Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519G04Rik |
T |
C |
5: 114,874,280 (GRCm38) |
V86A |
probably benign |
Het |
Abcc3 |
A |
T |
11: 94,364,417 (GRCm38) |
I601N |
probably damaging |
Het |
Abl2 |
T |
A |
1: 156,620,827 (GRCm38) |
|
probably null |
Het |
Adgrf4 |
C |
T |
17: 42,666,898 (GRCm38) |
R518Q |
possibly damaging |
Het |
Ahi1 |
C |
T |
10: 20,959,996 (GRCm38) |
T76I |
probably damaging |
Het |
Arhgap42 |
C |
T |
9: 9,035,600 (GRCm38) |
G247D |
probably damaging |
Het |
Arid2 |
C |
T |
15: 96,362,590 (GRCm38) |
L407F |
probably damaging |
Het |
Atp13a1 |
T |
C |
8: 69,799,773 (GRCm38) |
F606L |
probably benign |
Het |
Avl9 |
T |
A |
6: 56,736,435 (GRCm38) |
|
probably benign |
Het |
B3glct |
C |
T |
5: 149,709,380 (GRCm38) |
A65V |
probably damaging |
Het |
Bcorl1 |
T |
C |
X: 48,401,917 (GRCm38) |
|
probably benign |
Het |
Bdp1 |
T |
C |
13: 100,050,988 (GRCm38) |
T1624A |
probably benign |
Het |
Bmp15 |
A |
G |
X: 6,316,021 (GRCm38) |
M263T |
probably benign |
Het |
Brd8 |
T |
C |
18: 34,614,479 (GRCm38) |
K110E |
probably damaging |
Het |
Cachd1 |
A |
G |
4: 100,990,844 (GRCm38) |
D1052G |
probably damaging |
Het |
Capn9 |
G |
A |
8: 124,605,711 (GRCm38) |
G430R |
possibly damaging |
Het |
Ccdc113 |
G |
A |
8: 95,557,296 (GRCm38) |
E333K |
probably benign |
Het |
Ccnl2 |
A |
T |
4: 155,812,481 (GRCm38) |
|
probably null |
Het |
Ccr9 |
T |
C |
9: 123,779,364 (GRCm38) |
F37S |
probably benign |
Het |
Cdh7 |
A |
T |
1: 110,138,159 (GRCm38) |
D721V |
probably damaging |
Het |
Ceacam10 |
A |
T |
7: 24,778,372 (GRCm38) |
N104I |
probably damaging |
Het |
Cenpk |
T |
A |
13: 104,236,176 (GRCm38) |
|
probably benign |
Het |
Cfi |
A |
G |
3: 129,858,804 (GRCm38) |
|
probably null |
Het |
Chd1 |
T |
C |
17: 15,742,294 (GRCm38) |
F771S |
probably damaging |
Het |
Chil4 |
G |
A |
3: 106,219,455 (GRCm38) |
L4F |
probably benign |
Het |
Cilp |
G |
A |
9: 65,278,090 (GRCm38) |
R489Q |
possibly damaging |
Het |
Cntnap5b |
G |
A |
1: 100,358,725 (GRCm38) |
G402R |
probably benign |
Het |
Coq8b |
A |
G |
7: 27,257,377 (GRCm38) |
E485G |
probably damaging |
Het |
Cse1l |
A |
G |
2: 166,941,492 (GRCm38) |
S733G |
probably benign |
Het |
Dnah5 |
G |
A |
15: 28,312,388 (GRCm38) |
|
probably null |
Het |
Dnmt3l |
T |
C |
10: 78,052,732 (GRCm38) |
V156A |
probably damaging |
Het |
Duox1 |
A |
T |
2: 122,333,062 (GRCm38) |
T792S |
probably benign |
Het |
Duox2 |
T |
C |
2: 122,287,108 (GRCm38) |
D915G |
probably benign |
Het |
Efcab5 |
A |
T |
11: 77,172,321 (GRCm38) |
M115K |
probably benign |
Het |
Eif2s1 |
G |
A |
12: 78,877,185 (GRCm38) |
D139N |
probably benign |
Het |
Erg |
A |
G |
16: 95,361,078 (GRCm38) |
F390L |
probably damaging |
Het |
Fam193b |
A |
T |
13: 55,542,998 (GRCm38) |
S650R |
probably damaging |
Het |
Fbp2 |
T |
A |
13: 62,854,061 (GRCm38) |
K113N |
possibly damaging |
Het |
Fnbp4 |
T |
G |
2: 90,758,372 (GRCm38) |
S496A |
probably damaging |
Het |
Gab3 |
C |
A |
X: 75,000,095 (GRCm38) |
R475L |
probably damaging |
Het |
Gm7534 |
T |
G |
4: 134,201,941 (GRCm38) |
N351T |
possibly damaging |
Het |
Gsap |
T |
C |
5: 21,226,839 (GRCm38) |
|
probably benign |
Het |
Gucy1a2 |
C |
T |
9: 3,582,697 (GRCm38) |
L160F |
probably damaging |
Het |
Hivep1 |
C |
T |
13: 42,183,786 (GRCm38) |
A2447V |
possibly damaging |
Het |
Hrasls5 |
T |
C |
19: 7,612,638 (GRCm38) |
S10P |
possibly damaging |
Het |
Insc |
G |
T |
7: 114,804,593 (GRCm38) |
|
probably null |
Het |
Jph2 |
A |
G |
2: 163,339,685 (GRCm38) |
S520P |
possibly damaging |
Het |
Kidins220 |
T |
A |
12: 24,987,006 (GRCm38) |
|
probably benign |
Het |
Krtap29-1 |
A |
G |
11: 99,978,612 (GRCm38) |
S148P |
probably damaging |
Het |
Ltbp2 |
A |
C |
12: 84,793,733 (GRCm38) |
C1000G |
probably damaging |
Het |
Map2k3 |
T |
C |
11: 60,950,027 (GRCm38) |
F294S |
probably damaging |
Het |
Map4k2 |
C |
A |
19: 6,342,738 (GRCm38) |
|
probably benign |
Het |
Mboat2 |
T |
C |
12: 24,951,443 (GRCm38) |
V281A |
probably benign |
Het |
Mdga2 |
G |
A |
12: 66,568,917 (GRCm38) |
R570* |
probably null |
Het |
Mlxipl |
A |
G |
5: 135,107,005 (GRCm38) |
D28G |
probably damaging |
Het |
Morc2b |
T |
C |
17: 33,136,760 (GRCm38) |
I679M |
probably benign |
Het |
Myh4 |
T |
C |
11: 67,246,366 (GRCm38) |
|
probably benign |
Het |
Nfib |
A |
C |
4: 82,498,615 (GRCm38) |
L61R |
probably damaging |
Het |
Noc2l |
C |
A |
4: 156,241,450 (GRCm38) |
Y227* |
probably null |
Het |
Nrde2 |
A |
G |
12: 100,142,232 (GRCm38) |
S367P |
probably damaging |
Het |
Nup93 |
C |
A |
8: 94,243,739 (GRCm38) |
P89T |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Olfr1240 |
C |
T |
2: 89,439,583 (GRCm38) |
R232H |
probably benign |
Het |
Olfr1283 |
A |
G |
2: 111,369,095 (GRCm38) |
I154M |
probably benign |
Het |
Olfr6 |
A |
T |
7: 106,956,287 (GRCm38) |
Y216* |
probably null |
Het |
Olfr714 |
A |
T |
7: 107,074,619 (GRCm38) |
K264* |
probably null |
Het |
Olfr749 |
T |
A |
14: 50,736,576 (GRCm38) |
E195D |
possibly damaging |
Het |
Olfr824 |
A |
G |
10: 130,126,205 (GRCm38) |
I284T |
possibly damaging |
Het |
Oxct1 |
G |
T |
15: 4,092,525 (GRCm38) |
A319S |
probably null |
Het |
P2ry10 |
A |
G |
X: 107,103,253 (GRCm38) |
S265G |
probably benign |
Het |
Peak1 |
A |
T |
9: 56,258,759 (GRCm38) |
N628K |
probably damaging |
Het |
Pkdrej |
T |
A |
15: 85,821,231 (GRCm38) |
Q168L |
probably benign |
Het |
Plec |
A |
G |
15: 76,188,926 (GRCm38) |
M604T |
probably benign |
Het |
Pmfbp1 |
A |
T |
8: 109,532,103 (GRCm38) |
N680I |
possibly damaging |
Het |
Pnmal2 |
T |
C |
7: 16,945,789 (GRCm38) |
W233R |
probably damaging |
Het |
Pxn |
A |
G |
5: 115,545,667 (GRCm38) |
N186S |
probably benign |
Het |
Rsad1 |
A |
C |
11: 94,549,125 (GRCm38) |
|
probably benign |
Het |
Runx2 |
A |
G |
17: 44,735,342 (GRCm38) |
I112T |
probably benign |
Het |
S1pr2 |
A |
T |
9: 20,967,494 (GRCm38) |
L346Q |
probably damaging |
Het |
Skint6 |
A |
G |
4: 113,238,132 (GRCm38) |
I110T |
probably damaging |
Het |
Slc36a4 |
T |
A |
9: 15,726,980 (GRCm38) |
F234Y |
probably damaging |
Het |
Slitrk2 |
T |
A |
X: 66,654,629 (GRCm38) |
V242D |
probably damaging |
Het |
Sp100 |
A |
G |
1: 85,681,142 (GRCm38) |
|
probably null |
Het |
Spryd3 |
A |
C |
15: 102,118,181 (GRCm38) |
L352V |
probably benign |
Het |
Ssc4d |
A |
C |
5: 135,970,317 (GRCm38) |
W11G |
possibly damaging |
Het |
Stx17 |
T |
A |
4: 48,158,870 (GRCm38) |
D83E |
probably damaging |
Het |
Tlk2 |
A |
T |
11: 105,240,440 (GRCm38) |
Q204L |
probably benign |
Het |
Tnfrsf21 |
A |
T |
17: 43,037,938 (GRCm38) |
H147L |
possibly damaging |
Het |
Tnrc18 |
A |
T |
5: 142,766,087 (GRCm38) |
D1154E |
unknown |
Het |
Trap1 |
A |
G |
16: 4,068,336 (GRCm38) |
S86P |
probably benign |
Het |
Trim32 |
T |
A |
4: 65,614,776 (GRCm38) |
C523* |
probably null |
Het |
Ttc38 |
G |
T |
15: 85,838,788 (GRCm38) |
D146Y |
probably damaging |
Het |
Ttc9 |
T |
A |
12: 81,631,796 (GRCm38) |
L131Q |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,813,339 (GRCm38) |
G11436R |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,726,848 (GRCm38) |
|
probably benign |
Het |
Ubash3b |
G |
A |
9: 41,043,573 (GRCm38) |
P92S |
possibly damaging |
Het |
Ube4a |
T |
C |
9: 44,948,099 (GRCm38) |
N367S |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,479,540 (GRCm38) |
H4899Q |
possibly damaging |
Het |
Ufl1 |
C |
T |
4: 25,269,036 (GRCm38) |
G265D |
possibly damaging |
Het |
Vmn2r27 |
T |
A |
6: 124,224,483 (GRCm38) |
I172F |
probably damaging |
Het |
Vmn2r61 |
A |
G |
7: 42,300,001 (GRCm38) |
D615G |
probably benign |
Het |
Wdr24 |
T |
A |
17: 25,826,282 (GRCm38) |
D330E |
probably damaging |
Het |
Zbbx |
A |
T |
3: 75,078,412 (GRCm38) |
N444K |
probably benign |
Het |
Zc3h7b |
A |
T |
15: 81,792,328 (GRCm38) |
Q757L |
probably damaging |
Het |
|
Other mutations in Vmn2r6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01547:Vmn2r6
|
APN |
3 |
64,538,104 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01968:Vmn2r6
|
APN |
3 |
64,556,345 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL02009:Vmn2r6
|
APN |
3 |
64,537,902 (GRCm38) |
missense |
possibly damaging |
0.61 |
IGL02039:Vmn2r6
|
APN |
3 |
64,556,189 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02652:Vmn2r6
|
APN |
3 |
64,556,328 (GRCm38) |
missense |
probably benign |
0.24 |
IGL02737:Vmn2r6
|
APN |
3 |
64,556,490 (GRCm38) |
missense |
possibly damaging |
0.55 |
IGL02808:Vmn2r6
|
APN |
3 |
64,556,496 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03066:Vmn2r6
|
APN |
3 |
64,565,153 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03331:Vmn2r6
|
APN |
3 |
64,538,007 (GRCm38) |
missense |
probably damaging |
1.00 |
BB010:Vmn2r6
|
UTSW |
3 |
64,559,803 (GRCm38) |
missense |
probably benign |
0.02 |
BB020:Vmn2r6
|
UTSW |
3 |
64,559,803 (GRCm38) |
missense |
probably benign |
0.02 |
R0010:Vmn2r6
|
UTSW |
3 |
64,559,545 (GRCm38) |
nonsense |
probably null |
|
R0206:Vmn2r6
|
UTSW |
3 |
64,539,912 (GRCm38) |
missense |
probably benign |
|
R0206:Vmn2r6
|
UTSW |
3 |
64,539,912 (GRCm38) |
missense |
probably benign |
|
R0208:Vmn2r6
|
UTSW |
3 |
64,539,912 (GRCm38) |
missense |
probably benign |
|
R0427:Vmn2r6
|
UTSW |
3 |
64,559,587 (GRCm38) |
missense |
probably damaging |
1.00 |
R0466:Vmn2r6
|
UTSW |
3 |
64,556,302 (GRCm38) |
missense |
probably damaging |
1.00 |
R1018:Vmn2r6
|
UTSW |
3 |
64,556,840 (GRCm38) |
missense |
probably benign |
0.00 |
R1104:Vmn2r6
|
UTSW |
3 |
64,538,066 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1186:Vmn2r6
|
UTSW |
3 |
64,565,067 (GRCm38) |
missense |
probably benign |
0.01 |
R1245:Vmn2r6
|
UTSW |
3 |
64,556,790 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1295:Vmn2r6
|
UTSW |
3 |
64,538,273 (GRCm38) |
missense |
probably damaging |
1.00 |
R1473:Vmn2r6
|
UTSW |
3 |
64,538,158 (GRCm38) |
nonsense |
probably null |
|
R1498:Vmn2r6
|
UTSW |
3 |
64,556,469 (GRCm38) |
missense |
probably damaging |
1.00 |
R1925:Vmn2r6
|
UTSW |
3 |
64,556,277 (GRCm38) |
missense |
possibly damaging |
0.87 |
R2044:Vmn2r6
|
UTSW |
3 |
64,537,841 (GRCm38) |
missense |
probably damaging |
0.96 |
R2253:Vmn2r6
|
UTSW |
3 |
64,559,718 (GRCm38) |
missense |
probably damaging |
1.00 |
R2261:Vmn2r6
|
UTSW |
3 |
64,556,669 (GRCm38) |
missense |
probably benign |
0.24 |
R2262:Vmn2r6
|
UTSW |
3 |
64,556,669 (GRCm38) |
missense |
probably benign |
0.24 |
R2350:Vmn2r6
|
UTSW |
3 |
64,556,352 (GRCm38) |
missense |
probably benign |
0.01 |
R2680:Vmn2r6
|
UTSW |
3 |
64,538,286 (GRCm38) |
missense |
possibly damaging |
0.91 |
R2846:Vmn2r6
|
UTSW |
3 |
64,556,790 (GRCm38) |
missense |
possibly damaging |
0.53 |
R2860:Vmn2r6
|
UTSW |
3 |
64,547,339 (GRCm38) |
missense |
probably benign |
0.00 |
R2861:Vmn2r6
|
UTSW |
3 |
64,547,339 (GRCm38) |
missense |
probably benign |
0.00 |
R3766:Vmn2r6
|
UTSW |
3 |
64,556,508 (GRCm38) |
missense |
probably benign |
0.19 |
R3870:Vmn2r6
|
UTSW |
3 |
64,556,621 (GRCm38) |
missense |
probably damaging |
0.96 |
R4018:Vmn2r6
|
UTSW |
3 |
64,556,472 (GRCm38) |
missense |
probably benign |
0.05 |
R4024:Vmn2r6
|
UTSW |
3 |
64,538,250 (GRCm38) |
missense |
possibly damaging |
0.73 |
R4026:Vmn2r6
|
UTSW |
3 |
64,538,250 (GRCm38) |
missense |
possibly damaging |
0.73 |
R4227:Vmn2r6
|
UTSW |
3 |
64,537,948 (GRCm38) |
missense |
probably damaging |
0.99 |
R4526:Vmn2r6
|
UTSW |
3 |
64,537,724 (GRCm38) |
missense |
probably benign |
0.32 |
R4570:Vmn2r6
|
UTSW |
3 |
64,559,647 (GRCm38) |
missense |
probably benign |
0.31 |
R4894:Vmn2r6
|
UTSW |
3 |
64,547,408 (GRCm38) |
missense |
probably benign |
|
R4934:Vmn2r6
|
UTSW |
3 |
64,556,345 (GRCm38) |
missense |
probably damaging |
0.99 |
R5057:Vmn2r6
|
UTSW |
3 |
64,537,786 (GRCm38) |
missense |
probably damaging |
1.00 |
R5059:Vmn2r6
|
UTSW |
3 |
64,537,623 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5148:Vmn2r6
|
UTSW |
3 |
64,556,594 (GRCm38) |
missense |
probably damaging |
0.99 |
R5155:Vmn2r6
|
UTSW |
3 |
64,538,514 (GRCm38) |
missense |
probably benign |
0.44 |
R5179:Vmn2r6
|
UTSW |
3 |
64,537,990 (GRCm38) |
missense |
probably benign |
0.00 |
R5256:Vmn2r6
|
UTSW |
3 |
64,556,842 (GRCm38) |
missense |
probably benign |
0.33 |
R5861:Vmn2r6
|
UTSW |
3 |
64,556,033 (GRCm38) |
missense |
probably benign |
0.00 |
R5950:Vmn2r6
|
UTSW |
3 |
64,565,231 (GRCm38) |
missense |
probably benign |
0.05 |
R6081:Vmn2r6
|
UTSW |
3 |
64,556,532 (GRCm38) |
missense |
probably benign |
0.25 |
R6173:Vmn2r6
|
UTSW |
3 |
64,559,755 (GRCm38) |
missense |
probably damaging |
1.00 |
R6190:Vmn2r6
|
UTSW |
3 |
64,538,003 (GRCm38) |
missense |
probably benign |
0.04 |
R6240:Vmn2r6
|
UTSW |
3 |
64,556,805 (GRCm38) |
missense |
probably damaging |
1.00 |
R6433:Vmn2r6
|
UTSW |
3 |
64,547,380 (GRCm38) |
nonsense |
probably null |
|
R6645:Vmn2r6
|
UTSW |
3 |
64,556,876 (GRCm38) |
missense |
probably damaging |
1.00 |
R6791:Vmn2r6
|
UTSW |
3 |
64,538,159 (GRCm38) |
missense |
probably damaging |
1.00 |
R7265:Vmn2r6
|
UTSW |
3 |
64,556,774 (GRCm38) |
missense |
probably benign |
0.00 |
R7503:Vmn2r6
|
UTSW |
3 |
64,539,951 (GRCm38) |
nonsense |
probably null |
|
R7562:Vmn2r6
|
UTSW |
3 |
64,556,520 (GRCm38) |
missense |
probably benign |
0.00 |
R7584:Vmn2r6
|
UTSW |
3 |
64,565,262 (GRCm38) |
missense |
probably benign |
0.07 |
R7611:Vmn2r6
|
UTSW |
3 |
64,565,142 (GRCm38) |
missense |
probably damaging |
0.98 |
R7759:Vmn2r6
|
UTSW |
3 |
64,556,570 (GRCm38) |
missense |
probably damaging |
1.00 |
R7834:Vmn2r6
|
UTSW |
3 |
64,538,022 (GRCm38) |
missense |
probably damaging |
1.00 |
R7933:Vmn2r6
|
UTSW |
3 |
64,559,803 (GRCm38) |
missense |
probably benign |
0.02 |
R7982:Vmn2r6
|
UTSW |
3 |
64,559,820 (GRCm38) |
missense |
probably damaging |
1.00 |
R8024:Vmn2r6
|
UTSW |
3 |
64,559,824 (GRCm38) |
missense |
probably benign |
0.40 |
R8074:Vmn2r6
|
UTSW |
3 |
64,547,643 (GRCm38) |
intron |
probably benign |
|
R8169:Vmn2r6
|
UTSW |
3 |
64,539,889 (GRCm38) |
missense |
probably benign |
0.01 |
R8337:Vmn2r6
|
UTSW |
3 |
64,556,105 (GRCm38) |
nonsense |
probably null |
|
R8736:Vmn2r6
|
UTSW |
3 |
64,559,800 (GRCm38) |
missense |
probably damaging |
1.00 |
R8962:Vmn2r6
|
UTSW |
3 |
64,556,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R9139:Vmn2r6
|
UTSW |
3 |
64,556,856 (GRCm38) |
missense |
probably benign |
0.12 |
R9206:Vmn2r6
|
UTSW |
3 |
64,559,611 (GRCm38) |
missense |
probably damaging |
0.97 |
R9295:Vmn2r6
|
UTSW |
3 |
64,556,063 (GRCm38) |
missense |
probably benign |
0.00 |
R9332:Vmn2r6
|
UTSW |
3 |
64,547,250 (GRCm38) |
missense |
probably benign |
0.01 |
R9616:Vmn2r6
|
UTSW |
3 |
64,538,303 (GRCm38) |
missense |
probably damaging |
1.00 |
R9663:Vmn2r6
|
UTSW |
3 |
64,556,128 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9685:Vmn2r6
|
UTSW |
3 |
64,556,660 (GRCm38) |
missense |
probably benign |
0.19 |
X0020:Vmn2r6
|
UTSW |
3 |
64,538,450 (GRCm38) |
missense |
probably benign |
|
X0066:Vmn2r6
|
UTSW |
3 |
64,547,378 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r6
|
UTSW |
3 |
64,556,325 (GRCm38) |
missense |
probably damaging |
0.98 |
|