Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr6 |
A |
T |
10: 89,562,617 (GRCm39) |
D87E |
probably damaging |
Het |
Ano3 |
A |
T |
2: 110,491,616 (GRCm39) |
Y887N |
probably damaging |
Het |
Arid4a |
A |
G |
12: 71,106,867 (GRCm39) |
D313G |
probably damaging |
Het |
Armc2 |
A |
G |
10: 41,887,923 (GRCm39) |
V20A |
probably benign |
Het |
Bltp3b |
A |
G |
10: 89,623,061 (GRCm39) |
D312G |
possibly damaging |
Het |
C2 |
T |
A |
17: 35,095,432 (GRCm39) |
N171I |
possibly damaging |
Het |
Cdh1 |
C |
A |
8: 107,395,187 (GRCm39) |
N865K |
probably damaging |
Het |
Cep89 |
T |
A |
7: 35,117,070 (GRCm39) |
V224E |
probably damaging |
Het |
Cfap251 |
G |
A |
5: 123,436,584 (GRCm39) |
V1038I |
probably benign |
Het |
Dennd2d |
C |
T |
3: 106,395,131 (GRCm39) |
|
probably benign |
Het |
Diaph1 |
T |
A |
18: 37,986,408 (GRCm39) |
K1157N |
probably damaging |
Het |
Dsg4 |
T |
A |
18: 20,595,549 (GRCm39) |
L584* |
probably null |
Het |
Exoc4 |
G |
A |
6: 33,895,367 (GRCm39) |
A795T |
probably benign |
Het |
Fbln5 |
A |
T |
12: 101,731,468 (GRCm39) |
I242N |
probably damaging |
Het |
Gls2 |
A |
G |
10: 128,041,090 (GRCm39) |
H394R |
probably damaging |
Het |
Gm27013 |
C |
T |
6: 130,652,921 (GRCm39) |
C847Y |
possibly damaging |
Het |
Ifna5 |
C |
A |
4: 88,754,036 (GRCm39) |
T92K |
possibly damaging |
Het |
Ireb2 |
A |
G |
9: 54,807,800 (GRCm39) |
M674V |
probably benign |
Het |
Itga2 |
C |
T |
13: 114,976,106 (GRCm39) |
V1089M |
possibly damaging |
Het |
Kctd16 |
A |
T |
18: 40,391,922 (GRCm39) |
Y170F |
probably benign |
Het |
Kif15 |
A |
G |
9: 122,843,039 (GRCm39) |
N45D |
possibly damaging |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,496,901 (GRCm39) |
K420E |
possibly damaging |
Het |
Ms4a14 |
G |
T |
19: 11,279,391 (GRCm39) |
Q1056K |
probably benign |
Het |
Or11g1 |
T |
C |
14: 50,651,235 (GRCm39) |
V78A |
possibly damaging |
Het |
Or5k8 |
T |
C |
16: 58,644,316 (GRCm39) |
Y252C |
probably benign |
Het |
Or8k21 |
T |
A |
2: 86,144,742 (GRCm39) |
E296V |
probably damaging |
Het |
Ovch2 |
T |
C |
7: 107,381,185 (GRCm39) |
E571G |
probably benign |
Het |
Pmel |
T |
C |
10: 128,550,250 (GRCm39) |
V95A |
probably damaging |
Het |
Ptger2 |
G |
T |
14: 45,226,599 (GRCm39) |
G60C |
probably benign |
Het |
Ranbp2 |
T |
G |
10: 58,312,647 (GRCm39) |
S1122R |
probably benign |
Het |
Rasal2 |
T |
C |
1: 157,003,732 (GRCm39) |
D309G |
probably damaging |
Het |
Rcc2 |
T |
A |
4: 140,443,230 (GRCm39) |
C303S |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Serpini1 |
C |
T |
3: 75,520,388 (GRCm39) |
|
probably benign |
Het |
Sgo2a |
G |
T |
1: 58,058,819 (GRCm39) |
E1133* |
probably null |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Smarcc1 |
G |
A |
9: 109,961,251 (GRCm39) |
|
probably benign |
Het |
Tbcd |
A |
G |
11: 121,483,518 (GRCm39) |
E749G |
probably benign |
Het |
Tmc3 |
G |
A |
7: 83,249,190 (GRCm39) |
A260T |
probably benign |
Het |
Tnfrsf21 |
A |
G |
17: 43,348,550 (GRCm39) |
Y54C |
probably damaging |
Het |
Urb1 |
T |
A |
16: 90,573,051 (GRCm39) |
M994L |
probably benign |
Het |
Usp14 |
A |
T |
18: 10,009,935 (GRCm39) |
|
probably benign |
Het |
Vps13a |
T |
C |
19: 16,641,928 (GRCm39) |
Y2233C |
probably damaging |
Het |
Wnt2 |
G |
T |
6: 17,990,027 (GRCm39) |
A290E |
probably damaging |
Het |
Zc3h8 |
A |
T |
2: 128,772,812 (GRCm39) |
C225* |
probably null |
Het |
|
Other mutations in AI429214 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01962:AI429214
|
APN |
8 |
37,461,383 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02508:AI429214
|
APN |
8 |
37,461,240 (GRCm39) |
missense |
probably benign |
|
R0973:AI429214
|
UTSW |
8 |
37,461,473 (GRCm39) |
missense |
probably benign |
0.29 |
R0973:AI429214
|
UTSW |
8 |
37,461,473 (GRCm39) |
missense |
probably benign |
0.29 |
R0974:AI429214
|
UTSW |
8 |
37,461,473 (GRCm39) |
missense |
probably benign |
0.29 |
R2007:AI429214
|
UTSW |
8 |
37,460,923 (GRCm39) |
missense |
probably benign |
0.29 |
R2113:AI429214
|
UTSW |
8 |
37,461,154 (GRCm39) |
nonsense |
probably null |
|
R2126:AI429214
|
UTSW |
8 |
37,461,362 (GRCm39) |
missense |
probably benign |
0.00 |
R2254:AI429214
|
UTSW |
8 |
37,460,920 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3409:AI429214
|
UTSW |
8 |
37,461,071 (GRCm39) |
missense |
probably benign |
0.00 |
R3411:AI429214
|
UTSW |
8 |
37,461,071 (GRCm39) |
missense |
probably benign |
0.00 |
R3852:AI429214
|
UTSW |
8 |
37,461,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R4657:AI429214
|
UTSW |
8 |
37,461,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:AI429214
|
UTSW |
8 |
37,461,383 (GRCm39) |
frame shift |
probably null |
|
R6248:AI429214
|
UTSW |
8 |
37,461,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:AI429214
|
UTSW |
8 |
37,460,987 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8018:AI429214
|
UTSW |
8 |
37,460,820 (GRCm39) |
start gained |
probably benign |
|
R8817:AI429214
|
UTSW |
8 |
37,461,268 (GRCm39) |
missense |
probably benign |
0.05 |
R8985:AI429214
|
UTSW |
8 |
37,460,820 (GRCm39) |
start gained |
probably benign |
|
R9564:AI429214
|
UTSW |
8 |
37,461,067 (GRCm39) |
missense |
possibly damaging |
0.92 |
|