Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
A |
G |
15: 76,834,578 (GRCm39) |
N158S |
probably damaging |
Het |
Ankrd17 |
A |
C |
5: 90,412,010 (GRCm39) |
L1285V |
probably damaging |
Het |
Atp8b2 |
G |
A |
3: 89,861,546 (GRCm39) |
T267I |
probably damaging |
Het |
Becn1 |
C |
T |
11: 101,182,224 (GRCm39) |
G115D |
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Chd6 |
A |
C |
2: 160,826,372 (GRCm39) |
|
probably benign |
Het |
Col22a1 |
A |
G |
15: 71,699,602 (GRCm39) |
|
probably benign |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Dnm2 |
A |
G |
9: 21,397,004 (GRCm39) |
I494V |
possibly damaging |
Het |
Dock2 |
T |
A |
11: 34,199,801 (GRCm39) |
E1416D |
probably benign |
Het |
Eif2ak1 |
A |
G |
5: 143,821,701 (GRCm39) |
H339R |
probably benign |
Het |
Espnl |
C |
T |
1: 91,268,256 (GRCm39) |
P294L |
probably benign |
Het |
Ftmt |
T |
A |
18: 52,464,912 (GRCm39) |
I76N |
possibly damaging |
Het |
Gorasp2 |
T |
G |
2: 70,506,803 (GRCm39) |
|
probably benign |
Het |
Hadhb |
T |
A |
5: 30,389,061 (GRCm39) |
M468K |
possibly damaging |
Het |
Hfm1 |
A |
G |
5: 107,021,794 (GRCm39) |
|
probably benign |
Het |
Inpp5j |
T |
C |
11: 3,445,338 (GRCm39) |
|
probably benign |
Het |
Ipo7 |
T |
A |
7: 109,640,060 (GRCm39) |
F288I |
probably damaging |
Het |
Kcnv1 |
T |
A |
15: 44,972,519 (GRCm39) |
K455* |
probably null |
Het |
Kdm5a |
A |
G |
6: 120,383,691 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,747,958 (GRCm39) |
S3122F |
probably benign |
Het |
Kndc1 |
A |
G |
7: 139,490,817 (GRCm39) |
I440V |
probably benign |
Het |
Mib2 |
T |
A |
4: 155,741,203 (GRCm39) |
I545F |
probably damaging |
Het |
Nav2 |
C |
T |
7: 49,195,789 (GRCm39) |
P1055L |
probably damaging |
Het |
Or4c10b |
T |
A |
2: 89,711,755 (GRCm39) |
I195N |
probably benign |
Het |
Or5v1b |
C |
A |
17: 37,841,640 (GRCm39) |
F257L |
probably damaging |
Het |
Plch1 |
A |
T |
3: 63,609,270 (GRCm39) |
L65Q |
probably damaging |
Het |
Polr1g |
T |
C |
7: 19,093,030 (GRCm39) |
D50G |
probably damaging |
Het |
Ppp3ca |
A |
G |
3: 136,627,623 (GRCm39) |
I396V |
possibly damaging |
Het |
Ryr1 |
A |
T |
7: 28,740,269 (GRCm39) |
N3917K |
probably damaging |
Het |
Scn7a |
T |
C |
2: 66,582,658 (GRCm39) |
T80A |
probably damaging |
Het |
Sema3f |
C |
T |
9: 107,564,935 (GRCm39) |
E307K |
probably damaging |
Het |
Serpinb9b |
A |
T |
13: 33,223,953 (GRCm39) |
|
probably benign |
Het |
Siglec15 |
T |
A |
18: 78,086,832 (GRCm39) |
K342N |
possibly damaging |
Het |
Slc2a12 |
T |
C |
10: 22,541,054 (GRCm39) |
F303S |
probably damaging |
Het |
Slc9c1 |
T |
C |
16: 45,400,505 (GRCm39) |
V705A |
probably benign |
Het |
Tenm4 |
T |
C |
7: 96,423,383 (GRCm39) |
|
probably benign |
Het |
Tm6sf1 |
A |
T |
7: 81,525,572 (GRCm39) |
|
probably benign |
Het |
Tmem245 |
T |
C |
4: 56,899,119 (GRCm39) |
Y269C |
probably damaging |
Het |
Txndc2 |
A |
G |
17: 65,944,971 (GRCm39) |
I402T |
possibly damaging |
Het |
Ube4b |
A |
G |
4: 149,471,536 (GRCm39) |
|
probably null |
Het |
Usp28 |
T |
A |
9: 48,949,069 (GRCm39) |
Y863N |
possibly damaging |
Het |
Vmn2r69 |
T |
C |
7: 85,058,960 (GRCm39) |
I534V |
probably benign |
Het |
Zfp280d |
C |
A |
9: 72,208,993 (GRCm39) |
N74K |
probably damaging |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
|
Other mutations in Wdr89 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00837:Wdr89
|
APN |
12 |
75,679,825 (GRCm39) |
nonsense |
probably null |
|
IGL02176:Wdr89
|
APN |
12 |
75,679,897 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02973:Wdr89
|
APN |
12 |
75,679,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R0003:Wdr89
|
UTSW |
12 |
75,679,367 (GRCm39) |
missense |
probably benign |
0.00 |
R2060:Wdr89
|
UTSW |
12 |
75,679,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4494:Wdr89
|
UTSW |
12 |
75,679,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5120:Wdr89
|
UTSW |
12 |
75,679,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R5195:Wdr89
|
UTSW |
12 |
75,680,062 (GRCm39) |
missense |
probably benign |
0.23 |
R6572:Wdr89
|
UTSW |
12 |
75,680,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R7487:Wdr89
|
UTSW |
12 |
75,679,388 (GRCm39) |
missense |
probably benign |
|
R7835:Wdr89
|
UTSW |
12 |
75,679,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R8445:Wdr89
|
UTSW |
12 |
75,679,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R8765:Wdr89
|
UTSW |
12 |
75,679,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Wdr89
|
UTSW |
12 |
75,679,943 (GRCm39) |
missense |
probably benign |
0.00 |
R9269:Wdr89
|
UTSW |
12 |
75,679,564 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9340:Wdr89
|
UTSW |
12 |
75,679,937 (GRCm39) |
missense |
probably benign |
0.11 |
R9522:Wdr89
|
UTSW |
12 |
75,679,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R9557:Wdr89
|
UTSW |
12 |
75,679,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R9760:Wdr89
|
UTSW |
12 |
75,680,026 (GRCm39) |
missense |
probably damaging |
0.99 |
X0023:Wdr89
|
UTSW |
12 |
75,679,951 (GRCm39) |
missense |
probably benign |
|
|