Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap4e1 |
T |
A |
2: 126,889,061 (GRCm39) |
F509I |
probably damaging |
Het |
Asmt |
A |
T |
X: 169,106,456 (GRCm39) |
M19L |
probably benign |
Het |
Atf6 |
C |
T |
1: 170,621,608 (GRCm39) |
R471Q |
probably damaging |
Het |
Atp4a |
G |
A |
7: 30,419,650 (GRCm39) |
R671Q |
probably benign |
Het |
Baiap3 |
T |
A |
17: 25,468,510 (GRCm39) |
D250V |
probably damaging |
Het |
C2cd4d |
T |
A |
3: 94,271,054 (GRCm39) |
F107I |
probably damaging |
Het |
Cdkn2d |
C |
G |
9: 21,202,185 (GRCm39) |
V21L |
probably benign |
Het |
Cldn6 |
T |
C |
17: 23,900,060 (GRCm39) |
|
probably null |
Het |
Cpa5 |
A |
G |
6: 30,626,323 (GRCm39) |
N228S |
possibly damaging |
Het |
Cracdl |
T |
C |
1: 37,663,834 (GRCm39) |
E163G |
probably damaging |
Het |
Crocc |
T |
C |
4: 140,747,716 (GRCm39) |
S1478G |
possibly damaging |
Het |
Csmd1 |
A |
T |
8: 15,995,011 (GRCm39) |
C2675S |
probably damaging |
Het |
Cthrc1 |
C |
A |
15: 38,940,408 (GRCm39) |
Q4K |
probably benign |
Het |
Ddo |
A |
T |
10: 40,523,543 (GRCm39) |
I178F |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 50,026,399 (GRCm39) |
T1836A |
probably benign |
Het |
Dnah9 |
T |
G |
11: 66,038,215 (GRCm39) |
Q107P |
probably damaging |
Het |
Dusp26 |
A |
G |
8: 31,584,172 (GRCm39) |
N93S |
probably damaging |
Het |
Egr2 |
GAA |
GA |
10: 67,375,733 (GRCm39) |
|
probably null |
Het |
Epha5 |
T |
C |
5: 84,304,303 (GRCm39) |
I501V |
probably damaging |
Het |
Eya1 |
C |
T |
1: 14,253,420 (GRCm39) |
V519M |
probably damaging |
Het |
Fam227b |
T |
A |
2: 125,988,188 (GRCm39) |
|
probably benign |
Het |
Fgd5 |
C |
T |
6: 91,966,167 (GRCm39) |
S642F |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,821,120 (GRCm39) |
A5618S |
possibly damaging |
Het |
Gm12034 |
T |
A |
11: 20,396,476 (GRCm39) |
|
noncoding transcript |
Het |
Liph |
T |
C |
16: 21,803,018 (GRCm39) |
D17G |
probably benign |
Het |
Mbd3 |
A |
T |
10: 80,229,817 (GRCm39) |
L164H |
probably damaging |
Het |
Med4 |
A |
G |
14: 73,755,502 (GRCm39) |
|
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Nav2 |
A |
T |
7: 49,198,292 (GRCm39) |
|
probably null |
Het |
Or4k1 |
T |
C |
14: 50,377,953 (GRCm39) |
I48V |
probably benign |
Het |
Or8b1b |
C |
A |
9: 38,375,938 (GRCm39) |
F200L |
probably benign |
Het |
Pcdha11 |
G |
A |
18: 37,140,426 (GRCm39) |
G685D |
probably benign |
Het |
Pgc |
A |
G |
17: 48,043,335 (GRCm39) |
I228V |
probably benign |
Het |
Pramel25 |
A |
G |
4: 143,519,394 (GRCm39) |
S52G |
probably benign |
Het |
Rad51 |
C |
T |
2: 118,962,049 (GRCm39) |
H199Y |
probably damaging |
Het |
Robo2 |
A |
T |
16: 74,149,407 (GRCm39) |
|
probably benign |
Het |
Sap130 |
C |
T |
18: 31,844,413 (GRCm39) |
T861I |
probably damaging |
Het |
Sh3tc2 |
A |
T |
18: 62,140,844 (GRCm39) |
D1061V |
probably damaging |
Het |
Shoc1 |
T |
C |
4: 59,092,383 (GRCm39) |
D266G |
possibly damaging |
Het |
Snapc3 |
A |
G |
4: 83,336,996 (GRCm39) |
E119G |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,464,159 (GRCm39) |
G3862D |
probably benign |
Het |
Tbc1d16 |
G |
A |
11: 119,048,699 (GRCm39) |
T318M |
possibly damaging |
Het |
Thrb |
T |
A |
14: 18,011,187 (GRCm38) |
W188R |
probably damaging |
Het |
Thsd1 |
T |
C |
8: 22,733,594 (GRCm39) |
Y214H |
probably damaging |
Het |
Tnfrsf13b |
T |
C |
11: 61,032,264 (GRCm39) |
V98A |
probably benign |
Het |
Topbp1 |
T |
C |
9: 103,222,070 (GRCm39) |
Y1314H |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,616,150 (GRCm39) |
V8271L |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,777,257 (GRCm39) |
M1382V |
probably benign |
Het |
Utrn |
G |
T |
10: 12,603,584 (GRCm39) |
Q599K |
possibly damaging |
Het |
Zfp995 |
G |
A |
17: 22,098,932 (GRCm39) |
T434I |
probably benign |
Het |
|
Other mutations in Zfy1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0149:Zfy1
|
UTSW |
Y |
726,121 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0361:Zfy1
|
UTSW |
Y |
726,121 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0529:Zfy1
|
UTSW |
Y |
726,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0837:Zfy1
|
UTSW |
Y |
725,850 (GRCm39) |
nonsense |
probably null |
|
R0945:Zfy1
|
UTSW |
Y |
725,983 (GRCm39) |
missense |
probably damaging |
0.98 |
R1163:Zfy1
|
UTSW |
Y |
725,611 (GRCm39) |
missense |
probably damaging |
0.98 |
R1394:Zfy1
|
UTSW |
Y |
725,957 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1806:Zfy1
|
UTSW |
Y |
725,620 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1928:Zfy1
|
UTSW |
Y |
729,733 (GRCm39) |
missense |
unknown |
|
R2374:Zfy1
|
UTSW |
Y |
726,392 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2374:Zfy1
|
UTSW |
Y |
726,391 (GRCm39) |
missense |
probably damaging |
0.99 |
R2889:Zfy1
|
UTSW |
Y |
726,307 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2980:Zfy1
|
UTSW |
Y |
739,054 (GRCm39) |
missense |
unknown |
|
R3437:Zfy1
|
UTSW |
Y |
726,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4529:Zfy1
|
UTSW |
Y |
726,511 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4656:Zfy1
|
UTSW |
Y |
729,626 (GRCm39) |
missense |
unknown |
|
R5049:Zfy1
|
UTSW |
Y |
726,004 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5087:Zfy1
|
UTSW |
Y |
732,964 (GRCm39) |
missense |
unknown |
|
R5347:Zfy1
|
UTSW |
Y |
725,950 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5428:Zfy1
|
UTSW |
Y |
726,205 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5825:Zfy1
|
UTSW |
Y |
726,531 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6256:Zfy1
|
UTSW |
Y |
738,765 (GRCm39) |
missense |
unknown |
|
R7065:Zfy1
|
UTSW |
Y |
725,428 (GRCm39) |
missense |
probably benign |
0.33 |
R7134:Zfy1
|
UTSW |
Y |
725,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R7185:Zfy1
|
UTSW |
Y |
725,464 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7358:Zfy1
|
UTSW |
Y |
735,141 (GRCm39) |
missense |
unknown |
|
R7513:Zfy1
|
UTSW |
Y |
759,852 (GRCm39) |
missense |
unknown |
|
R7747:Zfy1
|
UTSW |
Y |
725,496 (GRCm39) |
nonsense |
probably null |
|
R7900:Zfy1
|
UTSW |
Y |
725,519 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8052:Zfy1
|
UTSW |
Y |
726,004 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8377:Zfy1
|
UTSW |
Y |
725,723 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8795:Zfy1
|
UTSW |
Y |
738,945 (GRCm39) |
missense |
unknown |
|
R8854:Zfy1
|
UTSW |
Y |
726,501 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8936:Zfy1
|
UTSW |
Y |
738,726 (GRCm39) |
missense |
unknown |
|
R9098:Zfy1
|
UTSW |
Y |
725,987 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9146:Zfy1
|
UTSW |
Y |
726,033 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9209:Zfy1
|
UTSW |
Y |
732,990 (GRCm39) |
missense |
unknown |
|
R9310:Zfy1
|
UTSW |
Y |
727,634 (GRCm39) |
missense |
unknown |
|
R9726:Zfy1
|
UTSW |
Y |
725,476 (GRCm39) |
missense |
possibly damaging |
0.53 |
|