Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
A |
G |
11: 84,168,628 (GRCm39) |
I1085V |
possibly damaging |
Het |
Adamts16 |
T |
C |
13: 70,941,260 (GRCm39) |
T376A |
probably benign |
Het |
Aifm3 |
T |
A |
16: 17,320,650 (GRCm39) |
|
probably null |
Het |
Ankrd16 |
A |
G |
2: 11,783,473 (GRCm39) |
E25G |
probably damaging |
Het |
Ano6 |
T |
A |
15: 95,865,495 (GRCm39) |
|
probably null |
Het |
Cdh18 |
T |
C |
15: 23,446,077 (GRCm39) |
I509T |
possibly damaging |
Het |
Cdon |
A |
G |
9: 35,394,510 (GRCm39) |
T919A |
possibly damaging |
Het |
Clca3a2 |
G |
A |
3: 144,522,916 (GRCm39) |
P148L |
probably damaging |
Het |
Dnph1 |
G |
T |
17: 46,809,408 (GRCm39) |
R74L |
probably benign |
Het |
Epha6 |
C |
T |
16: 59,596,007 (GRCm39) |
A895T |
probably damaging |
Het |
Exoc3l4 |
T |
A |
12: 111,395,845 (GRCm39) |
|
probably benign |
Het |
Fbll1 |
A |
G |
11: 35,688,648 (GRCm39) |
I205T |
probably damaging |
Het |
Frem2 |
T |
A |
3: 53,424,434 (GRCm39) |
H3001L |
probably damaging |
Het |
Galk2 |
A |
G |
2: 125,825,099 (GRCm39) |
N432D |
probably benign |
Het |
Il10 |
A |
G |
1: 130,949,151 (GRCm39) |
E104G |
probably benign |
Het |
Il1a |
T |
C |
2: 129,146,637 (GRCm39) |
K152R |
probably benign |
Het |
Kdm1b |
T |
A |
13: 47,227,213 (GRCm39) |
N568K |
probably damaging |
Het |
Kmt2c |
A |
C |
5: 25,515,668 (GRCm39) |
L2725R |
probably damaging |
Het |
Krba1 |
G |
T |
6: 48,388,688 (GRCm39) |
L527F |
probably damaging |
Het |
Lrp2 |
A |
G |
2: 69,259,050 (GRCm39) |
S4547P |
probably benign |
Het |
Nin |
G |
T |
12: 70,090,439 (GRCm39) |
A992E |
possibly damaging |
Het |
Or11g7 |
G |
A |
14: 50,690,607 (GRCm39) |
V33M |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,267,098 (GRCm39) |
H158Q |
probably benign |
Het |
Pcdhb1 |
A |
G |
18: 37,400,186 (GRCm39) |
I712M |
possibly damaging |
Het |
Prmt2 |
C |
T |
10: 76,053,143 (GRCm39) |
|
probably null |
Het |
Rbm20 |
T |
G |
19: 53,829,426 (GRCm39) |
V608G |
probably damaging |
Het |
Smarcc2 |
C |
T |
10: 128,324,846 (GRCm39) |
|
probably benign |
Het |
Speer3 |
A |
T |
5: 13,843,236 (GRCm39) |
R48* |
probably null |
Het |
Tlr1 |
A |
T |
5: 65,082,416 (GRCm39) |
N720K |
possibly damaging |
Het |
Tnfrsf21 |
A |
T |
17: 43,398,702 (GRCm39) |
M603L |
probably benign |
Het |
Ttc3 |
T |
A |
16: 94,210,590 (GRCm39) |
|
probably null |
Het |
Usp4 |
C |
A |
9: 108,243,079 (GRCm39) |
A249E |
possibly damaging |
Het |
Wdr20 |
T |
A |
12: 110,759,948 (GRCm39) |
V278E |
probably damaging |
Het |
|
Other mutations in Gm7535 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Gm7535
|
APN |
17 |
18,132,150 (GRCm39) |
intron |
probably benign |
|
R0165:Gm7535
|
UTSW |
17 |
18,131,437 (GRCm39) |
intron |
probably benign |
|
R0335:Gm7535
|
UTSW |
17 |
18,131,374 (GRCm39) |
intron |
probably benign |
|
R1985:Gm7535
|
UTSW |
17 |
18,131,800 (GRCm39) |
intron |
probably benign |
|
R2217:Gm7535
|
UTSW |
17 |
18,131,936 (GRCm39) |
intron |
probably benign |
|
R2218:Gm7535
|
UTSW |
17 |
18,131,936 (GRCm39) |
intron |
probably benign |
|
R4464:Gm7535
|
UTSW |
17 |
18,131,924 (GRCm39) |
intron |
probably benign |
|
R4581:Gm7535
|
UTSW |
17 |
18,131,345 (GRCm39) |
intron |
probably benign |
|
R4887:Gm7535
|
UTSW |
17 |
18,131,333 (GRCm39) |
intron |
probably benign |
|
R5225:Gm7535
|
UTSW |
17 |
18,131,809 (GRCm39) |
intron |
probably benign |
|
R5305:Gm7535
|
UTSW |
17 |
18,132,061 (GRCm39) |
intron |
probably benign |
|
R5641:Gm7535
|
UTSW |
17 |
18,131,788 (GRCm39) |
intron |
probably benign |
|
R5658:Gm7535
|
UTSW |
17 |
18,131,582 (GRCm39) |
intron |
probably benign |
|
R5760:Gm7535
|
UTSW |
17 |
18,132,080 (GRCm39) |
intron |
probably benign |
|
|