Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028K03Rik |
A |
T |
5: 107,693,575 (GRCm39) |
D64V |
probably damaging |
Het |
Ankdd1a |
A |
C |
9: 65,414,932 (GRCm39) |
I268S |
possibly damaging |
Het |
Atad3a |
C |
T |
4: 155,834,595 (GRCm39) |
R402Q |
probably benign |
Het |
C3ar1 |
A |
G |
6: 122,827,746 (GRCm39) |
V157A |
probably benign |
Het |
Cd200l1 |
A |
G |
16: 45,264,297 (GRCm39) |
F87S |
probably benign |
Het |
Cd55 |
C |
T |
1: 130,384,606 (GRCm39) |
V206I |
probably benign |
Het |
Cd8a |
A |
G |
6: 71,350,661 (GRCm39) |
D42G |
possibly damaging |
Het |
Cemip |
G |
T |
7: 83,593,147 (GRCm39) |
F1185L |
probably benign |
Het |
Cfap58 |
A |
G |
19: 47,963,953 (GRCm39) |
D527G |
probably damaging |
Het |
Cyp2a12 |
C |
A |
7: 26,734,198 (GRCm39) |
S377Y |
probably benign |
Het |
Dapk2 |
A |
G |
9: 66,175,968 (GRCm39) |
D289G |
probably benign |
Het |
Efcab6 |
G |
A |
15: 83,867,647 (GRCm39) |
A277V |
probably benign |
Het |
Ephx2 |
A |
T |
14: 66,339,671 (GRCm39) |
F250L |
probably damaging |
Het |
Flg2 |
A |
T |
3: 93,111,088 (GRCm39) |
S1039C |
unknown |
Het |
Gramd1a |
A |
G |
7: 30,832,021 (GRCm39) |
V674A |
probably benign |
Het |
Gtf2a1 |
A |
C |
12: 91,534,543 (GRCm39) |
V237G |
probably benign |
Het |
I830077J02Rik |
G |
A |
3: 105,833,886 (GRCm39) |
T90M |
probably damaging |
Het |
Jagn1 |
T |
A |
6: 113,424,398 (GRCm39) |
L90H |
probably damaging |
Het |
Mdn1 |
G |
T |
4: 32,746,527 (GRCm39) |
A4158S |
probably benign |
Het |
Myh11 |
G |
A |
16: 14,018,930 (GRCm39) |
A1839V |
|
Het |
Olr1 |
G |
A |
6: 129,476,869 (GRCm39) |
A132V |
probably damaging |
Het |
Paqr3 |
A |
T |
5: 97,251,330 (GRCm39) |
H131Q |
possibly damaging |
Het |
Pde4b |
A |
T |
4: 102,460,009 (GRCm39) |
T397S |
probably benign |
Het |
Pon1 |
A |
G |
6: 5,168,349 (GRCm39) |
C353R |
probably damaging |
Het |
Ppie |
G |
A |
4: 123,032,661 (GRCm39) |
T43I |
probably null |
Het |
Prr5l |
A |
G |
2: 101,588,875 (GRCm39) |
F92L |
probably damaging |
Het |
Rai14 |
T |
C |
15: 10,575,242 (GRCm39) |
Y601C |
probably damaging |
Het |
Rasal1 |
A |
G |
5: 120,808,441 (GRCm39) |
D491G |
probably damaging |
Het |
Rbm12b1 |
T |
A |
4: 12,145,441 (GRCm39) |
V471E |
probably damaging |
Het |
Scgb2b24 |
A |
T |
7: 33,438,036 (GRCm39) |
C24S |
probably damaging |
Het |
Slc17a5 |
C |
T |
9: 78,445,530 (GRCm39) |
V468M |
possibly damaging |
Het |
Tcp10c |
A |
G |
17: 13,576,772 (GRCm39) |
K117R |
possibly damaging |
Het |
Ubash3b |
A |
G |
9: 40,927,923 (GRCm39) |
S584P |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,709,386 (GRCm39) |
R1778C |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,967,665 (GRCm39) |
I220M |
probably benign |
Het |
Zfp474 |
C |
A |
18: 52,771,476 (GRCm39) |
T43K |
probably damaging |
Het |
Zscan4-ps3 |
G |
A |
7: 11,347,261 (GRCm39) |
M432I |
probably benign |
Het |
|
Other mutations in Rpusd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01729:Rpusd2
|
APN |
2 |
118,865,837 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02126:Rpusd2
|
APN |
2 |
118,869,119 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02136:Rpusd2
|
APN |
2 |
118,868,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Rpusd2
|
UTSW |
2 |
118,868,893 (GRCm39) |
missense |
probably benign |
|
R0211:Rpusd2
|
UTSW |
2 |
118,868,893 (GRCm39) |
missense |
probably benign |
|
R1295:Rpusd2
|
UTSW |
2 |
118,867,408 (GRCm39) |
missense |
probably benign |
0.39 |
R1866:Rpusd2
|
UTSW |
2 |
118,865,728 (GRCm39) |
missense |
probably benign |
0.13 |
R2060:Rpusd2
|
UTSW |
2 |
118,867,696 (GRCm39) |
critical splice donor site |
probably null |
|
R2567:Rpusd2
|
UTSW |
2 |
118,867,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Rpusd2
|
UTSW |
2 |
118,869,085 (GRCm39) |
missense |
probably benign |
0.00 |
R4133:Rpusd2
|
UTSW |
2 |
118,869,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R4486:Rpusd2
|
UTSW |
2 |
118,865,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R4874:Rpusd2
|
UTSW |
2 |
118,865,360 (GRCm39) |
missense |
probably benign |
0.00 |
R6235:Rpusd2
|
UTSW |
2 |
118,865,338 (GRCm39) |
missense |
probably benign |
|
R6801:Rpusd2
|
UTSW |
2 |
118,865,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R8505:Rpusd2
|
UTSW |
2 |
118,869,007 (GRCm39) |
missense |
probably benign |
0.00 |
R8802:Rpusd2
|
UTSW |
2 |
118,865,378 (GRCm39) |
missense |
probably benign |
|
|