Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26a |
T |
G |
8: 44,023,222 (GRCm39) |
Q89H |
probably benign |
Het |
Adgrb1 |
T |
C |
15: 74,415,511 (GRCm39) |
F697S |
probably damaging |
Het |
Adgrl2 |
A |
T |
3: 148,544,788 (GRCm39) |
V769E |
probably damaging |
Het |
Aldh7a1 |
A |
T |
18: 56,681,566 (GRCm39) |
F173L |
probably null |
Het |
Bcl3 |
G |
T |
7: 19,545,505 (GRCm39) |
C208* |
probably null |
Het |
Bmal1 |
A |
G |
7: 112,902,613 (GRCm39) |
I421V |
possibly damaging |
Het |
Casz1 |
T |
C |
4: 149,036,792 (GRCm39) |
S1685P |
unknown |
Het |
Cep250 |
A |
G |
2: 155,833,445 (GRCm39) |
E1789G |
probably damaging |
Het |
Cep76 |
A |
T |
18: 67,759,710 (GRCm39) |
D334E |
probably benign |
Het |
Clca3b |
A |
T |
3: 144,531,219 (GRCm39) |
|
probably null |
Het |
Col9a3 |
A |
G |
2: 180,248,271 (GRCm39) |
S208G |
probably benign |
Het |
Ddx47 |
T |
C |
6: 134,998,468 (GRCm39) |
V388A |
probably benign |
Het |
Dync1h1 |
C |
T |
12: 110,599,333 (GRCm39) |
A1896V |
possibly damaging |
Het |
Eif2ak2 |
T |
A |
17: 79,165,963 (GRCm39) |
R411S |
probably benign |
Het |
F7 |
A |
G |
8: 13,084,774 (GRCm39) |
T267A |
probably benign |
Het |
Fras1 |
C |
A |
5: 96,848,101 (GRCm39) |
D1770E |
probably benign |
Het |
G2e3 |
T |
A |
12: 51,412,120 (GRCm39) |
Y387N |
probably benign |
Het |
Hspg2 |
C |
T |
4: 137,256,729 (GRCm39) |
L1491F |
probably damaging |
Het |
Ighv3-4 |
T |
C |
12: 114,217,260 (GRCm39) |
I110M |
probably benign |
Het |
Itgb5 |
T |
A |
16: 33,665,367 (GRCm39) |
C28S |
probably damaging |
Het |
Itprid2 |
A |
G |
2: 79,472,342 (GRCm39) |
N132S |
probably benign |
Het |
Kbtbd11 |
C |
A |
8: 15,078,578 (GRCm39) |
N392K |
probably damaging |
Het |
Kcnmb4 |
A |
G |
10: 116,309,189 (GRCm39) |
S80P |
possibly damaging |
Het |
Kif21a |
C |
T |
15: 90,855,036 (GRCm39) |
C721Y |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Klrc3 |
T |
C |
6: 129,616,125 (GRCm39) |
M189V |
probably benign |
Het |
Macf1 |
T |
A |
4: 123,368,884 (GRCm39) |
E394V |
possibly damaging |
Het |
Myb |
A |
G |
10: 21,028,516 (GRCm39) |
S116P |
probably damaging |
Het |
Nf2 |
G |
A |
11: 4,730,613 (GRCm39) |
Q513* |
probably null |
Het |
Nmnat3 |
C |
T |
9: 98,292,205 (GRCm39) |
T150M |
possibly damaging |
Het |
Obi1 |
A |
G |
14: 104,716,693 (GRCm39) |
V560A |
probably benign |
Het |
Or11g27 |
T |
C |
14: 50,771,216 (GRCm39) |
C116R |
possibly damaging |
Het |
Or12k8 |
C |
A |
2: 36,974,942 (GRCm39) |
V273F |
probably benign |
Het |
Patj |
T |
G |
4: 98,538,691 (GRCm39) |
C210W |
possibly damaging |
Het |
Pde3b |
A |
G |
7: 114,015,522 (GRCm39) |
H246R |
probably benign |
Het |
Pnp2 |
A |
G |
14: 51,197,082 (GRCm39) |
H56R |
probably benign |
Het |
Prkg1 |
A |
G |
19: 30,546,629 (GRCm39) |
|
probably benign |
Het |
Rhbdf1 |
C |
T |
11: 32,166,236 (GRCm39) |
S8N |
probably damaging |
Het |
Rimbp3 |
A |
G |
16: 17,027,556 (GRCm39) |
K327E |
possibly damaging |
Het |
Rsph6a |
T |
A |
7: 18,801,003 (GRCm39) |
|
probably null |
Het |
Ryr2 |
T |
C |
13: 11,664,698 (GRCm39) |
N3535S |
probably benign |
Het |
Ston1 |
T |
G |
17: 88,944,436 (GRCm39) |
V614G |
probably damaging |
Het |
Svep1 |
T |
A |
4: 58,138,695 (GRCm39) |
T466S |
possibly damaging |
Het |
Tas2r109 |
A |
T |
6: 132,957,144 (GRCm39) |
I262N |
probably benign |
Het |
Tmtc1 |
T |
C |
6: 148,256,596 (GRCm39) |
|
probably benign |
Het |
Tshz2 |
G |
A |
2: 169,726,858 (GRCm39) |
E16K |
possibly damaging |
Het |
Ufsp2 |
T |
A |
8: 46,438,502 (GRCm39) |
S193R |
possibly damaging |
Het |
Ugt2b5 |
C |
A |
5: 87,287,622 (GRCm39) |
E182* |
probably null |
Het |
Usp43 |
A |
G |
11: 67,782,290 (GRCm39) |
V376A |
probably benign |
Het |
Utp15 |
A |
T |
13: 98,395,755 (GRCm39) |
F76I |
possibly damaging |
Het |
Wdr62 |
A |
C |
7: 29,941,673 (GRCm39) |
L1141R |
probably damaging |
Het |
Zfp418 |
T |
A |
7: 7,175,161 (GRCm39) |
M18K |
probably benign |
Het |
|
Other mutations in Mrgprb4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:Mrgprb4
|
APN |
7 |
47,848,649 (GRCm39) |
missense |
probably benign |
|
IGL02745:Mrgprb4
|
APN |
7 |
47,848,106 (GRCm39) |
missense |
probably damaging |
0.97 |
R0718:Mrgprb4
|
UTSW |
7 |
47,848,301 (GRCm39) |
missense |
probably benign |
0.10 |
R0849:Mrgprb4
|
UTSW |
7 |
47,848,868 (GRCm39) |
missense |
probably benign |
0.24 |
R1526:Mrgprb4
|
UTSW |
7 |
47,848,159 (GRCm39) |
nonsense |
probably null |
|
R2857:Mrgprb4
|
UTSW |
7 |
47,848,084 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2859:Mrgprb4
|
UTSW |
7 |
47,848,084 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5354:Mrgprb4
|
UTSW |
7 |
47,848,077 (GRCm39) |
missense |
probably benign |
0.07 |
R5636:Mrgprb4
|
UTSW |
7 |
47,848,218 (GRCm39) |
missense |
probably benign |
0.02 |
R5715:Mrgprb4
|
UTSW |
7 |
47,848,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R6180:Mrgprb4
|
UTSW |
7 |
47,848,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Mrgprb4
|
UTSW |
7 |
47,848,649 (GRCm39) |
missense |
probably benign |
|
R7092:Mrgprb4
|
UTSW |
7 |
47,847,984 (GRCm39) |
missense |
probably benign |
0.01 |
R7301:Mrgprb4
|
UTSW |
7 |
47,848,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R7779:Mrgprb4
|
UTSW |
7 |
47,848,895 (GRCm39) |
missense |
probably benign |
0.19 |
R8077:Mrgprb4
|
UTSW |
7 |
47,848,203 (GRCm39) |
missense |
probably benign |
0.00 |
R8292:Mrgprb4
|
UTSW |
7 |
47,848,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Mrgprb4
|
UTSW |
7 |
47,848,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9000:Mrgprb4
|
UTSW |
7 |
47,848,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R9006:Mrgprb4
|
UTSW |
7 |
47,848,343 (GRCm39) |
missense |
probably benign |
0.12 |
R9106:Mrgprb4
|
UTSW |
7 |
47,848,679 (GRCm39) |
missense |
probably benign |
0.43 |
R9717:Mrgprb4
|
UTSW |
7 |
47,848,583 (GRCm39) |
missense |
possibly damaging |
0.96 |
Z1088:Mrgprb4
|
UTSW |
7 |
47,848,430 (GRCm39) |
missense |
possibly damaging |
0.78 |
|