Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
G |
A |
5: 8,752,216 (GRCm39) |
G426S |
probably damaging |
Het |
Casp4 |
A |
T |
9: 5,328,573 (GRCm39) |
|
probably benign |
Het |
Ccdc40 |
T |
A |
11: 119,144,229 (GRCm39) |
F988Y |
probably damaging |
Het |
Ccdc9b |
T |
C |
2: 118,590,098 (GRCm39) |
T249A |
probably benign |
Het |
Chd5 |
T |
A |
4: 152,464,389 (GRCm39) |
V1516E |
probably benign |
Het |
Chrnd |
T |
A |
1: 87,123,389 (GRCm39) |
|
probably null |
Het |
Col5a3 |
C |
A |
9: 20,683,738 (GRCm39) |
G1506V |
unknown |
Het |
Csgalnact2 |
A |
T |
6: 118,106,215 (GRCm39) |
C34* |
probably null |
Het |
Ddx23 |
T |
C |
15: 98,549,832 (GRCm39) |
K195E |
probably benign |
Het |
Dhps |
T |
G |
8: 85,800,880 (GRCm39) |
S240A |
probably benign |
Het |
Dnah5 |
T |
A |
15: 28,234,599 (GRCm39) |
|
probably null |
Het |
Dock10 |
T |
C |
1: 80,514,676 (GRCm39) |
T1414A |
probably benign |
Het |
Dock4 |
A |
G |
12: 40,805,812 (GRCm39) |
D928G |
probably damaging |
Het |
Dolpp1 |
T |
C |
2: 30,285,658 (GRCm39) |
|
probably benign |
Het |
Dse |
T |
A |
10: 34,028,601 (GRCm39) |
I830F |
probably damaging |
Het |
Elmod1 |
C |
T |
9: 53,843,091 (GRCm39) |
R29Q |
probably damaging |
Het |
Ephx4 |
T |
A |
5: 107,577,518 (GRCm39) |
|
probably null |
Het |
Evi5 |
A |
T |
5: 107,968,302 (GRCm39) |
M215K |
probably damaging |
Het |
Fbxl4 |
T |
C |
4: 22,390,678 (GRCm39) |
L287P |
probably damaging |
Het |
Gbp9 |
G |
A |
5: 105,230,724 (GRCm39) |
S400L |
probably damaging |
Het |
Gm6291 |
T |
C |
18: 6,371,365 (GRCm39) |
|
noncoding transcript |
Het |
Gmcl1 |
A |
T |
6: 86,688,596 (GRCm39) |
D301E |
probably benign |
Het |
Gna14 |
C |
T |
19: 16,580,692 (GRCm39) |
R177C |
possibly damaging |
Het |
Golph3 |
C |
T |
15: 12,339,756 (GRCm39) |
R90C |
probably damaging |
Het |
Gpr142 |
T |
A |
11: 114,689,785 (GRCm39) |
C12* |
probably null |
Het |
Hat1 |
T |
A |
2: 71,239,357 (GRCm39) |
N43K |
possibly damaging |
Het |
Hivep1 |
A |
T |
13: 42,310,694 (GRCm39) |
E978V |
possibly damaging |
Het |
Hormad1 |
G |
A |
3: 95,467,044 (GRCm39) |
|
probably null |
Het |
Kalrn |
C |
T |
16: 33,795,805 (GRCm39) |
|
probably benign |
Het |
Mars1 |
T |
C |
10: 127,132,418 (GRCm39) |
T860A |
probably benign |
Het |
Mdn1 |
A |
T |
4: 32,695,400 (GRCm39) |
L1146F |
probably damaging |
Het |
Met |
A |
G |
6: 17,531,581 (GRCm39) |
T620A |
probably benign |
Het |
Mybpc3 |
T |
A |
2: 90,955,010 (GRCm39) |
V481D |
probably damaging |
Het |
Myh14 |
A |
T |
7: 44,256,133 (GRCm39) |
L1924Q |
probably damaging |
Het |
Mylip |
G |
T |
13: 45,562,178 (GRCm39) |
E327* |
probably null |
Het |
Naip1 |
C |
T |
13: 100,559,636 (GRCm39) |
G1123R |
probably benign |
Het |
Naip6 |
A |
G |
13: 100,452,500 (GRCm39) |
V187A |
possibly damaging |
Het |
Ncam1 |
T |
A |
9: 49,418,343 (GRCm39) |
T986S |
probably benign |
Het |
Or13p4 |
T |
C |
4: 118,547,314 (GRCm39) |
I112V |
probably damaging |
Het |
Or4x13 |
T |
C |
2: 90,231,800 (GRCm39) |
I265T |
probably benign |
Het |
Phactr2 |
C |
T |
10: 13,121,261 (GRCm39) |
G480S |
probably damaging |
Het |
Por |
A |
G |
5: 135,744,838 (GRCm39) |
I34V |
probably benign |
Het |
Ppp2r5b |
C |
T |
19: 6,284,764 (GRCm39) |
R33H |
probably damaging |
Het |
Prkdc |
C |
A |
16: 15,570,693 (GRCm39) |
Y2325* |
probably null |
Het |
Prx |
A |
G |
7: 27,214,709 (GRCm39) |
E73G |
probably damaging |
Het |
Rbms2 |
C |
A |
10: 127,981,556 (GRCm39) |
A126S |
possibly damaging |
Het |
Rhoq |
C |
T |
17: 87,302,117 (GRCm39) |
A111V |
probably damaging |
Het |
Rpl14 |
T |
A |
9: 120,403,240 (GRCm39) |
|
probably benign |
Het |
Serbp1 |
A |
G |
6: 67,249,870 (GRCm39) |
*75W |
probably null |
Het |
Sptbn1 |
C |
A |
11: 30,073,978 (GRCm39) |
V1351F |
probably damaging |
Het |
Supt16 |
A |
G |
14: 52,401,979 (GRCm39) |
V897A |
probably benign |
Het |
Tfdp1 |
T |
A |
8: 13,407,038 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,780,487 (GRCm39) |
Y1088F |
probably damaging |
Het |
Vmn2r105 |
G |
T |
17: 20,448,929 (GRCm39) |
Q83K |
probably benign |
Het |
Wdr76 |
A |
T |
2: 121,359,323 (GRCm39) |
S221C |
probably damaging |
Het |
Zfhx2 |
G |
T |
14: 55,303,348 (GRCm39) |
F1545L |
probably benign |
Het |
Zfp318 |
A |
G |
17: 46,709,959 (GRCm39) |
I561V |
probably damaging |
Het |
|
Other mutations in Mppe1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01129:Mppe1
|
APN |
18 |
67,370,515 (GRCm39) |
nonsense |
probably null |
|
IGL03028:Mppe1
|
APN |
18 |
67,360,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R0087:Mppe1
|
UTSW |
18 |
67,358,775 (GRCm39) |
makesense |
probably null |
|
R0538:Mppe1
|
UTSW |
18 |
67,370,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Mppe1
|
UTSW |
18 |
67,370,419 (GRCm39) |
critical splice donor site |
probably null |
|
R1170:Mppe1
|
UTSW |
18 |
67,360,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Mppe1
|
UTSW |
18 |
67,362,843 (GRCm39) |
missense |
probably benign |
0.07 |
R2229:Mppe1
|
UTSW |
18 |
67,361,082 (GRCm39) |
critical splice donor site |
probably null |
|
R3874:Mppe1
|
UTSW |
18 |
67,358,957 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4194:Mppe1
|
UTSW |
18 |
67,361,139 (GRCm39) |
missense |
probably benign |
0.27 |
R4775:Mppe1
|
UTSW |
18 |
67,359,930 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4940:Mppe1
|
UTSW |
18 |
67,361,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Mppe1
|
UTSW |
18 |
67,361,133 (GRCm39) |
missense |
probably benign |
|
R4979:Mppe1
|
UTSW |
18 |
67,362,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R5768:Mppe1
|
UTSW |
18 |
67,358,889 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5784:Mppe1
|
UTSW |
18 |
67,361,098 (GRCm39) |
missense |
probably benign |
0.12 |
R6547:Mppe1
|
UTSW |
18 |
67,362,059 (GRCm39) |
missense |
probably benign |
|
R7161:Mppe1
|
UTSW |
18 |
67,362,842 (GRCm39) |
missense |
probably benign |
0.10 |
R7580:Mppe1
|
UTSW |
18 |
67,370,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R7699:Mppe1
|
UTSW |
18 |
67,358,775 (GRCm39) |
makesense |
probably null |
|
R7700:Mppe1
|
UTSW |
18 |
67,358,775 (GRCm39) |
makesense |
probably null |
|
R7908:Mppe1
|
UTSW |
18 |
67,362,055 (GRCm39) |
missense |
probably benign |
0.01 |
R8399:Mppe1
|
UTSW |
18 |
67,358,946 (GRCm39) |
missense |
probably benign |
0.17 |
R8896:Mppe1
|
UTSW |
18 |
67,370,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R9002:Mppe1
|
UTSW |
18 |
67,358,925 (GRCm39) |
missense |
possibly damaging |
0.96 |
|