Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
C |
8: 111,774,575 (GRCm39) |
V568A |
possibly damaging |
Het |
Abcb11 |
T |
A |
2: 69,117,971 (GRCm39) |
Q469L |
probably damaging |
Het |
Ahsg |
G |
A |
16: 22,717,731 (GRCm39) |
G264E |
probably damaging |
Het |
Ankar |
T |
C |
1: 72,697,862 (GRCm39) |
Y788C |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,911,511 (GRCm39) |
F1508I |
possibly damaging |
Het |
Cd6 |
C |
A |
19: 10,776,601 (GRCm39) |
Q141H |
probably benign |
Het |
Cercam |
A |
C |
2: 29,771,015 (GRCm39) |
T471P |
probably damaging |
Het |
Cux1 |
T |
C |
5: 136,337,301 (GRCm39) |
D729G |
possibly damaging |
Het |
Dglucy |
T |
A |
12: 100,816,540 (GRCm39) |
F394Y |
probably damaging |
Het |
E130308A19Rik |
A |
G |
4: 59,720,004 (GRCm39) |
N512S |
probably benign |
Het |
Ephb4 |
T |
C |
5: 137,356,059 (GRCm39) |
C223R |
probably damaging |
Het |
Gcn1 |
T |
A |
5: 115,714,174 (GRCm39) |
|
probably null |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Hirip3 |
T |
A |
7: 126,463,381 (GRCm39) |
S446T |
probably benign |
Het |
Hoxa5 |
A |
T |
6: 52,179,647 (GRCm39) |
F243I |
probably damaging |
Het |
Iars1 |
T |
C |
13: 49,844,975 (GRCm39) |
V162A |
probably benign |
Het |
Lama2 |
G |
A |
10: 26,981,135 (GRCm39) |
R1840* |
probably null |
Het |
Lbp |
T |
A |
2: 158,166,493 (GRCm39) |
L349Q |
probably damaging |
Het |
Lrp4 |
T |
C |
2: 91,331,452 (GRCm39) |
I1604T |
probably benign |
Het |
Mapk10 |
T |
C |
5: 103,144,455 (GRCm39) |
K121E |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,578,521 (GRCm39) |
R1579* |
probably null |
Het |
Obscn |
T |
C |
11: 58,965,794 (GRCm39) |
D652G |
possibly damaging |
Het |
Or10x1 |
A |
G |
1: 174,196,967 (GRCm39) |
I161M |
probably damaging |
Het |
Or5b117 |
G |
A |
19: 13,431,449 (GRCm39) |
T144I |
probably benign |
Het |
Or7g30 |
A |
G |
9: 19,352,760 (GRCm39) |
I184V |
probably benign |
Het |
Ostm1 |
C |
T |
10: 42,574,147 (GRCm39) |
S280L |
possibly damaging |
Het |
Peak1 |
C |
T |
9: 56,167,388 (GRCm39) |
R180K |
probably damaging |
Het |
Plcz1 |
T |
C |
6: 139,947,837 (GRCm39) |
Y515C |
probably benign |
Het |
Postn |
T |
C |
3: 54,283,455 (GRCm39) |
|
probably benign |
Het |
Ptchd4 |
C |
T |
17: 42,814,493 (GRCm39) |
T798I |
probably damaging |
Het |
Rnf41 |
A |
T |
10: 128,271,344 (GRCm39) |
N85Y |
probably damaging |
Het |
Shisa7 |
A |
T |
7: 4,833,825 (GRCm39) |
H323Q |
probably damaging |
Het |
Slco2a1 |
T |
A |
9: 102,951,629 (GRCm39) |
M386K |
probably damaging |
Het |
St18 |
G |
A |
1: 6,914,596 (GRCm39) |
|
probably null |
Het |
Stra6 |
T |
A |
9: 58,048,431 (GRCm39) |
L175M |
probably damaging |
Het |
Tmem67 |
A |
G |
4: 12,057,389 (GRCm39) |
L600P |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Xpo7 |
G |
A |
14: 70,903,475 (GRCm39) |
T1078I |
probably benign |
Het |
Zan |
G |
A |
5: 137,462,386 (GRCm39) |
T931I |
unknown |
Het |
|
Other mutations in Try5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01837:Try5
|
APN |
6 |
41,290,358 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02652:Try5
|
APN |
6 |
41,288,342 (GRCm39) |
missense |
probably benign |
0.01 |
R1955:Try5
|
UTSW |
6 |
41,288,703 (GRCm39) |
missense |
probably benign |
0.17 |
R2014:Try5
|
UTSW |
6 |
41,291,585 (GRCm39) |
splice site |
probably null |
|
R2015:Try5
|
UTSW |
6 |
41,291,585 (GRCm39) |
splice site |
probably null |
|
R2848:Try5
|
UTSW |
6 |
41,290,410 (GRCm39) |
missense |
probably benign |
0.01 |
R4227:Try5
|
UTSW |
6 |
41,290,401 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4685:Try5
|
UTSW |
6 |
41,288,233 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4816:Try5
|
UTSW |
6 |
41,290,349 (GRCm39) |
missense |
probably benign |
0.18 |
R5230:Try5
|
UTSW |
6 |
41,289,312 (GRCm39) |
missense |
probably benign |
0.19 |
R5658:Try5
|
UTSW |
6 |
41,289,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R6518:Try5
|
UTSW |
6 |
41,291,613 (GRCm39) |
missense |
probably benign |
|
R6910:Try5
|
UTSW |
6 |
41,288,733 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6913:Try5
|
UTSW |
6 |
41,288,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7219:Try5
|
UTSW |
6 |
41,288,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Try5
|
UTSW |
6 |
41,290,388 (GRCm39) |
missense |
probably benign |
0.09 |
R7444:Try5
|
UTSW |
6 |
41,288,299 (GRCm39) |
missense |
probably benign |
0.00 |
R7575:Try5
|
UTSW |
6 |
41,288,748 (GRCm39) |
missense |
probably benign |
0.05 |
R7585:Try5
|
UTSW |
6 |
41,288,748 (GRCm39) |
missense |
probably benign |
0.14 |
R8011:Try5
|
UTSW |
6 |
41,290,421 (GRCm39) |
missense |
probably benign |
0.12 |
R8739:Try5
|
UTSW |
6 |
41,288,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R8991:Try5
|
UTSW |
6 |
41,289,295 (GRCm39) |
missense |
probably benign |
0.18 |
R9397:Try5
|
UTSW |
6 |
41,289,314 (GRCm39) |
missense |
probably benign |
0.00 |
|