Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apba1 |
T |
C |
19: 23,893,315 (GRCm39) |
S438P |
possibly damaging |
Het |
Atosa |
A |
G |
9: 74,926,265 (GRCm39) |
|
probably benign |
Het |
Atp2a1 |
A |
G |
7: 126,057,069 (GRCm39) |
|
probably benign |
Het |
Axin2 |
T |
C |
11: 108,840,096 (GRCm39) |
Y735H |
probably damaging |
Het |
Bicd2 |
T |
A |
13: 49,528,790 (GRCm39) |
L184Q |
probably damaging |
Het |
Bub1 |
G |
A |
2: 127,650,959 (GRCm39) |
T618I |
probably benign |
Het |
Catsperg2 |
A |
G |
7: 29,424,445 (GRCm39) |
|
probably benign |
Het |
Ccdc73 |
T |
A |
2: 104,759,915 (GRCm39) |
|
probably benign |
Het |
Crybg3 |
A |
T |
16: 59,386,019 (GRCm39) |
|
probably benign |
Het |
Dsp |
A |
G |
13: 38,381,340 (GRCm39) |
D2096G |
possibly damaging |
Het |
Eef2 |
C |
CN |
10: 81,014,602 (GRCm39) |
|
probably null |
Het |
Elp3 |
A |
G |
14: 65,768,975 (GRCm39) |
*548Q |
probably null |
Het |
Eno4 |
A |
G |
19: 58,956,985 (GRCm39) |
D357G |
probably damaging |
Het |
Fcrl2 |
A |
T |
3: 87,164,085 (GRCm39) |
I348N |
possibly damaging |
Het |
Fgl2 |
A |
T |
5: 21,580,347 (GRCm39) |
S230C |
probably damaging |
Het |
Ginm1 |
T |
A |
10: 7,655,070 (GRCm39) |
E57D |
possibly damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,267,143 (GRCm39) |
|
probably null |
Het |
Herc1 |
G |
T |
9: 66,307,438 (GRCm39) |
G1044V |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,553,157 (GRCm39) |
T2511M |
probably damaging |
Het |
Iba57 |
C |
T |
11: 59,049,727 (GRCm39) |
A207T |
probably benign |
Het |
Itga9 |
T |
A |
9: 118,465,617 (GRCm39) |
I157N |
probably damaging |
Het |
Kalrn |
A |
G |
16: 34,177,541 (GRCm39) |
L208P |
probably damaging |
Het |
Kcnj10 |
A |
G |
1: 172,196,491 (GRCm39) |
T2A |
probably benign |
Het |
Kdm1b |
T |
A |
13: 47,217,593 (GRCm39) |
C351S |
probably damaging |
Het |
Kif21a |
T |
C |
15: 90,855,060 (GRCm39) |
E700G |
probably damaging |
Het |
Mmd |
C |
T |
11: 90,150,824 (GRCm39) |
|
probably benign |
Het |
Mocs3 |
C |
T |
2: 168,073,602 (GRCm39) |
P350S |
probably benign |
Het |
Morn3 |
T |
C |
5: 123,184,726 (GRCm39) |
Y38C |
probably damaging |
Het |
Nacc1 |
A |
T |
8: 85,402,854 (GRCm39) |
V313D |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,267,771 (GRCm39) |
|
probably benign |
Het |
Neb |
T |
C |
2: 52,163,992 (GRCm39) |
K1989E |
possibly damaging |
Het |
Nlrp3 |
C |
T |
11: 59,455,954 (GRCm39) |
R917* |
probably null |
Het |
Nlrp4b |
T |
A |
7: 10,459,889 (GRCm39) |
Y463* |
probably null |
Het |
Perm1 |
A |
T |
4: 156,302,572 (GRCm39) |
D372V |
probably damaging |
Het |
Phf3 |
T |
C |
1: 30,847,848 (GRCm39) |
T1232A |
probably damaging |
Het |
Phldb3 |
G |
A |
7: 24,312,004 (GRCm39) |
R106Q |
probably benign |
Het |
Pld4 |
T |
A |
12: 112,734,291 (GRCm39) |
F386I |
probably benign |
Het |
Prex2 |
T |
A |
1: 11,230,380 (GRCm39) |
L802Q |
probably damaging |
Het |
Psd3 |
A |
G |
8: 68,335,631 (GRCm39) |
|
probably null |
Het |
Ralgds |
T |
A |
2: 28,434,400 (GRCm39) |
|
probably null |
Het |
Rnf111 |
A |
T |
9: 70,383,671 (GRCm39) |
S87R |
probably benign |
Het |
Slc4a4 |
A |
C |
5: 89,304,195 (GRCm39) |
H502P |
possibly damaging |
Het |
Slc9c1 |
A |
G |
16: 45,427,219 (GRCm39) |
|
probably benign |
Het |
Slco3a1 |
A |
T |
7: 74,154,074 (GRCm39) |
I166N |
probably benign |
Het |
Snx5 |
A |
T |
2: 144,101,112 (GRCm39) |
|
probably null |
Het |
Srgap1 |
T |
C |
10: 121,636,732 (GRCm39) |
D741G |
possibly damaging |
Het |
St8sia2 |
G |
T |
7: 73,593,038 (GRCm39) |
Y339* |
probably null |
Het |
St8sia2 |
A |
T |
7: 73,621,700 (GRCm39) |
W86R |
probably damaging |
Het |
Stk33 |
A |
G |
7: 108,878,876 (GRCm39) |
L491P |
possibly damaging |
Het |
Sult2a7 |
T |
C |
7: 14,199,133 (GRCm39) |
Y298C |
probably damaging |
Het |
Tdo2 |
T |
A |
3: 81,874,332 (GRCm39) |
N210I |
probably benign |
Het |
Thada |
A |
T |
17: 84,762,586 (GRCm39) |
N104K |
probably damaging |
Het |
Timm8b |
A |
T |
9: 50,516,330 (GRCm39) |
D61V |
possibly damaging |
Het |
Tshz1 |
G |
A |
18: 84,033,070 (GRCm39) |
T446I |
possibly damaging |
Het |
Ubap2l |
T |
C |
3: 89,946,235 (GRCm39) |
N123S |
possibly damaging |
Het |
Vmn1r48 |
T |
C |
6: 90,013,246 (GRCm39) |
E193G |
possibly damaging |
Het |
Vmn1r69 |
C |
T |
7: 10,314,327 (GRCm39) |
V135I |
probably benign |
Het |
Vmn2r103 |
G |
T |
17: 20,031,903 (GRCm39) |
G559V |
probably benign |
Het |
Vmn2r26 |
T |
A |
6: 124,038,992 (GRCm39) |
*856R |
probably null |
Het |
Vmn2r88 |
A |
G |
14: 51,656,157 (GRCm39) |
I798V |
possibly damaging |
Het |
Vsir |
C |
T |
10: 60,193,861 (GRCm39) |
A108V |
probably benign |
Het |
Zfp14 |
G |
T |
7: 29,737,753 (GRCm39) |
Q411K |
probably damaging |
Het |
Zfp236 |
A |
T |
18: 82,657,457 (GRCm39) |
M762K |
probably damaging |
Het |
Zfp462 |
G |
A |
4: 55,011,762 (GRCm39) |
G1243S |
probably benign |
Het |
|
Other mutations in Rmdn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01628:Rmdn2
|
APN |
17 |
79,979,817 (GRCm39) |
nonsense |
probably null |
|
R0052:Rmdn2
|
UTSW |
17 |
79,957,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R0127:Rmdn2
|
UTSW |
17 |
79,977,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Rmdn2
|
UTSW |
17 |
79,957,716 (GRCm39) |
splice site |
probably benign |
|
R0440:Rmdn2
|
UTSW |
17 |
79,975,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R0720:Rmdn2
|
UTSW |
17 |
79,975,458 (GRCm39) |
critical splice donor site |
probably null |
|
R1163:Rmdn2
|
UTSW |
17 |
79,966,880 (GRCm39) |
missense |
probably benign |
0.00 |
R3746:Rmdn2
|
UTSW |
17 |
79,977,981 (GRCm39) |
splice site |
probably null |
|
R4966:Rmdn2
|
UTSW |
17 |
79,974,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R5137:Rmdn2
|
UTSW |
17 |
79,975,418 (GRCm39) |
missense |
probably benign |
0.02 |
R5259:Rmdn2
|
UTSW |
17 |
79,975,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R6439:Rmdn2
|
UTSW |
17 |
79,934,971 (GRCm39) |
intron |
probably benign |
|
R6991:Rmdn2
|
UTSW |
17 |
79,928,739 (GRCm39) |
start gained |
probably benign |
|
R7046:Rmdn2
|
UTSW |
17 |
79,928,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Rmdn2
|
UTSW |
17 |
79,929,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R7541:Rmdn2
|
UTSW |
17 |
79,935,297 (GRCm39) |
missense |
|
|
R8246:Rmdn2
|
UTSW |
17 |
79,979,966 (GRCm39) |
nonsense |
probably null |
|
R8359:Rmdn2
|
UTSW |
17 |
79,935,580 (GRCm39) |
missense |
|
|
R8393:Rmdn2
|
UTSW |
17 |
79,975,459 (GRCm39) |
critical splice donor site |
probably null |
|
R8462:Rmdn2
|
UTSW |
17 |
79,978,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9472:Rmdn2
|
UTSW |
17 |
79,989,096 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9496:Rmdn2
|
UTSW |
17 |
79,975,425 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9549:Rmdn2
|
UTSW |
17 |
79,935,339 (GRCm39) |
missense |
|
|
R9602:Rmdn2
|
UTSW |
17 |
79,975,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9617:Rmdn2
|
UTSW |
17 |
79,928,790 (GRCm39) |
missense |
probably benign |
0.27 |
R9698:Rmdn2
|
UTSW |
17 |
79,957,729 (GRCm39) |
critical splice acceptor site |
probably null |
|
|