Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530053A07Rik |
T |
C |
7: 28,147,349 (GRCm38) |
V1119A |
possibly damaging |
Het |
Aadacl3 |
T |
C |
4: 144,456,190 (GRCm38) |
Y236C |
probably benign |
Het |
Arhgef2 |
T |
C |
3: 88,642,603 (GRCm38) |
L655P |
probably damaging |
Het |
Brsk2 |
T |
C |
7: 141,984,416 (GRCm38) |
S100P |
probably damaging |
Het |
Calb1 |
A |
G |
4: 15,898,926 (GRCm38) |
T141A |
probably benign |
Het |
Cog6 |
T |
C |
3: 52,993,517 (GRCm38) |
T447A |
probably benign |
Het |
Cyp4f13 |
A |
T |
17: 32,929,933 (GRCm38) |
N279K |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,878,524 (GRCm38) |
D4440G |
possibly damaging |
Het |
Dspp |
A |
T |
5: 104,175,328 (GRCm38) |
E112D |
possibly damaging |
Het |
Fam3c |
T |
A |
6: 22,328,676 (GRCm38) |
T71S |
possibly damaging |
Het |
Fdxr |
C |
A |
11: 115,271,318 (GRCm38) |
G188W |
probably damaging |
Het |
Fndc5 |
T |
C |
4: 129,138,721 (GRCm38) |
V39A |
possibly damaging |
Het |
Gm14226 |
T |
C |
2: 155,024,726 (GRCm38) |
I201T |
possibly damaging |
Het |
Gm853 |
C |
A |
4: 130,220,343 (GRCm38) |
A94S |
probably benign |
Het |
Grip1 |
C |
T |
10: 120,054,905 (GRCm38) |
Q950* |
probably null |
Het |
Haspin |
A |
T |
11: 73,136,746 (GRCm38) |
Y506N |
probably benign |
Het |
Itga2b |
C |
A |
11: 102,467,386 (GRCm38) |
R171L |
probably benign |
Het |
Kctd2 |
C |
T |
11: 115,420,348 (GRCm38) |
P61S |
unknown |
Het |
Kirrel2 |
A |
G |
7: 30,450,376 (GRCm38) |
|
probably null |
Het |
Lmx1b |
A |
G |
2: 33,565,114 (GRCm38) |
F310S |
|
Het |
Map4k4 |
A |
T |
1: 40,006,675 (GRCm38) |
I574F |
probably damaging |
Het |
Nrip1 |
T |
C |
16: 76,291,399 (GRCm38) |
K1090R |
probably benign |
Het |
Ntrk3 |
T |
C |
7: 78,192,578 (GRCm38) |
Y820C |
probably damaging |
Het |
Olfr1446 |
T |
C |
19: 12,890,485 (GRCm38) |
T31A |
probably benign |
Het |
Olfr209 |
T |
A |
16: 59,362,171 (GRCm38) |
I16L |
probably benign |
Het |
Pcdhb11 |
T |
C |
18: 37,422,189 (GRCm38) |
Y191H |
probably benign |
Het |
Pgm5 |
T |
C |
19: 24,727,725 (GRCm38) |
K475E |
probably benign |
Het |
Pi16 |
C |
A |
17: 29,319,234 (GRCm38) |
P7Q |
possibly damaging |
Het |
Psd4 |
A |
T |
2: 24,403,211 (GRCm38) |
D696V |
probably damaging |
Het |
Rere |
T |
C |
4: 150,612,672 (GRCm38) |
F556L |
unknown |
Het |
Sema4f |
A |
T |
6: 82,917,401 (GRCm38) |
C528S |
probably damaging |
Het |
Sorcs2 |
A |
G |
5: 36,038,206 (GRCm38) |
S680P |
probably benign |
Het |
Sv2c |
T |
C |
13: 96,088,565 (GRCm38) |
T79A |
probably damaging |
Het |
Tarsl2 |
A |
G |
7: 65,676,061 (GRCm38) |
N461S |
probably benign |
Het |
Thada |
T |
C |
17: 84,226,040 (GRCm38) |
N1661S |
probably benign |
Het |
Tubd1 |
A |
T |
11: 86,549,438 (GRCm38) |
Q96L |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,983,312 (GRCm38) |
|
probably benign |
Het |
Vwce |
C |
A |
19: 10,650,574 (GRCm38) |
S466Y |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,634,836 (GRCm38) |
I1178T |
probably benign |
Het |
Zfp568 |
A |
T |
7: 30,015,133 (GRCm38) |
H145L |
probably benign |
Het |
Zfp606 |
T |
C |
7: 12,492,861 (GRCm38) |
I303T |
possibly damaging |
Het |
Zfp846 |
A |
G |
9: 20,593,291 (GRCm38) |
D149G |
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 |
R7266:Vmn2r72
|
UTSW |
7 |
85,738,274 (GRCm38) |
nonsense |
probably null |
|
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 |
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 |
|