Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
G |
A |
5: 8,875,614 (GRCm39) |
V596I |
probably benign |
Het |
Acad8 |
A |
T |
9: 26,888,928 (GRCm39) |
H371Q |
probably damaging |
Het |
Actn3 |
G |
T |
19: 4,921,656 (GRCm39) |
R175S |
probably benign |
Het |
Adamts9 |
G |
T |
6: 92,864,371 (GRCm39) |
D780E |
probably benign |
Het |
AK157302 |
C |
A |
13: 21,679,537 (GRCm39) |
T21K |
probably benign |
Het |
Ank3 |
A |
T |
10: 69,706,872 (GRCm39) |
H329L |
unknown |
Het |
Ankrd36 |
A |
G |
11: 5,519,979 (GRCm39) |
H18R |
possibly damaging |
Het |
Anks1b |
T |
A |
10: 90,412,966 (GRCm39) |
V38D |
possibly damaging |
Het |
Apbb2 |
A |
T |
5: 66,470,677 (GRCm39) |
L520H |
probably damaging |
Het |
Arid1b |
C |
A |
17: 5,293,274 (GRCm39) |
P731T |
probably damaging |
Het |
Atp1a4 |
A |
G |
1: 172,067,398 (GRCm39) |
F578S |
probably damaging |
Het |
Atp6v0a2 |
A |
T |
5: 124,789,312 (GRCm39) |
I360F |
probably damaging |
Het |
Bcas3 |
A |
T |
11: 85,448,184 (GRCm39) |
I600F |
probably damaging |
Het |
C1qtnf7 |
T |
G |
5: 43,766,441 (GRCm39) |
C20W |
possibly damaging |
Het |
Cadm1 |
A |
T |
9: 47,708,821 (GRCm39) |
K184* |
probably null |
Het |
Ccdc138 |
A |
T |
10: 58,343,448 (GRCm39) |
H101L |
probably benign |
Het |
Cep120 |
T |
A |
18: 53,852,369 (GRCm39) |
N503I |
probably damaging |
Het |
Chil4 |
T |
C |
3: 106,109,874 (GRCm39) |
T380A |
probably benign |
Het |
Clip2 |
A |
G |
5: 134,526,942 (GRCm39) |
|
probably null |
Het |
Cyp3a11 |
G |
A |
5: 145,799,164 (GRCm39) |
P341L |
possibly damaging |
Het |
Cyp3a41a |
G |
C |
5: 145,656,906 (GRCm39) |
|
probably benign |
Het |
Dcaf1 |
A |
G |
9: 106,725,042 (GRCm39) |
I509M |
possibly damaging |
Het |
Dcaf13 |
T |
C |
15: 39,010,102 (GRCm39) |
S429P |
probably damaging |
Het |
Eln |
A |
G |
5: 134,758,220 (GRCm39) |
V151A |
unknown |
Het |
Endou |
T |
G |
15: 97,610,954 (GRCm39) |
M377L |
probably benign |
Het |
Etfa |
A |
G |
9: 55,396,152 (GRCm39) |
I138T |
probably damaging |
Het |
Fbxw10 |
T |
A |
11: 62,768,109 (GRCm39) |
S982T |
probably benign |
Het |
Gm9602 |
A |
T |
14: 15,933,435 (GRCm39) |
R47* |
probably null |
Het |
Hectd4 |
G |
A |
5: 121,486,952 (GRCm39) |
V3316I |
probably benign |
Het |
Hif1a |
T |
C |
12: 73,987,302 (GRCm39) |
L477S |
probably benign |
Het |
Icam5 |
G |
C |
9: 20,946,846 (GRCm39) |
G458A |
probably benign |
Het |
Itm2b |
A |
T |
14: 73,603,896 (GRCm39) |
D106E |
probably benign |
Het |
Kdm4d |
G |
A |
9: 14,375,336 (GRCm39) |
T174M |
probably damaging |
Het |
Kif16b |
G |
T |
2: 142,541,207 (GRCm39) |
D1364E |
probably benign |
Het |
Lbhd1 |
G |
A |
19: 8,861,550 (GRCm39) |
V61M |
probably damaging |
Het |
Lclat1 |
T |
A |
17: 73,546,919 (GRCm39) |
S279T |
probably benign |
Het |
Lhx4 |
G |
A |
1: 155,580,956 (GRCm39) |
L190F |
probably damaging |
Het |
Lima1 |
C |
T |
15: 99,704,320 (GRCm39) |
S283N |
probably benign |
Het |
Magi1 |
C |
A |
6: 93,724,209 (GRCm39) |
D496Y |
probably damaging |
Het |
Map1a |
T |
C |
2: 121,133,446 (GRCm39) |
S1421P |
probably damaging |
Het |
Map3k20 |
C |
T |
2: 72,202,257 (GRCm39) |
H163Y |
probably damaging |
Het |
Mier3 |
T |
G |
13: 111,822,890 (GRCm39) |
|
probably null |
Het |
Mllt3 |
G |
A |
4: 87,692,284 (GRCm39) |
Q560* |
probably null |
Het |
Mmp25 |
T |
A |
17: 23,851,728 (GRCm39) |
D327V |
probably benign |
Het |
Nckap5 |
G |
A |
1: 125,909,423 (GRCm39) |
Q1603* |
probably null |
Het |
Nell1 |
G |
A |
7: 49,712,368 (GRCm39) |
V63I |
probably benign |
Het |
Or10al3 |
C |
T |
17: 38,011,815 (GRCm39) |
P85S |
probably damaging |
Het |
Or2ag2b |
A |
T |
7: 106,418,111 (GRCm39) |
I274F |
probably benign |
Het |
Or8a1 |
A |
C |
9: 37,641,578 (GRCm39) |
S234A |
probably benign |
Het |
Pde12 |
C |
T |
14: 26,386,931 (GRCm39) |
E526K |
probably damaging |
Het |
Pfn4 |
T |
C |
12: 4,825,442 (GRCm39) |
V93A |
possibly damaging |
Het |
Poglut2 |
A |
G |
1: 44,156,362 (GRCm39) |
I75T |
possibly damaging |
Het |
Ppp2r3d |
A |
G |
9: 124,423,977 (GRCm38) |
S60P |
unknown |
Het |
Prelp |
T |
C |
1: 133,842,257 (GRCm39) |
H296R |
probably damaging |
Het |
Prickle1 |
T |
C |
15: 93,398,749 (GRCm39) |
E693G |
possibly damaging |
Het |
Rars1 |
A |
G |
11: 35,706,488 (GRCm39) |
L477P |
probably damaging |
Het |
Rasal1 |
G |
A |
5: 120,802,172 (GRCm39) |
R328H |
probably damaging |
Het |
Rasef |
A |
G |
4: 73,659,393 (GRCm39) |
F220S |
probably benign |
Het |
Rif1 |
C |
T |
2: 52,001,151 (GRCm39) |
S1535L |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,697,495 (GRCm39) |
I463T |
possibly damaging |
Het |
Ryr3 |
A |
T |
2: 112,690,695 (GRCm39) |
D1138E |
probably benign |
Het |
Scn9a |
T |
A |
2: 66,335,236 (GRCm39) |
Y1251F |
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,715,856 (GRCm39) |
W1568R |
possibly damaging |
Het |
Senp6 |
A |
G |
9: 80,049,433 (GRCm39) |
E1019G |
probably damaging |
Het |
Shh |
A |
G |
5: 28,663,461 (GRCm39) |
Y236H |
probably damaging |
Het |
Sin3a |
A |
G |
9: 57,014,744 (GRCm39) |
D655G |
probably damaging |
Het |
Slc35a4 |
C |
T |
18: 36,815,274 (GRCm39) |
P35S |
probably damaging |
Het |
Slc35g1 |
T |
C |
19: 38,384,633 (GRCm39) |
L24P |
probably benign |
Het |
Slc39a4 |
G |
T |
15: 76,498,759 (GRCm39) |
Q312K |
probably damaging |
Het |
Slc6a5 |
A |
T |
7: 49,601,175 (GRCm39) |
I659F |
probably damaging |
Het |
Slc7a4 |
T |
C |
16: 17,392,399 (GRCm39) |
Y345C |
probably benign |
Het |
Slco6c1 |
G |
T |
1: 96,993,809 (GRCm39) |
R645S |
probably benign |
Het |
Soat1 |
T |
C |
1: 156,268,923 (GRCm39) |
Y209C |
probably benign |
Het |
Tbc1d9b |
T |
C |
11: 50,054,714 (GRCm39) |
S953P |
probably benign |
Het |
Tgm1 |
G |
A |
14: 55,942,303 (GRCm39) |
H683Y |
probably benign |
Het |
Tmem98 |
G |
A |
11: 80,708,432 (GRCm39) |
R134Q |
probably damaging |
Het |
Trpm3 |
A |
C |
19: 22,955,745 (GRCm39) |
M1107L |
possibly damaging |
Het |
Vmn1r11 |
G |
A |
6: 57,114,872 (GRCm39) |
V179I |
probably benign |
Het |
Vmn1r119 |
G |
T |
7: 20,745,638 (GRCm39) |
T248K |
probably damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,506,945 (GRCm39) |
I21N |
possibly damaging |
Het |
Vstm5 |
A |
T |
9: 15,168,585 (GRCm39) |
I50F |
probably damaging |
Het |
Wdr1 |
T |
C |
5: 38,685,255 (GRCm39) |
D572G |
probably damaging |
Het |
Xaf1 |
T |
C |
11: 72,192,517 (GRCm39) |
F5S |
probably benign |
Het |
Zan |
A |
T |
5: 137,468,519 (GRCm39) |
|
probably null |
Het |
Zfp697 |
T |
C |
3: 98,334,979 (GRCm39) |
V248A |
possibly damaging |
Het |
Zftraf1 |
C |
A |
15: 76,530,541 (GRCm39) |
V260L |
probably benign |
Het |
Zkscan3 |
T |
A |
13: 21,577,667 (GRCm39) |
T249S |
unknown |
Het |
Znfx1 |
A |
G |
2: 166,897,860 (GRCm39) |
Y355H |
probably damaging |
Het |
|
Other mutations in Vmn2r24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00954:Vmn2r24
|
APN |
6 |
123,792,596 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01382:Vmn2r24
|
APN |
6 |
123,763,938 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01592:Vmn2r24
|
APN |
6 |
123,764,445 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01754:Vmn2r24
|
APN |
6 |
123,781,120 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01939:Vmn2r24
|
APN |
6 |
123,764,404 (GRCm39) |
missense |
probably benign |
|
IGL02140:Vmn2r24
|
APN |
6 |
123,757,631 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02272:Vmn2r24
|
APN |
6 |
123,763,843 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02568:Vmn2r24
|
APN |
6 |
123,792,812 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02748:Vmn2r24
|
APN |
6 |
123,793,057 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03022:Vmn2r24
|
APN |
6 |
123,755,967 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03343:Vmn2r24
|
APN |
6 |
123,793,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R0357:Vmn2r24
|
UTSW |
6 |
123,792,369 (GRCm39) |
frame shift |
probably null |
|
R0453:Vmn2r24
|
UTSW |
6 |
123,757,350 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0538:Vmn2r24
|
UTSW |
6 |
123,793,012 (GRCm39) |
missense |
probably benign |
0.32 |
R0607:Vmn2r24
|
UTSW |
6 |
123,763,893 (GRCm39) |
missense |
probably benign |
|
R1381:Vmn2r24
|
UTSW |
6 |
123,763,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Vmn2r24
|
UTSW |
6 |
123,783,479 (GRCm39) |
splice site |
probably benign |
|
R1848:Vmn2r24
|
UTSW |
6 |
123,793,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Vmn2r24
|
UTSW |
6 |
123,793,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Vmn2r24
|
UTSW |
6 |
123,792,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Vmn2r24
|
UTSW |
6 |
123,792,353 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2145:Vmn2r24
|
UTSW |
6 |
123,755,972 (GRCm39) |
missense |
probably benign |
|
R2483:Vmn2r24
|
UTSW |
6 |
123,792,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Vmn2r24
|
UTSW |
6 |
123,763,985 (GRCm39) |
missense |
probably benign |
0.01 |
R3001:Vmn2r24
|
UTSW |
6 |
123,781,231 (GRCm39) |
missense |
probably benign |
0.00 |
R3002:Vmn2r24
|
UTSW |
6 |
123,781,231 (GRCm39) |
missense |
probably benign |
0.00 |
R3236:Vmn2r24
|
UTSW |
6 |
123,755,984 (GRCm39) |
nonsense |
probably null |
|
R3623:Vmn2r24
|
UTSW |
6 |
123,792,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R3624:Vmn2r24
|
UTSW |
6 |
123,792,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R3835:Vmn2r24
|
UTSW |
6 |
123,764,412 (GRCm39) |
missense |
probably benign |
0.33 |
R4074:Vmn2r24
|
UTSW |
6 |
123,764,374 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4075:Vmn2r24
|
UTSW |
6 |
123,764,374 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4812:Vmn2r24
|
UTSW |
6 |
123,756,144 (GRCm39) |
missense |
probably benign |
0.00 |
R4825:Vmn2r24
|
UTSW |
6 |
123,792,739 (GRCm39) |
missense |
probably benign |
0.02 |
R5351:Vmn2r24
|
UTSW |
6 |
123,793,223 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5665:Vmn2r24
|
UTSW |
6 |
123,763,938 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5790:Vmn2r24
|
UTSW |
6 |
123,792,499 (GRCm39) |
missense |
probably benign |
|
R5808:Vmn2r24
|
UTSW |
6 |
123,792,597 (GRCm39) |
nonsense |
probably null |
|
R5879:Vmn2r24
|
UTSW |
6 |
123,764,226 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5923:Vmn2r24
|
UTSW |
6 |
123,792,751 (GRCm39) |
missense |
probably damaging |
0.96 |
R5969:Vmn2r24
|
UTSW |
6 |
123,755,981 (GRCm39) |
missense |
probably benign |
0.00 |
R6050:Vmn2r24
|
UTSW |
6 |
123,792,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6171:Vmn2r24
|
UTSW |
6 |
123,764,205 (GRCm39) |
missense |
probably damaging |
0.98 |
R6174:Vmn2r24
|
UTSW |
6 |
123,793,236 (GRCm39) |
missense |
probably benign |
0.00 |
R6356:Vmn2r24
|
UTSW |
6 |
123,783,368 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6562:Vmn2r24
|
UTSW |
6 |
123,757,386 (GRCm39) |
missense |
probably benign |
0.01 |
R6563:Vmn2r24
|
UTSW |
6 |
123,781,137 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6584:Vmn2r24
|
UTSW |
6 |
123,792,764 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6630:Vmn2r24
|
UTSW |
6 |
123,763,981 (GRCm39) |
missense |
probably benign |
0.00 |
R6803:Vmn2r24
|
UTSW |
6 |
123,755,960 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6864:Vmn2r24
|
UTSW |
6 |
123,756,117 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7252:Vmn2r24
|
UTSW |
6 |
123,764,191 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7369:Vmn2r24
|
UTSW |
6 |
123,792,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R7646:Vmn2r24
|
UTSW |
6 |
123,793,169 (GRCm39) |
missense |
probably benign |
0.20 |
R7799:Vmn2r24
|
UTSW |
6 |
123,757,422 (GRCm39) |
missense |
probably benign |
0.00 |
R7803:Vmn2r24
|
UTSW |
6 |
123,757,438 (GRCm39) |
missense |
probably benign |
0.00 |
R7959:Vmn2r24
|
UTSW |
6 |
123,755,949 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8215:Vmn2r24
|
UTSW |
6 |
123,756,077 (GRCm39) |
missense |
probably benign |
0.10 |
R8796:Vmn2r24
|
UTSW |
6 |
123,757,500 (GRCm39) |
missense |
probably benign |
|
R9172:Vmn2r24
|
UTSW |
6 |
123,783,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Vmn2r24
|
UTSW |
6 |
123,792,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R9375:Vmn2r24
|
UTSW |
6 |
123,792,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Vmn2r24
|
UTSW |
6 |
123,763,950 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9546:Vmn2r24
|
UTSW |
6 |
123,764,266 (GRCm39) |
missense |
probably damaging |
0.98 |
RF006:Vmn2r24
|
UTSW |
6 |
123,783,378 (GRCm39) |
missense |
probably damaging |
1.00 |
RF016:Vmn2r24
|
UTSW |
6 |
123,781,174 (GRCm39) |
missense |
probably benign |
0.04 |
X0023:Vmn2r24
|
UTSW |
6 |
123,764,359 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Vmn2r24
|
UTSW |
6 |
123,781,155 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Vmn2r24
|
UTSW |
6 |
123,763,719 (GRCm39) |
missense |
probably benign |
0.00 |
|