Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
A |
G |
15: 91,033,184 (GRCm39) |
|
probably benign |
Het |
Abcg5 |
C |
T |
17: 84,977,827 (GRCm39) |
R143Q |
probably damaging |
Het |
Arap3 |
G |
A |
18: 38,129,711 (GRCm39) |
T150I |
probably benign |
Het |
Arhgap32 |
T |
C |
9: 32,158,490 (GRCm39) |
V175A |
probably damaging |
Het |
Bpifb3 |
A |
G |
2: 153,766,721 (GRCm39) |
E208G |
probably benign |
Het |
C2 |
T |
A |
17: 35,083,325 (GRCm39) |
D518V |
possibly damaging |
Het |
C6 |
T |
A |
15: 4,820,646 (GRCm39) |
C552* |
probably null |
Het |
Ccdc38 |
A |
T |
10: 93,415,685 (GRCm39) |
D447V |
probably damaging |
Het |
Cept1 |
C |
T |
3: 106,411,035 (GRCm39) |
R386H |
probably benign |
Het |
Comt |
A |
G |
16: 18,230,454 (GRCm39) |
V85A |
probably damaging |
Het |
Ddx24 |
G |
T |
12: 103,383,571 (GRCm39) |
L627I |
probably damaging |
Het |
Efemp1 |
T |
C |
11: 28,866,971 (GRCm39) |
|
probably null |
Het |
Etf1 |
T |
C |
18: 35,046,714 (GRCm39) |
T99A |
possibly damaging |
Het |
Fhad1 |
T |
C |
4: 141,660,105 (GRCm39) |
E68G |
probably null |
Het |
Gins3 |
T |
C |
8: 96,364,606 (GRCm39) |
F119L |
probably benign |
Het |
Golga5 |
G |
T |
12: 102,438,338 (GRCm39) |
V18L |
probably benign |
Het |
Il16 |
C |
A |
7: 83,310,484 (GRCm39) |
R474M |
probably damaging |
Het |
Itpr1 |
C |
A |
6: 108,316,515 (GRCm39) |
Q71K |
possibly damaging |
Het |
Kif21b |
T |
G |
1: 136,100,605 (GRCm39) |
L1562R |
probably damaging |
Het |
Lamc2 |
T |
C |
1: 153,042,008 (GRCm39) |
E42G |
possibly damaging |
Het |
Mmp3 |
T |
G |
9: 7,446,001 (GRCm39) |
L35R |
probably benign |
Het |
Naip6 |
C |
A |
13: 100,452,780 (GRCm39) |
G94W |
probably damaging |
Het |
Nccrp1 |
G |
A |
7: 28,243,905 (GRCm39) |
A226V |
probably damaging |
Het |
Nckap5l |
A |
G |
15: 99,323,564 (GRCm39) |
Y980H |
probably damaging |
Het |
Ncoa3 |
T |
C |
2: 165,911,277 (GRCm39) |
S1345P |
probably damaging |
Het |
Nop2 |
T |
C |
6: 125,117,813 (GRCm39) |
S455P |
probably damaging |
Het |
Nup93 |
T |
C |
8: 95,036,263 (GRCm39) |
F689S |
probably damaging |
Het |
Or5b112 |
T |
C |
19: 13,319,583 (GRCm39) |
F154L |
probably benign |
Het |
Plekhm1 |
T |
A |
11: 103,285,876 (GRCm39) |
E186D |
probably damaging |
Het |
Plxdc1 |
T |
C |
11: 97,869,390 (GRCm39) |
Q66R |
probably damaging |
Het |
Prkdc |
T |
G |
16: 15,544,406 (GRCm39) |
Y1799D |
probably damaging |
Het |
Rasa2 |
A |
G |
9: 96,462,563 (GRCm39) |
F220L |
probably damaging |
Het |
Rftn1 |
T |
C |
17: 50,344,027 (GRCm39) |
D87G |
probably damaging |
Het |
Rgs6 |
C |
T |
12: 83,117,376 (GRCm39) |
T266M |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,326,054 (GRCm39) |
Y1208H |
probably damaging |
Het |
Slc12a1 |
G |
T |
2: 125,026,648 (GRCm39) |
V428L |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Svep1 |
T |
A |
4: 58,135,441 (GRCm39) |
T556S |
probably benign |
Het |
Tanc2 |
T |
A |
11: 105,667,777 (GRCm39) |
N119K |
probably benign |
Het |
Tpgs1 |
T |
A |
10: 79,505,238 (GRCm39) |
|
probably benign |
Het |
Tpm3-rs7 |
A |
G |
14: 113,552,370 (GRCm39) |
E88G |
probably damaging |
Het |
Tsr1 |
T |
C |
11: 74,791,204 (GRCm39) |
V261A |
probably benign |
Het |
Usp18 |
C |
T |
6: 121,238,050 (GRCm39) |
T143I |
probably benign |
Het |
Vmn2r24 |
T |
C |
6: 123,792,812 (GRCm39) |
I713T |
probably benign |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
|
Other mutations in Fzd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01987:Fzd3
|
APN |
14 |
65,477,347 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02505:Fzd3
|
APN |
14 |
65,490,555 (GRCm39) |
missense |
probably benign |
|
R1161:Fzd3
|
UTSW |
14 |
65,449,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Fzd3
|
UTSW |
14 |
65,473,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Fzd3
|
UTSW |
14 |
65,472,956 (GRCm39) |
missense |
probably benign |
|
R1636:Fzd3
|
UTSW |
14 |
65,490,555 (GRCm39) |
missense |
probably benign |
|
R1826:Fzd3
|
UTSW |
14 |
65,490,555 (GRCm39) |
missense |
probably benign |
|
R2071:Fzd3
|
UTSW |
14 |
65,473,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Fzd3
|
UTSW |
14 |
65,449,680 (GRCm39) |
splice site |
probably benign |
|
R3857:Fzd3
|
UTSW |
14 |
65,477,288 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3859:Fzd3
|
UTSW |
14 |
65,477,288 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3917:Fzd3
|
UTSW |
14 |
65,473,379 (GRCm39) |
missense |
probably damaging |
0.97 |
R4110:Fzd3
|
UTSW |
14 |
65,472,616 (GRCm39) |
missense |
probably benign |
0.00 |
R4396:Fzd3
|
UTSW |
14 |
65,473,054 (GRCm39) |
missense |
probably damaging |
0.99 |
R4740:Fzd3
|
UTSW |
14 |
65,473,193 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4796:Fzd3
|
UTSW |
14 |
65,472,607 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4838:Fzd3
|
UTSW |
14 |
65,477,269 (GRCm39) |
missense |
probably benign |
0.00 |
R5916:Fzd3
|
UTSW |
14 |
65,440,178 (GRCm39) |
missense |
probably benign |
0.29 |
R6240:Fzd3
|
UTSW |
14 |
65,447,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6732:Fzd3
|
UTSW |
14 |
65,473,252 (GRCm39) |
missense |
probably benign |
0.44 |
R6892:Fzd3
|
UTSW |
14 |
65,447,330 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7819:Fzd3
|
UTSW |
14 |
65,472,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R8113:Fzd3
|
UTSW |
14 |
65,440,262 (GRCm39) |
missense |
probably benign |
0.37 |
R8974:Fzd3
|
UTSW |
14 |
65,472,440 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9128:Fzd3
|
UTSW |
14 |
65,449,626 (GRCm39) |
missense |
probably damaging |
1.00 |
|