Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp6 |
T |
A |
3: 97,066,605 (GRCm39) |
L41Q |
probably damaging |
Het |
Aoc1 |
T |
C |
6: 48,882,589 (GRCm39) |
L177P |
probably damaging |
Het |
Btbd7 |
C |
T |
12: 102,804,411 (GRCm39) |
E210K |
probably benign |
Het |
C1qtnf12 |
G |
A |
4: 156,050,356 (GRCm39) |
R231H |
probably damaging |
Het |
Cenpf |
T |
A |
1: 189,390,534 (GRCm39) |
E1099D |
probably damaging |
Het |
Dennd3 |
T |
C |
15: 73,419,426 (GRCm39) |
V739A |
possibly damaging |
Het |
Dmxl1 |
G |
A |
18: 49,998,189 (GRCm39) |
S763N |
probably damaging |
Het |
Dzip3 |
C |
A |
16: 48,795,906 (GRCm39) |
C155F |
probably benign |
Het |
Fam161b |
A |
T |
12: 84,408,464 (GRCm39) |
|
probably null |
Het |
Fancd2 |
T |
G |
6: 113,542,165 (GRCm39) |
S770A |
probably damaging |
Het |
Gpt2 |
G |
T |
8: 86,252,202 (GRCm39) |
V506L |
probably benign |
Het |
Heatr1 |
G |
T |
13: 12,449,341 (GRCm39) |
L1946F |
probably damaging |
Het |
Hnrnpl |
A |
G |
7: 28,510,436 (GRCm39) |
|
probably benign |
Het |
Itgb1 |
T |
A |
8: 129,439,839 (GRCm39) |
I176N |
probably damaging |
Het |
Kif13b |
C |
T |
14: 65,037,849 (GRCm39) |
T1505I |
probably benign |
Het |
Magi2 |
C |
T |
5: 20,670,907 (GRCm39) |
T580M |
probably damaging |
Het |
Mettl3 |
A |
T |
14: 52,537,363 (GRCm39) |
I102N |
probably benign |
Het |
Mgat4c |
A |
G |
10: 102,220,931 (GRCm39) |
H71R |
probably damaging |
Het |
Misp |
G |
A |
10: 79,661,795 (GRCm39) |
V71I |
probably benign |
Het |
Muc2 |
A |
G |
7: 141,283,590 (GRCm39) |
Q734R |
probably benign |
Het |
Muc5b |
C |
T |
7: 141,418,853 (GRCm39) |
T3933I |
possibly damaging |
Het |
Myh13 |
A |
G |
11: 67,218,014 (GRCm39) |
N29S |
probably benign |
Het |
Myo15a |
A |
T |
11: 60,368,398 (GRCm39) |
Y386F |
probably damaging |
Het |
Neb |
C |
A |
2: 52,091,927 (GRCm39) |
V5046F |
probably damaging |
Het |
Neurod1 |
T |
A |
2: 79,284,939 (GRCm39) |
N148I |
probably damaging |
Het |
Nrg1 |
A |
T |
8: 32,311,411 (GRCm39) |
V376E |
probably damaging |
Het |
Nsa2 |
G |
T |
13: 97,272,042 (GRCm39) |
Q60K |
possibly damaging |
Het |
Odr4 |
A |
G |
1: 150,260,282 (GRCm39) |
I112T |
probably benign |
Het |
Ppp1r21 |
T |
A |
17: 88,884,555 (GRCm39) |
|
probably null |
Het |
Rala |
T |
A |
13: 18,057,031 (GRCm39) |
E185V |
probably benign |
Het |
Rhoc |
T |
C |
3: 104,700,003 (GRCm39) |
|
probably null |
Het |
Robo3 |
A |
G |
9: 37,333,521 (GRCm39) |
V708A |
probably damaging |
Het |
Rtcb |
G |
T |
10: 85,778,458 (GRCm39) |
T395K |
possibly damaging |
Het |
Rttn |
A |
G |
18: 89,056,018 (GRCm39) |
T967A |
probably benign |
Het |
Sacs |
C |
A |
14: 61,421,410 (GRCm39) |
Q116K |
probably damaging |
Het |
Smarca4 |
A |
G |
9: 21,583,355 (GRCm39) |
H1062R |
possibly damaging |
Het |
Spatc1l |
C |
T |
10: 76,399,736 (GRCm39) |
T86I |
probably benign |
Het |
Thbs4 |
T |
C |
13: 92,909,672 (GRCm39) |
N375S |
probably benign |
Het |
Tsc1 |
A |
G |
2: 28,577,154 (GRCm39) |
D1151G |
probably damaging |
Het |
Ttll1 |
T |
C |
15: 83,368,419 (GRCm39) |
D413G |
probably benign |
Het |
Wap |
G |
A |
11: 6,588,550 (GRCm39) |
Q25* |
probably null |
Het |
Wnt16 |
A |
G |
6: 22,298,021 (GRCm39) |
N296D |
probably benign |
Het |
|
Other mutations in Hao2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01933:Hao2
|
APN |
3 |
98,787,648 (GRCm39) |
splice site |
probably benign |
|
IGL03279:Hao2
|
APN |
3 |
98,787,712 (GRCm39) |
missense |
possibly damaging |
0.88 |
goatherd
|
UTSW |
3 |
98,784,451 (GRCm39) |
missense |
probably benign |
0.06 |
R0600:Hao2
|
UTSW |
3 |
98,790,876 (GRCm39) |
splice site |
probably benign |
|
R1298:Hao2
|
UTSW |
3 |
98,790,985 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3176:Hao2
|
UTSW |
3 |
98,787,644 (GRCm39) |
splice site |
probably benign |
|
R3177:Hao2
|
UTSW |
3 |
98,787,644 (GRCm39) |
splice site |
probably benign |
|
R4486:Hao2
|
UTSW |
3 |
98,789,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R4487:Hao2
|
UTSW |
3 |
98,789,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R4488:Hao2
|
UTSW |
3 |
98,789,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R5290:Hao2
|
UTSW |
3 |
98,784,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R5760:Hao2
|
UTSW |
3 |
98,787,748 (GRCm39) |
nonsense |
probably null |
|
R6129:Hao2
|
UTSW |
3 |
98,787,842 (GRCm39) |
missense |
probably benign |
0.00 |
R6720:Hao2
|
UTSW |
3 |
98,784,451 (GRCm39) |
missense |
probably benign |
0.06 |
R6861:Hao2
|
UTSW |
3 |
98,784,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Hao2
|
UTSW |
3 |
98,784,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Hao2
|
UTSW |
3 |
98,784,598 (GRCm39) |
splice site |
probably null |
|
R8277:Hao2
|
UTSW |
3 |
98,787,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R8515:Hao2
|
UTSW |
3 |
98,790,963 (GRCm39) |
missense |
probably benign |
0.00 |
R8848:Hao2
|
UTSW |
3 |
98,784,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R9335:Hao2
|
UTSW |
3 |
98,791,010 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9497:Hao2
|
UTSW |
3 |
98,784,462 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Hao2
|
UTSW |
3 |
98,782,668 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Hao2
|
UTSW |
3 |
98,789,357 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Hao2
|
UTSW |
3 |
98,789,258 (GRCm39) |
missense |
probably benign |
0.02 |
|