Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930555G01Rik |
T |
G |
14: 5,051,639 (GRCm38) |
V66G |
possibly damaging |
Het |
A630001G21Rik |
G |
T |
1: 85,653,002 (GRCm39) |
Y55* |
probably null |
Het |
Abca8a |
G |
A |
11: 109,921,173 (GRCm39) |
T1474I |
probably damaging |
Het |
Acaca |
T |
G |
11: 84,259,551 (GRCm39) |
I1962S |
probably damaging |
Het |
Acap1 |
A |
T |
11: 69,775,672 (GRCm39) |
S455T |
probably damaging |
Het |
Acbd7 |
G |
A |
2: 3,337,259 (GRCm39) |
|
probably null |
Het |
Adamts9 |
A |
G |
6: 92,878,444 (GRCm39) |
L541P |
probably damaging |
Het |
Ankrd49 |
T |
C |
9: 14,692,711 (GRCm39) |
N151S |
probably benign |
Het |
Apcdd1 |
C |
T |
18: 63,055,731 (GRCm39) |
|
probably benign |
Het |
Arhgap27 |
T |
C |
11: 103,231,115 (GRCm39) |
D58G |
probably damaging |
Het |
Btbd18 |
G |
T |
2: 84,497,810 (GRCm39) |
A483S |
probably damaging |
Het |
C2 |
A |
G |
17: 35,094,965 (GRCm39) |
S257P |
probably damaging |
Het |
Catsper3 |
T |
A |
13: 55,946,725 (GRCm39) |
Y141N |
probably damaging |
Het |
Cfap54 |
G |
A |
10: 92,833,147 (GRCm39) |
L1160F |
probably damaging |
Het |
Chst13 |
G |
A |
6: 90,286,506 (GRCm39) |
P152L |
probably damaging |
Het |
Cyp4f14 |
C |
T |
17: 33,130,516 (GRCm39) |
G141D |
probably damaging |
Het |
Duox1 |
C |
T |
2: 122,150,783 (GRCm39) |
T286I |
possibly damaging |
Het |
Epc2 |
G |
A |
2: 49,378,822 (GRCm39) |
G92E |
probably damaging |
Het |
Fmnl3 |
C |
T |
15: 99,225,938 (GRCm39) |
|
probably null |
Het |
Glyatl3 |
G |
A |
17: 41,223,565 (GRCm39) |
R59* |
probably null |
Het |
Gm3633 |
T |
A |
14: 42,460,400 (GRCm39) |
Q181L |
|
Het |
Guca1b |
C |
T |
17: 47,696,560 (GRCm39) |
T49M |
probably benign |
Het |
Hdac9 |
T |
A |
12: 34,353,275 (GRCm39) |
H645L |
probably damaging |
Het |
Hhip |
T |
C |
8: 80,719,112 (GRCm39) |
R472G |
probably benign |
Het |
Ifi203 |
A |
G |
1: 173,765,547 (GRCm39) |
V9A |
probably damaging |
Het |
Igkv9-123 |
A |
T |
6: 67,931,443 (GRCm39) |
V41D |
probably damaging |
Het |
Il5ra |
T |
A |
6: 106,721,258 (GRCm39) |
T14S |
probably benign |
Het |
Ints2 |
A |
G |
11: 86,135,311 (GRCm39) |
S368P |
probably benign |
Het |
Kat6b |
T |
A |
14: 21,675,244 (GRCm39) |
S470T |
possibly damaging |
Het |
Kmt2d |
A |
G |
15: 98,747,994 (GRCm39) |
V3110A |
unknown |
Het |
Lama2 |
T |
C |
10: 26,981,117 (GRCm39) |
N1846D |
probably benign |
Het |
Lrp1b |
T |
A |
2: 40,640,922 (GRCm39) |
E3507D |
|
Het |
Ly6g6c |
A |
G |
17: 35,288,317 (GRCm39) |
N63S |
probably benign |
Het |
Naprt |
C |
T |
15: 75,763,859 (GRCm39) |
V354I |
probably null |
Het |
Nars1 |
A |
G |
18: 64,642,327 (GRCm39) |
S172P |
probably benign |
Het |
Odr4 |
C |
T |
1: 150,238,616 (GRCm39) |
A434T |
probably damaging |
Het |
Or6c5b |
A |
G |
10: 129,245,909 (GRCm39) |
R225G |
possibly damaging |
Het |
Or7e177 |
T |
C |
9: 20,211,748 (GRCm39) |
I85T |
possibly damaging |
Het |
Pcdhb6 |
A |
G |
18: 37,469,353 (GRCm39) |
D758G |
probably benign |
Het |
Pkp4 |
G |
A |
2: 59,148,856 (GRCm39) |
W536* |
probably null |
Het |
Polr3b |
C |
T |
10: 84,467,653 (GRCm39) |
L78F |
possibly damaging |
Het |
Rasa4 |
T |
A |
5: 136,129,836 (GRCm39) |
V272E |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,040,849 (GRCm39) |
T3836A |
possibly damaging |
Het |
Tbpl2 |
C |
T |
2: 23,966,070 (GRCm39) |
V308I |
possibly damaging |
Het |
Tcea1 |
T |
A |
1: 4,962,141 (GRCm39) |
I176K |
probably damaging |
Het |
Ttc8 |
G |
T |
12: 98,942,692 (GRCm39) |
G411* |
probably null |
Het |
Vmn2r115 |
G |
A |
17: 23,564,152 (GRCm39) |
W108* |
probably null |
Het |
Zdhhc13 |
C |
T |
7: 48,476,628 (GRCm39) |
T581I |
probably benign |
Het |
Zfp777 |
G |
T |
6: 48,021,190 (GRCm39) |
T144K |
probably benign |
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 |
IGL01885:Try5
|
APN |
6 |
41,288,672 (GRCm39) |
missense |
possibly damaging |
0.93 |
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 |
|