Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
T |
6: 128,524,190 (GRCm39) |
F1147L |
probably damaging |
Het |
Abca2 |
T |
C |
2: 25,332,006 (GRCm39) |
S1373P |
probably damaging |
Het |
Abca9 |
A |
T |
11: 110,042,874 (GRCm39) |
S392T |
probably benign |
Het |
Abcd2 |
T |
C |
15: 91,047,313 (GRCm39) |
D580G |
probably benign |
Het |
Actl9 |
T |
A |
17: 33,652,882 (GRCm39) |
L314H |
probably damaging |
Het |
Adamtsl1 |
T |
C |
4: 86,255,168 (GRCm39) |
F746L |
probably damaging |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Cdkl3 |
T |
C |
11: 51,901,995 (GRCm39) |
V68A |
possibly damaging |
Het |
Cnot1 |
A |
G |
8: 96,448,254 (GRCm39) |
F2266S |
probably damaging |
Het |
Colq |
T |
C |
14: 31,267,034 (GRCm39) |
R159G |
probably damaging |
Het |
Ctse |
A |
T |
1: 131,592,130 (GRCm39) |
D152V |
probably damaging |
Het |
Cul7 |
G |
T |
17: 46,970,045 (GRCm39) |
M1011I |
probably benign |
Het |
Cyb5r4 |
G |
T |
9: 86,939,224 (GRCm39) |
V336L |
possibly damaging |
Het |
Dync2h1 |
A |
T |
9: 7,131,949 (GRCm39) |
H1619Q |
probably benign |
Het |
Eif2ak1 |
A |
G |
5: 143,818,986 (GRCm39) |
K216E |
probably damaging |
Het |
F5 |
A |
T |
1: 164,021,755 (GRCm39) |
H1410L |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,446,604 (GRCm39) |
Y2388C |
probably damaging |
Het |
Fsip2 |
C |
T |
2: 82,816,222 (GRCm39) |
T3985M |
probably benign |
Het |
Gak |
T |
C |
5: 108,744,672 (GRCm39) |
Y535C |
probably damaging |
Het |
Gzmc |
G |
T |
14: 56,469,826 (GRCm39) |
P158Q |
probably damaging |
Het |
Hook3 |
A |
G |
8: 26,572,607 (GRCm39) |
Y135H |
probably benign |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Ing4 |
A |
T |
6: 125,020,961 (GRCm39) |
M28L |
probably benign |
Het |
Irs3 |
T |
A |
5: 137,642,754 (GRCm39) |
D228V |
probably damaging |
Het |
Jade1 |
T |
A |
3: 41,555,836 (GRCm39) |
I301N |
probably damaging |
Het |
Kif13b |
T |
A |
14: 64,995,011 (GRCm39) |
M921K |
possibly damaging |
Het |
Kmt2c |
A |
G |
5: 25,515,870 (GRCm39) |
S2658P |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,468,382 (GRCm39) |
|
probably null |
Het |
Map4k5 |
C |
T |
12: 69,899,493 (GRCm39) |
V53I |
possibly damaging |
Het |
Mdn1 |
T |
C |
4: 32,739,827 (GRCm39) |
S3694P |
probably damaging |
Het |
Mroh7 |
A |
G |
4: 106,548,749 (GRCm39) |
V1038A |
probably benign |
Het |
Muc5ac |
T |
C |
7: 141,370,015 (GRCm39) |
V3185A |
possibly damaging |
Het |
Myo19 |
T |
A |
11: 84,783,023 (GRCm39) |
M179K |
probably damaging |
Het |
Myo1c |
A |
G |
11: 75,562,414 (GRCm39) |
Y902C |
probably damaging |
Het |
Nf1 |
T |
A |
11: 79,335,469 (GRCm39) |
I977K |
probably damaging |
Het |
Nos1 |
T |
C |
5: 118,081,899 (GRCm39) |
V1240A |
probably benign |
Het |
Nr3c1 |
T |
C |
18: 39,619,930 (GRCm39) |
D119G |
probably damaging |
Het |
Oga |
C |
A |
19: 45,758,485 (GRCm39) |
|
probably null |
Het |
Or4c107 |
A |
T |
2: 88,788,863 (GRCm39) |
N18Y |
probably damaging |
Het |
Pdlim2 |
A |
G |
14: 70,405,208 (GRCm39) |
V219A |
probably damaging |
Het |
Pira13 |
T |
A |
7: 3,825,805 (GRCm39) |
M355L |
probably benign |
Het |
Polr1g |
T |
C |
7: 19,091,487 (GRCm39) |
N207D |
probably benign |
Het |
Prdx1 |
T |
C |
4: 116,549,128 (GRCm39) |
|
probably null |
Het |
Rbfox1 |
C |
T |
16: 7,111,952 (GRCm39) |
R173C |
probably damaging |
Het |
Rbp3 |
T |
A |
14: 33,676,427 (GRCm39) |
V125D |
probably damaging |
Het |
Resf1 |
T |
C |
6: 149,227,097 (GRCm39) |
|
probably benign |
Het |
Rhot1 |
T |
A |
11: 80,124,300 (GRCm39) |
I154K |
probably damaging |
Het |
Runx1t1 |
C |
T |
4: 13,837,978 (GRCm39) |
R129C |
probably damaging |
Het |
Setbp1 |
A |
G |
18: 78,901,382 (GRCm39) |
S762P |
probably benign |
Het |
Slc13a3 |
A |
G |
2: 165,290,619 (GRCm39) |
I67T |
probably damaging |
Het |
Tbc1d2b |
A |
T |
9: 90,100,923 (GRCm39) |
M689K |
probably benign |
Het |
Top2a |
T |
C |
11: 98,884,667 (GRCm39) |
Y1517C |
probably damaging |
Het |
Txndc2 |
A |
T |
17: 65,945,849 (GRCm39) |
N109K |
probably damaging |
Het |
Tyk2 |
A |
G |
9: 21,031,797 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
T |
5: 102,096,838 (GRCm39) |
L320* |
probably null |
Het |
Zfp456 |
T |
C |
13: 67,514,995 (GRCm39) |
E237G |
probably benign |
Het |
Zscan10 |
A |
G |
17: 23,826,147 (GRCm39) |
E103G |
possibly damaging |
Het |
|
Other mutations in Mup5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0167:Mup5
|
UTSW |
4 |
61,752,019 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0485:Mup5
|
UTSW |
4 |
61,751,229 (GRCm39) |
splice site |
probably null |
|
R0547:Mup5
|
UTSW |
4 |
61,751,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Mup5
|
UTSW |
4 |
61,750,871 (GRCm39) |
missense |
probably benign |
0.07 |
R1597:Mup5
|
UTSW |
4 |
61,753,317 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1721:Mup5
|
UTSW |
4 |
61,750,607 (GRCm39) |
nonsense |
probably null |
|
R1772:Mup5
|
UTSW |
4 |
61,750,578 (GRCm39) |
critical splice donor site |
probably null |
|
R1881:Mup5
|
UTSW |
4 |
61,752,868 (GRCm39) |
nonsense |
probably null |
|
R2104:Mup5
|
UTSW |
4 |
61,751,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R2384:Mup5
|
UTSW |
4 |
61,753,261 (GRCm39) |
splice site |
probably null |
|
R5246:Mup5
|
UTSW |
4 |
61,752,874 (GRCm39) |
missense |
probably benign |
0.04 |
R5926:Mup5
|
UTSW |
4 |
61,751,286 (GRCm39) |
missense |
probably benign |
0.03 |
R6905:Mup5
|
UTSW |
4 |
61,751,340 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6912:Mup5
|
UTSW |
4 |
61,752,806 (GRCm39) |
missense |
probably benign |
0.03 |
R6957:Mup5
|
UTSW |
4 |
61,751,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Mup5
|
UTSW |
4 |
61,751,992 (GRCm39) |
missense |
probably damaging |
0.96 |
R7224:Mup5
|
UTSW |
4 |
61,750,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7244:Mup5
|
UTSW |
4 |
61,749,818 (GRCm39) |
splice site |
probably null |
|
R7570:Mup5
|
UTSW |
4 |
61,752,911 (GRCm39) |
nonsense |
probably null |
|
R8253:Mup5
|
UTSW |
4 |
61,752,811 (GRCm39) |
missense |
probably benign |
0.00 |
R8465:Mup5
|
UTSW |
4 |
61,752,015 (GRCm39) |
missense |
probably benign |
|
R9048:Mup5
|
UTSW |
4 |
61,750,612 (GRCm39) |
missense |
probably benign |
0.20 |
R9571:Mup5
|
UTSW |
4 |
61,750,787 (GRCm39) |
critical splice donor site |
probably null |
|
|