Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace3 |
A |
G |
11: 105,885,768 (GRCm39) |
E58G |
probably damaging |
Het |
Ank1 |
T |
A |
8: 23,629,302 (GRCm39) |
F4I |
possibly damaging |
Het |
Arih2 |
T |
C |
9: 108,488,872 (GRCm39) |
D282G |
possibly damaging |
Het |
Atp7b |
C |
T |
8: 22,503,556 (GRCm39) |
V733I |
probably damaging |
Het |
Avil |
A |
G |
10: 126,845,861 (GRCm39) |
D370G |
probably benign |
Het |
Ccdc88b |
T |
C |
19: 6,833,213 (GRCm39) |
E278G |
probably damaging |
Het |
Cdkl3 |
A |
G |
11: 51,975,260 (GRCm39) |
H74R |
|
Het |
Clec9a |
C |
A |
6: 129,387,292 (GRCm39) |
A49E |
probably damaging |
Het |
Cntn5 |
A |
G |
9: 9,666,840 (GRCm39) |
|
probably null |
Het |
Cyp11b2 |
A |
G |
15: 74,723,428 (GRCm39) |
M412T |
possibly damaging |
Het |
Dhrs7l |
T |
C |
12: 72,659,340 (GRCm39) |
N145D |
probably damaging |
Het |
Dync1i1 |
A |
G |
6: 5,966,815 (GRCm39) |
Q399R |
possibly damaging |
Het |
Fam47e |
C |
A |
5: 92,702,990 (GRCm39) |
R21S |
probably benign |
Het |
Gimap4 |
A |
G |
6: 48,667,694 (GRCm39) |
I150V |
probably damaging |
Het |
Gm7361 |
T |
A |
5: 26,465,387 (GRCm39) |
M128K |
possibly damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,468,068 (GRCm39) |
E190K |
probably damaging |
Het |
Hells |
T |
C |
19: 38,940,286 (GRCm39) |
S396P |
probably damaging |
Het |
Hrg |
T |
A |
16: 22,780,286 (GRCm39) |
S521R |
unknown |
Het |
Itih5 |
A |
G |
2: 10,191,800 (GRCm39) |
T112A |
probably benign |
Het |
Ly9 |
T |
A |
1: 171,421,586 (GRCm39) |
N555I |
probably damaging |
Het |
Morc2b |
C |
T |
17: 33,355,775 (GRCm39) |
E666K |
probably benign |
Het |
Nebl |
T |
A |
2: 17,418,593 (GRCm39) |
E268D |
probably damaging |
Het |
Nr4a3 |
G |
T |
4: 48,052,170 (GRCm39) |
R308L |
probably benign |
Het |
Or10k2 |
A |
T |
8: 84,268,301 (GRCm39) |
H176L |
probably damaging |
Het |
Or14j1 |
A |
G |
17: 38,146,561 (GRCm39) |
R224G |
probably damaging |
Het |
Or4c10 |
A |
T |
2: 89,760,878 (GRCm39) |
I242L |
possibly damaging |
Het |
Or6d14 |
G |
T |
6: 116,534,289 (GRCm39) |
R301L |
probably damaging |
Het |
Or8k33 |
T |
G |
2: 86,383,980 (GRCm39) |
I163L |
probably benign |
Het |
Plcd3 |
A |
G |
11: 102,965,496 (GRCm39) |
Y530H |
probably damaging |
Het |
Pou2af1 |
A |
T |
9: 51,144,326 (GRCm39) |
E80V |
probably damaging |
Het |
Scgb2b18 |
C |
T |
7: 32,872,656 (GRCm39) |
D50N |
probably benign |
Het |
Shisa6 |
G |
C |
11: 66,416,556 (GRCm39) |
Q79E |
probably benign |
Het |
Sis |
C |
T |
3: 72,810,984 (GRCm39) |
G1679D |
probably damaging |
Het |
Sorcs2 |
A |
T |
5: 36,386,519 (GRCm39) |
M173K |
possibly damaging |
Het |
Ston2 |
T |
C |
12: 91,608,649 (GRCm39) |
D817G |
probably damaging |
Het |
Ticrr |
T |
A |
7: 79,344,428 (GRCm39) |
F1431Y |
probably benign |
Het |
Uevld |
T |
A |
7: 46,595,055 (GRCm39) |
N179I |
probably damaging |
Het |
Utp6 |
G |
T |
11: 79,836,610 (GRCm39) |
Q375K |
probably benign |
Het |
Vmn2r68 |
T |
A |
7: 84,882,785 (GRCm39) |
E322D |
probably damaging |
Het |
Wnt5a |
A |
G |
14: 28,235,108 (GRCm39) |
M51V |
probably benign |
Het |
Zfp202 |
A |
T |
9: 40,118,976 (GRCm39) |
R130* |
probably null |
Het |
Zfp949 |
G |
T |
9: 88,449,302 (GRCm39) |
V36L |
possibly damaging |
Het |
|
Other mutations in Mup8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02442:Mup8
|
APN |
4 |
60,219,695 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03102:Mup8
|
APN |
4 |
60,219,746 (GRCm39) |
missense |
probably benign |
0.29 |
IGL03291:Mup8
|
APN |
4 |
60,221,950 (GRCm39) |
missense |
probably damaging |
0.99 |
R5159:Mup8
|
UTSW |
4 |
60,221,062 (GRCm39) |
missense |
probably benign |
0.34 |
R5371:Mup8
|
UTSW |
4 |
60,222,423 (GRCm39) |
missense |
probably benign |
0.00 |
R6006:Mup8
|
UTSW |
4 |
60,220,403 (GRCm39) |
missense |
probably benign |
0.43 |
R6407:Mup8
|
UTSW |
4 |
60,220,394 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6931:Mup8
|
UTSW |
4 |
60,220,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R7172:Mup8
|
UTSW |
4 |
60,222,425 (GRCm39) |
nonsense |
probably null |
|
R7607:Mup8
|
UTSW |
4 |
60,222,035 (GRCm39) |
missense |
probably benign |
0.01 |
R7757:Mup8
|
UTSW |
4 |
60,220,333 (GRCm39) |
missense |
probably benign |
0.03 |
R7757:Mup8
|
UTSW |
4 |
60,220,332 (GRCm39) |
missense |
probably benign |
0.14 |
R7874:Mup8
|
UTSW |
4 |
60,222,420 (GRCm39) |
missense |
probably damaging |
0.99 |
R8349:Mup8
|
UTSW |
4 |
60,222,382 (GRCm39) |
missense |
probably benign |
|
R9283:Mup8
|
UTSW |
4 |
60,221,903 (GRCm39) |
missense |
probably benign |
|
R9306:Mup8
|
UTSW |
4 |
60,219,682 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1176:Mup8
|
UTSW |
4 |
60,222,542 (GRCm39) |
start gained |
probably benign |
|
Z1176:Mup8
|
UTSW |
4 |
60,222,378 (GRCm39) |
missense |
probably benign |
0.01 |
|