Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
T |
A |
8: 24,667,623 (GRCm38) |
I104F |
probably benign |
Het |
Adgrg7 |
C |
T |
16: 56,770,311 (GRCm38) |
V166I |
probably benign |
Het |
Agfg1 |
G |
T |
1: 82,882,245 (GRCm38) |
V278L |
probably benign |
Het |
Alpk3 |
A |
G |
7: 81,092,580 (GRCm38) |
E715G |
possibly damaging |
Het |
Ap2m1 |
A |
G |
16: 20,543,345 (GRCm38) |
Y401C |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 97,965,452 (GRCm38) |
S838N |
probably benign |
Het |
Ash2l |
A |
T |
8: 25,827,205 (GRCm38) |
Y373* |
probably null |
Het |
Best2 |
C |
T |
8: 85,007,764 (GRCm38) |
V442I |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,425,542 (GRCm38) |
|
probably null |
Het |
Fat2 |
T |
A |
11: 55,285,030 (GRCm38) |
D1619V |
probably damaging |
Het |
Fer1l6 |
A |
T |
15: 58,627,597 (GRCm38) |
N1272I |
probably benign |
Het |
Gcc1 |
T |
A |
6: 28,417,996 (GRCm38) |
*779C |
probably null |
Het |
Gm12216 |
G |
A |
11: 53,859,251 (GRCm38) |
|
probably benign |
Het |
Gm17657 |
C |
A |
17: 29,519,373 (GRCm38) |
V140L |
probably benign |
Het |
Gm7102 |
A |
G |
19: 61,175,535 (GRCm38) |
V154A |
possibly damaging |
Het |
Grm2 |
C |
T |
9: 106,647,171 (GRCm38) |
V311I |
|
Het |
Immt |
T |
A |
6: 71,874,705 (GRCm38) |
D683E |
probably benign |
Het |
Itga8 |
T |
G |
2: 12,232,901 (GRCm38) |
D336A |
probably damaging |
Het |
Jhy |
T |
C |
9: 40,961,157 (GRCm38) |
T19A |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 181,135,092 (GRCm38) |
M1V |
probably null |
Het |
Kctd17 |
A |
T |
15: 78,433,014 (GRCm38) |
I117F |
probably damaging |
Het |
Lrp6 |
T |
C |
6: 134,507,401 (GRCm38) |
T420A |
probably damaging |
Het |
Manba |
T |
C |
3: 135,517,912 (GRCm38) |
S187P |
probably damaging |
Het |
Mef2b |
A |
T |
8: 70,164,288 (GRCm38) |
D13V |
probably damaging |
Het |
Mical2 |
T |
C |
7: 112,303,756 (GRCm38) |
F145L |
probably damaging |
Het |
Mphosph8 |
T |
A |
14: 56,685,040 (GRCm38) |
D551E |
possibly damaging |
Het |
Myo10 |
C |
G |
15: 25,782,981 (GRCm38) |
R1170G |
probably damaging |
Het |
Myo16 |
A |
C |
8: 10,272,687 (GRCm38) |
Q39P |
unknown |
Het |
Myo1f |
A |
G |
17: 33,601,694 (GRCm38) |
E837G |
probably benign |
Het |
Nell2 |
T |
A |
15: 95,435,393 (GRCm38) |
I128F |
possibly damaging |
Het |
Olfr1357 |
A |
G |
10: 78,612,614 (GRCm38) |
V9A |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,379,390 (GRCm38) |
R659* |
probably null |
Het |
Pcdhga1 |
A |
G |
18: 37,839,975 (GRCm38) |
Q881R |
possibly damaging |
Het |
Plekhm2 |
T |
G |
4: 141,642,459 (GRCm38) |
E75A |
possibly damaging |
Het |
Prc1 |
A |
G |
7: 80,307,657 (GRCm38) |
K357E |
possibly damaging |
Het |
Pxk |
T |
A |
14: 8,146,220 (GRCm38) |
C377S |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,334,568 (GRCm38) |
E1696G |
probably damaging |
Het |
Rbbp6 |
T |
A |
7: 123,001,367 (GRCm38) |
S1532R |
unknown |
Het |
Scn5a |
G |
T |
9: 119,562,560 (GRCm38) |
A22E |
probably benign |
Het |
Sctr |
G |
A |
1: 120,022,225 (GRCm38) |
R48Q |
probably benign |
Het |
Siae |
T |
C |
9: 37,623,013 (GRCm38) |
V115A |
probably damaging |
Het |
Slc16a6 |
A |
G |
11: 109,453,281 (GRCm38) |
C563R |
probably benign |
Het |
Sntg1 |
A |
C |
1: 8,682,019 (GRCm38) |
V58G |
possibly damaging |
Het |
Snx11 |
C |
T |
11: 96,773,159 (GRCm38) |
V36M |
probably damaging |
Het |
Stk3 |
C |
A |
15: 34,959,036 (GRCm38) |
S330I |
probably benign |
Het |
Synpo |
A |
G |
18: 60,629,559 (GRCm38) |
F92S |
probably benign |
Het |
Tle1 |
A |
G |
4: 72,139,687 (GRCm38) |
|
probably null |
Het |
Tmem117 |
A |
G |
15: 94,931,803 (GRCm38) |
D173G |
possibly damaging |
Het |
Tmprss5 |
T |
C |
9: 49,114,541 (GRCm38) |
W338R |
probably benign |
Het |
Tnfrsf19 |
T |
C |
14: 60,974,698 (GRCm38) |
T168A |
possibly damaging |
Het |
Trhde |
C |
T |
10: 114,800,871 (GRCm38) |
G144S |
possibly damaging |
Het |
Trim56 |
G |
T |
5: 137,114,243 (GRCm38) |
Q140K |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,732,574 (GRCm38) |
V28679M |
probably damaging |
Het |
Ubxn8 |
G |
A |
8: 33,623,203 (GRCm38) |
R208C |
probably damaging |
Het |
Wdr38 |
T |
A |
2: 39,000,264 (GRCm38) |
W137R |
probably damaging |
Het |
Zdhhc6 |
G |
T |
19: 55,304,500 (GRCm38) |
N271K |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,718,547 (GRCm38) |
S446P |
possibly damaging |
Het |
Zmynd8 |
T |
C |
2: 165,807,572 (GRCm38) |
Q867R |
possibly damaging |
Het |
Zswim3 |
T |
C |
2: 164,820,482 (GRCm38) |
I294T |
probably benign |
Het |
|
Other mutations in Vmn2r72 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00931:Vmn2r72
|
APN |
7 |
85,749,646 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01019:Vmn2r72
|
APN |
7 |
85,738,334 (GRCm38) |
missense |
probably benign |
0.26 |
IGL01445:Vmn2r72
|
APN |
7 |
85,749,646 (GRCm38) |
missense |
probably benign |
0.06 |
IGL02076:Vmn2r72
|
APN |
7 |
85,738,367 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02082:Vmn2r72
|
APN |
7 |
85,738,166 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02086:Vmn2r72
|
APN |
7 |
85,738,166 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02089:Vmn2r72
|
APN |
7 |
85,738,166 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02125:Vmn2r72
|
APN |
7 |
85,750,711 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02146:Vmn2r72
|
APN |
7 |
85,737,962 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02272:Vmn2r72
|
APN |
7 |
85,750,693 (GRCm38) |
missense |
probably benign |
|
IGL02514:Vmn2r72
|
APN |
7 |
85,738,699 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL02662:Vmn2r72
|
APN |
7 |
85,738,183 (GRCm38) |
missense |
probably benign |
0.26 |
IGL02697:Vmn2r72
|
APN |
7 |
85,738,671 (GRCm38) |
missense |
probably benign |
0.36 |
IGL02733:Vmn2r72
|
APN |
7 |
85,751,813 (GRCm38) |
missense |
probably benign |
0.05 |
IGL03070:Vmn2r72
|
APN |
7 |
85,752,041 (GRCm38) |
splice site |
probably benign |
|
IGL03150:Vmn2r72
|
APN |
7 |
85,751,176 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03159:Vmn2r72
|
APN |
7 |
85,754,954 (GRCm38) |
missense |
probably benign |
0.05 |
IGL03333:Vmn2r72
|
APN |
7 |
85,750,867 (GRCm38) |
missense |
probably benign |
0.10 |
R0081:Vmn2r72
|
UTSW |
7 |
85,751,836 (GRCm38) |
missense |
probably benign |
0.01 |
R0090:Vmn2r72
|
UTSW |
7 |
85,754,876 (GRCm38) |
missense |
probably benign |
|
R0655:Vmn2r72
|
UTSW |
7 |
85,738,111 (GRCm38) |
nonsense |
probably null |
|
R0778:Vmn2r72
|
UTSW |
7 |
85,749,739 (GRCm38) |
missense |
probably benign |
0.00 |
R1169:Vmn2r72
|
UTSW |
7 |
85,751,309 (GRCm38) |
missense |
probably benign |
0.01 |
R1172:Vmn2r72
|
UTSW |
7 |
85,751,944 (GRCm38) |
missense |
probably damaging |
1.00 |
R1173:Vmn2r72
|
UTSW |
7 |
85,751,944 (GRCm38) |
missense |
probably damaging |
1.00 |
R1175:Vmn2r72
|
UTSW |
7 |
85,751,944 (GRCm38) |
missense |
probably damaging |
1.00 |
R1248:Vmn2r72
|
UTSW |
7 |
85,749,188 (GRCm38) |
missense |
probably benign |
0.02 |
R1302:Vmn2r72
|
UTSW |
7 |
85,738,257 (GRCm38) |
missense |
probably damaging |
1.00 |
R1506:Vmn2r72
|
UTSW |
7 |
85,749,211 (GRCm38) |
missense |
probably benign |
|
R1632:Vmn2r72
|
UTSW |
7 |
85,751,792 (GRCm38) |
missense |
probably benign |
0.13 |
R1775:Vmn2r72
|
UTSW |
7 |
85,738,170 (GRCm38) |
missense |
probably benign |
0.01 |
R1962:Vmn2r72
|
UTSW |
7 |
85,749,161 (GRCm38) |
missense |
probably benign |
0.00 |
R2201:Vmn2r72
|
UTSW |
7 |
85,738,236 (GRCm38) |
missense |
probably benign |
0.12 |
R2290:Vmn2r72
|
UTSW |
7 |
85,738,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R2327:Vmn2r72
|
UTSW |
7 |
85,738,256 (GRCm38) |
missense |
probably damaging |
1.00 |
R2424:Vmn2r72
|
UTSW |
7 |
85,750,953 (GRCm38) |
missense |
probably damaging |
1.00 |
R2655:Vmn2r72
|
UTSW |
7 |
85,751,269 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2860:Vmn2r72
|
UTSW |
7 |
85,750,836 (GRCm38) |
missense |
probably damaging |
0.99 |
R2861:Vmn2r72
|
UTSW |
7 |
85,750,836 (GRCm38) |
missense |
probably damaging |
0.99 |
R2862:Vmn2r72
|
UTSW |
7 |
85,750,836 (GRCm38) |
missense |
probably damaging |
0.99 |
R3009:Vmn2r72
|
UTSW |
7 |
85,749,642 (GRCm38) |
missense |
probably benign |
0.00 |
R3797:Vmn2r72
|
UTSW |
7 |
85,738,077 (GRCm38) |
missense |
probably benign |
0.44 |
R3798:Vmn2r72
|
UTSW |
7 |
85,738,077 (GRCm38) |
missense |
probably benign |
0.44 |
R3902:Vmn2r72
|
UTSW |
7 |
85,749,735 (GRCm38) |
missense |
possibly damaging |
0.52 |
R3959:Vmn2r72
|
UTSW |
7 |
85,751,131 (GRCm38) |
missense |
probably benign |
0.36 |
R3974:Vmn2r72
|
UTSW |
7 |
85,749,809 (GRCm38) |
missense |
probably damaging |
1.00 |
R4399:Vmn2r72
|
UTSW |
7 |
85,738,500 (GRCm38) |
missense |
probably damaging |
1.00 |
R4421:Vmn2r72
|
UTSW |
7 |
85,738,500 (GRCm38) |
missense |
probably damaging |
1.00 |
R4426:Vmn2r72
|
UTSW |
7 |
85,737,828 (GRCm38) |
nonsense |
probably null |
|
R4522:Vmn2r72
|
UTSW |
7 |
85,751,926 (GRCm38) |
missense |
probably benign |
0.44 |
R4523:Vmn2r72
|
UTSW |
7 |
85,751,926 (GRCm38) |
missense |
probably benign |
0.44 |
R4533:Vmn2r72
|
UTSW |
7 |
85,751,926 (GRCm38) |
missense |
probably benign |
0.44 |
R4691:Vmn2r72
|
UTSW |
7 |
85,737,911 (GRCm38) |
nonsense |
probably null |
|
R4781:Vmn2r72
|
UTSW |
7 |
85,737,861 (GRCm38) |
missense |
probably benign |
0.14 |
R4863:Vmn2r72
|
UTSW |
7 |
85,750,598 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4952:Vmn2r72
|
UTSW |
7 |
85,751,109 (GRCm38) |
missense |
probably benign |
|
R4991:Vmn2r72
|
UTSW |
7 |
85,751,130 (GRCm38) |
missense |
probably damaging |
0.99 |
R4995:Vmn2r72
|
UTSW |
7 |
85,738,485 (GRCm38) |
missense |
probably damaging |
1.00 |
R5095:Vmn2r72
|
UTSW |
7 |
85,737,853 (GRCm38) |
missense |
probably damaging |
0.98 |
R5174:Vmn2r72
|
UTSW |
7 |
85,737,840 (GRCm38) |
missense |
probably benign |
0.00 |
R5276:Vmn2r72
|
UTSW |
7 |
85,738,254 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5395:Vmn2r72
|
UTSW |
7 |
85,750,897 (GRCm38) |
missense |
possibly damaging |
0.71 |
R5560:Vmn2r72
|
UTSW |
7 |
85,751,942 (GRCm38) |
missense |
probably damaging |
0.96 |
R5933:Vmn2r72
|
UTSW |
7 |
85,737,850 (GRCm38) |
missense |
probably benign |
0.05 |
R6033:Vmn2r72
|
UTSW |
7 |
85,737,929 (GRCm38) |
missense |
probably damaging |
1.00 |
R6033:Vmn2r72
|
UTSW |
7 |
85,737,929 (GRCm38) |
missense |
probably damaging |
1.00 |
R6354:Vmn2r72
|
UTSW |
7 |
85,750,539 (GRCm38) |
critical splice donor site |
probably null |
|
R6362:Vmn2r72
|
UTSW |
7 |
85,751,174 (GRCm38) |
missense |
probably damaging |
1.00 |
R6594:Vmn2r72
|
UTSW |
7 |
85,749,684 (GRCm38) |
missense |
probably benign |
0.32 |
R6794:Vmn2r72
|
UTSW |
7 |
85,737,996 (GRCm38) |
missense |
probably damaging |
1.00 |
R7113:Vmn2r72
|
UTSW |
7 |
85,749,803 (GRCm38) |
splice site |
probably null |
|
R7189:Vmn2r72
|
UTSW |
7 |
85,754,917 (GRCm38) |
missense |
probably benign |
0.36 |
R7323:Vmn2r72
|
UTSW |
7 |
85,750,563 (GRCm38) |
missense |
probably benign |
|
R7426:Vmn2r72
|
UTSW |
7 |
85,751,140 (GRCm38) |
missense |
probably benign |
|
R7606:Vmn2r72
|
UTSW |
7 |
85,751,154 (GRCm38) |
missense |
possibly damaging |
0.91 |
R7651:Vmn2r72
|
UTSW |
7 |
85,751,938 (GRCm38) |
missense |
probably damaging |
1.00 |
R7688:Vmn2r72
|
UTSW |
7 |
85,754,890 (GRCm38) |
missense |
probably benign |
0.32 |
R7753:Vmn2r72
|
UTSW |
7 |
85,750,626 (GRCm38) |
missense |
probably damaging |
1.00 |
R7843:Vmn2r72
|
UTSW |
7 |
85,749,630 (GRCm38) |
missense |
probably benign |
0.01 |
R8157:Vmn2r72
|
UTSW |
7 |
85,751,233 (GRCm38) |
missense |
probably benign |
0.09 |
R8254:Vmn2r72
|
UTSW |
7 |
85,751,019 (GRCm38) |
missense |
probably damaging |
1.00 |
R8389:Vmn2r72
|
UTSW |
7 |
85,751,960 (GRCm38) |
missense |
probably damaging |
0.99 |
R8444:Vmn2r72
|
UTSW |
7 |
85,738,175 (GRCm38) |
missense |
probably benign |
|
R8989:Vmn2r72
|
UTSW |
7 |
85,754,926 (GRCm38) |
missense |
probably benign |
0.10 |
R9015:Vmn2r72
|
UTSW |
7 |
85,749,180 (GRCm38) |
missense |
probably benign |
0.01 |
R9080:Vmn2r72
|
UTSW |
7 |
85,738,256 (GRCm38) |
missense |
probably damaging |
1.00 |
R9269:Vmn2r72
|
UTSW |
7 |
85,751,203 (GRCm38) |
missense |
probably benign |
0.03 |
R9317:Vmn2r72
|
UTSW |
7 |
85,754,814 (GRCm38) |
missense |
probably benign |
0.04 |
R9509:Vmn2r72
|
UTSW |
7 |
85,754,867 (GRCm38) |
missense |
probably benign |
|
Z1176:Vmn2r72
|
UTSW |
7 |
85,749,191 (GRCm38) |
missense |
probably damaging |
0.99 |
|