Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810459M11Rik |
T |
A |
1: 85,980,664 (GRCm39) |
|
probably null |
Het |
Abca8b |
A |
G |
11: 109,864,634 (GRCm39) |
V316A |
probably benign |
Het |
Acad10 |
A |
T |
5: 121,760,096 (GRCm39) |
V999D |
probably damaging |
Het |
Acot8 |
A |
G |
2: 164,644,985 (GRCm39) |
V66A |
probably benign |
Het |
Anxa6 |
A |
G |
11: 54,885,730 (GRCm39) |
F405S |
probably damaging |
Het |
Asmt |
G |
A |
X: 169,108,398 (GRCm39) |
V101I |
probably damaging |
Het |
Atp1a2 |
C |
T |
1: 172,114,805 (GRCm39) |
V327I |
probably damaging |
Het |
Brdt |
A |
G |
5: 107,525,865 (GRCm39) |
E906G |
possibly damaging |
Het |
Cacna1g |
A |
T |
11: 94,353,087 (GRCm39) |
C313S |
probably damaging |
Het |
Camk2d |
T |
C |
3: 126,599,507 (GRCm39) |
I329T |
probably benign |
Het |
Cavin4 |
A |
T |
4: 48,663,794 (GRCm39) |
H58L |
probably damaging |
Het |
Ccdc78 |
C |
A |
17: 26,008,039 (GRCm39) |
P317T |
probably benign |
Het |
Cdc16 |
T |
G |
8: 13,817,573 (GRCm39) |
Y295D |
possibly damaging |
Het |
Cdyl2 |
T |
A |
8: 117,321,717 (GRCm39) |
N270I |
probably damaging |
Het |
Cfap221 |
T |
A |
1: 119,912,546 (GRCm39) |
I114F |
possibly damaging |
Het |
Dmxl1 |
A |
G |
18: 50,045,833 (GRCm39) |
E2414G |
possibly damaging |
Het |
Dnaaf9 |
T |
C |
2: 130,620,393 (GRCm39) |
I247V |
probably benign |
Het |
Dnah1 |
C |
A |
14: 31,022,927 (GRCm39) |
R1070L |
probably benign |
Het |
Dnah14 |
T |
C |
1: 181,493,982 (GRCm39) |
S1713P |
probably benign |
Het |
Dock10 |
C |
A |
1: 80,553,621 (GRCm39) |
G602* |
probably null |
Het |
Ep400 |
A |
T |
5: 110,904,569 (GRCm39) |
V10D |
possibly damaging |
Het |
Epas1 |
T |
C |
17: 87,136,857 (GRCm39) |
C807R |
probably benign |
Het |
Esrrb |
C |
T |
12: 86,552,673 (GRCm39) |
P200L |
probably benign |
Het |
Fbxw26 |
T |
C |
9: 109,561,691 (GRCm39) |
I168V |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,824,112 (GRCm39) |
H6615L |
possibly damaging |
Het |
Galk2 |
A |
T |
2: 125,788,762 (GRCm39) |
Q272L |
possibly damaging |
Het |
Gas7 |
A |
C |
11: 67,520,438 (GRCm39) |
T43P |
probably damaging |
Het |
Gm5134 |
A |
T |
10: 75,831,673 (GRCm39) |
I371F |
probably damaging |
Het |
Gpr31b |
C |
T |
17: 13,270,266 (GRCm39) |
R301Q |
possibly damaging |
Het |
Grk1 |
T |
A |
8: 13,455,765 (GRCm39) |
Y216* |
probably null |
Het |
Grm5 |
T |
A |
7: 87,675,809 (GRCm39) |
M441K |
probably damaging |
Het |
Heatr6 |
A |
G |
11: 83,656,962 (GRCm39) |
E408G |
probably damaging |
Het |
Hoxc9 |
G |
T |
15: 102,892,391 (GRCm39) |
K201N |
probably damaging |
Het |
Igsf10 |
T |
A |
3: 59,239,077 (GRCm39) |
Y368F |
possibly damaging |
Het |
Il2ra |
A |
T |
2: 11,685,057 (GRCm39) |
D131V |
probably damaging |
Het |
Imp4 |
A |
G |
1: 34,479,177 (GRCm39) |
E19G |
probably benign |
Het |
Kcnk18 |
T |
C |
19: 59,224,039 (GRCm39) |
*395Q |
probably null |
Het |
Kdm6b |
A |
T |
11: 69,295,852 (GRCm39) |
L805Q |
unknown |
Het |
Lgr4 |
T |
A |
2: 109,837,588 (GRCm39) |
L427* |
probably null |
Het |
Myt1l |
G |
A |
12: 29,882,380 (GRCm39) |
S525N |
unknown |
Het |
Nasp |
G |
A |
4: 116,468,274 (GRCm39) |
T237I |
probably benign |
Het |
Nell2 |
G |
T |
15: 95,371,442 (GRCm39) |
Q98K |
probably damaging |
Het |
Nfasc |
C |
T |
1: 132,562,455 (GRCm39) |
G107R |
probably damaging |
Het |
Nsun4 |
A |
G |
4: 115,897,403 (GRCm39) |
S203P |
probably damaging |
Het |
Or1m1 |
T |
G |
9: 18,666,865 (GRCm39) |
D22A |
probably benign |
Het |
Or7g35 |
T |
C |
9: 19,496,184 (GRCm39) |
V117A |
probably benign |
Het |
Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
Pde10a |
T |
C |
17: 9,147,949 (GRCm39) |
V366A |
probably damaging |
Het |
Pdxk |
T |
A |
10: 78,279,625 (GRCm39) |
D250V |
probably benign |
Het |
Pih1d1 |
T |
A |
7: 44,808,468 (GRCm39) |
I179N |
probably damaging |
Het |
Plaa |
T |
A |
4: 94,472,229 (GRCm39) |
I294F |
probably damaging |
Het |
Pmel |
C |
A |
10: 128,551,804 (GRCm39) |
P213T |
probably damaging |
Het |
Pom121l2 |
A |
T |
13: 22,166,472 (GRCm39) |
R248* |
probably null |
Het |
Pou2f1 |
T |
C |
1: 165,703,002 (GRCm39) |
|
probably benign |
Het |
Ppm1j |
G |
A |
3: 104,688,695 (GRCm39) |
R98H |
probably damaging |
Het |
Prkdc |
C |
T |
16: 15,589,937 (GRCm39) |
P2600L |
probably damaging |
Het |
Prom1 |
T |
C |
5: 44,186,991 (GRCm39) |
N422S |
probably benign |
Het |
Pspn |
C |
T |
17: 57,306,467 (GRCm39) |
C154Y |
probably damaging |
Het |
Ptdss1 |
T |
C |
13: 67,120,701 (GRCm39) |
|
probably null |
Het |
Rapgef1 |
A |
G |
2: 29,626,678 (GRCm39) |
Y993C |
probably damaging |
Het |
Scrn2 |
A |
C |
11: 96,923,679 (GRCm39) |
T219P |
probably benign |
Het |
Sec23ip |
T |
G |
7: 128,380,208 (GRCm39) |
S874R |
probably damaging |
Het |
Septin4 |
G |
A |
11: 87,476,072 (GRCm39) |
|
probably null |
Het |
Slc15a3 |
C |
T |
19: 10,834,615 (GRCm39) |
L499F |
probably damaging |
Het |
Spaca9 |
G |
A |
2: 28,583,793 (GRCm39) |
R64W |
probably damaging |
Het |
Sra1 |
A |
G |
18: 36,800,628 (GRCm39) |
M193T |
probably damaging |
Het |
Srsf4 |
G |
T |
4: 131,627,605 (GRCm39) |
|
probably benign |
Het |
Syne1 |
T |
C |
10: 5,002,750 (GRCm39) |
D8055G |
probably damaging |
Het |
Syne4 |
T |
A |
7: 30,015,988 (GRCm39) |
|
probably null |
Het |
Tbc1d24 |
C |
A |
17: 24,427,203 (GRCm39) |
G253V |
probably damaging |
Het |
Tbck |
T |
A |
3: 132,437,976 (GRCm39) |
I467N |
probably damaging |
Het |
Tln1 |
T |
A |
4: 43,538,030 (GRCm39) |
M1857L |
possibly damaging |
Het |
Ttll2 |
T |
C |
17: 7,619,031 (GRCm39) |
R299G |
probably benign |
Het |
Ugt2b36 |
T |
G |
5: 87,214,072 (GRCm39) |
E524A |
probably benign |
Het |
Vmn2r124 |
C |
T |
17: 18,283,113 (GRCm39) |
T269I |
probably benign |
Het |
Vmn2r4 |
A |
G |
3: 64,314,364 (GRCm39) |
F206L |
probably benign |
Het |
Zfp346 |
A |
G |
13: 55,263,387 (GRCm39) |
K156R |
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 |
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 |
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 |
|