Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy4 |
T |
A |
14: 56,007,553 (GRCm39) |
I926F |
probably damaging |
Het |
Agap3 |
A |
G |
5: 24,692,820 (GRCm39) |
N418D |
probably damaging |
Het |
Alms1 |
T |
C |
6: 85,655,579 (GRCm39) |
V3375A |
possibly damaging |
Het |
Ankrd6 |
T |
A |
4: 32,860,441 (GRCm39) |
M1L |
possibly damaging |
Het |
Aox4 |
A |
G |
1: 58,303,526 (GRCm39) |
D1188G |
probably damaging |
Het |
Car2 |
T |
A |
3: 14,952,999 (GRCm39) |
L47Q |
probably damaging |
Het |
Catsper2 |
A |
G |
2: 121,240,681 (GRCm39) |
V107A |
probably benign |
Het |
Catsperg2 |
T |
C |
7: 29,416,473 (GRCm39) |
N313S |
possibly damaging |
Het |
Dolk |
T |
C |
2: 30,175,523 (GRCm39) |
Y174C |
probably damaging |
Het |
Erfe |
A |
G |
1: 91,298,147 (GRCm39) |
E219G |
probably benign |
Het |
Ern2 |
T |
C |
7: 121,770,894 (GRCm39) |
E733G |
probably benign |
Het |
Fam228a |
A |
G |
12: 4,787,734 (GRCm39) |
F13S |
probably damaging |
Het |
Fancd2 |
T |
C |
6: 113,545,169 (GRCm39) |
V829A |
probably benign |
Het |
Gid4 |
C |
A |
11: 60,323,169 (GRCm39) |
T87N |
probably benign |
Het |
H2-Ob |
A |
G |
17: 34,462,466 (GRCm39) |
K152R |
probably benign |
Het |
Ifna2 |
T |
A |
4: 88,601,614 (GRCm39) |
T135S |
probably benign |
Het |
Il1rapl2 |
G |
A |
X: 137,690,429 (GRCm39) |
G298D |
probably damaging |
Het |
Mbd1 |
T |
A |
18: 74,407,825 (GRCm39) |
L174* |
probably null |
Het |
Mga |
T |
A |
2: 119,765,994 (GRCm39) |
D1341E |
possibly damaging |
Het |
Mmp12 |
T |
A |
9: 7,348,631 (GRCm39) |
M54K |
probably benign |
Het |
Mphosph8 |
T |
A |
14: 56,916,277 (GRCm39) |
|
probably null |
Het |
Mrps23 |
A |
G |
11: 88,100,922 (GRCm39) |
|
probably benign |
Het |
Necab1 |
C |
T |
4: 14,960,046 (GRCm39) |
M300I |
probably benign |
Het |
Nid2 |
G |
A |
14: 19,829,688 (GRCm39) |
D660N |
probably damaging |
Het |
Or2ag12 |
T |
A |
7: 106,276,754 (GRCm39) |
H313L |
probably benign |
Het |
Or9r7 |
T |
A |
10: 129,962,584 (GRCm39) |
E114V |
probably damaging |
Het |
P2ry13 |
A |
T |
3: 59,117,013 (GRCm39) |
V255D |
possibly damaging |
Het |
Peak1 |
C |
T |
9: 56,165,214 (GRCm39) |
E905K |
probably damaging |
Het |
Picalm |
C |
A |
7: 89,843,499 (GRCm39) |
Q550K |
probably benign |
Het |
Rnf103 |
T |
A |
6: 71,487,289 (GRCm39) |
V640E |
possibly damaging |
Het |
Sec31b |
T |
G |
19: 44,507,379 (GRCm39) |
K817N |
possibly damaging |
Het |
Shisal2a |
A |
T |
4: 108,225,098 (GRCm39) |
C155S |
probably benign |
Het |
Skint2 |
C |
A |
4: 112,483,223 (GRCm39) |
H209Q |
probably benign |
Het |
Skint5 |
T |
C |
4: 113,798,005 (GRCm39) |
S193G |
probably damaging |
Het |
Tacr3 |
A |
G |
3: 134,635,852 (GRCm39) |
|
probably benign |
Het |
Tek |
A |
G |
4: 94,753,680 (GRCm39) |
M1041V |
possibly damaging |
Het |
Tm4sf1 |
A |
G |
3: 57,200,436 (GRCm39) |
S89P |
possibly damaging |
Het |
Tusc3 |
T |
A |
8: 39,597,931 (GRCm39) |
N299K |
possibly damaging |
Het |
|
Other mutations in Washc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00979:Washc4
|
APN |
10 |
83,386,747 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01370:Washc4
|
APN |
10 |
83,394,694 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01524:Washc4
|
APN |
10 |
83,411,996 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01682:Washc4
|
APN |
10 |
83,416,170 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01973:Washc4
|
APN |
10 |
83,391,973 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02002:Washc4
|
APN |
10 |
83,415,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02020:Washc4
|
APN |
10 |
83,400,336 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02230:Washc4
|
APN |
10 |
83,417,233 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02421:Washc4
|
APN |
10 |
83,415,414 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02514:Washc4
|
APN |
10 |
83,405,947 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02619:Washc4
|
APN |
10 |
83,394,717 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02852:Washc4
|
APN |
10 |
83,419,173 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02870:Washc4
|
APN |
10 |
83,421,740 (GRCm39) |
missense |
probably benign |
|
IGL03181:Washc4
|
APN |
10 |
83,426,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0458:Washc4
|
UTSW |
10 |
83,382,663 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0462:Washc4
|
UTSW |
10 |
83,392,777 (GRCm39) |
missense |
probably benign |
0.00 |
R0471:Washc4
|
UTSW |
10 |
83,394,598 (GRCm39) |
splice site |
probably benign |
|
R1144:Washc4
|
UTSW |
10 |
83,416,194 (GRCm39) |
missense |
probably damaging |
0.97 |
R1560:Washc4
|
UTSW |
10 |
83,391,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R1789:Washc4
|
UTSW |
10 |
83,415,389 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1819:Washc4
|
UTSW |
10 |
83,386,748 (GRCm39) |
missense |
probably benign |
0.08 |
R2421:Washc4
|
UTSW |
10 |
83,415,385 (GRCm39) |
missense |
probably damaging |
0.97 |
R2882:Washc4
|
UTSW |
10 |
83,415,365 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2902:Washc4
|
UTSW |
10 |
83,390,627 (GRCm39) |
nonsense |
probably null |
|
R3436:Washc4
|
UTSW |
10 |
83,405,866 (GRCm39) |
missense |
probably benign |
0.33 |
R3437:Washc4
|
UTSW |
10 |
83,405,866 (GRCm39) |
missense |
probably benign |
0.33 |
R3552:Washc4
|
UTSW |
10 |
83,382,720 (GRCm39) |
missense |
probably benign |
0.45 |
R4646:Washc4
|
UTSW |
10 |
83,410,407 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4647:Washc4
|
UTSW |
10 |
83,410,407 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4648:Washc4
|
UTSW |
10 |
83,410,407 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4732:Washc4
|
UTSW |
10 |
83,410,343 (GRCm39) |
missense |
probably benign |
|
R4733:Washc4
|
UTSW |
10 |
83,410,343 (GRCm39) |
missense |
probably benign |
|
R4750:Washc4
|
UTSW |
10 |
83,426,916 (GRCm39) |
missense |
probably damaging |
0.99 |
R4835:Washc4
|
UTSW |
10 |
83,415,376 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5024:Washc4
|
UTSW |
10 |
83,419,200 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5055:Washc4
|
UTSW |
10 |
83,392,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R5414:Washc4
|
UTSW |
10 |
83,391,967 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5423:Washc4
|
UTSW |
10 |
83,415,418 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5428:Washc4
|
UTSW |
10 |
83,410,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5506:Washc4
|
UTSW |
10 |
83,417,201 (GRCm39) |
missense |
probably damaging |
0.97 |
R5540:Washc4
|
UTSW |
10 |
83,409,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R5667:Washc4
|
UTSW |
10 |
83,405,892 (GRCm39) |
missense |
probably damaging |
0.97 |
R5671:Washc4
|
UTSW |
10 |
83,405,892 (GRCm39) |
missense |
probably damaging |
0.97 |
R5777:Washc4
|
UTSW |
10 |
83,391,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R6369:Washc4
|
UTSW |
10 |
83,410,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6370:Washc4
|
UTSW |
10 |
83,407,226 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6500:Washc4
|
UTSW |
10 |
83,394,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Washc4
|
UTSW |
10 |
83,408,059 (GRCm39) |
nonsense |
probably null |
|
R6657:Washc4
|
UTSW |
10 |
83,394,482 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6829:Washc4
|
UTSW |
10 |
83,396,380 (GRCm39) |
missense |
probably damaging |
0.97 |
R6862:Washc4
|
UTSW |
10 |
83,394,757 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6899:Washc4
|
UTSW |
10 |
83,411,919 (GRCm39) |
missense |
probably benign |
0.07 |
R7144:Washc4
|
UTSW |
10 |
83,409,638 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7163:Washc4
|
UTSW |
10 |
83,426,897 (GRCm39) |
missense |
probably damaging |
0.99 |
R7477:Washc4
|
UTSW |
10 |
83,410,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R7900:Washc4
|
UTSW |
10 |
83,409,637 (GRCm39) |
splice site |
probably null |
|
R8194:Washc4
|
UTSW |
10 |
83,416,163 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8491:Washc4
|
UTSW |
10 |
83,411,987 (GRCm39) |
missense |
probably benign |
0.24 |
R8791:Washc4
|
UTSW |
10 |
83,386,748 (GRCm39) |
missense |
probably benign |
0.08 |
R8804:Washc4
|
UTSW |
10 |
83,408,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R8896:Washc4
|
UTSW |
10 |
83,405,882 (GRCm39) |
missense |
probably damaging |
0.98 |
R8961:Washc4
|
UTSW |
10 |
83,409,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R9084:Washc4
|
UTSW |
10 |
83,422,499 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9452:Washc4
|
UTSW |
10 |
83,396,387 (GRCm39) |
missense |
probably benign |
|
R9532:Washc4
|
UTSW |
10 |
83,417,258 (GRCm39) |
splice site |
probably benign |
|
X0017:Washc4
|
UTSW |
10 |
83,427,007 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Washc4
|
UTSW |
10 |
83,394,693 (GRCm39) |
frame shift |
probably null |
|
Z1088:Washc4
|
UTSW |
10 |
83,412,605 (GRCm39) |
missense |
probably benign |
0.07 |
|