Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
G |
A |
17: 24,619,424 (GRCm39) |
G921S |
probably benign |
Het |
Abca8b |
T |
C |
11: 109,838,007 (GRCm39) |
T1082A |
possibly damaging |
Het |
B9d2 |
T |
C |
7: 25,380,901 (GRCm39) |
|
probably null |
Het |
Bfsp1 |
T |
C |
2: 143,669,253 (GRCm39) |
E442G |
possibly damaging |
Het |
Bpifb5 |
C |
T |
2: 154,078,673 (GRCm39) |
|
probably benign |
Het |
Ccl1 |
A |
G |
11: 82,068,896 (GRCm39) |
I47T |
probably damaging |
Het |
Cln3 |
T |
C |
7: 126,174,569 (GRCm39) |
I285V |
probably null |
Het |
Cyp4a12b |
G |
T |
4: 115,290,173 (GRCm39) |
R242I |
possibly damaging |
Het |
Dcc |
T |
C |
18: 71,553,344 (GRCm39) |
T771A |
probably benign |
Het |
Erbb4 |
T |
C |
1: 68,081,878 (GRCm39) |
D1052G |
probably benign |
Het |
Fcnb |
T |
C |
2: 27,966,630 (GRCm39) |
N301S |
probably benign |
Het |
Gm28043 |
A |
C |
17: 29,853,705 (GRCm39) |
E403A |
probably damaging |
Het |
Gria4 |
A |
G |
9: 4,793,804 (GRCm39) |
|
probably benign |
Het |
Ighv5-12 |
T |
A |
12: 113,666,198 (GRCm39) |
M1L |
probably benign |
Het |
Il17rd |
A |
G |
14: 26,815,352 (GRCm39) |
|
probably null |
Het |
Kcnn3 |
T |
A |
3: 89,574,468 (GRCm39) |
L660Q |
probably damaging |
Het |
Lcor |
C |
T |
19: 41,546,808 (GRCm39) |
P131S |
probably damaging |
Het |
Leng1 |
T |
C |
7: 3,668,409 (GRCm39) |
N13S |
probably damaging |
Het |
Loxhd1 |
T |
C |
18: 77,468,160 (GRCm39) |
V827A |
probably damaging |
Het |
Mapk13 |
A |
G |
17: 28,996,709 (GRCm39) |
Y208C |
probably benign |
Het |
Mybpc3 |
T |
C |
2: 90,954,848 (GRCm39) |
V453A |
probably damaging |
Het |
Odam |
T |
C |
5: 88,033,613 (GRCm39) |
S15P |
unknown |
Het |
Or11l3 |
A |
T |
11: 58,516,269 (GRCm39) |
V201D |
probably damaging |
Het |
Or8d1 |
A |
T |
9: 38,766,526 (GRCm39) |
H56L |
probably damaging |
Het |
Pcdhb19 |
T |
C |
18: 37,632,618 (GRCm39) |
|
probably benign |
Het |
Per2 |
G |
T |
1: 91,372,341 (GRCm39) |
Y244* |
probably null |
Het |
Pik3ca |
A |
T |
3: 32,514,084 (GRCm39) |
I857F |
probably damaging |
Het |
Pold1 |
T |
A |
7: 44,188,824 (GRCm39) |
I447F |
probably benign |
Het |
Ppm1f |
T |
A |
16: 16,731,942 (GRCm39) |
W131R |
probably null |
Het |
Ppp2r2c |
A |
G |
5: 37,083,660 (GRCm39) |
Y67C |
probably damaging |
Het |
Psmb10 |
A |
T |
8: 106,663,532 (GRCm39) |
H155Q |
probably damaging |
Het |
Ptbp3 |
G |
A |
4: 59,501,470 (GRCm39) |
A149V |
probably benign |
Het |
Pygb |
T |
A |
2: 150,662,731 (GRCm39) |
V566E |
probably benign |
Het |
Rictor |
G |
A |
15: 6,788,999 (GRCm39) |
R205Q |
possibly damaging |
Het |
Ryr1 |
T |
A |
7: 28,715,211 (GRCm39) |
R4638W |
unknown |
Het |
Semp2l2a |
C |
T |
8: 13,888,096 (GRCm39) |
|
probably benign |
Het |
Septin3 |
G |
A |
15: 82,168,715 (GRCm39) |
|
probably null |
Het |
Serpina3b |
A |
T |
12: 104,097,313 (GRCm39) |
D198V |
probably benign |
Het |
Slc27a6 |
C |
A |
18: 58,689,815 (GRCm39) |
H94N |
probably benign |
Het |
Taf2 |
C |
T |
15: 54,915,559 (GRCm39) |
V456M |
probably damaging |
Het |
Tbpl2 |
T |
C |
2: 23,977,301 (GRCm39) |
E238G |
probably benign |
Het |
Ttn |
C |
T |
2: 76,584,551 (GRCm39) |
V20440I |
possibly damaging |
Het |
Zfp638 |
T |
A |
6: 83,912,000 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp865 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01731:Zfp865
|
APN |
7 |
5,032,875 (GRCm39) |
missense |
probably benign |
|
IGL02041:Zfp865
|
APN |
7 |
5,034,372 (GRCm39) |
missense |
probably benign |
|
R0613:Zfp865
|
UTSW |
7 |
5,032,090 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0879:Zfp865
|
UTSW |
7 |
5,034,342 (GRCm39) |
missense |
probably benign |
|
R0938:Zfp865
|
UTSW |
7 |
5,034,403 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1448:Zfp865
|
UTSW |
7 |
5,032,278 (GRCm39) |
nonsense |
probably null |
|
R3955:Zfp865
|
UTSW |
7 |
5,035,013 (GRCm39) |
missense |
probably damaging |
0.96 |
R4841:Zfp865
|
UTSW |
7 |
5,034,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Zfp865
|
UTSW |
7 |
5,034,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Zfp865
|
UTSW |
7 |
5,037,668 (GRCm39) |
intron |
probably benign |
|
R5773:Zfp865
|
UTSW |
7 |
5,037,693 (GRCm39) |
intron |
probably benign |
|
R5843:Zfp865
|
UTSW |
7 |
5,033,416 (GRCm39) |
missense |
probably benign |
0.03 |
R5849:Zfp865
|
UTSW |
7 |
5,034,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Zfp865
|
UTSW |
7 |
5,033,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6480:Zfp865
|
UTSW |
7 |
5,032,782 (GRCm39) |
missense |
probably damaging |
0.98 |
R6681:Zfp865
|
UTSW |
7 |
5,032,450 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6880:Zfp865
|
UTSW |
7 |
5,033,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R7252:Zfp865
|
UTSW |
7 |
5,037,416 (GRCm39) |
intron |
probably benign |
|
R7302:Zfp865
|
UTSW |
7 |
5,032,252 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7486:Zfp865
|
UTSW |
7 |
5,034,259 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7611:Zfp865
|
UTSW |
7 |
5,034,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R8058:Zfp865
|
UTSW |
7 |
5,033,445 (GRCm39) |
missense |
probably benign |
|
R8327:Zfp865
|
UTSW |
7 |
5,034,058 (GRCm39) |
missense |
probably benign |
0.08 |
R8728:Zfp865
|
UTSW |
7 |
5,034,819 (GRCm39) |
missense |
probably damaging |
0.99 |
R9650:Zfp865
|
UTSW |
7 |
5,037,683 (GRCm39) |
missense |
unknown |
|
|