Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,126,398 (GRCm39) |
T1186A |
probably benign |
Het |
Adprhl1 |
C |
T |
8: 13,298,682 (GRCm39) |
V83I |
probably damaging |
Het |
Afap1 |
A |
G |
5: 36,092,995 (GRCm39) |
N33S |
probably benign |
Het |
Afap1 |
G |
A |
5: 36,141,396 (GRCm39) |
|
probably null |
Het |
Ampd3 |
A |
G |
7: 110,377,147 (GRCm39) |
D46G |
probably damaging |
Het |
Anks4b |
A |
G |
7: 119,781,707 (GRCm39) |
K246R |
probably benign |
Het |
Aqp9 |
C |
T |
9: 71,030,290 (GRCm39) |
V192M |
probably damaging |
Het |
Aspscr1 |
T |
G |
11: 120,599,443 (GRCm39) |
S132A |
|
Het |
Atp2b4 |
C |
A |
1: 133,658,320 (GRCm39) |
R530L |
probably damaging |
Het |
Bahcc1 |
T |
C |
11: 120,163,325 (GRCm39) |
V541A |
probably benign |
Het |
Caprin1 |
A |
T |
2: 103,603,093 (GRCm39) |
V490E |
probably damaging |
Het |
Ccdc7a |
T |
A |
8: 129,643,627 (GRCm39) |
K734M |
probably damaging |
Het |
Ccdc9b |
G |
T |
2: 118,590,146 (GRCm39) |
P233T |
probably benign |
Het |
Cdc16 |
A |
G |
8: 13,812,882 (GRCm39) |
K138R |
probably benign |
Het |
Cela2a |
A |
G |
4: 141,549,617 (GRCm39) |
S53P |
possibly damaging |
Het |
Clca3a2 |
A |
G |
3: 144,513,075 (GRCm39) |
|
probably null |
Het |
Cntrob |
T |
C |
11: 69,206,047 (GRCm39) |
E373G |
possibly damaging |
Het |
Csmd2 |
T |
C |
4: 128,414,058 (GRCm39) |
Y2633H |
|
Het |
Ctbp1 |
A |
T |
5: 33,407,688 (GRCm39) |
M296K |
probably benign |
Het |
Dido1 |
G |
T |
2: 180,303,501 (GRCm39) |
Q1468K |
possibly damaging |
Het |
Dnah7b |
T |
C |
1: 46,272,739 (GRCm39) |
F2289S |
probably damaging |
Het |
Fndc7 |
T |
A |
3: 108,779,452 (GRCm39) |
D364V |
possibly damaging |
Het |
Ggt7 |
G |
T |
2: 155,347,892 (GRCm39) |
H180Q |
probably damaging |
Het |
Gm14399 |
A |
T |
2: 174,973,273 (GRCm39) |
C161S |
probably damaging |
Het |
Gm17324 |
T |
C |
9: 78,355,794 (GRCm39) |
T62A |
unknown |
Het |
Gpr107 |
A |
G |
2: 31,078,716 (GRCm39) |
I384V |
probably damaging |
Het |
Igsf10 |
C |
A |
3: 59,227,125 (GRCm39) |
V2183L |
possibly damaging |
Het |
Il23r |
T |
A |
6: 67,411,648 (GRCm39) |
H363L |
possibly damaging |
Het |
Inka2 |
T |
A |
3: 105,623,761 (GRCm39) |
L45H |
probably damaging |
Het |
Iqsec1 |
A |
T |
6: 90,667,252 (GRCm39) |
I291N |
probably damaging |
Het |
Kcnc3 |
A |
T |
7: 44,245,569 (GRCm39) |
T620S |
probably benign |
Het |
Kif2b |
T |
C |
11: 91,466,571 (GRCm39) |
N571D |
probably benign |
Het |
Klrb1c |
T |
A |
6: 128,766,072 (GRCm39) |
|
probably benign |
Het |
Mgst2 |
A |
G |
3: 51,584,991 (GRCm39) |
N55S |
probably damaging |
Het |
Neb |
T |
C |
2: 52,102,746 (GRCm39) |
D4509G |
probably damaging |
Het |
Obox1 |
G |
T |
7: 15,289,456 (GRCm39) |
V82F |
probably benign |
Het |
Or4k51 |
A |
T |
2: 111,585,163 (GRCm39) |
M190L |
probably benign |
Het |
Or5p59 |
A |
G |
7: 107,703,053 (GRCm39) |
D179G |
probably benign |
Het |
Or7e174 |
T |
C |
9: 20,012,780 (GRCm39) |
S242P |
probably damaging |
Het |
Pakap |
A |
T |
4: 57,710,045 (GRCm39) |
N330I |
probably damaging |
Het |
Phf21a |
A |
T |
2: 92,189,512 (GRCm39) |
E590D |
probably damaging |
Het |
Rai14 |
T |
C |
15: 10,574,287 (GRCm39) |
|
probably null |
Het |
Rfx7 |
T |
C |
9: 72,524,096 (GRCm39) |
Y429H |
probably damaging |
Het |
Spata31d1d |
G |
T |
13: 59,878,606 (GRCm39) |
A77E |
probably benign |
Het |
Stra8 |
A |
G |
6: 34,907,816 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
G |
10: 5,200,919 (GRCm39) |
S3550P |
possibly damaging |
Het |
Tars2 |
A |
T |
3: 95,657,693 (GRCm39) |
H249Q |
probably damaging |
Het |
Tomm5 |
T |
C |
4: 45,107,969 (GRCm39) |
E22G |
probably benign |
Het |
Tor1a |
A |
G |
2: 30,853,704 (GRCm39) |
|
probably null |
Het |
Trim43b |
A |
G |
9: 88,973,538 (GRCm39) |
I65T |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,781,739 (GRCm39) |
M640T |
possibly damaging |
Het |
Vegfa |
A |
T |
17: 46,336,377 (GRCm39) |
Y248N |
probably damaging |
Het |
Vmn1r29 |
G |
T |
6: 58,284,834 (GRCm39) |
V185F |
probably benign |
Het |
Wdfy4 |
G |
A |
14: 32,826,072 (GRCm39) |
P1193L |
|
Het |
Wdfy4 |
T |
C |
14: 32,792,705 (GRCm39) |
K2114E |
|
Het |
|
Other mutations in Vmn1r172 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02295:Vmn1r172
|
APN |
7 |
23,359,342 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02407:Vmn1r172
|
APN |
7 |
23,359,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Vmn1r172
|
APN |
7 |
23,359,350 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03090:Vmn1r172
|
APN |
7 |
23,359,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R0396:Vmn1r172
|
UTSW |
7 |
23,359,957 (GRCm39) |
missense |
probably benign |
0.06 |
R1087:Vmn1r172
|
UTSW |
7 |
23,359,673 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1502:Vmn1r172
|
UTSW |
7 |
23,359,681 (GRCm39) |
nonsense |
probably null |
|
R1701:Vmn1r172
|
UTSW |
7 |
23,359,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R1882:Vmn1r172
|
UTSW |
7 |
23,359,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R2272:Vmn1r172
|
UTSW |
7 |
23,359,616 (GRCm39) |
missense |
probably damaging |
0.98 |
R4646:Vmn1r172
|
UTSW |
7 |
23,359,919 (GRCm39) |
missense |
probably benign |
0.03 |
R4653:Vmn1r172
|
UTSW |
7 |
23,359,997 (GRCm39) |
missense |
probably damaging |
0.96 |
R4709:Vmn1r172
|
UTSW |
7 |
23,359,606 (GRCm39) |
missense |
probably benign |
0.25 |
R4937:Vmn1r172
|
UTSW |
7 |
23,359,312 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4945:Vmn1r172
|
UTSW |
7 |
23,359,745 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5840:Vmn1r172
|
UTSW |
7 |
23,359,600 (GRCm39) |
missense |
probably benign |
0.03 |
R6154:Vmn1r172
|
UTSW |
7 |
23,359,583 (GRCm39) |
missense |
probably damaging |
0.96 |
R6317:Vmn1r172
|
UTSW |
7 |
23,359,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7206:Vmn1r172
|
UTSW |
7 |
23,359,582 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7290:Vmn1r172
|
UTSW |
7 |
23,360,048 (GRCm39) |
missense |
unknown |
|
R7362:Vmn1r172
|
UTSW |
7 |
23,359,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R7369:Vmn1r172
|
UTSW |
7 |
23,360,030 (GRCm39) |
missense |
unknown |
|
R7528:Vmn1r172
|
UTSW |
7 |
23,359,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R8193:Vmn1r172
|
UTSW |
7 |
23,359,752 (GRCm39) |
nonsense |
probably null |
|
R8540:Vmn1r172
|
UTSW |
7 |
23,359,498 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8863:Vmn1r172
|
UTSW |
7 |
23,359,210 (GRCm39) |
missense |
probably benign |
0.08 |
R8974:Vmn1r172
|
UTSW |
7 |
23,359,840 (GRCm39) |
missense |
probably benign |
0.06 |
R9006:Vmn1r172
|
UTSW |
7 |
23,359,402 (GRCm39) |
missense |
probably benign |
0.04 |
R9021:Vmn1r172
|
UTSW |
7 |
23,359,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Vmn1r172
|
UTSW |
7 |
23,359,593 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9604:Vmn1r172
|
UTSW |
7 |
23,359,193 (GRCm39) |
missense |
possibly damaging |
0.68 |
U24488:Vmn1r172
|
UTSW |
7 |
23,359,171 (GRCm39) |
missense |
probably benign |
0.02 |
|