Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430038I01Rik |
A |
T |
7: 136,978,069 (GRCm39) |
N102K |
possibly damaging |
Het |
Abca1 |
C |
T |
4: 53,061,481 (GRCm39) |
|
probably benign |
Het |
Adamts17 |
T |
A |
7: 66,490,215 (GRCm39) |
L99Q |
possibly damaging |
Het |
Adamtsl1 |
A |
T |
4: 86,336,783 (GRCm39) |
Q1564L |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,386,024 (GRCm39) |
V556E |
probably benign |
Het |
Axin1 |
T |
A |
17: 26,406,771 (GRCm39) |
Y455N |
probably benign |
Het |
Cacna2d3 |
A |
G |
14: 29,069,077 (GRCm39) |
|
probably null |
Het |
Car8 |
T |
A |
4: 8,189,353 (GRCm39) |
I154F |
probably benign |
Het |
Ccl27a |
T |
A |
4: 41,773,232 (GRCm39) |
T76S |
probably benign |
Het |
Cep170 |
G |
A |
1: 176,583,409 (GRCm39) |
A990V |
probably benign |
Het |
Chd1 |
A |
T |
17: 15,952,133 (GRCm39) |
T291S |
probably damaging |
Het |
Col3a1 |
C |
A |
1: 45,361,150 (GRCm39) |
P112T |
unknown |
Het |
Cul5 |
T |
G |
9: 53,529,286 (GRCm39) |
M800L |
probably benign |
Het |
Dst |
C |
T |
1: 34,251,400 (GRCm39) |
S4165F |
probably damaging |
Het |
Dusp8 |
T |
C |
7: 141,643,802 (GRCm39) |
E37G |
probably damaging |
Het |
Efr3b |
T |
C |
12: 4,033,414 (GRCm39) |
N131S |
probably benign |
Het |
Fan1 |
T |
C |
7: 64,022,119 (GRCm39) |
Y378C |
probably damaging |
Het |
Fcgr2b |
T |
C |
1: 170,795,704 (GRCm39) |
N75S |
possibly damaging |
Het |
Foxp4 |
A |
G |
17: 48,186,453 (GRCm39) |
I442T |
unknown |
Het |
Gp9 |
A |
G |
6: 87,756,133 (GRCm39) |
I49M |
probably benign |
Het |
Grip1 |
G |
A |
10: 119,765,863 (GRCm39) |
G65D |
probably damaging |
Het |
Hoxc10 |
T |
C |
15: 102,875,879 (GRCm39) |
V196A |
probably benign |
Het |
Hpx |
A |
G |
7: 105,245,498 (GRCm39) |
C92R |
probably damaging |
Het |
Ighv1-22 |
A |
G |
12: 114,710,301 (GRCm39) |
F9S |
possibly damaging |
Het |
Kif24 |
C |
T |
4: 41,404,734 (GRCm39) |
R422H |
probably damaging |
Het |
Klk1b1 |
T |
C |
7: 43,618,751 (GRCm39) |
Y43H |
probably damaging |
Het |
Lmo7 |
A |
G |
14: 102,159,531 (GRCm39) |
|
probably null |
Het |
Lrguk |
A |
G |
6: 34,050,703 (GRCm39) |
D387G |
probably damaging |
Het |
Lysmd1 |
G |
A |
3: 95,045,772 (GRCm39) |
G203D |
probably damaging |
Het |
Mpnd |
T |
C |
17: 56,318,692 (GRCm39) |
S150P |
probably damaging |
Het |
Mrc2 |
T |
C |
11: 105,183,729 (GRCm39) |
|
probably null |
Het |
Mtr |
A |
G |
13: 12,262,251 (GRCm39) |
S152P |
probably benign |
Het |
Naip2 |
A |
T |
13: 100,315,940 (GRCm39) |
L280Q |
probably damaging |
Het |
Naip2 |
G |
C |
13: 100,315,941 (GRCm39) |
L280V |
probably damaging |
Het |
Ndufa13 |
T |
C |
8: 70,354,260 (GRCm39) |
D9G |
probably damaging |
Het |
Nek1 |
T |
A |
8: 61,525,349 (GRCm39) |
F596I |
probably damaging |
Het |
Nsd1 |
A |
G |
13: 55,394,504 (GRCm39) |
T702A |
probably benign |
Het |
Or7d10 |
A |
T |
9: 19,832,105 (GRCm39) |
Y200F |
probably damaging |
Het |
Pam |
T |
A |
1: 97,782,481 (GRCm39) |
|
probably benign |
Het |
Plxna1 |
C |
A |
6: 89,333,501 (GRCm39) |
R376L |
probably damaging |
Het |
Plxnc1 |
A |
G |
10: 94,630,294 (GRCm39) |
V1535A |
probably benign |
Het |
Prdx5 |
A |
G |
19: 6,884,218 (GRCm39) |
L166P |
probably damaging |
Het |
Prol1 |
A |
T |
5: 88,476,476 (GRCm39) |
I289F |
unknown |
Het |
Prss23 |
T |
C |
7: 89,158,959 (GRCm39) |
Y370C |
probably damaging |
Het |
Rimbp3 |
A |
T |
16: 17,028,163 (GRCm39) |
H529L |
probably benign |
Het |
Rnase2b |
T |
A |
14: 51,400,205 (GRCm39) |
H95Q |
probably damaging |
Het |
Rnf103 |
C |
G |
6: 71,485,859 (GRCm39) |
C163W |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,749,753 (GRCm39) |
V1433A |
probably damaging |
Het |
Rusf1 |
C |
T |
7: 127,884,380 (GRCm39) |
V201I |
probably damaging |
Het |
Syne2 |
C |
T |
12: 76,092,839 (GRCm39) |
Q5150* |
probably null |
Het |
Tas2r110 |
T |
A |
6: 132,845,638 (GRCm39) |
I223N |
probably damaging |
Het |
Tead2 |
T |
A |
7: 44,881,752 (GRCm39) |
|
probably null |
Het |
Vwa3a |
A |
T |
7: 120,361,687 (GRCm39) |
K133* |
probably null |
Het |
Vwce |
T |
C |
19: 10,624,269 (GRCm39) |
S387P |
probably damaging |
Het |
Zbtb41 |
T |
A |
1: 139,351,734 (GRCm39) |
H282Q |
probably benign |
Het |
|
Other mutations in Cpa4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01404:Cpa4
|
APN |
6 |
30,581,701 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01621:Cpa4
|
APN |
6 |
30,574,415 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01712:Cpa4
|
APN |
6 |
30,590,815 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01970:Cpa4
|
APN |
6 |
30,579,645 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02751:Cpa4
|
APN |
6 |
30,581,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Cpa4
|
UTSW |
6 |
30,585,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Cpa4
|
UTSW |
6 |
30,585,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Cpa4
|
UTSW |
6 |
30,579,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Cpa4
|
UTSW |
6 |
30,580,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Cpa4
|
UTSW |
6 |
30,583,649 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4876:Cpa4
|
UTSW |
6 |
30,590,814 (GRCm39) |
missense |
probably benign |
0.01 |
R4920:Cpa4
|
UTSW |
6 |
30,568,462 (GRCm39) |
critical splice donor site |
probably null |
|
R6144:Cpa4
|
UTSW |
6 |
30,585,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R6892:Cpa4
|
UTSW |
6 |
30,583,628 (GRCm39) |
missense |
probably benign |
|
R7567:Cpa4
|
UTSW |
6 |
30,573,889 (GRCm39) |
missense |
probably benign |
0.03 |
R7763:Cpa4
|
UTSW |
6 |
30,583,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R8033:Cpa4
|
UTSW |
6 |
30,590,799 (GRCm39) |
missense |
probably benign |
|
R8679:Cpa4
|
UTSW |
6 |
30,585,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R9094:Cpa4
|
UTSW |
6 |
30,574,393 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9566:Cpa4
|
UTSW |
6 |
30,579,608 (GRCm39) |
missense |
probably benign |
|
X0061:Cpa4
|
UTSW |
6 |
30,590,962 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cpa4
|
UTSW |
6 |
30,574,402 (GRCm39) |
missense |
possibly damaging |
0.85 |
|