Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
A |
T |
8: 73,205,272 (GRCm39) |
Q361L |
probably damaging |
Het |
Abca7 |
A |
G |
10: 79,838,456 (GRCm39) |
T577A |
probably damaging |
Het |
Acad12 |
A |
T |
5: 121,752,149 (GRCm39) |
V54E |
probably benign |
Het |
Ago4 |
A |
G |
4: 126,414,019 (GRCm39) |
Y91H |
probably damaging |
Het |
Akr1b10 |
T |
C |
6: 34,364,623 (GRCm39) |
V28A |
probably damaging |
Het |
Ccdc33 |
T |
A |
9: 58,009,201 (GRCm39) |
|
probably null |
Het |
Ccdc7a |
T |
C |
8: 129,662,074 (GRCm39) |
|
probably null |
Het |
Ces1f |
A |
T |
8: 93,992,422 (GRCm39) |
V343E |
probably damaging |
Het |
Cftr |
T |
C |
6: 18,274,660 (GRCm39) |
L896P |
probably damaging |
Het |
Csmd3 |
G |
A |
15: 47,533,125 (GRCm39) |
P2375S |
probably damaging |
Het |
Dnajb14 |
C |
T |
3: 137,614,124 (GRCm39) |
A345V |
probably damaging |
Het |
Dnajb14 |
G |
C |
3: 137,614,123 (GRCm39) |
A345P |
probably damaging |
Het |
Dnase1 |
G |
A |
16: 3,855,485 (GRCm39) |
R24K |
probably benign |
Het |
Dnmbp |
C |
T |
19: 43,840,720 (GRCm39) |
V560M |
probably damaging |
Het |
Dop1b |
T |
A |
16: 93,604,102 (GRCm39) |
I1981N |
possibly damaging |
Het |
Eif3a |
A |
C |
19: 60,759,464 (GRCm39) |
S770A |
possibly damaging |
Het |
Fbxl7 |
A |
T |
15: 26,553,088 (GRCm39) |
C60S |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,881,702 (GRCm39) |
D2478V |
possibly damaging |
Het |
Hrnr |
A |
G |
3: 93,229,918 (GRCm39) |
D52G |
probably damaging |
Het |
Jmjd1c |
T |
A |
10: 67,056,187 (GRCm39) |
L823M |
probably damaging |
Het |
Kdm1a |
G |
T |
4: 136,295,911 (GRCm39) |
C172* |
probably null |
Het |
Kdm6b |
C |
T |
11: 69,297,555 (GRCm39) |
E295K |
probably damaging |
Het |
Mepe |
A |
T |
5: 104,484,940 (GRCm39) |
M27L |
probably benign |
Het |
Mogat2 |
A |
T |
7: 98,869,102 (GRCm39) |
H305Q |
probably damaging |
Het |
Mst1r |
T |
A |
9: 107,794,465 (GRCm39) |
Y1215N |
probably damaging |
Het |
Muc5ac |
A |
T |
7: 141,343,532 (GRCm39) |
H48L |
possibly damaging |
Het |
Myo7b |
T |
C |
18: 32,116,748 (GRCm39) |
D953G |
probably damaging |
Het |
Ocel1 |
T |
C |
8: 71,824,472 (GRCm39) |
|
probably benign |
Het |
Pcdhb6 |
A |
G |
18: 37,468,978 (GRCm39) |
D633G |
probably damaging |
Het |
Ppm1l |
A |
G |
3: 69,405,230 (GRCm39) |
I176V |
probably benign |
Het |
Sall3 |
C |
T |
18: 81,013,076 (GRCm39) |
R1120H |
possibly damaging |
Het |
Sbf1 |
G |
A |
15: 89,185,070 (GRCm39) |
P1018S |
probably benign |
Het |
Setbp1 |
T |
C |
18: 78,900,472 (GRCm39) |
Y1065C |
probably damaging |
Het |
Slc25a2 |
T |
C |
18: 37,770,776 (GRCm39) |
|
probably null |
Het |
Slc4a2 |
C |
A |
5: 24,640,888 (GRCm39) |
T729K |
probably damaging |
Het |
Sptlc2 |
T |
C |
12: 87,402,305 (GRCm39) |
E207G |
probably damaging |
Het |
Sult6b1 |
A |
T |
17: 79,214,343 (GRCm39) |
F27I |
probably benign |
Het |
Syf2 |
A |
T |
4: 134,661,889 (GRCm39) |
K84N |
probably damaging |
Het |
Tmem209 |
A |
T |
6: 30,497,166 (GRCm39) |
N183K |
probably benign |
Het |
Tmem232 |
G |
T |
17: 65,785,397 (GRCm39) |
Q188K |
possibly damaging |
Het |
Tomm70a |
A |
T |
16: 56,973,055 (GRCm39) |
T598S |
probably benign |
Het |
Ttll13 |
A |
G |
7: 79,908,052 (GRCm39) |
T556A |
probably benign |
Het |
Vmn2r120 |
A |
T |
17: 57,831,700 (GRCm39) |
L363* |
probably null |
Het |
Xpo6 |
G |
T |
7: 125,707,791 (GRCm39) |
Q872K |
probably damaging |
Het |
Xrra1 |
A |
C |
7: 99,563,671 (GRCm39) |
S553R |
probably damaging |
Het |
Zfy2 |
T |
C |
Y: 2,116,267 (GRCm39) |
I258V |
probably benign |
Homo |
|
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 |
R4454:Zfy1
|
UTSW |
Y |
725,518 (GRCm39) |
missense |
possibly damaging |
0.86 |
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 |
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 |
|