Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
A |
C |
8: 25,119,681 (GRCm39) |
S533A |
probably benign |
Het |
Akap6 |
T |
G |
12: 53,187,952 (GRCm39) |
S1789A |
probably damaging |
Het |
Alox15 |
A |
G |
11: 70,236,011 (GRCm39) |
S519P |
probably damaging |
Het |
Anapc2 |
A |
G |
2: 25,175,407 (GRCm39) |
K816E |
probably benign |
Het |
Atp6v1a |
T |
C |
16: 43,919,121 (GRCm39) |
D488G |
probably benign |
Het |
Banp |
A |
G |
8: 122,718,176 (GRCm39) |
|
probably null |
Het |
Camsap1 |
A |
G |
2: 25,825,874 (GRCm39) |
C1367R |
possibly damaging |
Het |
Casz1 |
C |
A |
4: 149,021,535 (GRCm39) |
H539Q |
probably damaging |
Het |
Ccl5 |
A |
G |
11: 83,421,212 (GRCm39) |
Y26H |
probably benign |
Het |
Cops3 |
A |
T |
11: 59,723,898 (GRCm39) |
S86R |
probably benign |
Het |
Cts7 |
A |
G |
13: 61,503,455 (GRCm39) |
S170P |
probably benign |
Het |
Cxcl15 |
A |
T |
5: 90,943,104 (GRCm39) |
E35D |
possibly damaging |
Het |
Dennd1b |
C |
T |
1: 138,969,698 (GRCm39) |
|
probably benign |
Het |
Dicer1 |
T |
C |
12: 104,662,982 (GRCm39) |
D1533G |
probably damaging |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dock4 |
A |
G |
12: 40,878,954 (GRCm39) |
E1531G |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,811,612 (GRCm39) |
|
probably null |
Het |
Fsip2 |
A |
G |
2: 82,820,430 (GRCm39) |
T5388A |
possibly damaging |
Het |
Gab1 |
C |
A |
8: 81,515,226 (GRCm39) |
R364L |
possibly damaging |
Het |
Gm10309 |
A |
T |
17: 86,812,007 (GRCm39) |
M1K |
probably null |
Het |
Gm4884 |
A |
T |
7: 40,690,211 (GRCm39) |
N36Y |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,553,053 (GRCm39) |
R2546* |
probably null |
Het |
Hmcn2 |
A |
G |
2: 31,315,480 (GRCm39) |
D3743G |
probably damaging |
Het |
Hsd3b9 |
T |
A |
3: 98,354,157 (GRCm39) |
E114V |
possibly damaging |
Het |
Irak2 |
A |
T |
6: 113,663,902 (GRCm39) |
N423Y |
probably damaging |
Het |
Jarid2 |
G |
A |
13: 45,001,765 (GRCm39) |
G26D |
probably benign |
Het |
Kif13b |
A |
G |
14: 64,988,974 (GRCm39) |
K785R |
probably benign |
Het |
Lamc3 |
A |
T |
2: 31,777,413 (GRCm39) |
I20F |
probably benign |
Het |
Limk1 |
G |
A |
5: 134,690,373 (GRCm39) |
|
probably benign |
Het |
Lrp4 |
C |
T |
2: 91,317,429 (GRCm39) |
T851I |
probably damaging |
Het |
Megf10 |
T |
C |
18: 57,379,642 (GRCm39) |
F273L |
possibly damaging |
Het |
Meltf |
T |
A |
16: 31,700,700 (GRCm39) |
D73E |
probably damaging |
Het |
Mroh7 |
A |
G |
4: 106,560,385 (GRCm39) |
F640L |
possibly damaging |
Het |
Mtor |
T |
C |
4: 148,635,457 (GRCm39) |
S2448P |
probably benign |
Het |
Myo3a |
T |
C |
2: 22,467,877 (GRCm39) |
V377A |
probably benign |
Het |
Myo5b |
T |
C |
18: 74,750,086 (GRCm39) |
V183A |
probably damaging |
Het |
Nedd4l |
G |
A |
18: 65,342,752 (GRCm39) |
R755H |
probably damaging |
Het |
Nrde2 |
T |
C |
12: 100,110,207 (GRCm39) |
T275A |
probably benign |
Het |
Or52n4 |
A |
G |
7: 104,294,333 (GRCm39) |
I80T |
probably benign |
Het |
Osgepl1 |
T |
C |
1: 53,360,702 (GRCm39) |
V381A |
probably benign |
Het |
Pcdha1 |
C |
T |
18: 37,064,509 (GRCm39) |
T391I |
probably benign |
Het |
Pdp1 |
T |
C |
4: 11,961,327 (GRCm39) |
N328S |
probably damaging |
Het |
Pepd |
A |
G |
7: 34,740,147 (GRCm39) |
E340G |
probably benign |
Het |
Plch1 |
T |
C |
3: 63,651,931 (GRCm39) |
T387A |
probably benign |
Het |
Plxnb1 |
C |
A |
9: 108,940,733 (GRCm39) |
T1536K |
possibly damaging |
Het |
Rbp7 |
T |
C |
4: 149,534,347 (GRCm39) |
T130A |
probably benign |
Het |
Rhot2 |
A |
T |
17: 26,060,054 (GRCm39) |
V309E |
probably benign |
Het |
Slc37a1 |
A |
G |
17: 31,557,964 (GRCm39) |
I421M |
possibly damaging |
Het |
Slit2 |
T |
A |
5: 48,389,331 (GRCm39) |
L585H |
probably damaging |
Het |
Spint4 |
C |
A |
2: 164,542,764 (GRCm39) |
A119D |
probably benign |
Het |
Strip2 |
G |
T |
6: 29,944,496 (GRCm39) |
|
probably null |
Het |
Stxbp4 |
T |
C |
11: 90,510,013 (GRCm39) |
Y59C |
probably damaging |
Het |
Syne1 |
G |
A |
10: 5,181,679 (GRCm39) |
Q4219* |
probably null |
Het |
Syne1 |
A |
T |
10: 5,406,826 (GRCm39) |
I37N |
probably damaging |
Het |
Syne4 |
G |
T |
7: 30,016,340 (GRCm39) |
G179* |
probably null |
Het |
Tead1 |
T |
C |
7: 112,460,672 (GRCm39) |
V192A |
probably benign |
Het |
Trim37 |
G |
T |
11: 87,107,313 (GRCm39) |
E317* |
probably null |
Het |
Wdfy3 |
A |
C |
5: 102,061,045 (GRCm39) |
Y1390D |
probably damaging |
Het |
Wdr81 |
A |
G |
11: 75,342,931 (GRCm39) |
F779L |
possibly damaging |
Het |
Zfp1002 |
C |
T |
2: 150,096,511 (GRCm39) |
G306D |
probably damaging |
Het |
|
Other mutations in Med13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00960:Med13
|
APN |
11 |
86,181,866 (GRCm39) |
splice site |
probably benign |
|
IGL01391:Med13
|
APN |
11 |
86,219,323 (GRCm39) |
missense |
probably benign |
|
IGL01767:Med13
|
APN |
11 |
86,210,609 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01830:Med13
|
APN |
11 |
86,179,754 (GRCm39) |
splice site |
probably benign |
|
IGL01859:Med13
|
APN |
11 |
86,174,577 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01924:Med13
|
APN |
11 |
86,199,522 (GRCm39) |
splice site |
probably benign |
|
IGL02080:Med13
|
APN |
11 |
86,174,638 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02138:Med13
|
APN |
11 |
86,177,591 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02259:Med13
|
APN |
11 |
86,248,327 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02339:Med13
|
APN |
11 |
86,179,765 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02399:Med13
|
APN |
11 |
86,174,771 (GRCm39) |
splice site |
probably benign |
|
IGL02646:Med13
|
APN |
11 |
86,174,212 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03227:Med13
|
APN |
11 |
86,218,618 (GRCm39) |
splice site |
probably benign |
|
R0197_Med13_854
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R0360_Med13_060
|
UTSW |
11 |
86,219,987 (GRCm39) |
splice site |
probably benign |
|
R2359_Med13_079
|
UTSW |
11 |
86,181,861 (GRCm39) |
splice site |
probably benign |
|
R3735_Med13_085
|
UTSW |
11 |
86,170,484 (GRCm39) |
missense |
probably benign |
0.00 |
R4974_Med13_508
|
UTSW |
11 |
86,189,673 (GRCm39) |
missense |
probably damaging |
0.98 |
R0116:Med13
|
UTSW |
11 |
86,210,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R0189:Med13
|
UTSW |
11 |
86,210,702 (GRCm39) |
missense |
probably benign |
|
R0197:Med13
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R0206:Med13
|
UTSW |
11 |
86,191,682 (GRCm39) |
splice site |
probably benign |
|
R0208:Med13
|
UTSW |
11 |
86,191,682 (GRCm39) |
splice site |
probably benign |
|
R0310:Med13
|
UTSW |
11 |
86,236,829 (GRCm39) |
missense |
probably benign |
0.11 |
R0360:Med13
|
UTSW |
11 |
86,219,987 (GRCm39) |
splice site |
probably benign |
|
R0413:Med13
|
UTSW |
11 |
86,190,033 (GRCm39) |
splice site |
probably benign |
|
R0482:Med13
|
UTSW |
11 |
86,175,977 (GRCm39) |
missense |
probably benign |
0.41 |
R0497:Med13
|
UTSW |
11 |
86,167,809 (GRCm39) |
splice site |
probably benign |
|
R0589:Med13
|
UTSW |
11 |
86,174,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Med13
|
UTSW |
11 |
86,236,788 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0646:Med13
|
UTSW |
11 |
86,221,915 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0701:Med13
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R0709:Med13
|
UTSW |
11 |
86,210,422 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0711:Med13
|
UTSW |
11 |
86,192,179 (GRCm39) |
splice site |
probably benign |
|
R0734:Med13
|
UTSW |
11 |
86,192,063 (GRCm39) |
missense |
probably benign |
|
R0883:Med13
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R1793:Med13
|
UTSW |
11 |
86,220,177 (GRCm39) |
missense |
probably benign |
0.45 |
R1926:Med13
|
UTSW |
11 |
86,179,899 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1959:Med13
|
UTSW |
11 |
86,189,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R2286:Med13
|
UTSW |
11 |
86,210,515 (GRCm39) |
missense |
probably benign |
0.05 |
R2359:Med13
|
UTSW |
11 |
86,181,861 (GRCm39) |
splice site |
probably benign |
|
R2444:Med13
|
UTSW |
11 |
86,222,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Med13
|
UTSW |
11 |
86,189,403 (GRCm39) |
missense |
probably benign |
0.00 |
R2879:Med13
|
UTSW |
11 |
86,189,988 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3439:Med13
|
UTSW |
11 |
86,176,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R3735:Med13
|
UTSW |
11 |
86,170,484 (GRCm39) |
missense |
probably benign |
0.00 |
R4333:Med13
|
UTSW |
11 |
86,179,009 (GRCm39) |
missense |
probably benign |
|
R4558:Med13
|
UTSW |
11 |
86,189,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R4598:Med13
|
UTSW |
11 |
86,169,392 (GRCm39) |
missense |
probably damaging |
0.97 |
R4773:Med13
|
UTSW |
11 |
86,167,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R4801:Med13
|
UTSW |
11 |
86,169,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Med13
|
UTSW |
11 |
86,169,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Med13
|
UTSW |
11 |
86,189,403 (GRCm39) |
missense |
probably benign |
0.00 |
R4940:Med13
|
UTSW |
11 |
86,178,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Med13
|
UTSW |
11 |
86,189,673 (GRCm39) |
missense |
probably damaging |
0.98 |
R5056:Med13
|
UTSW |
11 |
86,219,391 (GRCm39) |
missense |
probably benign |
0.00 |
R5133:Med13
|
UTSW |
11 |
86,210,675 (GRCm39) |
missense |
probably benign |
0.32 |
R5206:Med13
|
UTSW |
11 |
86,210,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Med13
|
UTSW |
11 |
86,192,294 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5534:Med13
|
UTSW |
11 |
86,210,191 (GRCm39) |
missense |
probably benign |
0.09 |
R5556:Med13
|
UTSW |
11 |
86,218,664 (GRCm39) |
missense |
probably benign |
0.25 |
R5633:Med13
|
UTSW |
11 |
86,169,757 (GRCm39) |
splice site |
probably benign |
|
R5769:Med13
|
UTSW |
11 |
86,236,829 (GRCm39) |
missense |
probably benign |
0.11 |
R6236:Med13
|
UTSW |
11 |
86,219,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R6487:Med13
|
UTSW |
11 |
86,221,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Med13
|
UTSW |
11 |
86,192,293 (GRCm39) |
missense |
probably damaging |
0.98 |
R6528:Med13
|
UTSW |
11 |
86,189,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Med13
|
UTSW |
11 |
86,169,622 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6913:Med13
|
UTSW |
11 |
86,210,702 (GRCm39) |
missense |
probably benign |
|
R7221:Med13
|
UTSW |
11 |
86,178,921 (GRCm39) |
missense |
probably benign |
0.00 |
R7254:Med13
|
UTSW |
11 |
86,210,661 (GRCm39) |
missense |
probably benign |
|
R7267:Med13
|
UTSW |
11 |
86,199,652 (GRCm39) |
missense |
probably benign |
0.01 |
R7309:Med13
|
UTSW |
11 |
86,181,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7404:Med13
|
UTSW |
11 |
86,177,272 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7586:Med13
|
UTSW |
11 |
86,161,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R7704:Med13
|
UTSW |
11 |
86,236,744 (GRCm39) |
nonsense |
probably null |
|
R7922:Med13
|
UTSW |
11 |
86,161,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R7943:Med13
|
UTSW |
11 |
86,169,352 (GRCm39) |
missense |
probably damaging |
0.97 |
R8062:Med13
|
UTSW |
11 |
86,210,264 (GRCm39) |
missense |
probably benign |
|
R8075:Med13
|
UTSW |
11 |
86,163,296 (GRCm39) |
missense |
probably damaging |
0.98 |
R8207:Med13
|
UTSW |
11 |
86,194,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R8671:Med13
|
UTSW |
11 |
86,161,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R9056:Med13
|
UTSW |
11 |
86,189,660 (GRCm39) |
nonsense |
probably null |
|
R9084:Med13
|
UTSW |
11 |
86,191,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Med13
|
UTSW |
11 |
86,192,297 (GRCm39) |
missense |
probably benign |
0.27 |
R9329:Med13
|
UTSW |
11 |
86,189,283 (GRCm39) |
missense |
probably benign |
0.10 |
R9380:Med13
|
UTSW |
11 |
86,177,598 (GRCm39) |
missense |
probably benign |
0.42 |
R9515:Med13
|
UTSW |
11 |
86,199,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9516:Med13
|
UTSW |
11 |
86,179,801 (GRCm39) |
missense |
probably benign |
0.01 |
R9690:Med13
|
UTSW |
11 |
86,169,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R9751:Med13
|
UTSW |
11 |
86,189,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9752:Med13
|
UTSW |
11 |
86,174,147 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9764:Med13
|
UTSW |
11 |
86,177,345 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Med13
|
UTSW |
11 |
86,246,249 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Med13
|
UTSW |
11 |
86,236,688 (GRCm39) |
missense |
probably benign |
0.45 |
Z1176:Med13
|
UTSW |
11 |
86,219,370 (GRCm39) |
missense |
possibly damaging |
0.91 |
|