Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
A |
16: 4,665,292 (GRCm39) |
F141L |
unknown |
Het |
A2ml1 |
G |
T |
6: 128,529,219 (GRCm39) |
N974K |
probably damaging |
Het |
Abcg8 |
T |
C |
17: 84,999,246 (GRCm39) |
L114P |
probably damaging |
Het |
Akt3 |
A |
T |
1: 176,958,645 (GRCm39) |
W22R |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,736,396 (GRCm39) |
|
probably benign |
Het |
Arhgef19 |
T |
A |
4: 140,973,618 (GRCm39) |
V35E |
possibly damaging |
Het |
Baz2b |
T |
C |
2: 59,778,583 (GRCm39) |
D759G |
probably benign |
Het |
BC051665 |
C |
A |
13: 60,930,004 (GRCm39) |
G320W |
probably damaging |
Het |
Bche |
T |
A |
3: 73,608,761 (GRCm39) |
T222S |
probably damaging |
Het |
C8a |
T |
C |
4: 104,679,326 (GRCm39) |
D444G |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,277,896 (GRCm39) |
S2019T |
probably benign |
Het |
Carm1 |
T |
C |
9: 21,497,749 (GRCm39) |
I373T |
probably damaging |
Het |
Ccdc39 |
T |
C |
3: 33,869,609 (GRCm39) |
|
probably benign |
Het |
Clic5 |
A |
T |
17: 44,553,148 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
A |
G |
6: 102,414,864 (GRCm39) |
F28L |
probably damaging |
Het |
Col6a5 |
C |
T |
9: 105,822,833 (GRCm39) |
E175K |
unknown |
Het |
Cpb2 |
T |
C |
14: 75,515,627 (GRCm39) |
Y352H |
probably damaging |
Het |
Cpeb3 |
A |
T |
19: 37,152,366 (GRCm39) |
D3E |
probably damaging |
Het |
Ctsl |
T |
C |
13: 64,514,840 (GRCm39) |
T155A |
probably damaging |
Het |
Cygb |
C |
T |
11: 116,540,645 (GRCm39) |
A114T |
probably damaging |
Het |
Cyp11a1 |
T |
C |
9: 57,924,738 (GRCm39) |
V17A |
probably benign |
Het |
Dhcr7 |
T |
G |
7: 143,400,959 (GRCm39) |
I374S |
probably damaging |
Het |
Dhx36 |
T |
C |
3: 62,380,387 (GRCm39) |
R807G |
probably benign |
Het |
Diaph1 |
A |
T |
18: 37,986,754 (GRCm39) |
V1077E |
probably damaging |
Het |
Ehmt2 |
A |
G |
17: 35,127,280 (GRCm39) |
E131G |
possibly damaging |
Het |
Evpl |
A |
G |
11: 116,112,164 (GRCm39) |
I1842T |
probably damaging |
Het |
Fastk |
C |
A |
5: 24,646,649 (GRCm39) |
C294F |
probably damaging |
Het |
Fndc5 |
T |
C |
4: 129,030,929 (GRCm39) |
C20R |
probably benign |
Het |
Gm7298 |
C |
A |
6: 121,757,553 (GRCm39) |
Q1053K |
possibly damaging |
Het |
Gm8362 |
A |
G |
14: 18,151,405 (GRCm39) |
|
probably null |
Het |
Gmps |
T |
A |
3: 63,906,098 (GRCm39) |
I465N |
probably damaging |
Het |
Heatr4 |
T |
G |
12: 84,001,431 (GRCm39) |
M904L |
probably benign |
Het |
Hhip |
T |
A |
8: 80,771,785 (GRCm39) |
D175V |
probably damaging |
Het |
Hmcn2 |
G |
A |
2: 31,278,220 (GRCm39) |
V1641M |
probably damaging |
Het |
Hoxa5 |
T |
G |
6: 52,179,776 (GRCm39) |
T200P |
probably damaging |
Het |
Ift122 |
C |
A |
6: 115,901,368 (GRCm39) |
A1050D |
probably benign |
Het |
Igf2bp2 |
C |
A |
16: 21,897,473 (GRCm39) |
E247* |
probably null |
Het |
Irak1bp1 |
T |
A |
9: 82,728,846 (GRCm39) |
L259H |
probably damaging |
Het |
Irgm1 |
G |
A |
11: 48,759,575 (GRCm39) |
|
probably benign |
Het |
Itih1 |
A |
T |
14: 30,657,866 (GRCm39) |
|
probably benign |
Het |
Itpk1 |
A |
T |
12: 102,536,582 (GRCm39) |
C355S |
probably benign |
Het |
Kcng4 |
T |
C |
8: 120,352,452 (GRCm39) |
E486G |
possibly damaging |
Het |
Kif20b |
T |
C |
19: 34,918,629 (GRCm39) |
V671A |
possibly damaging |
Het |
Kif28 |
T |
G |
1: 179,544,320 (GRCm39) |
I345L |
possibly damaging |
Het |
Klri2 |
C |
G |
6: 129,710,742 (GRCm39) |
|
probably null |
Het |
Kntc1 |
T |
C |
5: 123,925,041 (GRCm39) |
V1118A |
probably benign |
Het |
Lpin2 |
T |
A |
17: 71,511,871 (GRCm39) |
I34N |
probably benign |
Het |
Lrch3 |
T |
A |
16: 32,802,199 (GRCm39) |
V264D |
possibly damaging |
Het |
Lrrk2 |
C |
T |
15: 91,586,473 (GRCm39) |
Q430* |
probably null |
Het |
Map10 |
T |
G |
8: 126,397,839 (GRCm39) |
S411A |
probably benign |
Het |
Map1a |
A |
T |
2: 121,135,450 (GRCm39) |
I2089F |
probably benign |
Het |
Med12l |
T |
A |
3: 58,984,443 (GRCm39) |
|
probably benign |
Het |
Mypn |
T |
A |
10: 63,005,156 (GRCm39) |
Q317L |
probably damaging |
Het |
Ncan |
T |
A |
8: 70,555,171 (GRCm39) |
I999F |
probably damaging |
Het |
Nmrk2 |
C |
A |
10: 81,035,539 (GRCm39) |
R134L |
probably damaging |
Het |
Or4k42 |
C |
T |
2: 111,320,042 (GRCm39) |
V154I |
probably benign |
Het |
Or51f1d |
T |
A |
7: 102,701,315 (GRCm39) |
V270E |
probably damaging |
Het |
Or5k17 |
T |
C |
16: 58,746,433 (GRCm39) |
N167S |
probably benign |
Het |
Or6z7 |
A |
G |
7: 6,483,246 (GRCm39) |
V303A |
probably benign |
Het |
Or8b1c |
T |
A |
9: 38,384,685 (GRCm39) |
I214N |
probably damaging |
Het |
Osbpl1a |
A |
G |
18: 12,899,858 (GRCm39) |
|
probably null |
Het |
Pcdh1 |
T |
C |
18: 38,332,073 (GRCm39) |
D310G |
possibly damaging |
Het |
Pkn2 |
C |
T |
3: 142,517,674 (GRCm39) |
|
probably null |
Het |
Plch1 |
T |
A |
3: 63,691,547 (GRCm39) |
M31L |
probably damaging |
Het |
Polg2 |
A |
G |
11: 106,659,170 (GRCm39) |
F448L |
probably damaging |
Het |
Ppp4r3b |
A |
G |
11: 29,150,758 (GRCm39) |
T475A |
possibly damaging |
Het |
Prdm13 |
C |
T |
4: 21,678,817 (GRCm39) |
E558K |
probably damaging |
Het |
Prdm9 |
T |
A |
17: 15,764,270 (GRCm39) |
I837F |
possibly damaging |
Het |
R3hdm1 |
T |
A |
1: 128,102,694 (GRCm39) |
M125K |
possibly damaging |
Het |
Rbm39 |
A |
T |
2: 155,990,276 (GRCm39) |
V468E |
probably damaging |
Het |
Rnasel |
T |
A |
1: 153,630,777 (GRCm39) |
V431E |
probably damaging |
Het |
Rps2 |
T |
A |
17: 24,940,227 (GRCm39) |
D220E |
probably benign |
Het |
Rsf1 |
T |
C |
7: 97,331,059 (GRCm39) |
|
probably benign |
Het |
Rsph10b |
G |
T |
5: 143,913,952 (GRCm39) |
A710S |
probably benign |
Het |
Sez6 |
A |
T |
11: 77,844,353 (GRCm39) |
T59S |
probably damaging |
Het |
Sf3b1 |
A |
T |
1: 55,039,444 (GRCm39) |
V727E |
probably damaging |
Het |
Slit2 |
T |
G |
5: 48,407,140 (GRCm39) |
L857R |
probably damaging |
Het |
Spata31g1 |
T |
A |
4: 42,972,097 (GRCm39) |
S477T |
probably benign |
Het |
Sspo |
T |
G |
6: 48,425,504 (GRCm39) |
C42G |
probably damaging |
Het |
Strc |
C |
T |
2: 121,201,470 (GRCm39) |
D1245N |
probably benign |
Het |
Supv3l1 |
T |
A |
10: 62,268,118 (GRCm39) |
T576S |
probably benign |
Het |
Tecrl |
C |
T |
5: 83,461,154 (GRCm39) |
R101Q |
probably benign |
Het |
Tmeff2 |
A |
G |
1: 51,220,952 (GRCm39) |
Y309C |
probably damaging |
Het |
Tmem43 |
T |
A |
6: 91,462,362 (GRCm39) |
W316R |
probably damaging |
Het |
Tmigd3 |
T |
C |
3: 105,821,554 (GRCm39) |
V141A |
probably benign |
Het |
Trav9-1 |
T |
C |
14: 53,725,584 (GRCm39) |
F8L |
probably benign |
Het |
Trbv5 |
T |
G |
6: 41,039,641 (GRCm39) |
F82C |
probably damaging |
Het |
Ubtf |
T |
C |
11: 102,205,802 (GRCm39) |
N41S |
possibly damaging |
Het |
Uggt1 |
T |
C |
1: 36,197,229 (GRCm39) |
T1225A |
probably benign |
Het |
Vmn1r72 |
T |
C |
7: 11,403,807 (GRCm39) |
R214G |
possibly damaging |
Het |
Vmn2r12 |
T |
G |
5: 109,234,522 (GRCm39) |
K563N |
possibly damaging |
Het |
Vmn2r83 |
T |
C |
10: 79,304,873 (GRCm39) |
S28P |
probably benign |
Het |
Vwa8 |
T |
G |
14: 79,438,552 (GRCm39) |
L1875R |
probably damaging |
Het |
Xrcc6 |
T |
A |
15: 81,913,866 (GRCm39) |
V64E |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,811,835 (GRCm39) |
Y403C |
probably damaging |
Het |
Zfp955a |
A |
T |
17: 33,460,955 (GRCm39) |
H392Q |
probably damaging |
Het |
Zfyve19 |
T |
C |
2: 119,041,290 (GRCm39) |
S69P |
probably damaging |
Het |
|
Other mutations in Ap1g1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01324:Ap1g1
|
APN |
8 |
110,559,414 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01907:Ap1g1
|
APN |
8 |
110,569,975 (GRCm39) |
splice site |
probably benign |
|
IGL02248:Ap1g1
|
APN |
8 |
110,590,065 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02548:Ap1g1
|
APN |
8 |
110,576,254 (GRCm39) |
missense |
probably damaging |
1.00 |
Collapse
|
UTSW |
8 |
110,554,968 (GRCm39) |
critical splice donor site |
probably null |
|
Deflate
|
UTSW |
8 |
110,577,764 (GRCm39) |
critical splice donor site |
probably null |
|
depress
|
UTSW |
8 |
110,565,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0158:Ap1g1
|
UTSW |
8 |
110,582,267 (GRCm39) |
missense |
probably benign |
0.00 |
R0226:Ap1g1
|
UTSW |
8 |
110,581,694 (GRCm39) |
missense |
probably benign |
0.39 |
R0254:Ap1g1
|
UTSW |
8 |
110,529,749 (GRCm39) |
missense |
probably benign |
0.01 |
R0315:Ap1g1
|
UTSW |
8 |
110,545,667 (GRCm39) |
missense |
probably benign |
|
R0380:Ap1g1
|
UTSW |
8 |
110,529,796 (GRCm39) |
splice site |
probably benign |
|
R0471:Ap1g1
|
UTSW |
8 |
110,580,275 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0508:Ap1g1
|
UTSW |
8 |
110,564,364 (GRCm39) |
splice site |
probably benign |
|
R0837:Ap1g1
|
UTSW |
8 |
110,577,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R1025:Ap1g1
|
UTSW |
8 |
110,545,571 (GRCm39) |
missense |
probably benign |
0.24 |
R1700:Ap1g1
|
UTSW |
8 |
110,580,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Ap1g1
|
UTSW |
8 |
110,559,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Ap1g1
|
UTSW |
8 |
110,559,814 (GRCm39) |
splice site |
probably benign |
|
R2161:Ap1g1
|
UTSW |
8 |
110,570,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R3428:Ap1g1
|
UTSW |
8 |
110,570,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R3772:Ap1g1
|
UTSW |
8 |
110,564,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R3897:Ap1g1
|
UTSW |
8 |
110,581,631 (GRCm39) |
missense |
probably damaging |
0.97 |
R4244:Ap1g1
|
UTSW |
8 |
110,560,122 (GRCm39) |
missense |
probably benign |
0.04 |
R4714:Ap1g1
|
UTSW |
8 |
110,556,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R4736:Ap1g1
|
UTSW |
8 |
110,581,714 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5173:Ap1g1
|
UTSW |
8 |
110,577,764 (GRCm39) |
critical splice donor site |
probably null |
|
R5185:Ap1g1
|
UTSW |
8 |
110,589,958 (GRCm39) |
utr 3 prime |
probably benign |
|
R5435:Ap1g1
|
UTSW |
8 |
110,565,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R5685:Ap1g1
|
UTSW |
8 |
110,564,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R5824:Ap1g1
|
UTSW |
8 |
110,565,544 (GRCm39) |
splice site |
probably null |
|
R5867:Ap1g1
|
UTSW |
8 |
110,545,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Ap1g1
|
UTSW |
8 |
110,571,000 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6978:Ap1g1
|
UTSW |
8 |
110,554,968 (GRCm39) |
critical splice donor site |
probably null |
|
R7440:Ap1g1
|
UTSW |
8 |
110,529,356 (GRCm39) |
splice site |
probably null |
|
R7532:Ap1g1
|
UTSW |
8 |
110,586,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Ap1g1
|
UTSW |
8 |
110,576,308 (GRCm39) |
missense |
probably benign |
0.01 |
R7978:Ap1g1
|
UTSW |
8 |
110,564,399 (GRCm39) |
nonsense |
probably null |
|
R8022:Ap1g1
|
UTSW |
8 |
110,559,367 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8743:Ap1g1
|
UTSW |
8 |
110,564,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R9002:Ap1g1
|
UTSW |
8 |
110,581,738 (GRCm39) |
missense |
probably benign |
|
R9225:Ap1g1
|
UTSW |
8 |
110,585,509 (GRCm39) |
missense |
probably benign |
0.27 |
R9512:Ap1g1
|
UTSW |
8 |
110,529,687 (GRCm39) |
missense |
probably damaging |
0.97 |
|