Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
G |
A |
7: 78,742,231 (GRCm39) |
V543I |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,118,960 (GRCm39) |
I1104V |
possibly damaging |
Het |
Adgrl4 |
A |
T |
3: 151,248,370 (GRCm39) |
I681F |
possibly damaging |
Het |
Adgrv1 |
T |
A |
13: 81,676,820 (GRCm39) |
M2004L |
probably benign |
Het |
Anapc1 |
A |
G |
2: 128,501,688 (GRCm39) |
S785P |
possibly damaging |
Het |
Arhgap5 |
T |
C |
12: 52,565,927 (GRCm39) |
L966P |
probably benign |
Het |
Atp8a1 |
T |
C |
5: 67,895,794 (GRCm39) |
T547A |
probably benign |
Het |
Cadps |
A |
G |
14: 12,505,811 (GRCm38) |
F753S |
probably damaging |
Het |
Cdc20b |
T |
C |
13: 113,215,187 (GRCm39) |
S252P |
possibly damaging |
Het |
Cep63 |
A |
G |
9: 102,503,126 (GRCm39) |
|
probably benign |
Het |
Chrna5 |
G |
T |
9: 54,912,417 (GRCm39) |
V302L |
probably benign |
Het |
Crtc2 |
A |
G |
3: 90,168,378 (GRCm39) |
T374A |
probably damaging |
Het |
Dmtf1 |
T |
G |
5: 9,187,149 (GRCm39) |
D140A |
probably damaging |
Het |
Exosc8 |
C |
T |
3: 54,641,120 (GRCm39) |
V39M |
probably damaging |
Het |
Fam135b |
A |
C |
15: 71,335,164 (GRCm39) |
S677A |
probably damaging |
Het |
Hif1an |
T |
C |
19: 44,551,828 (GRCm39) |
Y93H |
probably damaging |
Het |
Hrc |
T |
C |
7: 44,985,088 (GRCm39) |
F80L |
probably benign |
Het |
Jmjd1c |
A |
G |
10: 67,025,599 (GRCm39) |
T139A |
possibly damaging |
Het |
Kdr |
T |
G |
5: 76,129,111 (GRCm39) |
R178S |
probably benign |
Het |
Lrrc61 |
A |
C |
6: 48,545,366 (GRCm39) |
N63T |
probably damaging |
Het |
Mrc1 |
C |
T |
2: 14,330,048 (GRCm39) |
A1219V |
possibly damaging |
Het |
Neto1 |
T |
C |
18: 86,516,760 (GRCm39) |
V359A |
probably benign |
Het |
Ngly1 |
T |
C |
14: 16,281,836 (GRCm38) |
I364T |
probably benign |
Het |
Nisch |
C |
T |
14: 30,907,301 (GRCm39) |
|
probably benign |
Het |
Or2y8 |
C |
A |
11: 52,036,179 (GRCm39) |
M59I |
probably benign |
Het |
Prrc2a |
T |
C |
17: 35,374,651 (GRCm39) |
D1333G |
probably damaging |
Het |
Raly |
G |
T |
2: 154,703,830 (GRCm39) |
V134F |
probably damaging |
Het |
Rbm6 |
T |
C |
9: 107,729,430 (GRCm39) |
Y406C |
probably damaging |
Het |
Robo4 |
G |
C |
9: 37,313,363 (GRCm39) |
E6Q |
possibly damaging |
Het |
Scnn1g |
C |
A |
7: 121,359,667 (GRCm39) |
S383R |
probably benign |
Het |
Sgtb |
T |
C |
13: 104,247,659 (GRCm39) |
W13R |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,435,633 (GRCm39) |
|
probably null |
Het |
Tbc1d32 |
G |
A |
10: 56,027,907 (GRCm39) |
Q732* |
probably null |
Het |
Tek |
T |
A |
4: 94,693,181 (GRCm39) |
C247S |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,153,799 (GRCm39) |
D91E |
probably damaging |
Het |
Usp39 |
A |
G |
6: 72,310,140 (GRCm39) |
L326P |
probably damaging |
Het |
Vmn2r7 |
A |
T |
3: 64,598,248 (GRCm39) |
C770S |
probably damaging |
Het |
Wdr31 |
C |
T |
4: 62,375,802 (GRCm39) |
G58R |
probably benign |
Het |
Zfyve26 |
A |
G |
12: 79,313,223 (GRCm39) |
I54T |
probably damaging |
Het |
|
Other mutations in Ap3d1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Ap3d1
|
APN |
10 |
80,577,813 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00827:Ap3d1
|
APN |
10 |
80,549,393 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01668:Ap3d1
|
APN |
10 |
80,554,993 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01934:Ap3d1
|
APN |
10 |
80,545,092 (GRCm39) |
nonsense |
probably null |
|
IGL03404:Ap3d1
|
APN |
10 |
80,565,871 (GRCm39) |
missense |
probably damaging |
1.00 |
christian
|
UTSW |
10 |
80,565,876 (GRCm39) |
missense |
probably damaging |
1.00 |
Particle
|
UTSW |
10 |
80,546,328 (GRCm39) |
splice site |
probably null |
|
vesicle
|
UTSW |
10 |
80,559,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Ap3d1
|
UTSW |
10 |
80,559,449 (GRCm39) |
splice site |
probably benign |
|
R0197:Ap3d1
|
UTSW |
10 |
80,565,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R0356:Ap3d1
|
UTSW |
10 |
80,563,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R0372:Ap3d1
|
UTSW |
10 |
80,559,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Ap3d1
|
UTSW |
10 |
80,555,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Ap3d1
|
UTSW |
10 |
80,555,216 (GRCm39) |
nonsense |
probably null |
|
R0792:Ap3d1
|
UTSW |
10 |
80,544,313 (GRCm39) |
missense |
probably benign |
|
R0942:Ap3d1
|
UTSW |
10 |
80,568,789 (GRCm39) |
splice site |
probably benign |
|
R1015:Ap3d1
|
UTSW |
10 |
80,552,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Ap3d1
|
UTSW |
10 |
80,550,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Ap3d1
|
UTSW |
10 |
80,568,674 (GRCm39) |
splice site |
probably benign |
|
R1540:Ap3d1
|
UTSW |
10 |
80,551,775 (GRCm39) |
missense |
probably benign |
0.00 |
R1639:Ap3d1
|
UTSW |
10 |
80,565,844 (GRCm39) |
missense |
probably damaging |
0.98 |
R1664:Ap3d1
|
UTSW |
10 |
80,553,571 (GRCm39) |
nonsense |
probably null |
|
R1669:Ap3d1
|
UTSW |
10 |
80,546,670 (GRCm39) |
unclassified |
probably benign |
|
R1839:Ap3d1
|
UTSW |
10 |
80,562,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Ap3d1
|
UTSW |
10 |
80,545,607 (GRCm39) |
missense |
probably benign |
0.03 |
R2081:Ap3d1
|
UTSW |
10 |
80,568,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Ap3d1
|
UTSW |
10 |
80,556,966 (GRCm39) |
missense |
probably benign |
0.03 |
R2281:Ap3d1
|
UTSW |
10 |
80,549,832 (GRCm39) |
missense |
probably damaging |
0.96 |
R2398:Ap3d1
|
UTSW |
10 |
80,555,006 (GRCm39) |
nonsense |
probably null |
|
R2849:Ap3d1
|
UTSW |
10 |
80,577,742 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3856:Ap3d1
|
UTSW |
10 |
80,548,019 (GRCm39) |
missense |
probably benign |
|
R4350:Ap3d1
|
UTSW |
10 |
80,555,119 (GRCm39) |
missense |
probably benign |
0.15 |
R4590:Ap3d1
|
UTSW |
10 |
80,555,646 (GRCm39) |
nonsense |
probably null |
|
R4782:Ap3d1
|
UTSW |
10 |
80,557,420 (GRCm39) |
splice site |
probably null |
|
R4785:Ap3d1
|
UTSW |
10 |
80,548,612 (GRCm39) |
frame shift |
probably null |
|
R4834:Ap3d1
|
UTSW |
10 |
80,555,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Ap3d1
|
UTSW |
10 |
80,548,612 (GRCm39) |
frame shift |
probably null |
|
R5051:Ap3d1
|
UTSW |
10 |
80,555,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R5109:Ap3d1
|
UTSW |
10 |
80,545,284 (GRCm39) |
missense |
probably benign |
0.11 |
R5219:Ap3d1
|
UTSW |
10 |
80,545,651 (GRCm39) |
missense |
probably benign |
0.03 |
R5220:Ap3d1
|
UTSW |
10 |
80,563,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Ap3d1
|
UTSW |
10 |
80,559,383 (GRCm39) |
missense |
probably benign |
0.29 |
R5586:Ap3d1
|
UTSW |
10 |
80,554,964 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5796:Ap3d1
|
UTSW |
10 |
80,549,871 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5905:Ap3d1
|
UTSW |
10 |
80,558,761 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6025:Ap3d1
|
UTSW |
10 |
80,546,298 (GRCm39) |
missense |
probably benign |
0.01 |
R6028:Ap3d1
|
UTSW |
10 |
80,558,761 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6364:Ap3d1
|
UTSW |
10 |
80,546,328 (GRCm39) |
splice site |
probably null |
|
R6469:Ap3d1
|
UTSW |
10 |
80,547,992 (GRCm39) |
missense |
probably benign |
|
R6603:Ap3d1
|
UTSW |
10 |
80,549,881 (GRCm39) |
missense |
probably benign |
0.04 |
R6872:Ap3d1
|
UTSW |
10 |
80,550,156 (GRCm39) |
nonsense |
probably null |
|
R7249:Ap3d1
|
UTSW |
10 |
80,577,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R7316:Ap3d1
|
UTSW |
10 |
80,553,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7325:Ap3d1
|
UTSW |
10 |
80,559,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Ap3d1
|
UTSW |
10 |
80,566,716 (GRCm39) |
missense |
probably benign |
0.11 |
R7405:Ap3d1
|
UTSW |
10 |
80,577,734 (GRCm39) |
missense |
probably benign |
0.16 |
R7425:Ap3d1
|
UTSW |
10 |
80,557,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Ap3d1
|
UTSW |
10 |
80,558,755 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7583:Ap3d1
|
UTSW |
10 |
80,545,292 (GRCm39) |
missense |
probably benign |
0.13 |
R7703:Ap3d1
|
UTSW |
10 |
80,553,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R7964:Ap3d1
|
UTSW |
10 |
80,565,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R8021:Ap3d1
|
UTSW |
10 |
80,550,135 (GRCm39) |
missense |
probably benign |
0.30 |
R8200:Ap3d1
|
UTSW |
10 |
80,558,766 (GRCm39) |
nonsense |
probably null |
|
R8314:Ap3d1
|
UTSW |
10 |
80,559,373 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8356:Ap3d1
|
UTSW |
10 |
80,568,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Ap3d1
|
UTSW |
10 |
80,552,425 (GRCm39) |
missense |
probably benign |
0.01 |
R8936:Ap3d1
|
UTSW |
10 |
80,547,952 (GRCm39) |
missense |
probably benign |
0.02 |
R9183:Ap3d1
|
UTSW |
10 |
80,545,627 (GRCm39) |
missense |
probably null |
0.06 |
R9209:Ap3d1
|
UTSW |
10 |
80,554,918 (GRCm39) |
missense |
probably benign |
0.04 |
R9259:Ap3d1
|
UTSW |
10 |
80,559,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Ap3d1
|
UTSW |
10 |
80,545,655 (GRCm39) |
missense |
probably benign |
0.00 |
R9645:Ap3d1
|
UTSW |
10 |
80,545,062 (GRCm39) |
missense |
probably benign |
|
R9664:Ap3d1
|
UTSW |
10 |
80,548,639 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9781:Ap3d1
|
UTSW |
10 |
80,545,609 (GRCm39) |
missense |
possibly damaging |
0.51 |
X0019:Ap3d1
|
UTSW |
10 |
80,554,936 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Ap3d1
|
UTSW |
10 |
80,556,981 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1088:Ap3d1
|
UTSW |
10 |
80,555,071 (GRCm39) |
missense |
possibly damaging |
0.91 |
|