Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,195,749 (GRCm39) |
V570A |
probably damaging |
Het |
Abcb1a |
T |
C |
5: 8,748,637 (GRCm39) |
S323P |
possibly damaging |
Het |
Adcy8 |
C |
T |
15: 64,687,170 (GRCm39) |
D445N |
probably damaging |
Het |
Cdc14a |
A |
T |
3: 116,186,474 (GRCm39) |
Y102* |
probably null |
Het |
Cubn |
A |
G |
2: 13,313,472 (GRCm39) |
|
probably benign |
Het |
Dcaf7 |
T |
C |
11: 105,944,653 (GRCm39) |
S279P |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,511,567 (GRCm39) |
Q1514R |
probably damaging |
Het |
Dtx2 |
G |
A |
5: 136,055,420 (GRCm39) |
S369N |
possibly damaging |
Het |
Dusp11 |
A |
G |
6: 85,930,376 (GRCm39) |
F136S |
probably damaging |
Het |
Fbxo32 |
T |
C |
15: 58,047,632 (GRCm39) |
D227G |
probably damaging |
Het |
Flg2 |
T |
A |
3: 93,120,773 (GRCm39) |
V1215E |
unknown |
Het |
Flg2 |
A |
T |
3: 93,122,777 (GRCm39) |
D1649V |
unknown |
Het |
Gabbr2 |
T |
C |
4: 46,674,524 (GRCm39) |
K821R |
probably damaging |
Het |
Gga2 |
T |
C |
7: 121,590,761 (GRCm39) |
T516A |
probably benign |
Het |
Gm15446 |
T |
A |
5: 110,088,668 (GRCm39) |
*64K |
probably null |
Het |
Gm5900 |
T |
C |
7: 104,599,361 (GRCm39) |
|
noncoding transcript |
Het |
Il17rb |
A |
G |
14: 29,725,637 (GRCm39) |
F121S |
probably damaging |
Het |
Ip6k3 |
C |
A |
17: 27,370,034 (GRCm39) |
R128L |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,754,250 (GRCm39) |
|
probably benign |
Het |
Lrrn4 |
A |
G |
2: 132,719,996 (GRCm39) |
L268P |
probably damaging |
Het |
Mthfd1l |
C |
A |
10: 3,966,738 (GRCm39) |
S332R |
probably damaging |
Het |
Or12d12 |
C |
T |
17: 37,610,629 (GRCm39) |
R228H |
probably benign |
Het |
Or5t17 |
G |
A |
2: 86,832,495 (GRCm39) |
V61I |
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,592,569 (GRCm39) |
E25G |
probably damaging |
Het |
Prima1 |
A |
T |
12: 103,169,047 (GRCm39) |
|
probably null |
Het |
Rbm26 |
A |
G |
14: 105,368,968 (GRCm39) |
V737A |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,616,644 (GRCm39) |
|
probably null |
Het |
Sema5b |
G |
T |
16: 35,465,793 (GRCm39) |
C114F |
probably damaging |
Het |
Spata31f1e |
A |
C |
4: 42,794,014 (GRCm39) |
S39R |
probably damaging |
Het |
Speg |
T |
C |
1: 75,407,581 (GRCm39) |
V3196A |
probably damaging |
Het |
Svs3b |
T |
C |
2: 164,097,943 (GRCm39) |
Y126C |
probably benign |
Het |
Tmem171 |
T |
C |
13: 98,828,683 (GRCm39) |
|
probably null |
Het |
Tnrc6b |
T |
A |
15: 80,763,883 (GRCm39) |
W462R |
probably benign |
Het |
Trdmt1 |
T |
C |
2: 13,524,739 (GRCm39) |
R239G |
probably benign |
Het |
Usp5 |
A |
T |
6: 124,796,350 (GRCm39) |
V583E |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,602,111 (GRCm39) |
V639A |
probably benign |
Het |
Vwa3a |
A |
G |
7: 120,383,197 (GRCm39) |
I599M |
probably benign |
Het |
|
Other mutations in Vmn1r206 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02016:Vmn1r206
|
APN |
13 |
22,804,334 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02754:Vmn1r206
|
APN |
13 |
22,805,060 (GRCm39) |
nonsense |
probably null |
|
R0317:Vmn1r206
|
UTSW |
13 |
22,805,130 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0570:Vmn1r206
|
UTSW |
13 |
22,804,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1056:Vmn1r206
|
UTSW |
13 |
22,804,784 (GRCm39) |
missense |
probably benign |
0.10 |
R1497:Vmn1r206
|
UTSW |
13 |
22,805,160 (GRCm39) |
missense |
probably benign |
0.23 |
R2018:Vmn1r206
|
UTSW |
13 |
22,804,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Vmn1r206
|
UTSW |
13 |
22,804,782 (GRCm39) |
missense |
probably benign |
0.09 |
R2129:Vmn1r206
|
UTSW |
13 |
22,804,782 (GRCm39) |
missense |
probably benign |
0.09 |
R5159:Vmn1r206
|
UTSW |
13 |
22,804,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7692:Vmn1r206
|
UTSW |
13 |
22,804,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Vmn1r206
|
UTSW |
13 |
22,804,839 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7910:Vmn1r206
|
UTSW |
13 |
22,804,471 (GRCm39) |
nonsense |
probably null |
|
R9580:Vmn1r206
|
UTSW |
13 |
22,804,890 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Vmn1r206
|
UTSW |
13 |
22,804,724 (GRCm39) |
missense |
possibly damaging |
0.53 |
|