Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
T |
C |
11: 94,242,636 (GRCm39) |
I1364V |
possibly damaging |
Het |
Adamts19 |
T |
A |
18: 59,122,037 (GRCm39) |
I813K |
probably damaging |
Het |
Adamtsl1 |
G |
T |
4: 86,342,594 (GRCm39) |
C1703F |
probably damaging |
Het |
Atp2b4 |
T |
A |
1: 133,658,303 (GRCm39) |
T536S |
probably damaging |
Het |
Capg |
T |
A |
6: 72,539,827 (GRCm39) |
I340N |
probably damaging |
Het |
Casc3 |
T |
A |
11: 98,719,749 (GRCm39) |
M567K |
probably damaging |
Het |
Chmp1a |
T |
C |
8: 123,934,806 (GRCm39) |
E50G |
probably damaging |
Het |
Cryba1 |
T |
C |
11: 77,610,207 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,965,735 (GRCm39) |
Y2356N |
probably damaging |
Het |
Ercc6 |
T |
G |
14: 32,292,060 (GRCm39) |
S1141R |
probably benign |
Het |
Exd2 |
T |
A |
12: 80,527,302 (GRCm39) |
V165D |
probably damaging |
Het |
Fbln1 |
A |
T |
15: 85,115,663 (GRCm39) |
E233V |
probably damaging |
Het |
Ftsj3 |
T |
C |
11: 106,143,163 (GRCm39) |
K384E |
probably damaging |
Het |
Ggt5 |
A |
G |
10: 75,439,962 (GRCm39) |
I188V |
probably benign |
Het |
Gm42742 |
A |
T |
7: 126,616,018 (GRCm39) |
S26T |
probably damaging |
Het |
Gucy1a2 |
T |
A |
9: 3,759,542 (GRCm39) |
D449E |
probably damaging |
Het |
Igfbp7 |
C |
T |
5: 77,499,188 (GRCm39) |
S239N |
possibly damaging |
Het |
Klf11 |
C |
T |
12: 24,705,626 (GRCm39) |
A360V |
probably damaging |
Het |
Kmt2e |
T |
A |
5: 23,672,098 (GRCm39) |
|
probably benign |
Het |
Magea8 |
A |
T |
X: 153,769,678 (GRCm39) |
C144S |
probably damaging |
Het |
Med4 |
A |
G |
14: 73,755,361 (GRCm39) |
Q223R |
probably damaging |
Het |
Mmd2 |
G |
T |
5: 142,555,232 (GRCm39) |
F153L |
probably damaging |
Het |
Nav3 |
C |
A |
10: 109,572,814 (GRCm39) |
R1615L |
probably damaging |
Het |
Nisch |
A |
G |
14: 30,902,769 (GRCm39) |
|
probably benign |
Het |
Nr1i3 |
A |
T |
1: 171,041,964 (GRCm39) |
Y16F |
probably benign |
Het |
Or5w1 |
C |
A |
2: 87,487,058 (GRCm39) |
C69F |
probably damaging |
Het |
Or7e169 |
G |
A |
9: 19,757,550 (GRCm39) |
R122* |
probably null |
Het |
Or7g16 |
A |
G |
9: 18,727,024 (GRCm39) |
C189R |
probably damaging |
Het |
Or8g34 |
A |
G |
9: 39,373,077 (GRCm39) |
T117A |
possibly damaging |
Het |
Ppil6 |
C |
A |
10: 41,383,479 (GRCm39) |
H252N |
probably benign |
Het |
Ppp6r2 |
C |
T |
15: 89,143,378 (GRCm39) |
P175L |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,741,095 (GRCm39) |
Y90* |
probably null |
Het |
Rbm20 |
C |
A |
19: 53,802,133 (GRCm39) |
L214I |
probably benign |
Het |
Rhox2f |
T |
C |
X: 36,753,334 (GRCm39) |
V24A |
probably benign |
Het |
Scnm1 |
T |
C |
3: 95,040,348 (GRCm39) |
K96E |
probably benign |
Het |
Sec16a |
A |
C |
2: 26,309,735 (GRCm39) |
D2090E |
probably benign |
Het |
Smg6 |
T |
C |
11: 74,821,576 (GRCm39) |
|
probably null |
Het |
Snx2 |
T |
C |
18: 53,327,630 (GRCm39) |
S119P |
probably benign |
Het |
Stam |
A |
G |
2: 14,120,779 (GRCm39) |
|
probably benign |
Het |
Sult2b1 |
T |
A |
7: 45,384,698 (GRCm39) |
E126V |
probably benign |
Het |
Tor1aip1 |
T |
C |
1: 155,911,590 (GRCm39) |
E131G |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,619,040 (GRCm39) |
C14367Y |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,135,131 (GRCm39) |
F821S |
possibly damaging |
Het |
Vmn1r32 |
T |
C |
6: 66,529,922 (GRCm39) |
N285D |
probably benign |
Het |
Vmn2r23 |
T |
C |
6: 123,718,741 (GRCm39) |
L698P |
possibly damaging |
Het |
Zfp747 |
T |
C |
7: 126,973,666 (GRCm39) |
E168G |
probably benign |
Het |
|
Other mutations in Wnt8a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01592:Wnt8a
|
APN |
18 |
34,677,846 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01823:Wnt8a
|
APN |
18 |
34,677,846 (GRCm39) |
missense |
possibly damaging |
0.85 |
PIT4486001:Wnt8a
|
UTSW |
18 |
34,680,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R0496:Wnt8a
|
UTSW |
18 |
34,677,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Wnt8a
|
UTSW |
18 |
34,680,618 (GRCm39) |
missense |
probably benign |
0.02 |
R1813:Wnt8a
|
UTSW |
18 |
34,675,422 (GRCm39) |
start codon destroyed |
probably null |
0.89 |
R1990:Wnt8a
|
UTSW |
18 |
34,677,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Wnt8a
|
UTSW |
18 |
34,677,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Wnt8a
|
UTSW |
18 |
34,677,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4927:Wnt8a
|
UTSW |
18 |
34,680,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R5085:Wnt8a
|
UTSW |
18 |
34,678,656 (GRCm39) |
nonsense |
probably null |
|
R6161:Wnt8a
|
UTSW |
18 |
34,678,599 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7719:Wnt8a
|
UTSW |
18 |
34,680,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R8001:Wnt8a
|
UTSW |
18 |
34,678,569 (GRCm39) |
missense |
probably damaging |
0.98 |
R9022:Wnt8a
|
UTSW |
18 |
34,680,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R9617:Wnt8a
|
UTSW |
18 |
34,680,163 (GRCm39) |
missense |
probably benign |
0.00 |
|