Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004B18Rik |
T |
A |
3: 145,644,018 (GRCm39) |
F69I |
possibly damaging |
Het |
Acot12 |
C |
T |
13: 91,932,882 (GRCm39) |
L552F |
probably benign |
Het |
Aff4 |
T |
A |
11: 53,301,726 (GRCm39) |
|
probably benign |
Het |
Aldh18a1 |
A |
G |
19: 40,539,725 (GRCm39) |
V750A |
probably damaging |
Het |
Anapc1 |
A |
G |
2: 128,469,149 (GRCm39) |
|
probably benign |
Het |
Arl6ip1 |
AAAATAAATAAATAAATAAATAAATA |
AAAATAAATAAATAAATAAATAAATAAATA |
7: 117,721,122 (GRCm39) |
|
probably benign |
Het |
Bcl11b |
A |
T |
12: 107,883,684 (GRCm39) |
|
probably null |
Het |
Ccpg1 |
C |
A |
9: 72,919,449 (GRCm39) |
Q355K |
probably benign |
Het |
Cdc42bpb |
G |
A |
12: 111,260,573 (GRCm39) |
P1702S |
probably benign |
Het |
Ddx20 |
G |
T |
3: 105,586,249 (GRCm39) |
Q699K |
probably benign |
Het |
Ecd |
A |
G |
14: 20,374,632 (GRCm39) |
S503P |
probably damaging |
Het |
Etaa1 |
C |
T |
11: 17,890,281 (GRCm39) |
R860Q |
probably damaging |
Het |
Ffar2 |
T |
A |
7: 30,519,093 (GRCm39) |
Y149F |
probably damaging |
Het |
Gamt |
T |
A |
10: 80,096,558 (GRCm39) |
R60* |
probably null |
Het |
Gm6871 |
T |
C |
7: 41,195,510 (GRCm39) |
N302S |
probably damaging |
Het |
Hps3 |
A |
G |
3: 20,083,393 (GRCm39) |
S135P |
probably damaging |
Het |
Ifi203 |
T |
A |
1: 173,764,106 (GRCm39) |
N122I |
probably damaging |
Het |
Leng9 |
T |
C |
7: 4,152,433 (GRCm39) |
D81G |
possibly damaging |
Het |
Lrrc23 |
T |
A |
6: 124,747,804 (GRCm39) |
K262* |
probably null |
Het |
Morc2b |
T |
A |
17: 33,357,401 (GRCm39) |
T124S |
probably benign |
Het |
Mroh1 |
G |
A |
15: 76,286,326 (GRCm39) |
|
probably null |
Het |
Naxe |
T |
C |
3: 87,964,011 (GRCm39) |
K240R |
probably benign |
Het |
Ncan |
C |
A |
8: 70,562,727 (GRCm39) |
E510D |
possibly damaging |
Het |
Ndufs4 |
A |
T |
13: 114,444,390 (GRCm39) |
S129R |
probably benign |
Het |
Oog2 |
A |
G |
4: 143,920,523 (GRCm39) |
|
probably benign |
Het |
Or5h18 |
A |
T |
16: 58,847,931 (GRCm39) |
F113Y |
probably damaging |
Het |
Or8h8 |
T |
C |
2: 86,753,222 (GRCm39) |
Y218C |
probably damaging |
Het |
Or8j3c |
C |
A |
2: 86,253,544 (GRCm39) |
V159L |
possibly damaging |
Het |
Papola |
G |
A |
12: 105,767,010 (GRCm39) |
|
probably null |
Het |
Pasd1 |
T |
C |
X: 70,983,161 (GRCm39) |
C378R |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,056,453 (GRCm39) |
S4517P |
probably damaging |
Het |
Rpap1 |
C |
T |
2: 119,604,660 (GRCm39) |
R416H |
probably damaging |
Het |
Rpl31-ps17 |
C |
T |
12: 54,748,397 (GRCm39) |
|
noncoding transcript |
Het |
Rxfp2 |
G |
A |
5: 149,975,020 (GRCm39) |
V210I |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,484,020 (GRCm39) |
D3909G |
probably damaging |
Het |
Spata31d1a |
T |
A |
13: 59,852,861 (GRCm39) |
K76N |
possibly damaging |
Het |
Srgn |
A |
G |
10: 62,333,613 (GRCm39) |
F55L |
possibly damaging |
Het |
Tmem54 |
G |
A |
4: 129,004,504 (GRCm39) |
R151Q |
probably damaging |
Het |
Tns1 |
T |
A |
1: 73,953,790 (GRCm39) |
N1848Y |
probably damaging |
Het |
Trim33 |
G |
T |
3: 103,217,630 (GRCm39) |
V192L |
possibly damaging |
Het |
Trpm5 |
G |
T |
7: 142,642,792 (GRCm39) |
L52I |
probably benign |
Het |
Uaca |
A |
G |
9: 60,779,035 (GRCm39) |
S1141G |
probably benign |
Het |
Vmn2r50 |
T |
C |
7: 9,774,309 (GRCm39) |
K529R |
probably benign |
Het |
Vmn2r9 |
T |
C |
5: 108,995,743 (GRCm39) |
T302A |
possibly damaging |
Het |
Ylpm1 |
T |
C |
12: 85,104,177 (GRCm39) |
|
probably benign |
Het |
Zfp410 |
G |
A |
12: 84,374,206 (GRCm39) |
R181H |
probably damaging |
Het |
|
Other mutations in Vmn1r63 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02465:Vmn1r63
|
APN |
7 |
5,806,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02897:Vmn1r63
|
APN |
7 |
5,805,744 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03032:Vmn1r63
|
APN |
7 |
5,806,350 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03190:Vmn1r63
|
APN |
7 |
5,806,110 (GRCm39) |
missense |
probably benign |
0.00 |
R0118:Vmn1r63
|
UTSW |
7 |
5,805,838 (GRCm39) |
missense |
probably benign |
0.00 |
R0227:Vmn1r63
|
UTSW |
7 |
5,805,741 (GRCm39) |
nonsense |
probably null |
|
R0323:Vmn1r63
|
UTSW |
7 |
5,806,335 (GRCm39) |
missense |
probably benign |
0.03 |
R0610:Vmn1r63
|
UTSW |
7 |
5,806,063 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0630:Vmn1r63
|
UTSW |
7 |
5,806,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Vmn1r63
|
UTSW |
7 |
5,806,609 (GRCm39) |
missense |
probably benign |
0.24 |
R1916:Vmn1r63
|
UTSW |
7 |
5,806,225 (GRCm39) |
missense |
probably damaging |
0.96 |
R1993:Vmn1r63
|
UTSW |
7 |
5,806,254 (GRCm39) |
missense |
probably benign |
0.12 |
R1994:Vmn1r63
|
UTSW |
7 |
5,806,254 (GRCm39) |
missense |
probably benign |
0.12 |
R2209:Vmn1r63
|
UTSW |
7 |
5,806,212 (GRCm39) |
missense |
probably damaging |
0.99 |
R3787:Vmn1r63
|
UTSW |
7 |
5,805,751 (GRCm39) |
missense |
probably benign |
|
R4702:Vmn1r63
|
UTSW |
7 |
5,806,516 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4728:Vmn1r63
|
UTSW |
7 |
5,806,362 (GRCm39) |
missense |
probably damaging |
0.99 |
R5410:Vmn1r63
|
UTSW |
7 |
5,806,189 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5796:Vmn1r63
|
UTSW |
7 |
5,806,140 (GRCm39) |
missense |
probably benign |
|
R6580:Vmn1r63
|
UTSW |
7 |
5,805,913 (GRCm39) |
missense |
probably benign |
0.02 |
R6723:Vmn1r63
|
UTSW |
7 |
5,805,948 (GRCm39) |
missense |
probably damaging |
0.96 |
R7418:Vmn1r63
|
UTSW |
7 |
5,806,554 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7476:Vmn1r63
|
UTSW |
7 |
5,806,000 (GRCm39) |
missense |
probably benign |
0.13 |
R7769:Vmn1r63
|
UTSW |
7 |
5,806,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8912:Vmn1r63
|
UTSW |
7 |
5,806,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9684:Vmn1r63
|
UTSW |
7 |
5,805,913 (GRCm39) |
missense |
probably benign |
0.02 |
X0027:Vmn1r63
|
UTSW |
7 |
5,805,930 (GRCm39) |
missense |
probably damaging |
1.00 |
|