Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700062C07Rik |
A |
G |
18: 24,608,580 (GRCm39) |
|
probably null |
Het |
Alms1 |
T |
C |
6: 85,604,986 (GRCm39) |
F2212S |
possibly damaging |
Het |
Anpep |
T |
C |
7: 79,475,098 (GRCm39) |
I155V |
possibly damaging |
Het |
Aoc1 |
G |
A |
6: 48,885,223 (GRCm39) |
V653M |
probably damaging |
Het |
Arl8b |
T |
C |
6: 108,798,518 (GRCm39) |
|
probably benign |
Het |
Bax |
A |
C |
7: 45,115,552 (GRCm39) |
|
probably null |
Het |
Cpne7 |
G |
A |
8: 123,852,382 (GRCm39) |
E195K |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,539,168 (GRCm39) |
I2330T |
possibly damaging |
Het |
Dnajc16 |
A |
G |
4: 141,501,940 (GRCm39) |
S297P |
probably benign |
Het |
Farp2 |
A |
G |
1: 93,504,155 (GRCm39) |
K311E |
probably damaging |
Het |
Fhad1 |
A |
G |
4: 141,691,906 (GRCm39) |
L410P |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,798,886 (GRCm39) |
T536A |
possibly damaging |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Hydin |
C |
T |
8: 111,245,806 (GRCm39) |
T2173I |
possibly damaging |
Het |
Kpnb1 |
A |
G |
11: 97,055,556 (GRCm39) |
V783A |
probably benign |
Het |
Krt1 |
A |
G |
15: 101,754,811 (GRCm39) |
V509A |
unknown |
Het |
Lrwd1 |
A |
T |
5: 136,164,729 (GRCm39) |
L26* |
probably null |
Het |
Mal2 |
T |
A |
15: 54,451,728 (GRCm39) |
W50R |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 126,668,871 (GRCm39) |
E819V |
probably damaging |
Het |
Mrgprx3-ps |
T |
C |
7: 46,959,959 (GRCm39) |
T11A |
probably benign |
Het |
Mylip |
G |
A |
13: 45,562,178 (GRCm39) |
E327K |
probably damaging |
Het |
Nfix |
T |
C |
8: 85,453,103 (GRCm39) |
D308G |
probably damaging |
Het |
Or1l8 |
G |
A |
2: 36,817,824 (GRCm39) |
Q101* |
probably null |
Het |
Or7e166 |
G |
A |
9: 19,624,638 (GRCm39) |
V172I |
probably benign |
Het |
Psma6 |
A |
G |
12: 55,454,254 (GRCm39) |
E26G |
probably damaging |
Het |
Rgs16 |
T |
A |
1: 153,617,804 (GRCm39) |
S105T |
probably damaging |
Het |
Slc25a23 |
T |
A |
17: 57,354,291 (GRCm39) |
N372Y |
possibly damaging |
Het |
Slc35e2 |
A |
G |
4: 155,697,187 (GRCm39) |
M234V |
probably benign |
Het |
Tbc1d8 |
A |
G |
1: 39,431,334 (GRCm39) |
V346A |
probably damaging |
Het |
Tgfb1i1 |
C |
T |
7: 127,847,654 (GRCm39) |
|
probably benign |
Het |
Triml2 |
A |
C |
8: 43,643,349 (GRCm39) |
T177P |
probably damaging |
Het |
Uba6 |
T |
C |
5: 86,267,245 (GRCm39) |
T959A |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (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 |
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 |
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 |
|