Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambn |
G |
A |
5: 88,604,807 (GRCm39) |
V27M |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,578,015 (GRCm39) |
N222D |
probably damaging |
Het |
Bcas3 |
A |
T |
11: 85,422,756 (GRCm39) |
T542S |
probably damaging |
Het |
Btbd1 |
A |
T |
7: 81,455,507 (GRCm39) |
I288N |
probably damaging |
Het |
Ctps1 |
C |
T |
4: 120,399,776 (GRCm39) |
V500I |
possibly damaging |
Het |
Cul5 |
A |
C |
9: 53,546,337 (GRCm39) |
V345G |
probably damaging |
Het |
Dchs1 |
A |
G |
7: 105,421,776 (GRCm39) |
Y215H |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 49,973,566 (GRCm39) |
M67K |
possibly damaging |
Het |
Egln2 |
C |
T |
7: 26,859,291 (GRCm39) |
E353K |
possibly damaging |
Het |
Fbxw5 |
G |
T |
2: 25,393,746 (GRCm39) |
A325S |
probably benign |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Gaa |
A |
G |
11: 119,172,091 (GRCm39) |
*207W |
probably null |
Het |
Herc2 |
A |
G |
7: 55,856,492 (GRCm39) |
T3947A |
probably damaging |
Het |
Ifit2 |
T |
A |
19: 34,551,624 (GRCm39) |
I388N |
probably damaging |
Het |
Ikzf4 |
T |
C |
10: 128,472,591 (GRCm39) |
T209A |
possibly damaging |
Het |
Il17re |
A |
T |
6: 113,445,472 (GRCm39) |
|
probably benign |
Het |
Insrr |
T |
A |
3: 87,708,029 (GRCm39) |
L157Q |
probably damaging |
Het |
Kcnq2 |
T |
G |
2: 180,723,483 (GRCm39) |
Y631S |
probably damaging |
Het |
Lrrfip1 |
A |
G |
1: 91,039,890 (GRCm39) |
I198V |
probably benign |
Het |
Mir7684 |
A |
T |
15: 82,273,345 (GRCm39) |
|
probably benign |
Het |
Mphosph9 |
C |
T |
5: 124,398,150 (GRCm39) |
E1049K |
probably damaging |
Het |
Mroh1 |
G |
A |
15: 76,313,360 (GRCm39) |
R611Q |
probably benign |
Het |
Mynn |
A |
T |
3: 30,661,280 (GRCm39) |
I121F |
possibly damaging |
Het |
Ndrg2 |
G |
A |
14: 52,148,566 (GRCm39) |
R32C |
probably damaging |
Het |
Or2ab1 |
T |
C |
11: 58,488,630 (GRCm39) |
I138T |
probably benign |
Het |
Or4p7 |
A |
G |
2: 88,221,725 (GRCm39) |
I45V |
probably benign |
Het |
Ppp1r9b |
A |
G |
11: 94,892,936 (GRCm39) |
E260G |
probably damaging |
Het |
Psd4 |
A |
G |
2: 24,291,756 (GRCm39) |
S652G |
probably damaging |
Het |
Psg25 |
C |
T |
7: 18,255,268 (GRCm39) |
R416H |
probably benign |
Het |
Pygm |
T |
A |
19: 6,438,301 (GRCm39) |
N171K |
probably damaging |
Het |
Rbm46 |
A |
T |
3: 82,771,723 (GRCm39) |
D297E |
possibly damaging |
Het |
Selenov |
T |
A |
7: 27,990,004 (GRCm39) |
T167S |
probably benign |
Het |
Serpina10 |
T |
C |
12: 103,583,208 (GRCm39) |
Y358C |
probably damaging |
Het |
Slc27a3 |
T |
C |
3: 90,295,002 (GRCm39) |
R352G |
probably benign |
Het |
Snx33 |
T |
C |
9: 56,833,862 (GRCm39) |
D69G |
probably benign |
Het |
St8sia2 |
G |
T |
7: 73,616,594 (GRCm39) |
P127H |
probably damaging |
Het |
Thbd |
T |
C |
2: 148,248,401 (GRCm39) |
K489R |
probably benign |
Het |
Ttn |
A |
T |
2: 76,767,049 (GRCm39) |
C3039S |
probably damaging |
Het |
Xdh |
A |
G |
17: 74,220,960 (GRCm39) |
S590P |
possibly damaging |
Het |
Zfp827 |
G |
A |
8: 79,906,708 (GRCm39) |
V907I |
probably damaging |
Het |
|
Other mutations in Vmn1r167 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02137:Vmn1r167
|
APN |
7 |
23,204,864 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02963:Vmn1r167
|
APN |
7 |
23,204,975 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0054:Vmn1r167
|
UTSW |
7 |
23,204,334 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0555:Vmn1r167
|
UTSW |
7 |
23,204,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Vmn1r167
|
UTSW |
7 |
23,204,548 (GRCm39) |
missense |
probably benign |
0.01 |
R1312:Vmn1r167
|
UTSW |
7 |
23,204,548 (GRCm39) |
missense |
probably benign |
0.01 |
R1464:Vmn1r167
|
UTSW |
7 |
23,204,681 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1464:Vmn1r167
|
UTSW |
7 |
23,204,681 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1532:Vmn1r167
|
UTSW |
7 |
23,204,204 (GRCm39) |
missense |
probably benign |
0.01 |
R1937:Vmn1r167
|
UTSW |
7 |
23,204,452 (GRCm39) |
missense |
probably benign |
0.25 |
R2162:Vmn1r167
|
UTSW |
7 |
23,204,224 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4639:Vmn1r167
|
UTSW |
7 |
23,205,011 (GRCm39) |
missense |
probably benign |
0.00 |
R4661:Vmn1r167
|
UTSW |
7 |
23,204,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R4845:Vmn1r167
|
UTSW |
7 |
23,204,158 (GRCm39) |
missense |
probably benign |
0.01 |
R4868:Vmn1r167
|
UTSW |
7 |
23,204,161 (GRCm39) |
missense |
probably benign |
|
R4993:Vmn1r167
|
UTSW |
7 |
23,204,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Vmn1r167
|
UTSW |
7 |
23,204,646 (GRCm39) |
nonsense |
probably null |
|
R6622:Vmn1r167
|
UTSW |
7 |
23,205,014 (GRCm39) |
start codon destroyed |
probably null |
|
R7800:Vmn1r167
|
UTSW |
7 |
23,204,069 (GRCm39) |
makesense |
probably null |
|
R8297:Vmn1r167
|
UTSW |
7 |
23,204,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8365:Vmn1r167
|
UTSW |
7 |
23,204,200 (GRCm39) |
missense |
probably benign |
0.03 |
R8411:Vmn1r167
|
UTSW |
7 |
23,204,981 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9667:Vmn1r167
|
UTSW |
7 |
23,204,990 (GRCm39) |
missense |
probably benign |
0.06 |
|