Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
C |
T |
15: 11,071,853 (GRCm38) |
A161V |
probably benign |
Het |
Bptf |
A |
T |
11: 107,054,853 (GRCm38) |
V2520E |
probably damaging |
Het |
C87436 |
T |
C |
6: 86,457,855 (GRCm38) |
F395S |
probably damaging |
Het |
Capn1 |
T |
C |
19: 5,989,984 (GRCm38) |
|
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,747,256 (GRCm38) |
Y309* |
probably null |
Het |
Clasp2 |
A |
G |
9: 113,906,127 (GRCm38) |
D1011G |
possibly damaging |
Het |
Csmd3 |
A |
G |
15: 47,849,755 (GRCm38) |
Y1608H |
probably damaging |
Het |
Dcaf1 |
T |
C |
9: 106,834,191 (GRCm38) |
I77T |
probably benign |
Het |
Dcdc2a |
T |
C |
13: 25,102,604 (GRCm38) |
L170P |
probably damaging |
Het |
Ddx28 |
A |
G |
8: 106,010,580 (GRCm38) |
F282S |
probably damaging |
Het |
Egf |
A |
G |
3: 129,686,260 (GRCm38) |
I497T |
probably benign |
Het |
Emsy |
A |
G |
7: 98,593,455 (GRCm38) |
V1159A |
probably benign |
Het |
Hk3 |
C |
A |
13: 55,007,063 (GRCm38) |
|
probably benign |
Het |
Htt |
A |
G |
5: 34,878,856 (GRCm38) |
D2049G |
probably benign |
Het |
Inpp5d |
C |
A |
1: 87,683,750 (GRCm38) |
S45* |
probably null |
Het |
Irf8 |
A |
G |
8: 120,753,380 (GRCm38) |
Y119C |
probably damaging |
Het |
Klk1b4 |
T |
C |
7: 44,211,176 (GRCm38) |
|
probably null |
Het |
Macf1 |
A |
G |
4: 123,486,720 (GRCm38) |
S1273P |
probably damaging |
Het |
Man2c1 |
A |
T |
9: 57,141,819 (GRCm38) |
H867L |
probably benign |
Het |
Mgat4e |
T |
C |
1: 134,541,449 (GRCm38) |
T286A |
probably damaging |
Het |
Necab1 |
T |
A |
4: 15,005,079 (GRCm38) |
E128D |
probably damaging |
Het |
Or10ak9 |
G |
A |
4: 118,869,131 (GRCm38) |
V117I |
probably benign |
Het |
Pds5a |
A |
G |
5: 65,615,294 (GRCm38) |
V1322A |
probably benign |
Het |
Poc1b |
C |
T |
10: 99,129,641 (GRCm38) |
T144I |
probably damaging |
Het |
Prcc |
T |
A |
3: 87,870,080 (GRCm38) |
N196Y |
probably damaging |
Het |
Psma5 |
G |
A |
3: 108,279,795 (GRCm38) |
V237M |
possibly damaging |
Het |
Rap1gds1 |
A |
G |
3: 139,050,561 (GRCm38) |
L11P |
probably damaging |
Het |
Rapgef3 |
A |
G |
15: 97,748,223 (GRCm38) |
F132S |
probably damaging |
Het |
Rgs13 |
T |
G |
1: 144,171,441 (GRCm38) |
D14A |
probably benign |
Het |
Rlig1 |
A |
C |
10: 100,573,611 (GRCm38) |
D313E |
probably damaging |
Het |
Stxbp4 |
A |
G |
11: 90,621,649 (GRCm38) |
|
probably benign |
Het |
Tcerg1 |
C |
A |
18: 42,573,309 (GRCm38) |
A1017D |
probably damaging |
Het |
Tent5c |
T |
C |
3: 100,473,174 (GRCm38) |
K89E |
probably benign |
Het |
Tmem79 |
T |
C |
3: 88,332,576 (GRCm38) |
I276V |
possibly damaging |
Het |
Tmem94 |
C |
A |
11: 115,790,009 (GRCm38) |
H113N |
probably damaging |
Het |
Vil1 |
G |
A |
1: 74,428,238 (GRCm38) |
D715N |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,582,964 (GRCm38) |
T187A |
probably benign |
Het |
Zfhx4 |
T |
A |
3: 5,413,094 (GRCm38) |
S3590T |
probably damaging |
Het |
|
Other mutations in Mug2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00708:Mug2
|
APN |
6 |
122,047,487 (GRCm38) |
missense |
possibly damaging |
0.83 |
IGL00957:Mug2
|
APN |
6 |
122,040,654 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01338:Mug2
|
APN |
6 |
122,049,628 (GRCm38) |
splice site |
probably benign |
|
IGL01477:Mug2
|
APN |
6 |
122,081,684 (GRCm38) |
splice site |
probably benign |
|
IGL01926:Mug2
|
APN |
6 |
122,036,104 (GRCm38) |
splice site |
probably benign |
|
IGL02019:Mug2
|
APN |
6 |
122,047,435 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02305:Mug2
|
APN |
6 |
122,036,056 (GRCm38) |
missense |
probably benign |
|
IGL02310:Mug2
|
APN |
6 |
122,059,123 (GRCm38) |
splice site |
probably benign |
|
IGL02484:Mug2
|
APN |
6 |
122,072,753 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02516:Mug2
|
APN |
6 |
122,070,843 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02531:Mug2
|
APN |
6 |
122,072,771 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02666:Mug2
|
APN |
6 |
122,081,326 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02936:Mug2
|
APN |
6 |
122,081,387 (GRCm38) |
critical splice donor site |
probably null |
|
R0114:Mug2
|
UTSW |
6 |
122,040,648 (GRCm38) |
missense |
probably damaging |
1.00 |
R0119:Mug2
|
UTSW |
6 |
122,036,063 (GRCm38) |
missense |
probably benign |
0.00 |
R0123:Mug2
|
UTSW |
6 |
122,074,714 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0144:Mug2
|
UTSW |
6 |
122,071,011 (GRCm38) |
splice site |
probably benign |
|
R0225:Mug2
|
UTSW |
6 |
122,074,714 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0514:Mug2
|
UTSW |
6 |
122,081,599 (GRCm38) |
missense |
probably damaging |
1.00 |
R0763:Mug2
|
UTSW |
6 |
122,075,294 (GRCm38) |
missense |
probably benign |
|
R0959:Mug2
|
UTSW |
6 |
122,085,495 (GRCm38) |
missense |
probably benign |
0.33 |
R1104:Mug2
|
UTSW |
6 |
122,059,055 (GRCm38) |
missense |
probably benign |
|
R1239:Mug2
|
UTSW |
6 |
122,081,678 (GRCm38) |
splice site |
probably benign |
|
R1318:Mug2
|
UTSW |
6 |
122,077,402 (GRCm38) |
missense |
probably damaging |
1.00 |
R1460:Mug2
|
UTSW |
6 |
122,040,533 (GRCm38) |
splice site |
probably benign |
|
R1706:Mug2
|
UTSW |
6 |
122,036,232 (GRCm38) |
splice site |
probably benign |
|
R1761:Mug2
|
UTSW |
6 |
122,074,705 (GRCm38) |
missense |
probably benign |
0.20 |
R1901:Mug2
|
UTSW |
6 |
122,071,842 (GRCm38) |
missense |
probably benign |
0.02 |
R1913:Mug2
|
UTSW |
6 |
122,070,870 (GRCm38) |
missense |
probably damaging |
1.00 |
R1943:Mug2
|
UTSW |
6 |
122,079,639 (GRCm38) |
missense |
probably benign |
|
R2054:Mug2
|
UTSW |
6 |
122,077,492 (GRCm38) |
missense |
probably damaging |
1.00 |
R2060:Mug2
|
UTSW |
6 |
122,079,612 (GRCm38) |
missense |
probably benign |
|
R2420:Mug2
|
UTSW |
6 |
122,083,460 (GRCm38) |
missense |
probably damaging |
1.00 |
R2432:Mug2
|
UTSW |
6 |
122,084,376 (GRCm38) |
missense |
possibly damaging |
0.93 |
R2916:Mug2
|
UTSW |
6 |
122,074,724 (GRCm38) |
splice site |
probably null |
|
R2918:Mug2
|
UTSW |
6 |
122,074,724 (GRCm38) |
splice site |
probably null |
|
R3423:Mug2
|
UTSW |
6 |
122,047,506 (GRCm38) |
splice site |
probably benign |
|
R3834:Mug2
|
UTSW |
6 |
122,049,787 (GRCm38) |
critical splice donor site |
probably null |
|
R3902:Mug2
|
UTSW |
6 |
122,075,567 (GRCm38) |
missense |
probably damaging |
1.00 |
R3941:Mug2
|
UTSW |
6 |
122,063,563 (GRCm38) |
missense |
probably benign |
|
R4227:Mug2
|
UTSW |
6 |
122,040,732 (GRCm38) |
missense |
probably benign |
0.10 |
R4284:Mug2
|
UTSW |
6 |
122,063,673 (GRCm38) |
missense |
probably benign |
0.00 |
R4287:Mug2
|
UTSW |
6 |
122,063,673 (GRCm38) |
missense |
probably benign |
0.00 |
R4377:Mug2
|
UTSW |
6 |
122,071,007 (GRCm38) |
critical splice donor site |
probably null |
|
R4419:Mug2
|
UTSW |
6 |
122,079,630 (GRCm38) |
missense |
probably damaging |
1.00 |
R4498:Mug2
|
UTSW |
6 |
122,082,752 (GRCm38) |
missense |
probably damaging |
0.99 |
R4566:Mug2
|
UTSW |
6 |
122,079,638 (GRCm38) |
missense |
probably benign |
0.00 |
R4690:Mug2
|
UTSW |
6 |
122,036,296 (GRCm38) |
missense |
probably benign |
|
R4732:Mug2
|
UTSW |
6 |
122,071,872 (GRCm38) |
missense |
probably damaging |
0.99 |
R4733:Mug2
|
UTSW |
6 |
122,071,872 (GRCm38) |
missense |
probably damaging |
0.99 |
R4741:Mug2
|
UTSW |
6 |
122,079,613 (GRCm38) |
missense |
probably benign |
|
R4888:Mug2
|
UTSW |
6 |
122,081,195 (GRCm38) |
missense |
probably damaging |
1.00 |
R5199:Mug2
|
UTSW |
6 |
122,040,660 (GRCm38) |
missense |
probably benign |
|
R5347:Mug2
|
UTSW |
6 |
122,081,592 (GRCm38) |
missense |
probably damaging |
1.00 |
R5457:Mug2
|
UTSW |
6 |
122,049,729 (GRCm38) |
nonsense |
probably null |
|
R5495:Mug2
|
UTSW |
6 |
122,079,650 (GRCm38) |
missense |
probably damaging |
0.96 |
R5509:Mug2
|
UTSW |
6 |
122,084,381 (GRCm38) |
missense |
possibly damaging |
0.84 |
R6006:Mug2
|
UTSW |
6 |
122,083,500 (GRCm38) |
missense |
probably null |
0.98 |
R6180:Mug2
|
UTSW |
6 |
122,079,606 (GRCm38) |
missense |
probably benign |
0.01 |
R6184:Mug2
|
UTSW |
6 |
122,037,046 (GRCm38) |
missense |
probably benign |
|
R6199:Mug2
|
UTSW |
6 |
122,047,439 (GRCm38) |
missense |
probably benign |
0.05 |
R6262:Mug2
|
UTSW |
6 |
122,075,255 (GRCm38) |
missense |
probably damaging |
1.00 |
R6416:Mug2
|
UTSW |
6 |
122,082,754 (GRCm38) |
missense |
probably damaging |
1.00 |
R6548:Mug2
|
UTSW |
6 |
122,047,442 (GRCm38) |
missense |
probably damaging |
1.00 |
R6703:Mug2
|
UTSW |
6 |
122,078,694 (GRCm38) |
missense |
probably benign |
0.25 |
R7106:Mug2
|
UTSW |
6 |
122,082,721 (GRCm38) |
missense |
probably damaging |
1.00 |
R7131:Mug2
|
UTSW |
6 |
122,075,247 (GRCm38) |
missense |
probably damaging |
1.00 |
R7372:Mug2
|
UTSW |
6 |
122,083,466 (GRCm38) |
missense |
possibly damaging |
0.88 |
R7379:Mug2
|
UTSW |
6 |
122,047,487 (GRCm38) |
missense |
possibly damaging |
0.83 |
R7419:Mug2
|
UTSW |
6 |
122,040,570 (GRCm38) |
missense |
possibly damaging |
0.86 |
R7423:Mug2
|
UTSW |
6 |
122,079,726 (GRCm38) |
missense |
probably benign |
0.00 |
R7581:Mug2
|
UTSW |
6 |
122,063,711 (GRCm38) |
missense |
probably damaging |
1.00 |
R7582:Mug2
|
UTSW |
6 |
122,079,644 (GRCm38) |
missense |
probably damaging |
0.99 |
R7672:Mug2
|
UTSW |
6 |
122,040,719 (GRCm38) |
missense |
probably benign |
0.37 |
R7713:Mug2
|
UTSW |
6 |
122,078,795 (GRCm38) |
missense |
possibly damaging |
0.83 |
R7759:Mug2
|
UTSW |
6 |
122,081,358 (GRCm38) |
missense |
probably damaging |
1.00 |
R7834:Mug2
|
UTSW |
6 |
122,036,282 (GRCm38) |
missense |
probably benign |
|
R7850:Mug2
|
UTSW |
6 |
122,075,211 (GRCm38) |
missense |
probably damaging |
1.00 |
R8029:Mug2
|
UTSW |
6 |
122,081,545 (GRCm38) |
critical splice acceptor site |
probably null |
|
R8127:Mug2
|
UTSW |
6 |
122,075,608 (GRCm38) |
missense |
probably benign |
0.01 |
R8335:Mug2
|
UTSW |
6 |
122,040,584 (GRCm38) |
missense |
probably benign |
|
R8348:Mug2
|
UTSW |
6 |
122,072,233 (GRCm38) |
nonsense |
probably null |
|
R8557:Mug2
|
UTSW |
6 |
122,063,701 (GRCm38) |
missense |
probably damaging |
0.99 |
R8798:Mug2
|
UTSW |
6 |
122,081,610 (GRCm38) |
missense |
probably damaging |
1.00 |
R8823:Mug2
|
UTSW |
6 |
122,063,689 (GRCm38) |
missense |
possibly damaging |
0.89 |
R9029:Mug2
|
UTSW |
6 |
122,084,369 (GRCm38) |
missense |
probably damaging |
1.00 |
R9153:Mug2
|
UTSW |
6 |
122,040,668 (GRCm38) |
missense |
possibly damaging |
0.71 |
R9185:Mug2
|
UTSW |
6 |
122,077,483 (GRCm38) |
missense |
probably benign |
0.06 |
R9186:Mug2
|
UTSW |
6 |
122,075,289 (GRCm38) |
missense |
probably damaging |
0.99 |
R9418:Mug2
|
UTSW |
6 |
122,040,741 (GRCm38) |
missense |
probably benign |
0.00 |
R9464:Mug2
|
UTSW |
6 |
122,051,731 (GRCm38) |
missense |
probably benign |
0.01 |
R9622:Mug2
|
UTSW |
6 |
122,051,792 (GRCm38) |
missense |
probably benign |
0.29 |
Z1177:Mug2
|
UTSW |
6 |
122,037,121 (GRCm38) |
missense |
probably damaging |
1.00 |
|