Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
T |
C |
5: 138,644,793 (GRCm39) |
V226A |
probably benign |
Het |
Acan |
G |
T |
7: 78,749,653 (GRCm39) |
V1475F |
probably benign |
Het |
Acin1 |
T |
A |
14: 54,901,913 (GRCm39) |
R626S |
probably benign |
Het |
Aff3 |
T |
C |
1: 38,249,121 (GRCm39) |
K662R |
probably damaging |
Het |
Ano9 |
T |
G |
7: 140,687,388 (GRCm39) |
N309T |
probably benign |
Het |
Ap3d1 |
G |
A |
10: 80,545,062 (GRCm39) |
S1092L |
probably benign |
Het |
B4galt7 |
C |
T |
13: 55,756,556 (GRCm39) |
H257Y |
probably damaging |
Het |
BC051665 |
G |
T |
13: 60,932,545 (GRCm39) |
Q47K |
possibly damaging |
Het |
Brip1 |
A |
G |
11: 85,952,512 (GRCm39) |
F1090L |
probably benign |
Het |
Cabin1 |
A |
G |
10: 75,494,543 (GRCm39) |
V1612A |
probably benign |
Het |
Ccar1 |
A |
T |
10: 62,602,369 (GRCm39) |
D434E |
probably benign |
Het |
Ccdc15 |
T |
C |
9: 37,227,083 (GRCm39) |
D297G |
probably benign |
Het |
Celsr3 |
C |
A |
9: 108,704,691 (GRCm39) |
Y391* |
probably null |
Het |
Cfap52 |
A |
G |
11: 67,837,179 (GRCm39) |
I194T |
possibly damaging |
Het |
Ctif |
T |
C |
18: 75,757,352 (GRCm39) |
E67G |
probably benign |
Het |
Cxcr6 |
T |
C |
9: 123,639,151 (GRCm39) |
F58L |
possibly damaging |
Het |
Cyp2c69 |
T |
C |
19: 39,869,593 (GRCm39) |
E142G |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,115,750 (GRCm39) |
R1549S |
possibly damaging |
Het |
Duxf3 |
A |
T |
10: 58,066,803 (GRCm39) |
H75Q |
probably benign |
Het |
Ehbp1 |
A |
T |
11: 22,051,052 (GRCm39) |
I500N |
probably damaging |
Het |
F13a1 |
A |
T |
13: 37,082,154 (GRCm39) |
S517T |
probably benign |
Het |
Fbln7 |
C |
T |
2: 128,719,316 (GRCm39) |
R38C |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,667,629 (GRCm39) |
N788S |
probably benign |
Het |
Foxc1 |
A |
T |
13: 31,991,882 (GRCm39) |
E231V |
probably damaging |
Het |
Gal3st2b |
T |
C |
1: 93,866,328 (GRCm39) |
S10P |
probably damaging |
Het |
Gm6899 |
G |
A |
11: 26,543,592 (GRCm39) |
C53Y |
unknown |
Het |
Hps3 |
T |
C |
3: 20,084,831 (GRCm39) |
E119G |
probably benign |
Het |
Impg2 |
A |
G |
16: 56,038,767 (GRCm39) |
E135G |
probably damaging |
Het |
Kalrn |
G |
A |
16: 34,032,583 (GRCm39) |
T1155M |
probably benign |
Het |
Kcna6 |
G |
A |
6: 126,716,022 (GRCm39) |
A289V |
probably benign |
Het |
Kcnh5 |
T |
C |
12: 75,134,191 (GRCm39) |
M453V |
probably benign |
Het |
Krt222 |
A |
G |
11: 99,131,320 (GRCm39) |
V75A |
possibly damaging |
Het |
Lmtk3 |
A |
T |
7: 45,450,431 (GRCm39) |
T1432S |
unknown |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Ltbp3 |
C |
G |
19: 5,802,099 (GRCm39) |
N758K |
probably damaging |
Het |
Map6d1 |
T |
A |
16: 20,055,377 (GRCm39) |
H153L |
possibly damaging |
Het |
Mefv |
A |
G |
16: 3,528,782 (GRCm39) |
L583P |
probably damaging |
Het |
Mrps28 |
T |
C |
3: 8,867,389 (GRCm39) |
T160A |
probably damaging |
Het |
Mtcl2 |
T |
C |
2: 156,869,390 (GRCm39) |
K1082E |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,217,783 (GRCm39) |
T2297A |
possibly damaging |
Het |
Mx1 |
G |
T |
16: 97,253,409 (GRCm39) |
D338E |
probably benign |
Het |
Myom1 |
G |
A |
17: 71,399,204 (GRCm39) |
R1120H |
probably benign |
Het |
Nif3l1 |
T |
C |
1: 58,487,074 (GRCm39) |
F87L |
probably benign |
Het |
Or1e35 |
T |
A |
11: 73,797,713 (GRCm39) |
M202L |
probably benign |
Het |
Or4p22 |
T |
C |
2: 88,317,373 (GRCm39) |
V99A |
possibly damaging |
Het |
Pex10 |
T |
A |
4: 155,153,264 (GRCm39) |
L111Q |
probably damaging |
Het |
Phf1 |
T |
C |
17: 27,154,130 (GRCm39) |
|
probably null |
Het |
Pigp |
A |
T |
16: 94,166,278 (GRCm39) |
Y143* |
probably null |
Het |
Pou2af2 |
A |
G |
9: 51,229,579 (GRCm39) |
|
probably null |
Het |
Prrc2a |
A |
G |
17: 35,381,176 (GRCm39) |
|
probably null |
Het |
Psd |
GCC |
GC |
19: 46,301,841 (GRCm39) |
|
probably null |
Het |
Pum3 |
A |
G |
19: 27,403,412 (GRCm39) |
S30P |
probably benign |
Het |
Rab12 |
A |
G |
17: 66,826,421 (GRCm39) |
S97P |
probably damaging |
Het |
Rigi |
T |
C |
4: 40,220,437 (GRCm39) |
E482G |
possibly damaging |
Het |
Ros1 |
A |
G |
10: 51,948,148 (GRCm39) |
|
probably null |
Het |
Scp2 |
A |
T |
4: 107,948,519 (GRCm39) |
Y197N |
probably benign |
Het |
Serpinb10 |
T |
C |
1: 107,474,488 (GRCm39) |
F217L |
possibly damaging |
Het |
Shank3 |
T |
G |
15: 89,409,453 (GRCm39) |
M604R |
possibly damaging |
Het |
Slc22a29 |
A |
G |
19: 8,184,488 (GRCm39) |
S238P |
probably benign |
Het |
Smarcc1 |
A |
G |
9: 109,986,410 (GRCm39) |
D237G |
probably damaging |
Het |
Stag3 |
T |
C |
5: 138,299,701 (GRCm39) |
S871P |
possibly damaging |
Het |
Tmem132d |
A |
G |
5: 128,346,075 (GRCm39) |
F149S |
probably damaging |
Het |
Tmem25 |
C |
T |
9: 44,706,515 (GRCm39) |
E333K |
|
Het |
Togaram1 |
T |
A |
12: 65,066,082 (GRCm39) |
Y1695* |
probably null |
Het |
Tox3 |
G |
A |
8: 90,984,574 (GRCm39) |
P202S |
probably damaging |
Het |
Trim34b |
T |
A |
7: 103,980,474 (GRCm39) |
N187K |
probably benign |
Het |
Vcan |
A |
G |
13: 89,841,081 (GRCm39) |
S1488P |
probably benign |
Het |
Vps26a |
A |
C |
10: 62,305,791 (GRCm39) |
V124G |
probably benign |
Het |
Vps50 |
T |
G |
6: 3,516,706 (GRCm39) |
S63A |
possibly damaging |
Het |
Wbp4 |
T |
A |
14: 79,707,553 (GRCm39) |
E186V |
possibly damaging |
Het |
Zfp52 |
A |
G |
17: 21,781,937 (GRCm39) |
D595G |
possibly damaging |
Het |
Zfr2 |
C |
A |
10: 81,084,252 (GRCm39) |
S1* |
probably null |
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 |
R6913:Ankrd11
|
UTSW |
8 |
123,621,650 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
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 |
|