Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
A |
T |
16: 20,197,494 (GRCm39) |
I619N |
possibly damaging |
Het |
Accsl |
T |
C |
2: 93,696,488 (GRCm39) |
K41E |
possibly damaging |
Het |
Actr6 |
T |
C |
10: 89,562,558 (GRCm39) |
E107G |
probably damaging |
Het |
Adam7 |
T |
A |
14: 68,771,100 (GRCm39) |
M9L |
probably benign |
Het |
Adamts12 |
T |
A |
15: 11,215,778 (GRCm39) |
H266Q |
probably damaging |
Het |
Adamts16 |
A |
G |
13: 70,877,017 (GRCm39) |
F1208S |
possibly damaging |
Het |
Ap1b1 |
T |
C |
11: 4,962,972 (GRCm39) |
V43A |
possibly damaging |
Het |
Asnsd1 |
A |
G |
1: 53,387,390 (GRCm39) |
V79A |
probably damaging |
Het |
Aste1 |
T |
A |
9: 105,274,607 (GRCm39) |
S221R |
probably benign |
Het |
Ccndbp1 |
G |
A |
2: 120,840,347 (GRCm39) |
E94K |
probably benign |
Het |
Cdc34 |
G |
A |
10: 79,520,937 (GRCm39) |
|
probably null |
Het |
Cdh16 |
T |
C |
8: 105,348,896 (GRCm39) |
D67G |
probably benign |
Het |
Chd8 |
T |
C |
14: 52,451,951 (GRCm39) |
E1348G |
probably damaging |
Het |
Chl1 |
C |
T |
6: 103,642,909 (GRCm39) |
Q216* |
probably null |
Het |
Cse1l |
G |
A |
2: 166,771,797 (GRCm39) |
V353I |
possibly damaging |
Het |
Ctbp2 |
G |
A |
7: 132,616,455 (GRCm39) |
S160F |
possibly damaging |
Het |
Cyp1a1 |
C |
A |
9: 57,607,576 (GRCm39) |
T68K |
probably damaging |
Het |
Dennd11 |
T |
C |
6: 40,383,851 (GRCm39) |
N397S |
possibly damaging |
Het |
Dlgap2 |
T |
A |
8: 14,828,374 (GRCm39) |
M594K |
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,189,505 (GRCm39) |
E48K |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,647,049 (GRCm39) |
V35A |
probably damaging |
Het |
Edem2 |
A |
T |
2: 155,568,594 (GRCm39) |
S73R |
probably damaging |
Het |
Eps15 |
T |
C |
4: 109,218,427 (GRCm39) |
V430A |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,424,242 (GRCm39) |
N3065S |
probably damaging |
Het |
Gal3st4 |
A |
T |
5: 138,269,090 (GRCm39) |
S123R |
possibly damaging |
Het |
Garnl3 |
T |
A |
2: 32,876,841 (GRCm39) |
I937F |
possibly damaging |
Het |
Gfod2 |
C |
T |
8: 106,443,995 (GRCm39) |
V183M |
possibly damaging |
Het |
Glipr1l1 |
T |
C |
10: 111,898,339 (GRCm39) |
|
probably null |
Het |
Gm7145 |
T |
G |
1: 117,913,711 (GRCm39) |
C198G |
probably damaging |
Het |
Gvin2 |
G |
A |
7: 105,551,187 (GRCm39) |
Q622* |
probably null |
Het |
H2-Eb2 |
G |
A |
17: 34,552,523 (GRCm39) |
A123T |
possibly damaging |
Het |
Ighv1-55 |
T |
C |
12: 115,172,129 (GRCm39) |
I7V |
probably benign |
Het |
Itpripl2 |
G |
T |
7: 118,090,332 (GRCm39) |
P76T |
possibly damaging |
Het |
Kat6a |
C |
A |
8: 23,393,215 (GRCm39) |
A231E |
possibly damaging |
Het |
Lipo3 |
C |
T |
19: 33,757,705 (GRCm39) |
V255I |
probably benign |
Het |
Mamstr |
A |
T |
7: 45,292,662 (GRCm39) |
M141L |
probably benign |
Het |
Med13 |
A |
G |
11: 86,210,702 (GRCm39) |
V480A |
probably benign |
Het |
Mei1 |
A |
G |
15: 81,973,810 (GRCm39) |
N523S |
probably benign |
Het |
Mill2 |
A |
G |
7: 18,590,351 (GRCm39) |
T144A |
probably null |
Het |
Muc16 |
C |
A |
9: 18,553,959 (GRCm39) |
L4111F |
unknown |
Het |
Mylk2 |
G |
A |
2: 152,755,610 (GRCm39) |
G258E |
possibly damaging |
Het |
Myom2 |
T |
G |
8: 15,115,710 (GRCm39) |
S42A |
probably benign |
Het |
Nab1 |
C |
A |
1: 52,503,995 (GRCm39) |
G401C |
possibly damaging |
Het |
Nifk |
T |
C |
1: 118,260,592 (GRCm39) |
V244A |
possibly damaging |
Het |
Nipsnap2 |
C |
A |
5: 129,830,357 (GRCm39) |
Q224K |
probably benign |
Het |
Nop16 |
T |
G |
13: 54,737,553 (GRCm39) |
K47Q |
probably damaging |
Het |
Nup153 |
A |
T |
13: 46,853,192 (GRCm39) |
S548R |
probably damaging |
Het |
Or2at1 |
A |
C |
7: 99,416,924 (GRCm39) |
D185A |
probably damaging |
Het |
Or4g17 |
A |
G |
2: 111,209,347 (GRCm39) |
M1V |
probably null |
Het |
Or5b111 |
A |
G |
19: 13,290,998 (GRCm39) |
I217T |
probably benign |
Het |
Pard6g |
G |
A |
18: 80,160,534 (GRCm39) |
V216I |
possibly damaging |
Het |
Pcdh20 |
C |
T |
14: 88,706,038 (GRCm39) |
V421I |
probably benign |
Het |
Pcif1 |
G |
A |
2: 164,726,224 (GRCm39) |
|
probably null |
Het |
Pde11a |
C |
A |
2: 76,168,084 (GRCm39) |
V290F |
probably damaging |
Het |
Pisd |
T |
C |
5: 32,894,773 (GRCm39) |
Y511C |
probably damaging |
Het |
Polg |
A |
T |
7: 79,110,405 (GRCm39) |
D276E |
probably damaging |
Het |
Polr3b |
T |
C |
10: 84,549,496 (GRCm39) |
V906A |
probably damaging |
Het |
Prkcg |
C |
T |
7: 3,362,335 (GRCm39) |
P270S |
probably benign |
Het |
Rapgef2 |
T |
A |
3: 78,993,281 (GRCm39) |
I884F |
probably damaging |
Het |
Rpl13 |
C |
A |
8: 123,830,014 (GRCm39) |
N113K |
possibly damaging |
Het |
Rxra |
T |
A |
2: 27,631,186 (GRCm39) |
I139N |
probably damaging |
Het |
Sf3b5 |
T |
A |
10: 12,884,487 (GRCm39) |
C41S |
probably benign |
Het |
Spata31e3 |
G |
T |
13: 50,399,293 (GRCm39) |
P1011H |
probably damaging |
Het |
Stk24 |
C |
T |
14: 121,540,221 (GRCm39) |
R126Q |
probably damaging |
Het |
Taar8b |
T |
C |
10: 23,967,963 (GRCm39) |
D77G |
possibly damaging |
Het |
Tbc1d1 |
T |
A |
5: 64,468,452 (GRCm39) |
C566S |
probably benign |
Het |
Tenm3 |
A |
T |
8: 48,751,972 (GRCm39) |
M948K |
probably damaging |
Het |
Thbs4 |
T |
A |
13: 92,894,444 (GRCm39) |
Q693L |
possibly damaging |
Het |
Tnfrsf26 |
A |
T |
7: 143,172,126 (GRCm39) |
C61* |
probably null |
Het |
Trp63 |
A |
G |
16: 25,707,918 (GRCm39) |
E636G |
probably damaging |
Het |
Try5 |
T |
C |
6: 41,288,266 (GRCm39) |
Y121C |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,660,755 (GRCm39) |
|
probably benign |
Het |
Vamp1 |
T |
A |
6: 125,195,908 (GRCm39) |
V55D |
probably damaging |
Het |
Vmn2r117 |
T |
C |
17: 23,698,537 (GRCm39) |
N12S |
probably damaging |
Het |
Vmn2r90 |
G |
A |
17: 17,924,323 (GRCm39) |
G41S |
probably damaging |
Het |
Zfp462 |
T |
A |
4: 55,007,775 (GRCm39) |
D71E |
probably benign |
Het |
|
Other mutations in Ankrd11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00949:Ankrd11
|
APN |
8 |
123,635,467 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL00971:Ankrd11
|
APN |
8 |
123,622,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01017:Ankrd11
|
APN |
8 |
123,621,467 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01137:Ankrd11
|
APN |
8 |
123,611,075 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01659:Ankrd11
|
APN |
8 |
123,622,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01920:Ankrd11
|
APN |
8 |
123,642,636 (GRCm39) |
splice site |
probably benign |
|
IGL01964:Ankrd11
|
APN |
8 |
123,616,475 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02131:Ankrd11
|
APN |
8 |
123,621,149 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02226:Ankrd11
|
APN |
8 |
123,618,984 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02549:Ankrd11
|
APN |
8 |
123,618,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02642:Ankrd11
|
APN |
8 |
123,617,390 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02643:Ankrd11
|
APN |
8 |
123,619,061 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02861:Ankrd11
|
APN |
8 |
123,622,566 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03086:Ankrd11
|
APN |
8 |
123,621,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03336:Ankrd11
|
APN |
8 |
123,618,582 (GRCm39) |
missense |
probably benign |
0.00 |
anchors
|
UTSW |
8 |
123,622,509 (GRCm39) |
missense |
probably damaging |
0.99 |
away
|
UTSW |
8 |
123,618,692 (GRCm39) |
missense |
probably damaging |
1.00 |
bluebell
|
UTSW |
8 |
123,618,524 (GRCm39) |
missense |
probably damaging |
0.97 |
Navy
|
UTSW |
8 |
123,635,473 (GRCm39) |
nonsense |
probably null |
|
BB001:Ankrd11
|
UTSW |
8 |
123,622,641 (GRCm39) |
missense |
possibly damaging |
0.95 |
BB011:Ankrd11
|
UTSW |
8 |
123,622,641 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0051:Ankrd11
|
UTSW |
8 |
123,616,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Ankrd11
|
UTSW |
8 |
123,616,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Ankrd11
|
UTSW |
8 |
123,618,914 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0281:Ankrd11
|
UTSW |
8 |
123,622,307 (GRCm39) |
missense |
probably benign |
0.01 |
R0450:Ankrd11
|
UTSW |
8 |
123,618,914 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0481:Ankrd11
|
UTSW |
8 |
123,626,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Ankrd11
|
UTSW |
8 |
123,622,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R0606:Ankrd11
|
UTSW |
8 |
123,619,571 (GRCm39) |
missense |
probably benign |
0.04 |
R0702:Ankrd11
|
UTSW |
8 |
123,616,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Ankrd11
|
UTSW |
8 |
123,618,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0737:Ankrd11
|
UTSW |
8 |
123,622,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R1401:Ankrd11
|
UTSW |
8 |
123,619,789 (GRCm39) |
missense |
probably benign |
0.23 |
R1464:Ankrd11
|
UTSW |
8 |
123,619,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Ankrd11
|
UTSW |
8 |
123,619,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Ankrd11
|
UTSW |
8 |
123,626,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Ankrd11
|
UTSW |
8 |
123,626,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R1641:Ankrd11
|
UTSW |
8 |
123,618,485 (GRCm39) |
missense |
probably benign |
0.03 |
R1950:Ankrd11
|
UTSW |
8 |
123,616,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Ankrd11
|
UTSW |
8 |
123,629,161 (GRCm39) |
critical splice donor site |
probably null |
|
R2401:Ankrd11
|
UTSW |
8 |
123,635,473 (GRCm39) |
nonsense |
probably null |
|
R2425:Ankrd11
|
UTSW |
8 |
123,619,902 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2830:Ankrd11
|
UTSW |
8 |
123,618,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:Ankrd11
|
UTSW |
8 |
123,635,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R2911:Ankrd11
|
UTSW |
8 |
123,635,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R3736:Ankrd11
|
UTSW |
8 |
123,618,524 (GRCm39) |
missense |
probably damaging |
0.97 |
R3738:Ankrd11
|
UTSW |
8 |
123,623,454 (GRCm39) |
unclassified |
probably benign |
|
R3739:Ankrd11
|
UTSW |
8 |
123,623,454 (GRCm39) |
unclassified |
probably benign |
|
R3813:Ankrd11
|
UTSW |
8 |
123,618,117 (GRCm39) |
missense |
probably benign |
|
R4012:Ankrd11
|
UTSW |
8 |
123,619,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R4183:Ankrd11
|
UTSW |
8 |
123,626,415 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4213:Ankrd11
|
UTSW |
8 |
123,617,765 (GRCm39) |
missense |
probably benign |
0.00 |
R4469:Ankrd11
|
UTSW |
8 |
123,623,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R4482:Ankrd11
|
UTSW |
8 |
123,620,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R4935:Ankrd11
|
UTSW |
8 |
123,626,922 (GRCm39) |
missense |
probably benign |
0.02 |
R4940:Ankrd11
|
UTSW |
8 |
123,616,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5145:Ankrd11
|
UTSW |
8 |
123,617,943 (GRCm39) |
utr 3 prime |
probably benign |
|
R5154:Ankrd11
|
UTSW |
8 |
123,619,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Ankrd11
|
UTSW |
8 |
123,617,216 (GRCm39) |
missense |
probably benign |
0.11 |
R5283:Ankrd11
|
UTSW |
8 |
123,610,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R5377:Ankrd11
|
UTSW |
8 |
123,620,453 (GRCm39) |
splice site |
probably null |
|
R5513:Ankrd11
|
UTSW |
8 |
123,619,259 (GRCm39) |
missense |
probably benign |
0.38 |
R5518:Ankrd11
|
UTSW |
8 |
123,617,733 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5549:Ankrd11
|
UTSW |
8 |
123,617,117 (GRCm39) |
missense |
probably benign |
0.02 |
R5579:Ankrd11
|
UTSW |
8 |
123,610,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R5595:Ankrd11
|
UTSW |
8 |
123,621,043 (GRCm39) |
nonsense |
probably null |
|
R5650:Ankrd11
|
UTSW |
8 |
123,614,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5717:Ankrd11
|
UTSW |
8 |
123,619,377 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5753:Ankrd11
|
UTSW |
8 |
123,622,043 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5782:Ankrd11
|
UTSW |
8 |
123,626,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R5812:Ankrd11
|
UTSW |
8 |
123,620,544 (GRCm39) |
splice site |
probably null |
|
R5823:Ankrd11
|
UTSW |
8 |
123,622,529 (GRCm39) |
missense |
probably benign |
0.12 |
R5900:Ankrd11
|
UTSW |
8 |
123,617,805 (GRCm39) |
missense |
probably benign |
0.00 |
R5975:Ankrd11
|
UTSW |
8 |
123,616,488 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5979:Ankrd11
|
UTSW |
8 |
123,619,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Ankrd11
|
UTSW |
8 |
123,617,934 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6145:Ankrd11
|
UTSW |
8 |
123,619,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R6252:Ankrd11
|
UTSW |
8 |
123,620,561 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6302:Ankrd11
|
UTSW |
8 |
123,616,728 (GRCm39) |
missense |
probably benign |
|
R6457:Ankrd11
|
UTSW |
8 |
123,635,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6513:Ankrd11
|
UTSW |
8 |
123,616,919 (GRCm39) |
missense |
probably benign |
0.02 |
R6582:Ankrd11
|
UTSW |
8 |
123,618,368 (GRCm39) |
missense |
probably benign |
0.00 |
R6738:Ankrd11
|
UTSW |
8 |
123,618,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R6865:Ankrd11
|
UTSW |
8 |
123,621,683 (GRCm39) |
missense |
probably benign |
0.41 |
R7101:Ankrd11
|
UTSW |
8 |
123,622,194 (GRCm39) |
missense |
probably benign |
0.35 |
R7116:Ankrd11
|
UTSW |
8 |
123,622,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R7477:Ankrd11
|
UTSW |
8 |
123,621,124 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7534:Ankrd11
|
UTSW |
8 |
123,621,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7555:Ankrd11
|
UTSW |
8 |
123,614,145 (GRCm39) |
missense |
probably damaging |
0.99 |
R7627:Ankrd11
|
UTSW |
8 |
123,617,690 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7658:Ankrd11
|
UTSW |
8 |
123,620,403 (GRCm39) |
missense |
probably benign |
|
R7721:Ankrd11
|
UTSW |
8 |
123,621,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7731:Ankrd11
|
UTSW |
8 |
123,622,172 (GRCm39) |
missense |
probably benign |
0.12 |
R7792:Ankrd11
|
UTSW |
8 |
123,610,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R7924:Ankrd11
|
UTSW |
8 |
123,622,641 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7939:Ankrd11
|
UTSW |
8 |
123,617,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Ankrd11
|
UTSW |
8 |
123,614,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R8222:Ankrd11
|
UTSW |
8 |
123,622,347 (GRCm39) |
missense |
probably damaging |
0.98 |
R8362:Ankrd11
|
UTSW |
8 |
123,618,797 (GRCm39) |
missense |
probably damaging |
0.96 |
R8430:Ankrd11
|
UTSW |
8 |
123,620,105 (GRCm39) |
missense |
probably benign |
0.01 |
R8511:Ankrd11
|
UTSW |
8 |
123,626,468 (GRCm39) |
missense |
|
|
R8726:Ankrd11
|
UTSW |
8 |
123,620,765 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8888:Ankrd11
|
UTSW |
8 |
123,621,014 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8895:Ankrd11
|
UTSW |
8 |
123,621,014 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8928:Ankrd11
|
UTSW |
8 |
123,622,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R8930:Ankrd11
|
UTSW |
8 |
123,622,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R8931:Ankrd11
|
UTSW |
8 |
123,622,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R8936:Ankrd11
|
UTSW |
8 |
123,621,840 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9018:Ankrd11
|
UTSW |
8 |
123,622,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9113:Ankrd11
|
UTSW |
8 |
123,614,072 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9399:Ankrd11
|
UTSW |
8 |
123,618,179 (GRCm39) |
missense |
probably benign |
|
R9644:Ankrd11
|
UTSW |
8 |
123,617,682 (GRCm39) |
missense |
probably benign |
0.00 |
R9645:Ankrd11
|
UTSW |
8 |
123,617,682 (GRCm39) |
missense |
probably benign |
0.00 |
R9647:Ankrd11
|
UTSW |
8 |
123,617,682 (GRCm39) |
missense |
probably benign |
0.00 |
R9683:Ankrd11
|
UTSW |
8 |
123,617,682 (GRCm39) |
missense |
probably benign |
0.00 |
RF019:Ankrd11
|
UTSW |
8 |
123,623,373 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ankrd11
|
UTSW |
8 |
123,622,542 (GRCm39) |
missense |
possibly damaging |
0.68 |
Z1177:Ankrd11
|
UTSW |
8 |
123,626,881 (GRCm39) |
missense |
probably damaging |
1.00 |
|