Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acoxl |
T |
A |
2: 127,720,701 (GRCm39) |
I188N |
probably damaging |
Het |
Akr1c14 |
T |
C |
13: 4,131,106 (GRCm39) |
V266A |
probably damaging |
Het |
Als2cl |
C |
A |
9: 110,717,810 (GRCm39) |
P301H |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Catspere2 |
C |
T |
1: 177,843,477 (GRCm39) |
|
probably benign |
Het |
Cpsf1 |
A |
T |
15: 76,487,937 (GRCm39) |
N53K |
possibly damaging |
Het |
Ctsll3 |
C |
T |
13: 60,948,749 (GRCm39) |
G69R |
possibly damaging |
Het |
F2 |
C |
T |
2: 91,458,693 (GRCm39) |
R539Q |
probably damaging |
Het |
Fam78b |
G |
A |
1: 166,906,219 (GRCm39) |
G126D |
probably damaging |
Het |
Fancd2 |
A |
G |
6: 113,568,120 (GRCm39) |
I1332V |
possibly damaging |
Het |
Flg2 |
C |
T |
3: 93,109,244 (GRCm39) |
S424L |
probably damaging |
Het |
Fpr1 |
T |
C |
17: 18,097,471 (GRCm39) |
T173A |
possibly damaging |
Het |
Gas2l3 |
A |
G |
10: 89,249,960 (GRCm39) |
V386A |
probably benign |
Het |
Gdap2 |
A |
C |
3: 100,095,199 (GRCm39) |
E269A |
probably benign |
Het |
Igf2bp2 |
T |
A |
16: 21,898,358 (GRCm39) |
|
probably null |
Het |
Ipo11 |
T |
C |
13: 107,016,118 (GRCm39) |
|
probably null |
Het |
Itpr2 |
G |
T |
6: 146,013,176 (GRCm39) |
P2667Q |
probably benign |
Het |
Itsn2 |
G |
T |
12: 4,683,044 (GRCm39) |
|
probably benign |
Het |
Jakmip2 |
A |
G |
18: 43,698,995 (GRCm39) |
L488P |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,265,858 (GRCm39) |
C248S |
probably damaging |
Het |
Lrrc17 |
A |
T |
5: 21,780,046 (GRCm39) |
D340V |
probably damaging |
Het |
Megf9 |
T |
C |
4: 70,351,679 (GRCm39) |
T481A |
probably damaging |
Het |
Mrc1 |
T |
C |
2: 14,249,015 (GRCm39) |
S184P |
possibly damaging |
Het |
Msh4 |
A |
T |
3: 153,573,472 (GRCm39) |
Y533* |
probably null |
Het |
Nectin2 |
G |
T |
7: 19,464,539 (GRCm39) |
S288R |
probably damaging |
Het |
Neurog2 |
A |
T |
3: 127,427,754 (GRCm39) |
H126L |
probably damaging |
Het |
Nol10 |
A |
T |
12: 17,423,585 (GRCm39) |
E310V |
probably damaging |
Het |
Or1f12 |
T |
G |
13: 21,721,422 (GRCm39) |
K251T |
probably damaging |
Het |
Or4c29 |
A |
G |
2: 88,740,522 (GRCm39) |
S72P |
probably damaging |
Het |
Or51h7 |
A |
T |
7: 102,591,678 (GRCm39) |
F35L |
probably benign |
Het |
Or5h23 |
T |
A |
16: 58,905,949 (GRCm39) |
K299I |
probably benign |
Het |
Pappa |
A |
C |
4: 65,074,682 (GRCm39) |
D412A |
probably damaging |
Het |
Pcdhb7 |
T |
A |
18: 37,476,335 (GRCm39) |
F490L |
probably benign |
Het |
Pcsk1 |
T |
A |
13: 75,260,653 (GRCm39) |
|
probably benign |
Het |
Plekhn1 |
T |
A |
4: 156,306,339 (GRCm39) |
D577V |
probably damaging |
Het |
Prrc2c |
C |
A |
1: 162,537,903 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Pzp |
G |
A |
6: 128,465,010 (GRCm39) |
T1288M |
probably damaging |
Het |
Radil |
A |
C |
5: 142,492,718 (GRCm39) |
H63Q |
probably benign |
Het |
Rai1 |
T |
C |
11: 60,078,422 (GRCm39) |
S829P |
probably benign |
Het |
Rd3 |
A |
G |
1: 191,715,488 (GRCm39) |
I88V |
probably damaging |
Het |
Rfesd |
T |
C |
13: 76,156,244 (GRCm39) |
D54G |
probably damaging |
Het |
Rnf213 |
A |
C |
11: 119,305,896 (GRCm39) |
K568T |
probably damaging |
Het |
Scaper |
T |
A |
9: 55,650,923 (GRCm39) |
K913N |
probably damaging |
Het |
Serpina3c |
T |
C |
12: 104,115,628 (GRCm39) |
|
probably null |
Het |
Serpinb6d |
A |
T |
13: 33,850,357 (GRCm39) |
K61N |
probably benign |
Het |
Skint4 |
A |
T |
4: 111,944,183 (GRCm39) |
|
probably null |
Het |
Sod1 |
T |
C |
16: 90,017,801 (GRCm39) |
I19T |
possibly damaging |
Het |
Stfa3 |
C |
A |
16: 36,271,042 (GRCm39) |
G81* |
probably null |
Het |
Ubr4 |
A |
G |
4: 139,137,960 (GRCm39) |
T1106A |
probably benign |
Het |
Uggt2 |
T |
A |
14: 119,256,917 (GRCm39) |
N1106Y |
probably damaging |
Het |
Vmn1r217 |
G |
A |
13: 23,298,714 (GRCm39) |
Q63* |
probably null |
Het |
Vmn2r129 |
A |
T |
4: 156,690,673 (GRCm39) |
|
noncoding transcript |
Het |
Vps13b |
C |
A |
15: 35,792,334 (GRCm39) |
P2201T |
probably damaging |
Het |
Vps13b |
C |
A |
15: 35,792,335 (GRCm39) |
P2201Q |
probably damaging |
Het |
Vps13d |
G |
T |
4: 144,813,893 (GRCm39) |
|
probably benign |
Het |
Zer1 |
A |
G |
2: 29,994,887 (GRCm39) |
C503R |
probably damaging |
Het |
Zfp369 |
T |
C |
13: 65,444,762 (GRCm39) |
V635A |
probably benign |
Het |
Zfp608 |
A |
T |
18: 55,031,125 (GRCm39) |
Y938* |
probably null |
Het |
|
Other mutations in Mug1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Mug1
|
APN |
6 |
121,842,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00485:Mug1
|
APN |
6 |
121,864,375 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00816:Mug1
|
APN |
6 |
121,859,597 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01140:Mug1
|
APN |
6 |
121,859,693 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01141:Mug1
|
APN |
6 |
121,847,458 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01384:Mug1
|
APN |
6 |
121,826,433 (GRCm39) |
splice site |
probably benign |
|
IGL01659:Mug1
|
APN |
6 |
121,847,619 (GRCm39) |
splice site |
probably benign |
|
IGL02049:Mug1
|
APN |
6 |
121,848,295 (GRCm39) |
missense |
probably benign |
|
IGL02151:Mug1
|
APN |
6 |
121,861,649 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02315:Mug1
|
APN |
6 |
121,817,126 (GRCm39) |
missense |
probably benign |
|
IGL02629:Mug1
|
APN |
6 |
121,817,024 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02642:Mug1
|
APN |
6 |
121,859,544 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02807:Mug1
|
APN |
6 |
121,863,531 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02932:Mug1
|
APN |
6 |
121,864,386 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03232:Mug1
|
APN |
6 |
121,855,494 (GRCm39) |
missense |
probably benign |
0.00 |
R1462_Mug1_304
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R2341_Mug1_749
|
UTSW |
6 |
121,861,588 (GRCm39) |
missense |
probably benign |
0.06 |
R4261_Mug1_652
|
UTSW |
6 |
121,850,693 (GRCm39) |
missense |
probably benign |
|
R6173_mug1_139
|
UTSW |
6 |
121,840,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03050:Mug1
|
UTSW |
6 |
121,857,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0101:Mug1
|
UTSW |
6 |
121,861,206 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0194:Mug1
|
UTSW |
6 |
121,817,066 (GRCm39) |
missense |
probably damaging |
0.98 |
R0196:Mug1
|
UTSW |
6 |
121,815,684 (GRCm39) |
critical splice donor site |
probably null |
|
R0325:Mug1
|
UTSW |
6 |
121,826,801 (GRCm39) |
missense |
probably benign |
|
R0332:Mug1
|
UTSW |
6 |
121,826,856 (GRCm39) |
splice site |
probably null |
|
R0377:Mug1
|
UTSW |
6 |
121,834,320 (GRCm39) |
missense |
probably benign |
0.02 |
R0393:Mug1
|
UTSW |
6 |
121,826,809 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0414:Mug1
|
UTSW |
6 |
121,833,513 (GRCm39) |
missense |
probably benign |
0.00 |
R0457:Mug1
|
UTSW |
6 |
121,838,514 (GRCm39) |
missense |
probably benign |
0.06 |
R0479:Mug1
|
UTSW |
6 |
121,817,186 (GRCm39) |
missense |
probably benign |
|
R0519:Mug1
|
UTSW |
6 |
121,828,383 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0535:Mug1
|
UTSW |
6 |
121,828,413 (GRCm39) |
missense |
probably benign |
|
R0745:Mug1
|
UTSW |
6 |
121,864,386 (GRCm39) |
missense |
probably benign |
0.35 |
R0939:Mug1
|
UTSW |
6 |
121,861,308 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0975:Mug1
|
UTSW |
6 |
121,855,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R1033:Mug1
|
UTSW |
6 |
121,857,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R1086:Mug1
|
UTSW |
6 |
121,862,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Mug1
|
UTSW |
6 |
121,847,604 (GRCm39) |
missense |
probably benign |
|
R1131:Mug1
|
UTSW |
6 |
121,838,144 (GRCm39) |
missense |
probably benign |
0.18 |
R1249:Mug1
|
UTSW |
6 |
121,826,420 (GRCm39) |
missense |
probably benign |
0.07 |
R1364:Mug1
|
UTSW |
6 |
121,858,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Mug1
|
UTSW |
6 |
121,815,635 (GRCm39) |
missense |
probably benign |
0.00 |
R1462:Mug1
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R1462:Mug1
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R1494:Mug1
|
UTSW |
6 |
121,856,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1639:Mug1
|
UTSW |
6 |
121,857,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Mug1
|
UTSW |
6 |
121,858,780 (GRCm39) |
missense |
probably benign |
|
R1902:Mug1
|
UTSW |
6 |
121,858,780 (GRCm39) |
missense |
probably benign |
|
R2087:Mug1
|
UTSW |
6 |
121,833,250 (GRCm39) |
missense |
probably benign |
0.00 |
R2249:Mug1
|
UTSW |
6 |
121,847,469 (GRCm39) |
missense |
probably benign |
|
R2341:Mug1
|
UTSW |
6 |
121,861,588 (GRCm39) |
missense |
probably benign |
0.06 |
R2888:Mug1
|
UTSW |
6 |
121,858,802 (GRCm39) |
missense |
probably benign |
0.44 |
R2892:Mug1
|
UTSW |
6 |
121,817,029 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3703:Mug1
|
UTSW |
6 |
121,865,515 (GRCm39) |
splice site |
probably benign |
|
R3789:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R3790:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R3950:Mug1
|
UTSW |
6 |
121,855,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:Mug1
|
UTSW |
6 |
121,850,693 (GRCm39) |
missense |
probably benign |
|
R4402:Mug1
|
UTSW |
6 |
121,856,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R4589:Mug1
|
UTSW |
6 |
121,834,310 (GRCm39) |
missense |
probably benign |
0.19 |
R4707:Mug1
|
UTSW |
6 |
121,861,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Mug1
|
UTSW |
6 |
121,861,213 (GRCm39) |
missense |
probably benign |
0.01 |
R4840:Mug1
|
UTSW |
6 |
121,862,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Mug1
|
UTSW |
6 |
121,815,576 (GRCm39) |
utr 5 prime |
probably benign |
|
R4999:Mug1
|
UTSW |
6 |
121,855,902 (GRCm39) |
nonsense |
probably null |
|
R5198:Mug1
|
UTSW |
6 |
121,851,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5220:Mug1
|
UTSW |
6 |
121,838,092 (GRCm39) |
missense |
probably benign |
0.03 |
R5253:Mug1
|
UTSW |
6 |
121,865,872 (GRCm39) |
missense |
probably benign |
0.03 |
R5273:Mug1
|
UTSW |
6 |
121,850,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R5285:Mug1
|
UTSW |
6 |
121,818,066 (GRCm39) |
missense |
probably benign |
0.45 |
R5387:Mug1
|
UTSW |
6 |
121,861,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R5560:Mug1
|
UTSW |
6 |
121,838,032 (GRCm39) |
missense |
probably damaging |
0.96 |
R5652:Mug1
|
UTSW |
6 |
121,817,140 (GRCm39) |
missense |
probably benign |
|
R5704:Mug1
|
UTSW |
6 |
121,828,392 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5732:Mug1
|
UTSW |
6 |
121,855,452 (GRCm39) |
missense |
probably benign |
0.00 |
R6053:Mug1
|
UTSW |
6 |
121,842,697 (GRCm39) |
missense |
probably benign |
0.00 |
R6173:Mug1
|
UTSW |
6 |
121,840,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R6578:Mug1
|
UTSW |
6 |
121,864,411 (GRCm39) |
missense |
probably benign |
0.00 |
R6647:Mug1
|
UTSW |
6 |
121,817,200 (GRCm39) |
missense |
probably benign |
0.02 |
R6681:Mug1
|
UTSW |
6 |
121,815,683 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6925:Mug1
|
UTSW |
6 |
121,858,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Mug1
|
UTSW |
6 |
121,838,084 (GRCm39) |
missense |
probably benign |
0.22 |
R7031:Mug1
|
UTSW |
6 |
121,815,673 (GRCm39) |
missense |
probably benign |
0.00 |
R7034:Mug1
|
UTSW |
6 |
121,850,603 (GRCm39) |
missense |
probably benign |
0.00 |
R7156:Mug1
|
UTSW |
6 |
121,861,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7156:Mug1
|
UTSW |
6 |
121,857,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Mug1
|
UTSW |
6 |
121,834,379 (GRCm39) |
missense |
probably benign |
0.00 |
R7211:Mug1
|
UTSW |
6 |
121,857,498 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7318:Mug1
|
UTSW |
6 |
121,847,611 (GRCm39) |
critical splice donor site |
probably null |
|
R7462:Mug1
|
UTSW |
6 |
121,852,399 (GRCm39) |
missense |
probably benign |
0.00 |
R7479:Mug1
|
UTSW |
6 |
121,855,467 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7588:Mug1
|
UTSW |
6 |
121,852,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R7611:Mug1
|
UTSW |
6 |
121,852,387 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7659:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7660:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7661:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7663:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7664:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7666:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7788:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7789:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7794:Mug1
|
UTSW |
6 |
121,833,247 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7809:Mug1
|
UTSW |
6 |
121,855,944 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7836:Mug1
|
UTSW |
6 |
121,847,611 (GRCm39) |
critical splice donor site |
probably null |
|
R7867:Mug1
|
UTSW |
6 |
121,850,593 (GRCm39) |
missense |
probably benign |
|
R7904:Mug1
|
UTSW |
6 |
121,828,424 (GRCm39) |
missense |
probably benign |
|
R7937:Mug1
|
UTSW |
6 |
121,838,128 (GRCm39) |
missense |
probably benign |
0.00 |
R7981:Mug1
|
UTSW |
6 |
121,858,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Mug1
|
UTSW |
6 |
121,857,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8070:Mug1
|
UTSW |
6 |
121,852,838 (GRCm39) |
missense |
probably benign |
0.26 |
R8071:Mug1
|
UTSW |
6 |
121,850,631 (GRCm39) |
missense |
probably benign |
|
R8151:Mug1
|
UTSW |
6 |
121,818,117 (GRCm39) |
missense |
probably benign |
0.01 |
R8491:Mug1
|
UTSW |
6 |
121,859,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8714:Mug1
|
UTSW |
6 |
121,859,681 (GRCm39) |
missense |
probably benign |
0.01 |
R8734:Mug1
|
UTSW |
6 |
121,848,340 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:Mug1
|
UTSW |
6 |
121,817,208 (GRCm39) |
splice site |
probably benign |
|
R8807:Mug1
|
UTSW |
6 |
121,851,434 (GRCm39) |
missense |
probably benign |
0.27 |
R8931:Mug1
|
UTSW |
6 |
121,861,296 (GRCm39) |
missense |
probably benign |
|
R8940:Mug1
|
UTSW |
6 |
121,858,642 (GRCm39) |
missense |
|
|
R9156:Mug1
|
UTSW |
6 |
121,851,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R9314:Mug1
|
UTSW |
6 |
121,834,296 (GRCm39) |
missense |
probably damaging |
0.97 |
R9315:Mug1
|
UTSW |
6 |
121,850,730 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9330:Mug1
|
UTSW |
6 |
121,859,723 (GRCm39) |
missense |
probably benign |
0.14 |
R9334:Mug1
|
UTSW |
6 |
121,838,490 (GRCm39) |
missense |
probably benign |
0.01 |
R9357:Mug1
|
UTSW |
6 |
121,852,450 (GRCm39) |
missense |
probably benign |
0.02 |
R9515:Mug1
|
UTSW |
6 |
121,861,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R9549:Mug1
|
UTSW |
6 |
121,858,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Mug1
|
UTSW |
6 |
121,859,699 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Mug1
|
UTSW |
6 |
121,857,463 (GRCm39) |
missense |
probably benign |
0.08 |
R9681:Mug1
|
UTSW |
6 |
121,833,254 (GRCm39) |
missense |
probably benign |
0.01 |
R9777:Mug1
|
UTSW |
6 |
121,857,864 (GRCm39) |
missense |
probably damaging |
1.00 |
RF017:Mug1
|
UTSW |
6 |
121,861,533 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Mug1
|
UTSW |
6 |
121,838,174 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Mug1
|
UTSW |
6 |
121,857,452 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mug1
|
UTSW |
6 |
121,818,253 (GRCm39) |
missense |
probably benign |
0.32 |
Z1177:Mug1
|
UTSW |
6 |
121,856,258 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Mug1
|
UTSW |
6 |
121,840,767 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Mug1
|
UTSW |
6 |
121,863,527 (GRCm39) |
missense |
probably damaging |
0.98 |
|