Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
T |
A |
12: 84,660,745 (GRCm39) |
H116L |
probably damaging |
Het |
Anapc4 |
C |
T |
5: 53,019,581 (GRCm39) |
S581L |
probably benign |
Het |
Ano8 |
A |
C |
8: 71,935,887 (GRCm39) |
D276E |
probably damaging |
Het |
Aspm |
G |
A |
1: 139,407,407 (GRCm39) |
R2098H |
probably benign |
Het |
Bend7 |
G |
A |
2: 4,768,052 (GRCm39) |
R336Q |
probably damaging |
Het |
Bpifb4 |
G |
A |
2: 153,784,843 (GRCm39) |
G184S |
probably damaging |
Het |
Cbx8 |
T |
C |
11: 118,930,137 (GRCm39) |
D152G |
probably benign |
Het |
Cdca2 |
A |
G |
14: 67,943,078 (GRCm39) |
|
probably null |
Het |
Cgn |
G |
A |
3: 94,680,945 (GRCm39) |
A531V |
probably benign |
Het |
Cmya5 |
C |
A |
13: 93,182,374 (GRCm39) |
|
probably null |
Het |
Cntnap3 |
A |
G |
13: 64,935,769 (GRCm39) |
S365P |
probably damaging |
Het |
Crnn |
A |
G |
3: 93,056,330 (GRCm39) |
Q372R |
probably damaging |
Het |
Ehf |
T |
A |
2: 103,097,124 (GRCm39) |
E276V |
probably damaging |
Het |
Eif4g3 |
T |
A |
4: 137,890,744 (GRCm39) |
|
probably null |
Het |
Enpep |
C |
T |
3: 129,102,748 (GRCm39) |
D403N |
probably damaging |
Het |
Enpp1 |
T |
C |
10: 24,530,806 (GRCm39) |
E550G |
probably damaging |
Het |
Entpd8 |
A |
G |
2: 24,974,346 (GRCm39) |
D377G |
probably benign |
Het |
Epc2 |
T |
A |
2: 49,437,619 (GRCm39) |
|
probably null |
Het |
Erich3 |
G |
T |
3: 154,439,210 (GRCm39) |
G481V |
probably damaging |
Het |
Fank1 |
A |
G |
7: 133,471,075 (GRCm39) |
Y156C |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,929,203 (GRCm39) |
D3869G |
probably damaging |
Het |
Gcnt2 |
A |
G |
13: 41,071,675 (GRCm39) |
D106G |
probably benign |
Het |
Gm20830 |
A |
T |
Y: 6,916,501 (GRCm39) |
V206E |
probably benign |
Het |
Gmpr2 |
T |
C |
14: 55,914,691 (GRCm39) |
V228A |
possibly damaging |
Het |
Gon4l |
TGAGCA |
TGAGCAGAGCA |
3: 88,803,523 (GRCm39) |
|
probably null |
Het |
Gtpbp1 |
G |
A |
15: 79,596,375 (GRCm39) |
|
probably null |
Het |
Hhat |
A |
T |
1: 192,399,327 (GRCm39) |
M271K |
probably damaging |
Het |
Hipk2 |
A |
T |
6: 38,795,810 (GRCm39) |
M153K |
possibly damaging |
Het |
Hydin |
A |
T |
8: 111,261,915 (GRCm39) |
H2672L |
probably benign |
Het |
Igfbpl1 |
A |
T |
4: 45,826,374 (GRCm39) |
D140E |
probably damaging |
Het |
Kctd1 |
T |
G |
18: 15,196,573 (GRCm39) |
|
probably benign |
Het |
Lax1 |
A |
T |
1: 133,608,316 (GRCm39) |
Y142N |
probably damaging |
Het |
Lpin2 |
C |
T |
17: 71,551,798 (GRCm39) |
R733C |
probably damaging |
Het |
Morn4 |
A |
G |
19: 42,064,556 (GRCm39) |
L144P |
possibly damaging |
Het |
Nup214 |
C |
A |
2: 31,924,385 (GRCm39) |
T1638K |
probably damaging |
Het |
Nyap1 |
C |
T |
5: 137,733,246 (GRCm39) |
A596T |
probably damaging |
Het |
Oas1d |
T |
C |
5: 121,053,074 (GRCm39) |
M43T |
probably benign |
Het |
Or4l15 |
T |
C |
14: 50,198,080 (GRCm39) |
T150A |
probably benign |
Het |
Or6x1 |
T |
C |
9: 40,098,897 (GRCm39) |
V162A |
probably benign |
Het |
Or8b42 |
A |
G |
9: 38,342,472 (GRCm39) |
H298R |
probably benign |
Het |
Pacs1 |
A |
G |
19: 5,186,819 (GRCm39) |
F851S |
probably damaging |
Het |
Pcdh17 |
A |
G |
14: 84,683,800 (GRCm39) |
Q89R |
probably damaging |
Het |
Phrf1 |
A |
G |
7: 140,838,378 (GRCm39) |
|
probably benign |
Het |
Plekhb1 |
A |
T |
7: 100,304,602 (GRCm39) |
I34N |
probably damaging |
Het |
Ralgapa2 |
T |
C |
2: 146,175,397 (GRCm39) |
E1800G |
probably damaging |
Het |
Rbm33 |
A |
T |
5: 28,544,010 (GRCm39) |
I89F |
probably damaging |
Het |
Rtl1 |
T |
A |
12: 109,560,531 (GRCm39) |
E436V |
probably damaging |
Het |
Slc2a4 |
G |
T |
11: 69,837,217 (GRCm39) |
P73Q |
probably damaging |
Het |
Sorbs2 |
A |
T |
8: 46,245,912 (GRCm39) |
T311S |
probably benign |
Het |
Sulf2 |
G |
A |
2: 165,974,678 (GRCm39) |
A2V |
probably benign |
Het |
Supt16 |
A |
T |
14: 52,411,601 (GRCm39) |
|
probably null |
Het |
Vmn2r39 |
T |
A |
7: 9,028,150 (GRCm39) |
H407L |
possibly damaging |
Het |
Vmn2r84 |
T |
A |
10: 130,225,064 (GRCm39) |
Y482F |
probably benign |
Het |
Vps9d1 |
T |
C |
8: 123,973,655 (GRCm39) |
E376G |
probably benign |
Het |
Wrn |
C |
A |
8: 33,814,346 (GRCm39) |
G366V |
probably benign |
Het |
|
Other mutations in Vmn1r26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02517:Vmn1r26
|
APN |
6 |
57,986,127 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02609:Vmn1r26
|
APN |
6 |
57,985,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R1121:Vmn1r26
|
UTSW |
6 |
57,985,647 (GRCm39) |
missense |
probably benign |
0.43 |
R1881:Vmn1r26
|
UTSW |
6 |
57,985,650 (GRCm39) |
missense |
probably benign |
0.20 |
R1958:Vmn1r26
|
UTSW |
6 |
57,985,286 (GRCm39) |
missense |
probably benign |
0.01 |
R1978:Vmn1r26
|
UTSW |
6 |
57,986,111 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2106:Vmn1r26
|
UTSW |
6 |
57,985,710 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2117:Vmn1r26
|
UTSW |
6 |
57,985,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2323:Vmn1r26
|
UTSW |
6 |
57,985,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Vmn1r26
|
UTSW |
6 |
57,985,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R6355:Vmn1r26
|
UTSW |
6 |
57,985,536 (GRCm39) |
missense |
probably benign |
0.02 |
R6948:Vmn1r26
|
UTSW |
6 |
57,985,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R7114:Vmn1r26
|
UTSW |
6 |
57,985,755 (GRCm39) |
missense |
probably benign |
0.02 |
R7977:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R7987:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R8311:Vmn1r26
|
UTSW |
6 |
57,985,518 (GRCm39) |
missense |
probably benign |
0.39 |
R8442:Vmn1r26
|
UTSW |
6 |
57,985,728 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8784:Vmn1r26
|
UTSW |
6 |
57,985,440 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9129:Vmn1r26
|
UTSW |
6 |
57,985,373 (GRCm39) |
missense |
|
|
RF020:Vmn1r26
|
UTSW |
6 |
57,985,705 (GRCm39) |
missense |
probably benign |
0.35 |
Z1176:Vmn1r26
|
UTSW |
6 |
57,985,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|