Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
T |
G |
11: 84,154,910 (GRCm39) |
D988E |
probably benign |
Het |
Als2 |
A |
G |
1: 59,219,760 (GRCm39) |
V1185A |
probably damaging |
Het |
Amdhd2 |
A |
G |
17: 24,375,029 (GRCm39) |
V391A |
probably damaging |
Het |
Armh4 |
G |
C |
14: 50,011,017 (GRCm39) |
T230S |
probably damaging |
Het |
Caprin1 |
A |
T |
2: 103,599,851 (GRCm39) |
V608E |
probably damaging |
Het |
Celsr3 |
T |
A |
9: 108,720,151 (GRCm39) |
C2512* |
probably null |
Het |
Cfl1 |
A |
T |
19: 5,543,583 (GRCm39) |
R187W |
probably damaging |
Het |
Cgnl1 |
C |
T |
9: 71,633,226 (GRCm39) |
V42I |
probably damaging |
Het |
Chd2 |
A |
G |
7: 73,130,178 (GRCm39) |
Y826H |
probably damaging |
Het |
Col9a2 |
C |
A |
4: 120,898,171 (GRCm39) |
P28T |
unknown |
Het |
Cyp3a44 |
G |
A |
5: 145,716,553 (GRCm39) |
P346S |
probably damaging |
Het |
Dact2 |
A |
G |
17: 14,418,252 (GRCm39) |
V151A |
probably benign |
Het |
Dhx29 |
T |
C |
13: 113,089,377 (GRCm39) |
I716T |
probably damaging |
Het |
Entrep1 |
C |
A |
19: 23,952,999 (GRCm39) |
C437F |
probably damaging |
Het |
Esam |
T |
C |
9: 37,448,917 (GRCm39) |
S342P |
probably damaging |
Het |
Fer1l4 |
A |
G |
2: 155,877,518 (GRCm39) |
V1053A |
possibly damaging |
Het |
Grk3 |
A |
G |
5: 113,114,848 (GRCm39) |
F124S |
probably damaging |
Het |
H2-DMa |
G |
A |
17: 34,356,373 (GRCm39) |
|
probably null |
Het |
Hsd3b5 |
T |
A |
3: 98,527,036 (GRCm39) |
I137F |
possibly damaging |
Het |
Itgav |
A |
T |
2: 83,632,123 (GRCm39) |
I902F |
probably benign |
Het |
Itsn1 |
G |
T |
16: 91,706,111 (GRCm39) |
C179F |
probably damaging |
Het |
Kcnh8 |
G |
A |
17: 53,146,153 (GRCm39) |
R347H |
probably damaging |
Het |
Kif9 |
T |
C |
9: 110,319,034 (GRCm39) |
M166T |
possibly damaging |
Het |
Kmt5c |
C |
T |
7: 4,749,453 (GRCm39) |
Q324* |
probably null |
Het |
Lcn9 |
G |
A |
2: 25,714,722 (GRCm39) |
E154K |
probably benign |
Het |
Mfge8 |
A |
T |
7: 78,791,521 (GRCm39) |
L227Q |
probably benign |
Het |
Mtif2 |
G |
A |
11: 29,490,721 (GRCm39) |
R475Q |
probably benign |
Het |
Nln |
C |
T |
13: 104,173,455 (GRCm39) |
V584I |
possibly damaging |
Het |
Nr2e3 |
T |
C |
9: 59,856,050 (GRCm39) |
E129G |
probably benign |
Het |
Ocstamp |
T |
C |
2: 165,239,436 (GRCm39) |
D250G |
probably damaging |
Het |
Or1a1 |
A |
T |
11: 74,086,722 (GRCm39) |
H131L |
probably damaging |
Het |
Or52n4b |
T |
C |
7: 108,144,584 (GRCm39) |
I284T |
possibly damaging |
Het |
Or8k27 |
A |
C |
2: 86,275,562 (GRCm39) |
L255V |
probably damaging |
Het |
Pld1 |
A |
T |
3: 28,125,336 (GRCm39) |
I417L |
probably benign |
Het |
Polr1a |
A |
T |
6: 71,918,519 (GRCm39) |
K692N |
probably damaging |
Het |
Qsox2 |
A |
T |
2: 26,110,759 (GRCm39) |
Y152* |
probably null |
Het |
Rpap1 |
T |
C |
2: 119,614,259 (GRCm39) |
D46G |
possibly damaging |
Het |
Rpe65 |
A |
G |
3: 159,320,085 (GRCm39) |
T246A |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,391,446 (GRCm39) |
D82G |
probably damaging |
Het |
Sema3d |
A |
G |
5: 12,634,941 (GRCm39) |
E669G |
possibly damaging |
Het |
Serpinb6c |
T |
C |
13: 34,064,209 (GRCm39) |
N282S |
probably benign |
Het |
Snap47 |
A |
T |
11: 59,319,596 (GRCm39) |
S181T |
probably benign |
Het |
Snx9 |
A |
C |
17: 5,968,711 (GRCm39) |
T336P |
possibly damaging |
Het |
Sphkap |
G |
A |
1: 83,255,236 (GRCm39) |
R838* |
probably null |
Het |
Terb1 |
A |
T |
8: 105,215,123 (GRCm39) |
D284E |
possibly damaging |
Het |
Tmem266 |
C |
T |
9: 55,325,292 (GRCm39) |
A153V |
probably damaging |
Het |
Trappc2b |
T |
C |
11: 51,576,505 (GRCm39) |
Q131R |
probably benign |
Het |
Ttn |
T |
C |
2: 76,573,148 (GRCm39) |
E25915G |
possibly damaging |
Het |
Tubal3 |
A |
G |
13: 3,983,011 (GRCm39) |
T264A |
possibly damaging |
Het |
Vldlr |
G |
A |
19: 27,223,070 (GRCm39) |
R747Q |
probably benign |
Het |
Zc3h8 |
G |
T |
2: 128,771,877 (GRCm39) |
|
probably benign |
Het |
Zfp184 |
C |
T |
13: 22,143,443 (GRCm39) |
T383M |
probably damaging |
Het |
Zfp455 |
T |
C |
13: 67,346,703 (GRCm39) |
F38S |
possibly damaging |
Het |
Zfp746 |
A |
G |
6: 48,059,108 (GRCm39) |
V167A |
possibly damaging |
Het |
Zfp985 |
T |
A |
4: 147,668,567 (GRCm39) |
N478K |
probably benign |
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 |
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 |
R4592:Mroh2b
|
UTSW |
15 |
4,947,772 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|