Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss3 |
T |
C |
10: 106,784,611 (GRCm39) |
Y537C |
probably damaging |
Het |
Ambra1 |
A |
G |
2: 91,717,265 (GRCm39) |
H854R |
probably damaging |
Het |
Atf7ip |
A |
G |
6: 136,570,116 (GRCm39) |
N981S |
probably benign |
Het |
Atp6v1d |
A |
G |
12: 78,908,230 (GRCm39) |
S2P |
probably damaging |
Het |
Cd59a |
A |
T |
2: 103,944,373 (GRCm39) |
I74F |
possibly damaging |
Het |
Chek2 |
T |
C |
5: 111,014,877 (GRCm39) |
Y449H |
possibly damaging |
Het |
Ctif |
C |
T |
18: 75,654,944 (GRCm39) |
|
probably benign |
Het |
Dnaaf3 |
T |
C |
7: 4,526,946 (GRCm39) |
E403G |
probably damaging |
Het |
Dock1 |
T |
G |
7: 134,374,178 (GRCm39) |
V608G |
possibly damaging |
Het |
Fcf1 |
T |
C |
12: 85,017,982 (GRCm39) |
|
probably null |
Het |
Fgf17 |
T |
G |
14: 70,874,183 (GRCm39) |
Q202P |
possibly damaging |
Het |
Hnrnpm |
A |
T |
17: 33,868,924 (GRCm39) |
L501Q |
probably damaging |
Het |
Itgb4 |
G |
A |
11: 115,879,752 (GRCm39) |
V635I |
probably damaging |
Het |
Klra6 |
A |
T |
6: 130,002,177 (GRCm39) |
S2R |
probably damaging |
Het |
Krtap19-9b |
T |
A |
16: 88,729,002 (GRCm39) |
Y33F |
unknown |
Het |
Lpcat4 |
G |
A |
2: 112,074,229 (GRCm39) |
V264M |
probably damaging |
Het |
Lyzl6 |
T |
C |
11: 103,525,862 (GRCm39) |
Y86C |
probably damaging |
Het |
Myo18b |
T |
C |
5: 112,939,005 (GRCm39) |
K1669E |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,893,159 (GRCm39) |
V1558A |
probably damaging |
Het |
Or51a42 |
A |
G |
7: 103,708,140 (GRCm39) |
I223T |
probably damaging |
Het |
Or51l14 |
G |
A |
7: 103,101,474 (GRCm39) |
C310Y |
probably benign |
Het |
Or5b105 |
A |
G |
19: 13,080,026 (GRCm39) |
I214T |
probably benign |
Het |
Or8b47 |
T |
A |
9: 38,435,166 (GRCm39) |
I46N |
probably damaging |
Het |
Pex11b |
T |
C |
3: 96,550,885 (GRCm39) |
|
probably benign |
Het |
Rbm5 |
A |
T |
9: 107,621,064 (GRCm39) |
L689* |
probably null |
Het |
Rd3 |
G |
T |
1: 191,715,452 (GRCm39) |
G76C |
probably null |
Het |
Rgs16 |
A |
T |
1: 153,617,852 (GRCm39) |
I121F |
probably damaging |
Het |
Tmem30a |
A |
T |
9: 79,681,485 (GRCm39) |
M264K |
probably damaging |
Het |
Traf2 |
T |
C |
2: 25,426,695 (GRCm39) |
E127G |
probably damaging |
Het |
Trmt11 |
A |
T |
10: 30,436,869 (GRCm39) |
D290E |
probably damaging |
Het |
Wnk2 |
A |
G |
13: 49,214,914 (GRCm39) |
S1211P |
possibly damaging |
Het |
|
Other mutations in Wdr35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Wdr35
|
APN |
12 |
9,069,900 (GRCm39) |
missense |
probably benign |
|
IGL00962:Wdr35
|
APN |
12 |
9,071,726 (GRCm39) |
splice site |
probably benign |
|
IGL01094:Wdr35
|
APN |
12 |
9,055,838 (GRCm39) |
splice site |
probably benign |
|
IGL01312:Wdr35
|
APN |
12 |
9,058,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01397:Wdr35
|
APN |
12 |
9,058,550 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01490:Wdr35
|
APN |
12 |
9,027,381 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02153:Wdr35
|
APN |
12 |
9,058,535 (GRCm39) |
missense |
probably null |
0.04 |
IGL02548:Wdr35
|
APN |
12 |
9,074,297 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02941:Wdr35
|
APN |
12 |
9,077,507 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03038:Wdr35
|
APN |
12 |
9,024,185 (GRCm39) |
splice site |
probably benign |
|
IGL03086:Wdr35
|
APN |
12 |
9,058,692 (GRCm39) |
splice site |
probably null |
|
IGL03207:Wdr35
|
APN |
12 |
9,039,936 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03327:Wdr35
|
APN |
12 |
9,028,694 (GRCm39) |
splice site |
probably benign |
|
R0362:Wdr35
|
UTSW |
12 |
9,045,625 (GRCm39) |
unclassified |
probably benign |
|
R0464:Wdr35
|
UTSW |
12 |
9,077,472 (GRCm39) |
unclassified |
probably benign |
|
R0487:Wdr35
|
UTSW |
12 |
9,062,743 (GRCm39) |
critical splice donor site |
probably null |
|
R0976:Wdr35
|
UTSW |
12 |
9,036,104 (GRCm39) |
missense |
probably benign |
0.03 |
R1349:Wdr35
|
UTSW |
12 |
9,069,870 (GRCm39) |
splice site |
probably benign |
|
R1663:Wdr35
|
UTSW |
12 |
9,070,000 (GRCm39) |
missense |
probably benign |
0.00 |
R1769:Wdr35
|
UTSW |
12 |
9,062,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Wdr35
|
UTSW |
12 |
9,035,772 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1789:Wdr35
|
UTSW |
12 |
9,027,435 (GRCm39) |
critical splice donor site |
probably null |
|
R1893:Wdr35
|
UTSW |
12 |
9,035,994 (GRCm39) |
missense |
probably benign |
|
R2076:Wdr35
|
UTSW |
12 |
9,074,281 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2228:Wdr35
|
UTSW |
12 |
9,024,955 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2280:Wdr35
|
UTSW |
12 |
9,028,628 (GRCm39) |
missense |
probably benign |
0.01 |
R2281:Wdr35
|
UTSW |
12 |
9,028,628 (GRCm39) |
missense |
probably benign |
0.01 |
R2863:Wdr35
|
UTSW |
12 |
9,078,060 (GRCm39) |
nonsense |
probably null |
|
R3713:Wdr35
|
UTSW |
12 |
9,077,648 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3911:Wdr35
|
UTSW |
12 |
9,036,077 (GRCm39) |
missense |
probably benign |
|
R3934:Wdr35
|
UTSW |
12 |
9,058,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R4360:Wdr35
|
UTSW |
12 |
9,024,149 (GRCm39) |
utr 5 prime |
probably benign |
|
R4402:Wdr35
|
UTSW |
12 |
9,039,981 (GRCm39) |
missense |
probably damaging |
0.98 |
R4473:Wdr35
|
UTSW |
12 |
9,065,995 (GRCm39) |
missense |
probably benign |
0.00 |
R4656:Wdr35
|
UTSW |
12 |
9,066,619 (GRCm39) |
missense |
probably benign |
0.00 |
R4780:Wdr35
|
UTSW |
12 |
9,068,150 (GRCm39) |
missense |
probably benign |
|
R5092:Wdr35
|
UTSW |
12 |
9,037,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R5160:Wdr35
|
UTSW |
12 |
9,058,487 (GRCm39) |
missense |
probably damaging |
0.99 |
R5184:Wdr35
|
UTSW |
12 |
9,068,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Wdr35
|
UTSW |
12 |
9,028,684 (GRCm39) |
missense |
probably benign |
0.00 |
R5435:Wdr35
|
UTSW |
12 |
9,039,951 (GRCm39) |
missense |
probably benign |
0.01 |
R5472:Wdr35
|
UTSW |
12 |
9,066,619 (GRCm39) |
missense |
probably benign |
0.00 |
R5682:Wdr35
|
UTSW |
12 |
9,031,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Wdr35
|
UTSW |
12 |
9,056,723 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5990:Wdr35
|
UTSW |
12 |
9,066,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R6196:Wdr35
|
UTSW |
12 |
9,077,632 (GRCm39) |
missense |
probably benign |
0.05 |
R6531:Wdr35
|
UTSW |
12 |
9,028,685 (GRCm39) |
missense |
probably benign |
0.00 |
R6746:Wdr35
|
UTSW |
12 |
9,053,982 (GRCm39) |
splice site |
probably null |
|
R6816:Wdr35
|
UTSW |
12 |
9,077,724 (GRCm39) |
critical splice donor site |
probably null |
|
R6863:Wdr35
|
UTSW |
12 |
9,040,047 (GRCm39) |
missense |
probably damaging |
0.97 |
R7088:Wdr35
|
UTSW |
12 |
9,028,659 (GRCm39) |
missense |
probably benign |
0.11 |
R7140:Wdr35
|
UTSW |
12 |
9,072,785 (GRCm39) |
missense |
probably damaging |
0.98 |
R7327:Wdr35
|
UTSW |
12 |
9,037,312 (GRCm39) |
missense |
probably benign |
0.10 |
R7403:Wdr35
|
UTSW |
12 |
9,062,685 (GRCm39) |
missense |
probably damaging |
0.98 |
R7422:Wdr35
|
UTSW |
12 |
9,054,105 (GRCm39) |
missense |
probably benign |
0.00 |
R7438:Wdr35
|
UTSW |
12 |
9,072,785 (GRCm39) |
missense |
probably damaging |
0.98 |
R7466:Wdr35
|
UTSW |
12 |
9,055,773 (GRCm39) |
missense |
probably benign |
|
R7491:Wdr35
|
UTSW |
12 |
9,036,000 (GRCm39) |
missense |
probably benign |
0.00 |
R7599:Wdr35
|
UTSW |
12 |
9,074,886 (GRCm39) |
missense |
probably benign |
0.01 |
R7620:Wdr35
|
UTSW |
12 |
9,066,042 (GRCm39) |
missense |
probably benign |
0.04 |
R7857:Wdr35
|
UTSW |
12 |
9,058,113 (GRCm39) |
critical splice donor site |
probably null |
|
R8289:Wdr35
|
UTSW |
12 |
9,058,020 (GRCm39) |
missense |
probably benign |
0.00 |
R8302:Wdr35
|
UTSW |
12 |
9,078,110 (GRCm39) |
missense |
probably benign |
0.09 |
R8433:Wdr35
|
UTSW |
12 |
9,058,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8479:Wdr35
|
UTSW |
12 |
9,035,985 (GRCm39) |
missense |
probably benign |
0.04 |
R8498:Wdr35
|
UTSW |
12 |
9,058,626 (GRCm39) |
missense |
probably damaging |
0.97 |
R8721:Wdr35
|
UTSW |
12 |
9,075,044 (GRCm39) |
critical splice donor site |
probably null |
|
R9220:Wdr35
|
UTSW |
12 |
9,036,000 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9368:Wdr35
|
UTSW |
12 |
9,071,826 (GRCm39) |
missense |
probably benign |
0.00 |
R9573:Wdr35
|
UTSW |
12 |
9,078,014 (GRCm39) |
missense |
probably benign |
0.00 |
R9596:Wdr35
|
UTSW |
12 |
9,036,092 (GRCm39) |
missense |
probably benign |
0.08 |
R9773:Wdr35
|
UTSW |
12 |
9,039,990 (GRCm39) |
missense |
probably benign |
0.03 |
X0066:Wdr35
|
UTSW |
12 |
9,040,029 (GRCm39) |
missense |
probably benign |
0.04 |
|