Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadl |
C |
T |
1: 66,854,747 (GRCm38) |
G83E |
probably damaging |
Het |
Adamtsl2 |
A |
G |
2: 27,103,124 (GRCm38) |
D722G |
possibly damaging |
Het |
Akap11 |
A |
T |
14: 78,518,882 (GRCm38) |
D25E |
|
Het |
Akr1c21 |
C |
T |
13: 4,576,279 (GRCm38) |
R101W |
probably damaging |
Het |
Ano2 |
T |
C |
6: 125,980,169 (GRCm38) |
Y634H |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,719,291 (GRCm38) |
R240Q |
probably benign |
Het |
C87414 |
A |
T |
5: 93,637,728 (GRCm38) |
F231Y |
probably benign |
Het |
Cfap221 |
T |
C |
1: 119,923,571 (GRCm38) |
E820G |
probably damaging |
Het |
Chad |
A |
G |
11: 94,567,892 (GRCm38) |
D289G |
probably benign |
Het |
Col4a2 |
C |
A |
8: 11,448,132 (GRCm38) |
A1647E |
probably damaging |
Het |
Dhx32 |
G |
T |
7: 133,725,206 (GRCm38) |
T522K |
possibly damaging |
Het |
E430018J23Rik |
C |
T |
7: 127,393,324 (GRCm38) |
C38Y |
probably null |
Het |
Eloa |
A |
G |
4: 136,006,311 (GRCm38) |
V707A |
probably benign |
Het |
Fam219a |
A |
G |
4: 41,520,935 (GRCm38) |
S109P |
probably damaging |
Het |
Ftl1 |
A |
T |
7: 45,459,227 (GRCm38) |
F36I |
probably benign |
Het |
Furin |
C |
T |
7: 80,390,879 (GRCm38) |
R737Q |
probably benign |
Het |
Gm40460 |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
7: 142,240,434 (GRCm38) |
|
probably benign |
Het |
Gpt |
C |
T |
15: 76,699,042 (GRCm38) |
T393M |
probably damaging |
Het |
Greb1l |
A |
T |
18: 10,529,613 (GRCm38) |
D865V |
probably benign |
Het |
Ifi207 |
GTT |
GT |
1: 173,729,450 (GRCm38) |
|
probably null |
Het |
Klk1b11 |
G |
A |
7: 43,999,696 (GRCm38) |
C219Y |
probably damaging |
Het |
Lcn11 |
A |
T |
2: 25,779,031 (GRCm38) |
D117V |
probably damaging |
Het |
Lrpprc |
A |
T |
17: 84,773,314 (GRCm38) |
V161D |
possibly damaging |
Het |
Lrrk2 |
T |
C |
15: 91,699,991 (GRCm38) |
L318S |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,861,779 (GRCm38) |
T2821A |
possibly damaging |
Het |
Mysm1 |
A |
G |
4: 94,965,612 (GRCm38) |
M250T |
probably benign |
Het |
Nol12 |
A |
G |
15: 78,935,068 (GRCm38) |
K27E |
probably damaging |
Het |
Olfr1186 |
G |
A |
2: 88,525,587 (GRCm38) |
M1I |
probably null |
Het |
Olfr951 |
A |
G |
9: 39,394,616 (GRCm38) |
K272R |
probably damaging |
Het |
Omg |
T |
A |
11: 79,502,175 (GRCm38) |
M286L |
probably benign |
Het |
Pdyn |
A |
G |
2: 129,688,437 (GRCm38) |
L104P |
probably benign |
Het |
Pira2 |
A |
C |
7: 3,843,889 (GRCm38) |
L218R |
probably damaging |
Het |
Pnpt1 |
A |
T |
11: 29,130,758 (GRCm38) |
M1L |
unknown |
Het |
Pofut2 |
C |
T |
10: 77,265,951 (GRCm38) |
T274M |
probably benign |
Het |
Rbm12b1 |
C |
A |
4: 12,146,363 (GRCm38) |
D778E |
probably damaging |
Het |
Srsf12 |
C |
G |
4: 33,226,070 (GRCm38) |
P111R |
probably damaging |
Het |
Tbc1d14 |
G |
A |
5: 36,530,448 (GRCm38) |
|
probably benign |
Het |
Tcf23 |
A |
G |
5: 30,970,120 (GRCm38) |
K89E |
probably benign |
Het |
Tmem74 |
C |
T |
15: 43,866,919 (GRCm38) |
G243R |
probably damaging |
Het |
Ufd1 |
T |
C |
16: 18,821,103 (GRCm38) |
V119A |
possibly damaging |
Het |
Zfp120 |
A |
T |
2: 150,117,407 (GRCm38) |
C354S |
probably damaging |
Het |
Zfp69 |
G |
A |
4: 120,949,352 (GRCm38) |
T28I |
possibly damaging |
Het |
Zfp959 |
T |
C |
17: 55,897,299 (GRCm38) |
V112A |
probably benign |
Het |
Zfr2 |
T |
A |
10: 81,245,489 (GRCm38) |
W458R |
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 |
R8254:Vmn2r72
|
UTSW |
7 |
85,751,019 (GRCm38) |
missense |
probably damaging |
1.00 |
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 |
|