Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110004E09Rik |
A |
C |
16: 90,926,062 (GRCm38) |
D261E |
probably benign |
Het |
1810041L15Rik |
A |
G |
15: 84,420,129 (GRCm38) |
|
probably benign |
Het |
4930404N11Rik |
A |
G |
10: 81,364,736 (GRCm38) |
|
probably benign |
Het |
A3galt2 |
T |
C |
4: 128,761,509 (GRCm38) |
|
probably benign |
Het |
Alk |
C |
T |
17: 71,869,536 (GRCm38) |
G1591D |
probably damaging |
Het |
Angptl2 |
T |
C |
2: 33,228,315 (GRCm38) |
S34P |
probably benign |
Het |
Atp2a2 |
A |
G |
5: 122,489,291 (GRCm38) |
V137A |
probably benign |
Het |
Atp8b5 |
A |
G |
4: 43,366,770 (GRCm38) |
M845V |
probably damaging |
Het |
Camk1d |
A |
G |
2: 5,565,760 (GRCm38) |
V30A |
possibly damaging |
Het |
Ceacam19 |
G |
A |
7: 19,882,610 (GRCm38) |
T193I |
probably benign |
Het |
Chst15 |
T |
A |
7: 132,266,746 (GRCm38) |
D315V |
probably damaging |
Het |
Cux1 |
G |
T |
5: 136,308,003 (GRCm38) |
P885Q |
probably damaging |
Het |
Cyth1 |
C |
T |
11: 118,185,481 (GRCm38) |
E88K |
possibly damaging |
Het |
Dido1 |
A |
G |
2: 180,683,958 (GRCm38) |
V479A |
probably benign |
Het |
Dlc1 |
G |
T |
8: 36,570,275 (GRCm38) |
|
probably benign |
Het |
H2-Ab1 |
G |
A |
17: 34,264,911 (GRCm38) |
R82Q |
probably damaging |
Het |
Hps6 |
T |
A |
19: 46,006,041 (GRCm38) |
*806K |
probably null |
Het |
Ilf3 |
T |
C |
9: 21,398,044 (GRCm38) |
S486P |
probably benign |
Het |
Kdm1b |
C |
A |
13: 47,080,467 (GRCm38) |
T759K |
probably damaging |
Het |
Kirrel |
C |
A |
3: 87,088,485 (GRCm38) |
V381F |
probably damaging |
Het |
Kmt2b |
A |
T |
7: 30,577,144 (GRCm38) |
V1701E |
probably damaging |
Het |
Lrmda |
T |
C |
14: 22,828,737 (GRCm38) |
Y100H |
probably damaging |
Het |
Mastl |
T |
C |
2: 23,145,409 (GRCm38) |
I169V |
probably damaging |
Het |
Nek3 |
A |
T |
8: 22,160,368 (GRCm38) |
|
probably null |
Het |
Nipal3 |
G |
T |
4: 135,468,550 (GRCm38) |
Y247* |
probably null |
Het |
Nt5e |
A |
C |
9: 88,355,705 (GRCm38) |
K229N |
probably damaging |
Het |
Olfr237-ps1 |
A |
G |
6: 43,153,577 (GRCm38) |
I91V |
possibly damaging |
Het |
Olfr974 |
G |
T |
9: 39,942,958 (GRCm38) |
G233C |
probably damaging |
Het |
Opa1 |
A |
G |
16: 29,610,887 (GRCm38) |
M290V |
probably null |
Het |
Parp2 |
T |
A |
14: 50,815,415 (GRCm38) |
I155K |
probably benign |
Het |
Pde4dip |
G |
T |
3: 97,767,087 (GRCm38) |
A171E |
probably damaging |
Het |
Prom2 |
C |
T |
2: 127,531,116 (GRCm38) |
E678K |
probably benign |
Het |
Rab12 |
A |
G |
17: 66,498,116 (GRCm38) |
|
probably benign |
Het |
Rgs8 |
A |
T |
1: 153,670,799 (GRCm38) |
T13S |
probably damaging |
Het |
Setd3 |
A |
G |
12: 108,112,124 (GRCm38) |
|
probably benign |
Het |
Slx4ip |
G |
A |
2: 137,004,973 (GRCm38) |
V53I |
probably damaging |
Het |
Stil |
A |
G |
4: 115,024,098 (GRCm38) |
D613G |
probably benign |
Het |
Tjp3 |
T |
A |
10: 81,273,689 (GRCm38) |
S858C |
probably damaging |
Het |
Tmem215 |
A |
G |
4: 40,474,632 (GRCm38) |
*236W |
probably null |
Het |
Ttbk1 |
A |
G |
17: 46,470,660 (GRCm38) |
V389A |
probably benign |
Het |
Wdfy4 |
A |
G |
14: 32,971,750 (GRCm38) |
F2706S |
possibly damaging |
Het |
Xpo4 |
C |
A |
14: 57,629,420 (GRCm38) |
V222L |
possibly damaging |
Het |
Zfc3h1 |
A |
G |
10: 115,400,904 (GRCm38) |
S428G |
probably benign |
Het |
Zfp286 |
T |
C |
11: 62,787,960 (GRCm38) |
Q47R |
probably damaging |
Het |
Zfp318 |
A |
G |
17: 46,398,754 (GRCm38) |
K468E |
probably damaging |
Het |
|
Other mutations in Mroh2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Mroh2b
|
APN |
15 |
4,899,197 (GRCm38) |
missense |
probably benign |
|
IGL00507:Mroh2b
|
APN |
15 |
4,962,127 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00548:Mroh2b
|
APN |
15 |
4,931,316 (GRCm38) |
missense |
probably benign |
0.35 |
IGL00902:Mroh2b
|
APN |
15 |
4,915,222 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00944:Mroh2b
|
APN |
15 |
4,951,127 (GRCm38) |
splice site |
probably benign |
|
IGL00954:Mroh2b
|
APN |
15 |
4,903,054 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01015:Mroh2b
|
APN |
15 |
4,941,542 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01134:Mroh2b
|
APN |
15 |
4,915,152 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01337:Mroh2b
|
APN |
15 |
4,905,024 (GRCm38) |
missense |
probably benign |
0.38 |
IGL01780:Mroh2b
|
APN |
15 |
4,912,000 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01919:Mroh2b
|
APN |
15 |
4,923,688 (GRCm38) |
missense |
probably benign |
0.10 |
IGL02069:Mroh2b
|
APN |
15 |
4,904,324 (GRCm38) |
splice site |
probably benign |
|
IGL02146:Mroh2b
|
APN |
15 |
4,951,294 (GRCm38) |
splice site |
probably null |
|
IGL02221:Mroh2b
|
APN |
15 |
4,923,641 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02281:Mroh2b
|
APN |
15 |
4,952,263 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02350:Mroh2b
|
APN |
15 |
4,912,000 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02357:Mroh2b
|
APN |
15 |
4,912,000 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02401:Mroh2b
|
APN |
15 |
4,900,501 (GRCm38) |
missense |
possibly damaging |
0.71 |
IGL02427:Mroh2b
|
APN |
15 |
4,951,560 (GRCm38) |
splice site |
probably benign |
|
IGL02432:Mroh2b
|
APN |
15 |
4,914,186 (GRCm38) |
missense |
probably benign |
|
IGL02582:Mroh2b
|
APN |
15 |
4,908,515 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02632:Mroh2b
|
APN |
15 |
4,931,101 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02741:Mroh2b
|
APN |
15 |
4,905,632 (GRCm38) |
missense |
probably benign |
|
IGL02811:Mroh2b
|
APN |
15 |
4,915,236 (GRCm38) |
missense |
possibly damaging |
0.55 |
IGL03412:Mroh2b
|
APN |
15 |
4,944,372 (GRCm38) |
missense |
probably benign |
0.14 |
PIT4468001:Mroh2b
|
UTSW |
15 |
4,912,812 (GRCm38) |
missense |
probably damaging |
1.00 |
R0024:Mroh2b
|
UTSW |
15 |
4,925,627 (GRCm38) |
missense |
probably damaging |
1.00 |
R0333:Mroh2b
|
UTSW |
15 |
4,931,118 (GRCm38) |
missense |
probably damaging |
1.00 |
R0433:Mroh2b
|
UTSW |
15 |
4,941,634 (GRCm38) |
missense |
probably benign |
0.01 |
R0530:Mroh2b
|
UTSW |
15 |
4,934,395 (GRCm38) |
missense |
probably damaging |
0.97 |
R1411:Mroh2b
|
UTSW |
15 |
4,918,317 (GRCm38) |
missense |
probably damaging |
1.00 |
R1457:Mroh2b
|
UTSW |
15 |
4,925,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R1466:Mroh2b
|
UTSW |
15 |
4,925,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R1466:Mroh2b
|
UTSW |
15 |
4,925,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R1472:Mroh2b
|
UTSW |
15 |
4,948,655 (GRCm38) |
missense |
probably benign |
0.00 |
R1525:Mroh2b
|
UTSW |
15 |
4,951,130 (GRCm38) |
splice site |
probably null |
|
R1584:Mroh2b
|
UTSW |
15 |
4,925,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R1605:Mroh2b
|
UTSW |
15 |
4,945,090 (GRCm38) |
missense |
probably benign |
0.08 |
R1657:Mroh2b
|
UTSW |
15 |
4,931,043 (GRCm38) |
nonsense |
probably null |
|
R1671:Mroh2b
|
UTSW |
15 |
4,951,294 (GRCm38) |
splice site |
probably null |
|
R1698:Mroh2b
|
UTSW |
15 |
4,914,140 (GRCm38) |
missense |
probably benign |
0.02 |
R2002:Mroh2b
|
UTSW |
15 |
4,925,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R2005:Mroh2b
|
UTSW |
15 |
4,917,158 (GRCm38) |
missense |
probably damaging |
1.00 |
R2077:Mroh2b
|
UTSW |
15 |
4,944,966 (GRCm38) |
missense |
probably damaging |
1.00 |
R2179:Mroh2b
|
UTSW |
15 |
4,921,446 (GRCm38) |
critical splice donor site |
probably null |
|
R2183:Mroh2b
|
UTSW |
15 |
4,918,225 (GRCm38) |
splice site |
probably null |
|
R3713:Mroh2b
|
UTSW |
15 |
4,943,649 (GRCm38) |
missense |
probably benign |
0.01 |
R3714:Mroh2b
|
UTSW |
15 |
4,943,649 (GRCm38) |
missense |
probably benign |
0.01 |
R3747:Mroh2b
|
UTSW |
15 |
4,952,246 (GRCm38) |
nonsense |
probably null |
|
R3748:Mroh2b
|
UTSW |
15 |
4,952,246 (GRCm38) |
nonsense |
probably null |
|
R3749:Mroh2b
|
UTSW |
15 |
4,952,246 (GRCm38) |
nonsense |
probably null |
|
R3750:Mroh2b
|
UTSW |
15 |
4,952,246 (GRCm38) |
nonsense |
probably null |
|
R3792:Mroh2b
|
UTSW |
15 |
4,923,620 (GRCm38) |
missense |
probably damaging |
1.00 |
R3872:Mroh2b
|
UTSW |
15 |
4,925,061 (GRCm38) |
nonsense |
probably null |
|
R4021:Mroh2b
|
UTSW |
15 |
4,925,100 (GRCm38) |
missense |
possibly damaging |
0.75 |
R4329:Mroh2b
|
UTSW |
15 |
4,931,379 (GRCm38) |
missense |
probably damaging |
0.99 |
R4456:Mroh2b
|
UTSW |
15 |
4,947,925 (GRCm38) |
missense |
probably benign |
0.21 |
R4592:Mroh2b
|
UTSW |
15 |
4,918,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R4836:Mroh2b
|
UTSW |
15 |
4,904,270 (GRCm38) |
missense |
probably damaging |
1.00 |
R5050:Mroh2b
|
UTSW |
15 |
4,900,450 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5230:Mroh2b
|
UTSW |
15 |
4,941,522 (GRCm38) |
missense |
probably benign |
0.07 |
R5342:Mroh2b
|
UTSW |
15 |
4,914,133 (GRCm38) |
nonsense |
probably null |
|
R5353:Mroh2b
|
UTSW |
15 |
4,917,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R5368:Mroh2b
|
UTSW |
15 |
4,905,572 (GRCm38) |
missense |
probably damaging |
1.00 |
R5424:Mroh2b
|
UTSW |
15 |
4,941,612 (GRCm38) |
missense |
probably damaging |
0.98 |
R5484:Mroh2b
|
UTSW |
15 |
4,908,981 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5999:Mroh2b
|
UTSW |
15 |
4,912,884 (GRCm38) |
splice site |
probably null |
|
R6046:Mroh2b
|
UTSW |
15 |
4,951,281 (GRCm38) |
missense |
probably benign |
0.01 |
R6081:Mroh2b
|
UTSW |
15 |
4,944,377 (GRCm38) |
missense |
probably damaging |
1.00 |
R6162:Mroh2b
|
UTSW |
15 |
4,915,225 (GRCm38) |
missense |
probably damaging |
1.00 |
R6165:Mroh2b
|
UTSW |
15 |
4,918,350 (GRCm38) |
missense |
probably benign |
0.23 |
R6240:Mroh2b
|
UTSW |
15 |
4,934,644 (GRCm38) |
missense |
probably benign |
0.38 |
R6487:Mroh2b
|
UTSW |
15 |
4,947,239 (GRCm38) |
missense |
probably damaging |
1.00 |
R6539:Mroh2b
|
UTSW |
15 |
4,905,574 (GRCm38) |
missense |
probably damaging |
1.00 |
R6616:Mroh2b
|
UTSW |
15 |
4,953,282 (GRCm38) |
missense |
probably benign |
0.36 |
R6663:Mroh2b
|
UTSW |
15 |
4,947,935 (GRCm38) |
missense |
probably benign |
0.21 |
R6820:Mroh2b
|
UTSW |
15 |
4,953,274 (GRCm38) |
missense |
probably damaging |
1.00 |
R6900:Mroh2b
|
UTSW |
15 |
4,908,987 (GRCm38) |
missense |
probably benign |
0.00 |
R6990:Mroh2b
|
UTSW |
15 |
4,912,802 (GRCm38) |
missense |
possibly damaging |
0.55 |
R7067:Mroh2b
|
UTSW |
15 |
4,900,504 (GRCm38) |
missense |
probably benign |
0.35 |
R7092:Mroh2b
|
UTSW |
15 |
4,934,678 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7102:Mroh2b
|
UTSW |
15 |
4,948,003 (GRCm38) |
missense |
probably benign |
0.06 |
R7264:Mroh2b
|
UTSW |
15 |
4,921,362 (GRCm38) |
missense |
possibly damaging |
0.81 |
R7436:Mroh2b
|
UTSW |
15 |
4,941,554 (GRCm38) |
missense |
probably benign |
0.21 |
R7462:Mroh2b
|
UTSW |
15 |
4,908,627 (GRCm38) |
missense |
probably damaging |
1.00 |
R7529:Mroh2b
|
UTSW |
15 |
4,949,009 (GRCm38) |
missense |
probably damaging |
1.00 |
R7575:Mroh2b
|
UTSW |
15 |
4,934,605 (GRCm38) |
missense |
probably damaging |
1.00 |
R7579:Mroh2b
|
UTSW |
15 |
4,931,061 (GRCm38) |
missense |
probably benign |
0.09 |
R7605:Mroh2b
|
UTSW |
15 |
4,945,023 (GRCm38) |
missense |
probably damaging |
1.00 |
R7624:Mroh2b
|
UTSW |
15 |
4,917,131 (GRCm38) |
missense |
probably damaging |
1.00 |
R7797:Mroh2b
|
UTSW |
15 |
4,949,105 (GRCm38) |
missense |
probably benign |
0.36 |
R7848:Mroh2b
|
UTSW |
15 |
4,938,379 (GRCm38) |
nonsense |
probably null |
|
R7952:Mroh2b
|
UTSW |
15 |
4,951,211 (GRCm38) |
missense |
probably damaging |
1.00 |
R7995:Mroh2b
|
UTSW |
15 |
4,921,357 (GRCm38) |
nonsense |
probably null |
|
R8088:Mroh2b
|
UTSW |
15 |
4,900,503 (GRCm38) |
missense |
possibly damaging |
0.57 |
R8207:Mroh2b
|
UTSW |
15 |
4,938,410 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8242:Mroh2b
|
UTSW |
15 |
4,909,040 (GRCm38) |
missense |
probably benign |
0.04 |
R8248:Mroh2b
|
UTSW |
15 |
4,931,104 (GRCm38) |
missense |
probably benign |
0.40 |
R8258:Mroh2b
|
UTSW |
15 |
4,911,909 (GRCm38) |
missense |
probably benign |
0.01 |
R8259:Mroh2b
|
UTSW |
15 |
4,911,909 (GRCm38) |
missense |
probably benign |
0.01 |
R8304:Mroh2b
|
UTSW |
15 |
4,925,637 (GRCm38) |
missense |
probably damaging |
0.99 |
R8316:Mroh2b
|
UTSW |
15 |
4,951,264 (GRCm38) |
nonsense |
probably null |
|
R8345:Mroh2b
|
UTSW |
15 |
4,944,326 (GRCm38) |
missense |
probably benign |
0.09 |
R8507:Mroh2b
|
UTSW |
15 |
4,949,090 (GRCm38) |
missense |
probably damaging |
1.00 |
R8728:Mroh2b
|
UTSW |
15 |
4,905,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R8747:Mroh2b
|
UTSW |
15 |
4,935,300 (GRCm38) |
missense |
probably damaging |
0.99 |
R8798:Mroh2b
|
UTSW |
15 |
4,948,709 (GRCm38) |
missense |
probably damaging |
1.00 |
R8814:Mroh2b
|
UTSW |
15 |
4,941,625 (GRCm38) |
missense |
possibly damaging |
0.61 |
R8856:Mroh2b
|
UTSW |
15 |
4,931,028 (GRCm38) |
nonsense |
probably null |
|
R8910:Mroh2b
|
UTSW |
15 |
4,931,373 (GRCm38) |
missense |
probably benign |
0.01 |
R8913:Mroh2b
|
UTSW |
15 |
4,917,528 (GRCm38) |
intron |
probably benign |
|
R8941:Mroh2b
|
UTSW |
15 |
4,962,124 (GRCm38) |
missense |
possibly damaging |
0.86 |
R9014:Mroh2b
|
UTSW |
15 |
4,899,188 (GRCm38) |
start codon destroyed |
probably null |
0.95 |
R9086:Mroh2b
|
UTSW |
15 |
4,953,272 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9101:Mroh2b
|
UTSW |
15 |
4,900,453 (GRCm38) |
missense |
probably benign |
0.20 |
R9118:Mroh2b
|
UTSW |
15 |
4,962,091 (GRCm38) |
missense |
possibly damaging |
0.86 |
R9393:Mroh2b
|
UTSW |
15 |
4,951,184 (GRCm38) |
missense |
probably benign |
|
R9429:Mroh2b
|
UTSW |
15 |
4,934,425 (GRCm38) |
missense |
probably damaging |
1.00 |
R9431:Mroh2b
|
UTSW |
15 |
4,934,470 (GRCm38) |
missense |
probably damaging |
1.00 |
R9443:Mroh2b
|
UTSW |
15 |
4,944,339 (GRCm38) |
missense |
probably damaging |
1.00 |
R9447:Mroh2b
|
UTSW |
15 |
4,931,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R9497:Mroh2b
|
UTSW |
15 |
4,921,363 (GRCm38) |
missense |
probably damaging |
0.98 |
R9588:Mroh2b
|
UTSW |
15 |
4,948,648 (GRCm38) |
missense |
probably benign |
0.00 |
R9631:Mroh2b
|
UTSW |
15 |
4,917,074 (GRCm38) |
missense |
probably damaging |
0.97 |
R9686:Mroh2b
|
UTSW |
15 |
4,945,123 (GRCm38) |
missense |
probably benign |
0.34 |
R9774:Mroh2b
|
UTSW |
15 |
4,914,131 (GRCm38) |
missense |
probably benign |
0.08 |
X0067:Mroh2b
|
UTSW |
15 |
4,951,591 (GRCm38) |
missense |
possibly damaging |
0.90 |
Z1177:Mroh2b
|
UTSW |
15 |
4,905,005 (GRCm38) |
missense |
probably damaging |
1.00 |
|