Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abra |
T |
A |
15: 41,732,512 (GRCm39) |
T185S |
possibly damaging |
Het |
Acad10 |
T |
A |
5: 121,767,981 (GRCm39) |
H823L |
probably benign |
Het |
Acly |
A |
G |
11: 100,407,657 (GRCm39) |
V231A |
probably benign |
Het |
Adamts9 |
T |
C |
6: 92,849,381 (GRCm39) |
N1026S |
probably benign |
Het |
Amot |
A |
T |
X: 144,244,745 (GRCm39) |
L435H |
|
Het |
Ankrd65 |
A |
G |
4: 155,875,800 (GRCm39) |
E7G |
probably benign |
Het |
Atp9a |
A |
G |
2: 168,485,780 (GRCm39) |
|
probably null |
Het |
Atxn10 |
T |
G |
15: 85,277,557 (GRCm39) |
H341Q |
probably damaging |
Het |
Cacng1 |
A |
G |
11: 107,607,060 (GRCm39) |
L53P |
probably damaging |
Het |
Cdh23 |
T |
C |
10: 60,161,810 (GRCm39) |
N2014S |
probably benign |
Het |
Cma1 |
T |
C |
14: 56,181,189 (GRCm39) |
N72S |
probably benign |
Het |
Col7a1 |
G |
A |
9: 108,807,953 (GRCm39) |
G2551D |
unknown |
Het |
Cyp20a1 |
T |
G |
1: 60,415,343 (GRCm39) |
L323R |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 117,894,918 (GRCm39) |
V3643E |
probably damaging |
Het |
Dnmt3l |
A |
C |
10: 77,895,518 (GRCm39) |
D352A |
probably benign |
Het |
Dock2 |
A |
T |
11: 34,589,670 (GRCm39) |
N462K |
probably benign |
Het |
Drc1 |
A |
G |
5: 30,513,794 (GRCm39) |
Q450R |
probably benign |
Het |
Drgx |
C |
T |
14: 32,330,339 (GRCm39) |
S152F |
probably damaging |
Het |
Efcab3 |
A |
G |
11: 104,800,708 (GRCm39) |
T2977A |
probably benign |
Het |
Eid3 |
C |
T |
10: 82,703,316 (GRCm39) |
T259M |
probably damaging |
Het |
Eif2ak3 |
T |
G |
6: 70,835,419 (GRCm39) |
D115E |
probably damaging |
Het |
Ezh2 |
A |
C |
6: 47,531,134 (GRCm39) |
D183E |
probably benign |
Het |
Fam114a1 |
A |
C |
5: 65,191,713 (GRCm39) |
|
probably null |
Het |
Fcho2 |
G |
A |
13: 98,891,607 (GRCm39) |
T385I |
probably benign |
Het |
Gm6882 |
C |
A |
7: 21,161,254 (GRCm39) |
E205* |
probably null |
Het |
Hexim2 |
G |
A |
11: 103,029,822 (GRCm39) |
W291* |
probably null |
Het |
Hnrnpab |
A |
C |
11: 51,492,710 (GRCm39) |
S265R |
unknown |
Het |
Hsd17b1 |
A |
G |
11: 100,969,832 (GRCm39) |
N115D |
probably damaging |
Het |
Ighmbp2 |
T |
C |
19: 3,315,641 (GRCm39) |
D593G |
possibly damaging |
Het |
Inf2 |
C |
A |
12: 112,567,965 (GRCm39) |
C172* |
probably null |
Het |
Invs |
A |
T |
4: 48,398,149 (GRCm39) |
N445I |
possibly damaging |
Het |
Izumo2 |
A |
G |
7: 44,369,184 (GRCm39) |
Q186R |
probably benign |
Het |
Kcnj15 |
T |
C |
16: 95,097,481 (GRCm39) |
F368L |
probably benign |
Het |
Kctd20 |
A |
G |
17: 29,185,866 (GRCm39) |
D403G |
probably damaging |
Het |
Kmt2c |
A |
C |
5: 25,486,309 (GRCm39) |
V4748G |
probably damaging |
Het |
Lrrc37a |
A |
G |
11: 103,393,140 (GRCm39) |
S762P |
probably benign |
Het |
Man2c1 |
C |
T |
9: 57,044,317 (GRCm39) |
Q324* |
probably null |
Het |
Mgam |
A |
G |
6: 40,745,146 (GRCm39) |
I1804M |
possibly damaging |
Het |
Mmp28 |
A |
G |
11: 83,335,661 (GRCm39) |
V279A |
probably benign |
Het |
Mrpl22 |
T |
C |
11: 58,070,185 (GRCm39) |
V164A |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,952,329 (GRCm39) |
H3913Q |
possibly damaging |
Het |
Or6e1 |
T |
C |
14: 54,520,329 (GRCm39) |
T8A |
probably benign |
Het |
Or8g50 |
C |
T |
9: 39,648,516 (GRCm39) |
T135I |
probably benign |
Het |
Paqr6 |
A |
G |
3: 88,273,066 (GRCm39) |
T46A |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,178,550 (GRCm39) |
D1789G |
probably benign |
Het |
Pou4f2 |
T |
C |
8: 79,162,748 (GRCm39) |
T96A |
probably benign |
Het |
Ppp1r12b |
A |
T |
1: 134,801,725 (GRCm39) |
V497E |
probably benign |
Het |
Prdm13 |
C |
G |
4: 21,679,659 (GRCm39) |
R277P |
unknown |
Het |
Rsph4a |
C |
T |
10: 33,785,438 (GRCm39) |
Q450* |
probably null |
Het |
Sh3d19 |
C |
T |
3: 85,990,918 (GRCm39) |
|
probably benign |
Het |
Slc39a14 |
T |
C |
14: 70,547,687 (GRCm39) |
T259A |
probably benign |
Het |
Snap91 |
T |
C |
9: 86,680,672 (GRCm39) |
T404A |
probably benign |
Het |
Sptbn4 |
A |
T |
7: 27,141,844 (GRCm39) |
C50S |
possibly damaging |
Het |
Stx8 |
A |
C |
11: 67,875,471 (GRCm39) |
N99H |
possibly damaging |
Het |
Tgfbi |
A |
T |
13: 56,773,526 (GRCm39) |
M175L |
probably damaging |
Het |
Themis |
C |
A |
10: 28,658,233 (GRCm39) |
T420N |
probably benign |
Het |
Tle1 |
A |
T |
4: 72,043,232 (GRCm39) |
C536S |
possibly damaging |
Het |
Tprn |
A |
G |
2: 25,152,799 (GRCm39) |
S34G |
probably benign |
Het |
Vmn1r80 |
A |
T |
7: 11,927,124 (GRCm39) |
D78V |
possibly damaging |
Het |
|
Other mutations in Ap1g2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01095:Ap1g2
|
APN |
14 |
55,342,571 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02421:Ap1g2
|
APN |
14 |
55,339,859 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02633:Ap1g2
|
APN |
14 |
55,338,104 (GRCm39) |
splice site |
probably null |
|
IGL02967:Ap1g2
|
APN |
14 |
55,342,479 (GRCm39) |
splice site |
probably benign |
|
IGL03030:Ap1g2
|
APN |
14 |
55,343,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03087:Ap1g2
|
APN |
14 |
55,340,493 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03261:Ap1g2
|
APN |
14 |
55,337,987 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03308:Ap1g2
|
APN |
14 |
55,342,333 (GRCm39) |
missense |
probably benign |
0.44 |
R0284:Ap1g2
|
UTSW |
14 |
55,339,149 (GRCm39) |
splice site |
probably benign |
|
R0614:Ap1g2
|
UTSW |
14 |
55,337,230 (GRCm39) |
missense |
probably benign |
0.00 |
R0762:Ap1g2
|
UTSW |
14 |
55,337,868 (GRCm39) |
splice site |
probably benign |
|
R1561:Ap1g2
|
UTSW |
14 |
55,342,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R1889:Ap1g2
|
UTSW |
14 |
55,338,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Ap1g2
|
UTSW |
14 |
55,337,229 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1997:Ap1g2
|
UTSW |
14 |
55,339,835 (GRCm39) |
missense |
probably benign |
0.00 |
R2169:Ap1g2
|
UTSW |
14 |
55,336,797 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3157:Ap1g2
|
UTSW |
14 |
55,336,731 (GRCm39) |
missense |
probably damaging |
0.96 |
R3820:Ap1g2
|
UTSW |
14 |
55,338,030 (GRCm39) |
splice site |
probably benign |
|
R3850:Ap1g2
|
UTSW |
14 |
55,342,363 (GRCm39) |
missense |
probably benign |
0.03 |
R4750:Ap1g2
|
UTSW |
14 |
55,341,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R4909:Ap1g2
|
UTSW |
14 |
55,342,483 (GRCm39) |
critical splice donor site |
probably null |
|
R5305:Ap1g2
|
UTSW |
14 |
55,336,533 (GRCm39) |
missense |
probably benign |
|
R5880:Ap1g2
|
UTSW |
14 |
55,340,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Ap1g2
|
UTSW |
14 |
55,336,530 (GRCm39) |
missense |
probably benign |
|
R6964:Ap1g2
|
UTSW |
14 |
55,336,722 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7039:Ap1g2
|
UTSW |
14 |
55,340,111 (GRCm39) |
nonsense |
probably null |
|
R7180:Ap1g2
|
UTSW |
14 |
55,341,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R7563:Ap1g2
|
UTSW |
14 |
55,337,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R7818:Ap1g2
|
UTSW |
14 |
55,337,181 (GRCm39) |
missense |
probably benign |
0.44 |
R7854:Ap1g2
|
UTSW |
14 |
55,343,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R9060:Ap1g2
|
UTSW |
14 |
55,337,887 (GRCm39) |
missense |
probably benign |
0.00 |
R9276:Ap1g2
|
UTSW |
14 |
55,339,818 (GRCm39) |
missense |
probably benign |
|
|