Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
A |
6: 142,591,656 (GRCm39) |
I791F |
probably damaging |
Het |
Adamts15 |
A |
G |
9: 30,822,498 (GRCm39) |
M389T |
probably damaging |
Het |
Adgrb2 |
G |
A |
4: 129,910,877 (GRCm39) |
V1065M |
probably damaging |
Het |
Agbl1 |
C |
A |
7: 76,239,225 (GRCm39) |
A827E |
unknown |
Het |
Alox5ap |
T |
C |
5: 149,216,015 (GRCm39) |
F67S |
probably damaging |
Het |
Arhgap10 |
T |
C |
8: 77,985,701 (GRCm39) |
D722G |
probably damaging |
Het |
Atp5mf |
A |
G |
5: 145,128,315 (GRCm39) |
L4P |
probably benign |
Het |
Bean1 |
T |
C |
8: 104,940,557 (GRCm39) |
V130A |
probably benign |
Het |
Ccdc88b |
T |
C |
19: 6,833,213 (GRCm39) |
E278G |
probably damaging |
Het |
Cdhr2 |
A |
G |
13: 54,882,700 (GRCm39) |
D1222G |
probably benign |
Het |
Chrm4 |
T |
A |
2: 91,758,075 (GRCm39) |
V161E |
probably benign |
Het |
Ckap5 |
T |
C |
2: 91,426,144 (GRCm39) |
S1335P |
probably damaging |
Het |
Col11a1 |
T |
A |
3: 113,888,192 (GRCm39) |
Y267* |
probably null |
Het |
Col14a1 |
T |
C |
15: 55,201,825 (GRCm39) |
Y38H |
unknown |
Het |
Coro2a |
C |
T |
4: 46,563,047 (GRCm39) |
G36S |
|
Het |
Ctsc |
A |
T |
7: 87,959,104 (GRCm39) |
K461N |
possibly damaging |
Het |
Dcaf1 |
A |
G |
9: 106,712,831 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
A |
G |
11: 65,880,713 (GRCm39) |
I2628T |
probably damaging |
Het |
Dnajb5 |
T |
C |
4: 42,953,233 (GRCm39) |
I20T |
probably damaging |
Het |
Dus2 |
C |
T |
8: 106,775,333 (GRCm39) |
Q287* |
probably null |
Het |
Fbxl17 |
A |
G |
17: 63,532,085 (GRCm39) |
V586A |
probably benign |
Het |
Glg1 |
A |
T |
8: 111,887,452 (GRCm39) |
|
probably benign |
Het |
Gm4924 |
G |
A |
10: 82,214,113 (GRCm39) |
C637Y |
unknown |
Het |
Gorasp1 |
A |
G |
9: 119,757,442 (GRCm39) |
F310S |
probably damaging |
Het |
Gsta5 |
A |
T |
9: 78,212,667 (GRCm39) |
I213F |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,883,328 (GRCm39) |
T2726I |
probably damaging |
Het |
Inppl1 |
G |
T |
7: 101,475,231 (GRCm39) |
P940Q |
probably benign |
Het |
Klk1b22 |
G |
A |
7: 43,765,692 (GRCm39) |
V183M |
possibly damaging |
Het |
Krt12 |
A |
G |
11: 99,309,378 (GRCm39) |
M294T |
probably damaging |
Het |
Krtap6-2 |
GAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCGTATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAACCATAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCA |
GAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCGTATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAACCATAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCA |
16: 89,216,613 (GRCm39) |
|
probably benign |
Het |
Lep |
T |
C |
6: 29,071,093 (GRCm39) |
L139P |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,224,532 (GRCm39) |
D64G |
probably damaging |
Het |
Lyzl1 |
C |
T |
18: 4,168,604 (GRCm39) |
A28V |
probably null |
Het |
Mcam |
T |
C |
9: 44,051,693 (GRCm39) |
V483A |
probably benign |
Het |
Mia2 |
C |
T |
12: 59,217,053 (GRCm39) |
|
probably benign |
Het |
Mzf1 |
T |
A |
7: 12,778,279 (GRCm39) |
H454L |
probably damaging |
Het |
Pde10a |
A |
G |
17: 9,197,782 (GRCm39) |
T742A |
probably benign |
Het |
Rapgef4 |
A |
G |
2: 71,861,493 (GRCm39) |
Y61C |
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,618,741 (GRCm39) |
|
probably benign |
Het |
Setbp1 |
G |
T |
18: 78,900,948 (GRCm39) |
H906Q |
probably damaging |
Het |
Slc12a4 |
A |
G |
8: 106,670,984 (GRCm39) |
V1032A |
probably benign |
Het |
Slc6a15 |
T |
C |
10: 103,236,140 (GRCm39) |
M285T |
probably damaging |
Het |
Spata31h1 |
G |
A |
10: 82,131,352 (GRCm39) |
Q553* |
probably null |
Het |
Steap2 |
A |
G |
5: 5,727,475 (GRCm39) |
Y287H |
probably damaging |
Het |
Tas2r135 |
T |
G |
6: 42,383,315 (GRCm39) |
F285V |
probably benign |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,618,538 (GRCm39) |
T16249A |
probably benign |
Het |
Usp8 |
A |
G |
2: 126,579,343 (GRCm39) |
T299A |
probably benign |
Het |
Vmn2r101 |
A |
G |
17: 19,811,288 (GRCm39) |
I457M |
possibly damaging |
Het |
Vps41 |
A |
G |
13: 19,023,883 (GRCm39) |
E437G |
probably benign |
Het |
Zfp638 |
A |
T |
6: 83,953,894 (GRCm39) |
E1333V |
probably damaging |
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 |
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 |
|