Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adss2 |
A |
T |
1: 177,612,508 (GRCm39) |
H80Q |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,847,959 (GRCm39) |
N456D |
probably damaging |
Het |
Alpk2 |
T |
G |
18: 65,439,673 (GRCm39) |
E573D |
probably damaging |
Het |
Axin2 |
G |
A |
11: 108,814,501 (GRCm39) |
V130M |
probably damaging |
Het |
Cadm4 |
T |
C |
7: 24,202,184 (GRCm39) |
L341P |
possibly damaging |
Het |
Col20a1 |
G |
A |
2: 180,641,559 (GRCm39) |
C625Y |
probably damaging |
Het |
Col6a3 |
T |
G |
1: 90,731,655 (GRCm39) |
I1533L |
possibly damaging |
Het |
Dusp10 |
A |
T |
1: 183,769,697 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
A |
6: 84,171,368 (GRCm39) |
I1837N |
probably damaging |
Het |
Fbxw19 |
A |
G |
9: 109,322,614 (GRCm39) |
S119P |
probably benign |
Het |
Il22ra1 |
C |
A |
4: 135,478,395 (GRCm39) |
P489T |
possibly damaging |
Het |
Il7r |
A |
T |
15: 9,508,085 (GRCm39) |
N412K |
possibly damaging |
Het |
Kdr |
A |
T |
5: 76,122,420 (GRCm39) |
Y502N |
probably benign |
Het |
Med12l |
T |
A |
3: 59,001,076 (GRCm39) |
L713H |
probably damaging |
Het |
Nfxl1 |
A |
G |
5: 72,707,771 (GRCm39) |
|
probably benign |
Het |
Or4a70 |
A |
G |
2: 89,324,182 (GRCm39) |
V158A |
probably benign |
Het |
Piezo1 |
T |
A |
8: 123,208,877 (GRCm39) |
E2495D |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,410,325 (GRCm39) |
F2611L |
probably benign |
Het |
Pld2 |
T |
C |
11: 70,432,132 (GRCm39) |
C84R |
probably damaging |
Het |
Prss3l |
A |
G |
6: 41,420,357 (GRCm39) |
V123A |
possibly damaging |
Het |
Scfd2 |
G |
T |
5: 74,691,707 (GRCm39) |
P192T |
possibly damaging |
Het |
Tm4sf19 |
A |
G |
16: 32,224,772 (GRCm39) |
N40S |
possibly damaging |
Het |
Tmc2 |
T |
C |
2: 130,102,086 (GRCm39) |
|
probably benign |
Het |
Tmem217 |
T |
C |
17: 29,745,566 (GRCm39) |
R55G |
probably benign |
Het |
Unc80 |
A |
G |
1: 66,734,592 (GRCm39) |
D3205G |
possibly damaging |
Het |
Vps13c |
A |
G |
9: 67,793,566 (GRCm39) |
N440D |
probably damaging |
Het |
Zfp110 |
T |
A |
7: 12,583,723 (GRCm39) |
H790Q |
probably 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 |
|
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 |
IGL02319:Wdr35
|
APN |
12 |
9,077,480 (GRCm39) |
unclassified |
probably benign |
|
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 |
|