Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdhppt |
A |
G |
9: 4,309,322 (GRCm39) |
S39P |
probably damaging |
Het |
Aif1 |
G |
A |
17: 35,391,127 (GRCm39) |
P44L |
probably benign |
Het |
Anxa6 |
T |
A |
11: 54,902,561 (GRCm39) |
I58F |
probably damaging |
Het |
Ccdc30 |
T |
A |
4: 119,181,763 (GRCm39) |
K582* |
probably null |
Het |
Cebpz |
A |
G |
17: 79,227,976 (GRCm39) |
|
probably null |
Het |
Clstn3 |
T |
A |
6: 124,427,676 (GRCm39) |
D473V |
probably benign |
Het |
Cry1 |
A |
T |
10: 84,969,175 (GRCm39) |
C550S |
probably benign |
Het |
Dclk2 |
G |
A |
3: 86,827,342 (GRCm39) |
P46S |
probably damaging |
Het |
Dolk |
G |
T |
2: 30,175,497 (GRCm39) |
L183M |
probably damaging |
Het |
Dpys |
T |
C |
15: 39,691,486 (GRCm39) |
T279A |
possibly damaging |
Het |
Drd4 |
T |
C |
7: 140,873,854 (GRCm39) |
Y140H |
probably damaging |
Het |
Duox1 |
C |
A |
2: 122,164,211 (GRCm39) |
C890* |
probably null |
Het |
Epha2 |
T |
A |
4: 141,046,325 (GRCm39) |
V508E |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fahd1 |
A |
T |
17: 25,068,570 (GRCm39) |
I169N |
probably damaging |
Het |
Fgfr1 |
C |
T |
8: 26,060,909 (GRCm39) |
S527F |
probably damaging |
Het |
Flywch1 |
A |
G |
17: 23,982,000 (GRCm39) |
V68A |
probably benign |
Het |
Gm21834 |
A |
T |
17: 58,049,210 (GRCm39) |
V2E |
possibly damaging |
Het |
Gm7853 |
A |
T |
14: 35,811,621 (GRCm39) |
|
noncoding transcript |
Het |
Igf2r |
T |
A |
17: 12,934,830 (GRCm39) |
H713L |
probably benign |
Het |
Iqgap3 |
T |
C |
3: 88,023,338 (GRCm39) |
V543A |
probably benign |
Het |
Kcnq5 |
T |
A |
1: 21,549,595 (GRCm39) |
|
probably null |
Het |
Lsm1 |
C |
T |
8: 26,275,712 (GRCm39) |
P5S |
possibly damaging |
Het |
Marchf1 |
T |
C |
8: 66,574,442 (GRCm39) |
M1T |
probably null |
Het |
Myocd |
T |
C |
11: 65,091,633 (GRCm39) |
H103R |
probably damaging |
Het |
Myom2 |
C |
T |
8: 15,113,927 (GRCm39) |
T25I |
probably damaging |
Het |
Nck1 |
T |
C |
9: 100,380,003 (GRCm39) |
K83E |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,839,829 (GRCm39) |
D806G |
probably benign |
Het |
Onecut2 |
G |
T |
18: 64,474,268 (GRCm39) |
R254L |
probably damaging |
Het |
Or51k1 |
T |
A |
7: 103,661,436 (GRCm39) |
M158L |
probably benign |
Het |
Plxna1 |
A |
C |
6: 89,301,298 (GRCm39) |
L1534R |
probably damaging |
Het |
Polb |
C |
A |
8: 23,130,018 (GRCm39) |
A185S |
possibly damaging |
Het |
Pou3f3 |
T |
C |
1: 42,737,651 (GRCm39) |
V449A |
probably damaging |
Het |
Pskh1 |
C |
T |
8: 106,640,145 (GRCm39) |
T275I |
probably damaging |
Het |
Rab18 |
C |
A |
18: 6,788,516 (GRCm39) |
A161D |
probably damaging |
Het |
Rrp8 |
T |
C |
7: 105,384,011 (GRCm39) |
R164G |
probably benign |
Het |
Sacs |
T |
A |
14: 61,445,208 (GRCm39) |
I2418K |
probably benign |
Het |
Scrn1 |
T |
C |
6: 54,502,631 (GRCm39) |
E136G |
probably benign |
Het |
Sgk1 |
C |
T |
10: 21,872,500 (GRCm39) |
R171W |
probably damaging |
Het |
Slitrk6 |
C |
T |
14: 110,989,387 (GRCm39) |
A107T |
probably damaging |
Het |
Spata31e2 |
T |
C |
1: 26,723,783 (GRCm39) |
S466G |
probably benign |
Het |
Tktl2 |
T |
A |
8: 66,965,795 (GRCm39) |
F451Y |
probably damaging |
Het |
Tnks1bp1 |
G |
A |
2: 84,889,259 (GRCm39) |
V529M |
probably benign |
Het |
Trps1 |
T |
C |
15: 50,524,742 (GRCm39) |
K874E |
probably damaging |
Het |
Ttll9 |
T |
A |
2: 152,825,047 (GRCm39) |
D75E |
probably benign |
Het |
Ttn |
A |
G |
2: 76,596,368 (GRCm39) |
Y20182H |
probably damaging |
Het |
Ufc1 |
A |
T |
1: 171,116,821 (GRCm39) |
C116S |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Zfp81 |
A |
G |
17: 33,553,597 (GRCm39) |
Y406H |
probably damaging |
Het |
|
Other mutations in Zfp809 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02967:Zfp809
|
APN |
9 |
22,146,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03117:Zfp809
|
APN |
9 |
22,149,950 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03177:Zfp809
|
APN |
9 |
22,146,347 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03250:Zfp809
|
APN |
9 |
22,149,931 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03265:Zfp809
|
APN |
9 |
22,154,339 (GRCm39) |
missense |
probably benign |
0.20 |
R1080:Zfp809
|
UTSW |
9 |
22,146,405 (GRCm39) |
missense |
probably damaging |
0.98 |
R1544:Zfp809
|
UTSW |
9 |
22,146,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Zfp809
|
UTSW |
9 |
22,150,027 (GRCm39) |
nonsense |
probably null |
|
R2137:Zfp809
|
UTSW |
9 |
22,146,434 (GRCm39) |
missense |
probably benign |
0.07 |
R2356:Zfp809
|
UTSW |
9 |
22,154,336 (GRCm39) |
missense |
probably benign |
0.00 |
R5019:Zfp809
|
UTSW |
9 |
22,148,998 (GRCm39) |
missense |
probably benign |
0.44 |
R5735:Zfp809
|
UTSW |
9 |
22,150,227 (GRCm39) |
nonsense |
probably null |
|
R6483:Zfp809
|
UTSW |
9 |
22,147,540 (GRCm39) |
missense |
probably benign |
|
R7106:Zfp809
|
UTSW |
9 |
22,147,520 (GRCm39) |
missense |
probably benign |
0.04 |
R8969:Zfp809
|
UTSW |
9 |
22,137,130 (GRCm39) |
critical splice donor site |
probably null |
|
R9364:Zfp809
|
UTSW |
9 |
22,150,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R9600:Zfp809
|
UTSW |
9 |
22,150,384 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9666:Zfp809
|
UTSW |
9 |
22,149,863 (GRCm39) |
missense |
probably benign |
0.07 |
R9700:Zfp809
|
UTSW |
9 |
22,154,470 (GRCm39) |
missense |
unknown |
|
|