Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
T |
C |
7: 119,195,143 (GRCm39) |
F552L |
probably damaging |
Het |
Actn2 |
A |
G |
13: 12,325,765 (GRCm39) |
L70P |
probably damaging |
Het |
Btbd7 |
A |
G |
12: 102,751,552 (GRCm39) |
S1071P |
probably benign |
Het |
Cd200r1 |
T |
A |
16: 44,586,417 (GRCm39) |
W16R |
probably benign |
Het |
Cdhr2 |
A |
G |
13: 54,863,478 (GRCm39) |
N120D |
probably damaging |
Het |
Col19a1 |
T |
C |
1: 24,549,947 (GRCm39) |
T317A |
unknown |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dmbt1 |
T |
C |
7: 130,718,361 (GRCm39) |
L1683P |
probably damaging |
Het |
Dynll1 |
A |
T |
5: 115,438,700 (GRCm39) |
C2S |
probably benign |
Het |
Elp2 |
T |
A |
18: 24,742,707 (GRCm39) |
S80T |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,405,383 (GRCm39) |
N711K |
probably damaging |
Het |
Fzd3 |
A |
G |
14: 65,473,054 (GRCm39) |
I238T |
probably damaging |
Het |
Galnt7 |
A |
T |
8: 57,991,215 (GRCm39) |
F432I |
probably damaging |
Het |
Gemin5 |
T |
A |
11: 58,030,375 (GRCm39) |
T817S |
probably benign |
Het |
H2-T5 |
C |
A |
17: 36,472,861 (GRCm39) |
|
probably benign |
Het |
Homer3 |
G |
A |
8: 70,742,793 (GRCm39) |
|
probably null |
Het |
Kcnj4 |
C |
A |
15: 79,368,874 (GRCm39) |
A369S |
probably benign |
Het |
Llgl1 |
T |
C |
11: 60,596,834 (GRCm39) |
V145A |
probably benign |
Het |
Mdga1 |
T |
C |
17: 30,069,491 (GRCm39) |
D185G |
probably damaging |
Het |
Mettl2 |
A |
G |
11: 105,017,604 (GRCm39) |
D38G |
probably damaging |
Het |
Mfsd13a |
C |
T |
19: 46,360,431 (GRCm39) |
R328C |
probably damaging |
Het |
Mpp4 |
T |
C |
1: 59,183,961 (GRCm39) |
I260V |
possibly damaging |
Het |
Mtcl1 |
T |
C |
17: 66,651,220 (GRCm39) |
E1112G |
probably damaging |
Het |
Mtus2 |
T |
A |
5: 148,140,748 (GRCm39) |
N871K |
possibly damaging |
Het |
Mylk |
C |
T |
16: 34,732,645 (GRCm39) |
Q642* |
probably null |
Het |
Naip6 |
C |
T |
13: 100,437,108 (GRCm39) |
A472T |
probably benign |
Het |
Or4f57 |
A |
G |
2: 111,790,560 (GRCm39) |
I286T |
probably damaging |
Het |
Pdzd2 |
A |
T |
15: 12,387,732 (GRCm39) |
D875E |
probably benign |
Het |
Piezo1 |
G |
T |
8: 123,225,413 (GRCm39) |
T557K |
probably damaging |
Het |
Plxna2 |
C |
T |
1: 194,431,625 (GRCm39) |
S538F |
probably damaging |
Het |
Plxnb1 |
T |
C |
9: 108,929,291 (GRCm39) |
V49A |
possibly damaging |
Het |
Pramel6 |
A |
T |
2: 87,338,874 (GRCm39) |
I25F |
probably damaging |
Het |
Rreb1 |
C |
T |
13: 38,114,419 (GRCm39) |
Q593* |
probably null |
Het |
Scn8a |
A |
G |
15: 100,870,711 (GRCm39) |
N254S |
probably damaging |
Het |
Scnn1g |
T |
G |
7: 121,339,650 (GRCm39) |
S150A |
probably benign |
Het |
Sec24a |
A |
G |
11: 51,605,991 (GRCm39) |
F686L |
possibly damaging |
Het |
Sirt1 |
T |
C |
10: 63,157,777 (GRCm39) |
T546A |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Traf5 |
A |
T |
1: 191,729,806 (GRCm39) |
V415E |
probably benign |
Het |
Traip |
C |
G |
9: 107,836,686 (GRCm39) |
T110S |
probably benign |
Het |
Treml2 |
T |
C |
17: 48,615,142 (GRCm39) |
V209A |
probably benign |
Het |
Trpv5 |
T |
C |
6: 41,634,830 (GRCm39) |
S500G |
probably benign |
Het |
Usp32 |
G |
A |
11: 84,944,801 (GRCm39) |
L296F |
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,651,099 (GRCm39) |
H166R |
possibly damaging |
Het |
Zswim1 |
A |
G |
2: 164,667,369 (GRCm39) |
D207G |
probably damaging |
Het |
|
Other mutations in Gm5414 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Gm5414
|
APN |
15 |
101,536,569 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Gm5414
|
APN |
15 |
101,535,410 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01939:Gm5414
|
APN |
15 |
101,534,105 (GRCm39) |
splice site |
probably benign |
|
IGL02205:Gm5414
|
APN |
15 |
101,534,304 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02411:Gm5414
|
APN |
15 |
101,536,269 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02720:Gm5414
|
APN |
15 |
101,533,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02900:Gm5414
|
APN |
15 |
101,536,242 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03283:Gm5414
|
APN |
15 |
101,535,522 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4480001:Gm5414
|
UTSW |
15 |
101,536,181 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4504001:Gm5414
|
UTSW |
15 |
101,534,258 (GRCm39) |
missense |
probably damaging |
0.98 |
R1905:Gm5414
|
UTSW |
15 |
101,533,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Gm5414
|
UTSW |
15 |
101,536,495 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3011:Gm5414
|
UTSW |
15 |
101,534,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R3033:Gm5414
|
UTSW |
15 |
101,533,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Gm5414
|
UTSW |
15 |
101,533,988 (GRCm39) |
missense |
probably benign |
|
R4257:Gm5414
|
UTSW |
15 |
101,533,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Gm5414
|
UTSW |
15 |
101,536,543 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4912:Gm5414
|
UTSW |
15 |
101,533,445 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5095:Gm5414
|
UTSW |
15 |
101,532,473 (GRCm39) |
missense |
probably benign |
0.01 |
R5135:Gm5414
|
UTSW |
15 |
101,536,203 (GRCm39) |
missense |
probably damaging |
0.97 |
R5177:Gm5414
|
UTSW |
15 |
101,534,252 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5330:Gm5414
|
UTSW |
15 |
101,533,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5331:Gm5414
|
UTSW |
15 |
101,533,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Gm5414
|
UTSW |
15 |
101,533,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Gm5414
|
UTSW |
15 |
101,536,422 (GRCm39) |
missense |
probably benign |
0.33 |
R5623:Gm5414
|
UTSW |
15 |
101,534,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6781:Gm5414
|
UTSW |
15 |
101,534,096 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8298:Gm5414
|
UTSW |
15 |
101,532,605 (GRCm39) |
missense |
unknown |
|
R8912:Gm5414
|
UTSW |
15 |
101,536,620 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9092:Gm5414
|
UTSW |
15 |
101,536,345 (GRCm39) |
missense |
probably benign |
0.01 |
R9721:Gm5414
|
UTSW |
15 |
101,536,582 (GRCm39) |
nonsense |
probably null |
|
RF001:Gm5414
|
UTSW |
15 |
101,536,388 (GRCm39) |
missense |
probably benign |
|
|