Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aen |
G |
A |
7: 78,552,491 (GRCm39) |
M150I |
possibly damaging |
Het |
Arhgef11 |
A |
G |
3: 87,606,082 (GRCm39) |
N279S |
possibly damaging |
Het |
Arid3a |
T |
C |
10: 79,786,760 (GRCm39) |
|
probably null |
Het |
Casp8ap2 |
A |
G |
4: 32,646,446 (GRCm39) |
T1840A |
possibly damaging |
Het |
Ccdc14 |
T |
A |
16: 34,525,413 (GRCm39) |
N235K |
possibly damaging |
Het |
Cdh20 |
T |
C |
1: 109,922,076 (GRCm39) |
V56A |
probably damaging |
Het |
Clec16a |
G |
A |
16: 10,512,574 (GRCm39) |
R837H |
probably damaging |
Het |
Clec16a |
A |
G |
16: 10,445,312 (GRCm39) |
N518S |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,576,515 (GRCm39) |
D137G |
possibly damaging |
Het |
Cpt1b |
T |
C |
15: 89,303,018 (GRCm39) |
T649A |
probably damaging |
Het |
Efcab8 |
C |
G |
2: 153,631,145 (GRCm39) |
L192V |
probably damaging |
Het |
Farp2 |
A |
G |
1: 93,548,965 (GRCm39) |
R1024G |
probably benign |
Het |
Flvcr2 |
GTAGTGTATA |
GTA |
12: 85,849,922 (GRCm39) |
|
probably null |
Het |
Fmo1 |
T |
A |
1: 162,677,676 (GRCm39) |
T147S |
probably benign |
Het |
Fryl |
A |
C |
5: 73,257,843 (GRCm39) |
|
probably null |
Het |
Galnt13 |
A |
C |
2: 54,770,122 (GRCm39) |
I305L |
probably benign |
Het |
Guca2a |
A |
G |
4: 119,494,951 (GRCm39) |
N2D |
unknown |
Het |
Iqcd |
C |
T |
5: 120,740,514 (GRCm39) |
R282W |
probably damaging |
Het |
Lamc1 |
A |
C |
1: 153,126,268 (GRCm39) |
C475G |
probably damaging |
Het |
Map3k5 |
AAAAGAAAAAGA |
AA |
10: 19,986,612 (GRCm39) |
|
probably null |
Het |
Mn1 |
A |
G |
5: 111,569,651 (GRCm39) |
Y1207C |
probably damaging |
Het |
Mroh2b |
A |
G |
15: 4,967,892 (GRCm39) |
D977G |
possibly damaging |
Het |
Mrpl53 |
A |
T |
6: 83,086,169 (GRCm39) |
N26I |
probably damaging |
Het |
Nell1 |
A |
T |
7: 49,869,760 (GRCm39) |
|
probably null |
Het |
Ogdh |
T |
G |
11: 6,299,329 (GRCm39) |
F743V |
probably benign |
Het |
Or4d10b |
A |
T |
19: 12,036,222 (GRCm39) |
M298K |
possibly damaging |
Het |
Or4n4 |
C |
T |
14: 50,519,036 (GRCm39) |
V225I |
probably benign |
Het |
Or6c3 |
A |
G |
10: 129,308,953 (GRCm39) |
T131A |
probably benign |
Het |
Plscr1l1 |
T |
A |
9: 92,233,061 (GRCm39) |
F61L |
probably benign |
Het |
Pmvk |
A |
G |
3: 89,375,899 (GRCm39) |
E174G |
probably benign |
Het |
Pou6f2 |
T |
C |
13: 18,414,158 (GRCm39) |
N206D |
|
Het |
Prelid3a |
A |
T |
18: 67,606,018 (GRCm39) |
S42C |
probably benign |
Het |
Riok1 |
T |
A |
13: 38,236,296 (GRCm39) |
H347Q |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,789,650 (GRCm39) |
L1488P |
probably damaging |
Het |
Shkbp1 |
A |
G |
7: 27,052,109 (GRCm39) |
V158A |
probably benign |
Het |
Slc9c1 |
A |
G |
16: 45,360,076 (GRCm39) |
I43M |
possibly damaging |
Het |
Smarca2 |
A |
G |
19: 26,654,080 (GRCm39) |
N755S |
possibly damaging |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Tfb2m |
G |
A |
1: 179,373,668 (GRCm39) |
P10L |
probably benign |
Het |
Trim30c |
T |
C |
7: 104,032,703 (GRCm39) |
M252V |
probably benign |
Het |
Ttll1 |
A |
G |
15: 83,384,279 (GRCm39) |
L116P |
probably damaging |
Het |
Tubd1 |
C |
T |
11: 86,440,248 (GRCm39) |
H91Y |
possibly damaging |
Het |
Vgll4 |
A |
G |
6: 114,839,786 (GRCm39) |
S175P |
probably damaging |
Het |
Vmn1r79 |
A |
G |
7: 11,910,415 (GRCm39) |
Y99C |
possibly damaging |
Het |
Vmn2r80 |
C |
T |
10: 79,030,150 (GRCm39) |
Q659* |
probably null |
Het |
Zfp382 |
A |
G |
7: 29,833,840 (GRCm39) |
D497G |
possibly damaging |
Het |
Zfp41 |
A |
G |
15: 75,490,384 (GRCm39) |
E112G |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,307,605 (GRCm39) |
S1754P |
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 |
R6479:Med13
|
UTSW |
11 |
86,248,353 (GRCm39) |
start gained |
probably benign |
|
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 |
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 |
|