Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anks1 |
A |
G |
17: 28,276,328 (GRCm39) |
N1024D |
probably damaging |
Het |
Cts7 |
A |
G |
13: 61,504,723 (GRCm39) |
|
probably null |
Het |
Dock3 |
T |
A |
9: 106,788,576 (GRCm39) |
|
probably benign |
Het |
Fbxo6 |
A |
G |
4: 148,230,567 (GRCm39) |
F232L |
probably benign |
Het |
Hsd3b6 |
A |
T |
3: 98,713,940 (GRCm39) |
F120I |
probably damaging |
Het |
Il4ra |
G |
A |
7: 125,168,347 (GRCm39) |
|
probably null |
Het |
Irs4 |
A |
T |
X: 140,505,140 (GRCm39) |
F1019I |
unknown |
Het |
Klc1 |
A |
G |
12: 111,753,932 (GRCm39) |
T464A |
probably damaging |
Het |
Mical3 |
T |
C |
6: 120,999,371 (GRCm39) |
T660A |
possibly damaging |
Het |
Ndufs7 |
T |
A |
10: 80,090,955 (GRCm39) |
V158E |
probably damaging |
Het |
Nhs |
T |
A |
X: 160,620,226 (GRCm39) |
N1510I |
probably damaging |
Het |
Or51e2 |
A |
G |
7: 102,391,469 (GRCm39) |
V247A |
probably damaging |
Het |
Or8k38 |
T |
G |
2: 86,488,070 (GRCm39) |
H244P |
probably damaging |
Het |
Pole2 |
G |
A |
12: 69,262,134 (GRCm39) |
T148I |
probably damaging |
Het |
Pramel1 |
T |
A |
4: 143,124,126 (GRCm39) |
L267H |
probably damaging |
Het |
Rag1 |
T |
C |
2: 101,472,733 (GRCm39) |
E803G |
probably damaging |
Het |
Rassf1 |
G |
T |
9: 107,435,510 (GRCm39) |
|
probably benign |
Het |
Rnf220 |
T |
C |
4: 117,164,872 (GRCm39) |
K210R |
probably benign |
Het |
Setd7 |
T |
A |
3: 51,440,459 (GRCm39) |
D194V |
probably damaging |
Het |
Snd1 |
T |
C |
6: 28,745,174 (GRCm39) |
|
probably benign |
Het |
Ssb |
T |
A |
2: 69,701,179 (GRCm39) |
|
probably null |
Het |
Tlr5 |
T |
C |
1: 182,801,761 (GRCm39) |
V355A |
possibly damaging |
Het |
Ush2a |
A |
T |
1: 188,090,158 (GRCm39) |
R414* |
probably null |
Het |
Zfyve26 |
A |
G |
12: 79,327,674 (GRCm39) |
S559P |
probably benign |
Het |
|
Other mutations in Spmip9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02323:Spmip9
|
APN |
6 |
70,890,679 (GRCm39) |
splice site |
probably benign |
|
IGL02693:Spmip9
|
APN |
6 |
70,890,488 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03161:Spmip9
|
APN |
6 |
70,890,519 (GRCm39) |
missense |
probably benign |
0.08 |
R1734:Spmip9
|
UTSW |
6 |
70,890,645 (GRCm39) |
missense |
probably benign |
0.12 |
R3408:Spmip9
|
UTSW |
6 |
70,892,690 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3956:Spmip9
|
UTSW |
6 |
70,890,469 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3981:Spmip9
|
UTSW |
6 |
70,890,283 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5084:Spmip9
|
UTSW |
6 |
70,892,688 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5376:Spmip9
|
UTSW |
6 |
70,890,466 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7532:Spmip9
|
UTSW |
6 |
70,890,621 (GRCm39) |
missense |
probably benign |
0.37 |
R8317:Spmip9
|
UTSW |
6 |
70,890,276 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9468:Spmip9
|
UTSW |
6 |
70,890,627 (GRCm39) |
missense |
probably benign |
|
|