Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf3 |
T |
C |
5: 30,401,821 (GRCm39) |
I736V |
possibly damaging |
Het |
Alpk3 |
C |
A |
7: 80,742,501 (GRCm39) |
P773T |
probably benign |
Het |
B4galt1 |
G |
A |
4: 40,807,258 (GRCm39) |
T376I |
probably benign |
Het |
Basp1 |
C |
A |
15: 25,364,398 (GRCm39) |
|
probably benign |
Het |
Capn5 |
C |
T |
7: 97,775,036 (GRCm39) |
G535R |
probably null |
Het |
Ccdc170 |
G |
A |
10: 4,510,920 (GRCm39) |
V660I |
possibly damaging |
Het |
Cdc73 |
A |
T |
1: 143,553,461 (GRCm39) |
D215E |
probably benign |
Het |
Clec14a |
G |
A |
12: 58,314,695 (GRCm39) |
A309V |
probably benign |
Het |
Clns1a |
G |
A |
7: 97,346,042 (GRCm39) |
G36R |
probably benign |
Het |
Cops7a |
C |
T |
6: 124,936,795 (GRCm39) |
R252H |
probably damaging |
Het |
Csmd2 |
C |
T |
4: 128,411,388 (GRCm39) |
P2469S |
probably benign |
Het |
Dsp |
T |
A |
13: 38,361,260 (GRCm39) |
|
probably null |
Het |
Eif3d |
A |
G |
15: 77,852,769 (GRCm39) |
F4S |
probably damaging |
Het |
Ephb1 |
T |
C |
9: 101,848,466 (GRCm39) |
T611A |
probably damaging |
Het |
Fgfr1 |
G |
A |
8: 26,062,453 (GRCm39) |
D663N |
probably damaging |
Het |
Gm5592 |
G |
A |
7: 40,807,259 (GRCm39) |
|
probably benign |
Het |
Itgb8 |
T |
C |
12: 119,127,204 (GRCm39) |
I683M |
possibly damaging |
Het |
Kcnip3 |
A |
G |
2: 127,323,934 (GRCm39) |
S32P |
probably benign |
Het |
Limch1 |
A |
G |
5: 67,126,422 (GRCm39) |
T8A |
probably damaging |
Het |
Lmf1 |
G |
A |
17: 25,873,445 (GRCm39) |
V317M |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,669,625 (GRCm39) |
Q1455R |
probably damaging |
Het |
Mtarc2 |
T |
C |
1: 184,573,505 (GRCm39) |
E131G |
possibly damaging |
Het |
Or51v14 |
C |
T |
7: 103,260,654 (GRCm39) |
R302Q |
probably benign |
Het |
Pak5 |
T |
C |
2: 135,942,746 (GRCm39) |
I465V |
probably benign |
Het |
Pcdhgb8 |
T |
C |
18: 37,895,728 (GRCm39) |
I266T |
probably benign |
Het |
Pde4d |
T |
C |
13: 109,769,431 (GRCm39) |
S40P |
probably benign |
Het |
Phrf1 |
C |
T |
7: 140,839,831 (GRCm39) |
R243* |
probably null |
Het |
Polk |
A |
T |
13: 96,623,490 (GRCm39) |
|
probably benign |
Het |
Ppl |
T |
C |
16: 4,922,414 (GRCm39) |
|
probably benign |
Het |
Rab11fip3 |
A |
G |
17: 26,287,500 (GRCm39) |
C218R |
possibly damaging |
Het |
Setd2 |
T |
C |
9: 110,378,639 (GRCm39) |
V818A |
probably benign |
Het |
Skida1 |
C |
A |
2: 18,050,708 (GRCm39) |
E815* |
probably null |
Het |
Slc35g3 |
A |
G |
11: 69,651,743 (GRCm39) |
F103L |
probably benign |
Het |
Svil |
T |
A |
18: 5,060,534 (GRCm39) |
C802S |
probably benign |
Het |
Trim7 |
A |
G |
11: 48,736,497 (GRCm39) |
|
probably null |
Het |
Ugt3a1 |
G |
A |
15: 9,310,727 (GRCm39) |
W336* |
probably null |
Het |
Vmn2r72 |
T |
C |
7: 85,387,285 (GRCm39) |
S760G |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,723,311 (GRCm39) |
|
probably null |
Het |
Wdfy4 |
A |
T |
14: 32,862,602 (GRCm39) |
I590N |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,214,653 (GRCm39) |
E764G |
probably damaging |
Het |
Xpnpep1 |
A |
T |
19: 52,994,773 (GRCm39) |
V285D |
probably benign |
Het |
Zfp934 |
T |
C |
13: 62,665,702 (GRCm39) |
K313R |
probably benign |
Het |
|
Other mutations in Fam43b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2128:Fam43b
|
UTSW |
4 |
138,123,299 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2258:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R2281:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R2413:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R2416:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R2417:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R3705:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R3715:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R3798:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R3854:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R3856:Fam43b
|
UTSW |
4 |
138,122,409 (GRCm39) |
missense |
probably benign |
0.25 |
R4639:Fam43b
|
UTSW |
4 |
138,123,278 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4868:Fam43b
|
UTSW |
4 |
138,123,108 (GRCm39) |
missense |
probably benign |
0.32 |
R5129:Fam43b
|
UTSW |
4 |
138,122,783 (GRCm39) |
nonsense |
probably null |
|
R6176:Fam43b
|
UTSW |
4 |
138,122,522 (GRCm39) |
missense |
probably damaging |
0.99 |
R7296:Fam43b
|
UTSW |
4 |
138,123,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R8280:Fam43b
|
UTSW |
4 |
138,123,281 (GRCm39) |
missense |
probably damaging |
0.99 |
|