |
4,935,114 (GRCm39) |
missense |
probably benign |
|
IGL02811:Mroh2b
|
APN |
15 |
4,944,718 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02826:Mroh2b
|
APN |
15 |
4,991,630 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03412:Mroh2b
|
APN |
15 |
4,973,854 (GRCm39) |
missense |
probably benign |
0.14 |
PIT4468001:Mroh2b
|
UTSW |
15 |
4,942,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R0024:Mroh2b
|
UTSW |
15 |
4,955,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R0333:Mroh2b
|
UTSW |
15 |
4,960,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Mroh2b
|
UTSW |
15 |
4,971,116 (GRCm39) |
missense |
probably benign |
0.01 |
R0530:Mroh2b
|
UTSW |
15 |
4,963,877 (GRCm39) |
missense |
probably damaging |
0.97 |
R1411:Mroh2b
|
UTSW |
15 |
4,947,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Mroh2b
|
UTSW |
15 |
4,978,137 (GRCm39) |
missense |
probably benign |
0.00 |
R1525:Mroh2b
|
UTSW |
15 |
4,980,612 (GRCm39) |
splice site |
probably null |
|
R1584:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Mroh2b
|
UTSW |
15 |
4,974,572 (GRCm39) |
missense |
probably benign |
0.08 |
R1657:Mroh2b
|
UTSW |
15 |
4,960,525 (GRCm39) |
nonsense |
probably null |
|
R1671:Mroh2b
|
UTSW |
15 |
4,980,776 (GRCm39) |
splice site |
probably null |
|
R1698:Mroh2b
|
UTSW |
15 |
4,943,622 (GRCm39) |
missense |
probably benign |
0.02 |
R2002:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Mroh2b
|
UTSW |
15 |
4,946,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Mroh2b
|
UTSW |
15 |
4,974,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R2179:Mroh2b
|
UTSW |
15 |
4,950,928 (GRCm39) |
critical splice donor site |
probably null |
|
R2183:Mroh2b
|
UTSW |
15 |
4,947,707 (GRCm39) |
splice site |
probably null |
|
R3713:Mroh2b
|
UTSW |
15 |
4,973,131 (GRCm39) |
missense |
probably benign |
0.01 |
R3714:Mroh2b
|
UTSW |
15 |
4,973,131 (GRCm39) |
missense |
probably benign |
0.01 |
R3747:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3748:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3749:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3750:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3792:Mroh2b
|
UTSW |
15 |
4,953,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R3872:Mroh2b
|
UTSW |
15 |
4,954,543 (GRCm39) |
nonsense |
probably null |
|
R4021:Mroh2b
|
UTSW |
15 |
4,954,582 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4329:Mroh2b
|
UTSW |
15 |
4,960,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R4456:Mroh2b
|
UTSW |
15 |
4,977,407 (GRCm39) |
missense |
probably benign |
0.21 |
R4836:Mroh2b
|
UTSW |
15 |
4,933,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5050:Mroh2b
|
UTSW |
15 |
4,929,932 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5230:Mroh2b
|
UTSW |
15 |
4,971,004 (GRCm39) |
missense |
probably benign |
0.07 |
R5342:Mroh2b
|
UTSW |
15 |
4,943,615 (GRCm39) |
nonsense |
probably null |
|
R5353:Mroh2b
|
UTSW |
15 |
4,946,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Mroh2b
|
UTSW |
15 |
4,935,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5424:Mroh2b
|
UTSW |
15 |
4,971,094 (GRCm39) |
missense |
probably damaging |
0.98 |
R5484:Mroh2b
|
UTSW |
15 |
4,938,463 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5999:Mroh2b
|
UTSW |
15 |
4,942,366 (GRCm39) |
splice site |
probably null |
|
R6046:Mroh2b
|
UTSW |
15 |
4,980,763 (GRCm39) |
missense |
probably benign |
0.01 |
R6081:Mroh2b
|
UTSW |
15 |
4,973,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Mroh2b
|
UTSW |
15 |
4,944,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6165:Mroh2b
|
UTSW |
15 |
4,947,832 (GRCm39) |
missense |
probably benign |
0.23 |
R6240:Mroh2b
|
UTSW |
15 |
4,964,126 (GRCm39) |
missense |
probably benign |
0.38 |
R6487:Mroh2b
|
UTSW |
15 |
4,976,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R6539:Mroh2b
|
UTSW |
15 |
4,935,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R6616:Mroh2b
|
UTSW |
15 |
4,982,764 (GRCm39) |
missense |
probably benign |
0.36 |
R6663:Mroh2b
|
UTSW |
15 |
4,977,417 (GRCm39) |
missense |
probably benign |
0.21 |
R6820:Mroh2b
|
UTSW |
15 |
4,982,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6900:Mroh2b
|
UTSW |
15 |
4,938,469 (GRCm39) |
missense |
probably benign |
0.00 |
R6990:Mroh2b
|
UTSW |
15 |
4,942,284 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7067:Mroh2b
|
UTSW |
15 |
4,929,986 (GRCm39) |
missense |
probably benign |
0.35 |
R7092:Mroh2b
|
UTSW |
15 |
4,964,160 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7102:Mroh2b
|
UTSW |
15 |
4,977,485 (GRCm39) |
missense |
probably benign |
0.06 |
R7264:Mroh2b
|
UTSW |
15 |
4,950,844 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7436:Mroh2b
|
UTSW |
15 |
4,971,036 (GRCm39) |
missense |
probably benign |
0.21 |
R7462:Mroh2b
|
UTSW |
15 |
4,938,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Mroh2b
|
UTSW |
15 |
4,978,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7575:Mroh2b
|
UTSW |
15 |
4,964,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R7579:Mroh2b
|
UTSW |
15 |
4,960,543 (GRCm39) |
missense |
probably benign |
0.09 |
R7605:Mroh2b
|
UTSW |
15 |
4,974,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R7624:Mroh2b
|
UTSW |
15 |
4,946,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R7797:Mroh2b
|
UTSW |
15 |
4,978,587 (GRCm39) |
missense |
probably benign |
0.36 |
R7848:Mroh2b
|
UTSW |
15 |
4,967,861 (GRCm39) |
nonsense |
probably null |
|
R7952:Mroh2b
|
UTSW |
15 |
4,980,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Mroh2b
|
UTSW |
15 |
4,950,839 (GRCm39) |
nonsense |
probably null |
|
R8088:Mroh2b
|
UTSW |
15 |
4,929,985 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8207:Mroh2b
|
UTSW |
15 |
4,967,892 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8242:Mroh2b
|
UTSW |
15 |
4,938,522 (GRCm39) |
missense |
probably benign |
0.04 |
R8248:Mroh2b
|
UTSW |
15 |
4,960,586 (GRCm39) |
missense |
probably benign |
0.40 |
R8258:Mroh2b
|
UTSW |
15 |
4,941,391 (GRCm39) |
missense |
probably benign |
0.01 |
R8259:Mroh2b
|
UTSW |
15 |
4,941,391 (GRCm39) |
missense |
probably benign |
0.01 |
R8304:Mroh2b
|
UTSW |
15 |
4,955,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R8316:Mroh2b
|
UTSW |
15 |
4,980,746 (GRCm39) |
nonsense |
probably null |
|
R8345:Mroh2b
|
UTSW |
15 |
4,973,808 (GRCm39) |
missense |
probably benign |
0.09 |
R8507:Mroh2b
|
UTSW |
15 |
4,978,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R8728:Mroh2b
|
UTSW |
15 |
4,935,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8747:Mroh2b
|
UTSW |
15 |
4,964,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Mroh2b
|
UTSW |
15 |
4,978,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R8814:Mroh2b
|
UTSW |
15 |
4,971,107 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8856:Mroh2b
|
UTSW |
15 |
4,960,510 (GRCm39) |
nonsense |
probably null |
|
R8910:Mroh2b
|
UTSW |
15 |
4,960,855 (GRCm39) |
missense |
probably benign |
0.01 |
R8913:Mroh2b
|
UTSW |
15 |
4,947,010 (GRCm39) |
intron |
probably benign |
|
R8941:Mroh2b
|
UTSW |
15 |
4,991,606 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9014:Mroh2b
|
UTSW |
15 |
4,928,670 (GRCm39) |
start codon destroyed |
probably null |
0.95 |
R9086:Mroh2b
|
UTSW |
15 |
4,982,754 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9101:Mroh2b
|
UTSW |
15 |
4,929,935 (GRCm39) |
missense |
probably benign |
0.20 |
R9118:Mroh2b
|
UTSW |
15 |
4,991,573 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9393:Mroh2b
|
UTSW |
15 |
4,980,666 (GRCm39) |
missense |
probably benign |
|
R9429:Mroh2b
|
UTSW |
15 |
4,963,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9431:Mroh2b
|
UTSW |
15 |
4,963,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R9443:Mroh2b
|
UTSW |
15 |
4,973,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R9447:Mroh2b
|
UTSW |
15 |
4,960,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R9497:Mroh2b
|
UTSW |
15 |
4,950,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R9588:Mroh2b
|
UTSW |
15 |
4,978,130 (GRCm39) |
missense |
probably benign |
0.00 |
R9631:Mroh2b
|
UTSW |
15 |
4,946,556 (GRCm39) |
missense |
probably damaging |
0.97 |
R9686:Mroh2b
|
UTSW |
15 |
4,974,605 (GRCm39) |
missense |
probably benign |
0.34 |
R9774:Mroh2b
|
UTSW |
15 |
4,943,613 (GRCm39) |
missense |
probably benign |
0.08 |
X0067:Mroh2b
|
UTSW |
15 |
4,981,073 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Mroh2b
|
UTSW |
15 |
4,934,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|