Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
C |
T |
6: 128,557,349 (GRCm39) |
A115T |
probably benign |
Het |
Alg11 |
T |
A |
8: 22,555,534 (GRCm39) |
I223N |
probably damaging |
Het |
Apbb1 |
T |
C |
7: 105,216,891 (GRCm39) |
D264G |
probably damaging |
Het |
Arhgap32 |
T |
C |
9: 32,168,770 (GRCm39) |
Y918H |
probably benign |
Het |
Astn2 |
T |
G |
4: 65,829,919 (GRCm39) |
T584P |
probably damaging |
Het |
Atxn7 |
G |
A |
14: 14,100,381 (GRCm38) |
S689N |
probably benign |
Het |
Cacna1h |
T |
C |
17: 25,606,837 (GRCm39) |
N873S |
probably damaging |
Het |
Cadps |
T |
A |
14: 12,488,987 (GRCm38) |
I857F |
probably damaging |
Het |
Cfap119 |
T |
A |
7: 127,186,002 (GRCm39) |
M102L |
probably benign |
Het |
Cog6 |
T |
C |
3: 52,900,229 (GRCm39) |
T511A |
probably benign |
Het |
Dppa3 |
A |
T |
6: 122,606,291 (GRCm39) |
N118I |
probably damaging |
Het |
Dst |
A |
G |
1: 34,234,909 (GRCm39) |
N3663D |
probably benign |
Het |
Eif1ad14 |
A |
T |
12: 87,886,567 (GRCm39) |
S21T |
unknown |
Het |
Eme1 |
G |
A |
11: 94,538,818 (GRCm39) |
T354M |
possibly damaging |
Het |
Gm10735 |
T |
C |
13: 113,177,743 (GRCm39) |
|
probably benign |
Het |
Ifi44l |
A |
T |
3: 151,468,514 (GRCm39) |
C5* |
probably null |
Het |
Itln1 |
G |
A |
1: 171,362,375 (GRCm39) |
T2I |
probably benign |
Het |
Jam2 |
T |
A |
16: 84,618,180 (GRCm39) |
M309K |
possibly damaging |
Het |
Kcnk5 |
C |
A |
14: 20,194,852 (GRCm39) |
C162F |
probably damaging |
Het |
Metrn |
A |
G |
17: 26,015,915 (GRCm39) |
|
probably benign |
Het |
Muc5b |
T |
A |
7: 141,417,259 (GRCm39) |
Y3402N |
probably benign |
Het |
Ncoa7 |
A |
T |
10: 30,574,253 (GRCm39) |
|
probably null |
Het |
Nxpe4 |
A |
G |
9: 48,304,122 (GRCm39) |
R70G |
possibly damaging |
Het |
Onecut3 |
T |
C |
10: 80,349,793 (GRCm39) |
I429T |
probably damaging |
Het |
Or2n1 |
A |
C |
17: 38,486,772 (GRCm39) |
I266L |
possibly damaging |
Het |
Or2z9 |
T |
C |
8: 72,854,188 (GRCm39) |
Y195H |
probably damaging |
Het |
Or4k37 |
T |
G |
2: 111,159,475 (GRCm39) |
L237R |
probably damaging |
Het |
Or52e18 |
A |
T |
7: 104,609,801 (GRCm39) |
I46N |
probably benign |
Het |
Pds5a |
A |
G |
5: 65,787,329 (GRCm39) |
S858P |
possibly damaging |
Het |
Phf11c |
A |
T |
14: 59,630,516 (GRCm39) |
V63E |
probably benign |
Het |
Rasa3 |
A |
G |
8: 13,620,264 (GRCm39) |
F802L |
possibly damaging |
Het |
Sec24b |
G |
T |
3: 129,834,368 (GRCm39) |
Q141K |
probably benign |
Het |
Sec61a1 |
A |
T |
6: 88,492,413 (GRCm39) |
|
probably null |
Het |
Slc45a3 |
T |
A |
1: 131,909,399 (GRCm39) |
L532Q |
probably damaging |
Het |
Slc46a2 |
T |
C |
4: 59,914,048 (GRCm39) |
I292V |
probably benign |
Het |
Smg1 |
C |
T |
7: 117,747,956 (GRCm39) |
|
probably null |
Het |
Spag6 |
T |
A |
2: 18,720,449 (GRCm39) |
|
probably null |
Het |
Spi1 |
T |
C |
2: 90,945,680 (GRCm39) |
F254L |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,467,868 (GRCm39) |
S4272P |
probably benign |
Het |
Tgm5 |
T |
C |
2: 120,901,216 (GRCm39) |
T292A |
probably damaging |
Het |
Tmem229a |
T |
A |
6: 24,954,831 (GRCm39) |
I308F |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,554,464 (GRCm39) |
I30784V |
possibly damaging |
Het |
Urod |
T |
A |
4: 116,849,880 (GRCm39) |
T173S |
probably benign |
Het |
Vmn1r223 |
A |
T |
13: 23,433,585 (GRCm39) |
M60L |
probably benign |
Het |
Vmn2r2 |
T |
A |
3: 64,041,912 (GRCm39) |
I268L |
probably benign |
Het |
Vwa8 |
C |
T |
14: 79,320,292 (GRCm39) |
T1101M |
probably benign |
Het |
Zc3h12c |
T |
A |
9: 52,055,728 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ankrd26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Ankrd26
|
APN |
6 |
118,536,319 (GRCm39) |
nonsense |
probably null |
|
IGL01286:Ankrd26
|
APN |
6 |
118,536,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01574:Ankrd26
|
APN |
6 |
118,516,659 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01727:Ankrd26
|
APN |
6 |
118,488,597 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01954:Ankrd26
|
APN |
6 |
118,535,966 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02200:Ankrd26
|
APN |
6 |
118,536,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Ankrd26
|
APN |
6 |
118,495,379 (GRCm39) |
splice site |
probably benign |
|
IGL02973:Ankrd26
|
APN |
6 |
118,500,511 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03233:Ankrd26
|
APN |
6 |
118,512,107 (GRCm39) |
splice site |
probably null |
|
guillemot
|
UTSW |
6 |
118,484,598 (GRCm39) |
critical splice donor site |
probably null |
|
Iceland
|
UTSW |
6 |
118,526,389 (GRCm39) |
missense |
probably benign |
0.30 |
murre
|
UTSW |
6 |
118,526,598 (GRCm39) |
critical splice donor site |
probably null |
|
ANU74:Ankrd26
|
UTSW |
6 |
118,529,736 (GRCm39) |
missense |
probably benign |
0.02 |
N/A:Ankrd26
|
UTSW |
6 |
118,506,535 (GRCm39) |
missense |
probably benign |
0.04 |
R0078:Ankrd26
|
UTSW |
6 |
118,512,030 (GRCm39) |
splice site |
probably benign |
|
R0083:Ankrd26
|
UTSW |
6 |
118,500,215 (GRCm39) |
missense |
probably benign |
0.36 |
R0165:Ankrd26
|
UTSW |
6 |
118,517,445 (GRCm39) |
missense |
probably benign |
0.01 |
R0344:Ankrd26
|
UTSW |
6 |
118,484,598 (GRCm39) |
critical splice donor site |
probably null |
|
R0828:Ankrd26
|
UTSW |
6 |
118,510,434 (GRCm39) |
splice site |
probably benign |
|
R1532:Ankrd26
|
UTSW |
6 |
118,499,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Ankrd26
|
UTSW |
6 |
118,502,883 (GRCm39) |
splice site |
probably benign |
|
R1875:Ankrd26
|
UTSW |
6 |
118,517,410 (GRCm39) |
critical splice donor site |
probably null |
|
R1940:Ankrd26
|
UTSW |
6 |
118,488,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2164:Ankrd26
|
UTSW |
6 |
118,502,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R2202:Ankrd26
|
UTSW |
6 |
118,500,843 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2204:Ankrd26
|
UTSW |
6 |
118,500,843 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2205:Ankrd26
|
UTSW |
6 |
118,500,843 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3107:Ankrd26
|
UTSW |
6 |
118,533,204 (GRCm39) |
missense |
probably benign |
0.01 |
R3419:Ankrd26
|
UTSW |
6 |
118,512,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R3552:Ankrd26
|
UTSW |
6 |
118,484,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R3899:Ankrd26
|
UTSW |
6 |
118,526,389 (GRCm39) |
missense |
probably benign |
0.30 |
R4157:Ankrd26
|
UTSW |
6 |
118,484,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R4194:Ankrd26
|
UTSW |
6 |
118,500,639 (GRCm39) |
missense |
probably benign |
0.21 |
R4651:Ankrd26
|
UTSW |
6 |
118,492,787 (GRCm39) |
missense |
probably benign |
0.03 |
R4701:Ankrd26
|
UTSW |
6 |
118,483,446 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4747:Ankrd26
|
UTSW |
6 |
118,504,718 (GRCm39) |
missense |
probably benign |
0.01 |
R4752:Ankrd26
|
UTSW |
6 |
118,517,426 (GRCm39) |
missense |
probably null |
1.00 |
R4834:Ankrd26
|
UTSW |
6 |
118,500,679 (GRCm39) |
missense |
probably benign |
0.08 |
R4835:Ankrd26
|
UTSW |
6 |
118,525,811 (GRCm39) |
nonsense |
probably null |
|
R4849:Ankrd26
|
UTSW |
6 |
118,509,257 (GRCm39) |
missense |
probably benign |
0.00 |
R5149:Ankrd26
|
UTSW |
6 |
118,535,957 (GRCm39) |
missense |
probably benign |
0.05 |
R5389:Ankrd26
|
UTSW |
6 |
118,485,536 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5473:Ankrd26
|
UTSW |
6 |
118,492,797 (GRCm39) |
missense |
probably benign |
0.04 |
R5518:Ankrd26
|
UTSW |
6 |
118,525,869 (GRCm39) |
missense |
probably benign |
0.00 |
R5525:Ankrd26
|
UTSW |
6 |
118,504,692 (GRCm39) |
missense |
probably benign |
0.00 |
R5608:Ankrd26
|
UTSW |
6 |
118,488,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R5639:Ankrd26
|
UTSW |
6 |
118,516,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5704:Ankrd26
|
UTSW |
6 |
118,500,843 (GRCm39) |
missense |
probably damaging |
0.96 |
R5927:Ankrd26
|
UTSW |
6 |
118,484,597 (GRCm39) |
critical splice donor site |
probably null |
|
R5943:Ankrd26
|
UTSW |
6 |
118,482,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Ankrd26
|
UTSW |
6 |
118,494,855 (GRCm39) |
critical splice donor site |
probably null |
|
R6181:Ankrd26
|
UTSW |
6 |
118,525,838 (GRCm39) |
missense |
probably benign |
0.15 |
R6478:Ankrd26
|
UTSW |
6 |
118,488,599 (GRCm39) |
missense |
probably benign |
0.28 |
R6667:Ankrd26
|
UTSW |
6 |
118,484,749 (GRCm39) |
missense |
probably benign |
0.02 |
R6865:Ankrd26
|
UTSW |
6 |
118,500,442 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7224:Ankrd26
|
UTSW |
6 |
118,516,688 (GRCm39) |
missense |
probably benign |
0.07 |
R7287:Ankrd26
|
UTSW |
6 |
118,526,598 (GRCm39) |
critical splice donor site |
probably null |
|
R7301:Ankrd26
|
UTSW |
6 |
118,488,624 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7348:Ankrd26
|
UTSW |
6 |
118,485,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R7414:Ankrd26
|
UTSW |
6 |
118,485,741 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7789:Ankrd26
|
UTSW |
6 |
118,504,760 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7789:Ankrd26
|
UTSW |
6 |
118,504,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R7964:Ankrd26
|
UTSW |
6 |
118,500,160 (GRCm39) |
missense |
probably benign |
0.03 |
R8078:Ankrd26
|
UTSW |
6 |
118,494,854 (GRCm39) |
splice site |
probably null |
|
R8224:Ankrd26
|
UTSW |
6 |
118,502,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R8917:Ankrd26
|
UTSW |
6 |
118,535,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Ankrd26
|
UTSW |
6 |
118,512,104 (GRCm39) |
missense |
probably benign |
0.02 |
R9072:Ankrd26
|
UTSW |
6 |
118,500,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R9073:Ankrd26
|
UTSW |
6 |
118,500,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R9087:Ankrd26
|
UTSW |
6 |
118,536,230 (GRCm39) |
critical splice donor site |
probably null |
|
R9334:Ankrd26
|
UTSW |
6 |
118,509,262 (GRCm39) |
missense |
probably benign |
|
R9417:Ankrd26
|
UTSW |
6 |
118,504,725 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9521:Ankrd26
|
UTSW |
6 |
118,517,420 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9720:Ankrd26
|
UTSW |
6 |
118,498,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R9766:Ankrd26
|
UTSW |
6 |
118,500,067 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0028:Ankrd26
|
UTSW |
6 |
118,484,722 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ankrd26
|
UTSW |
6 |
118,500,493 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1177:Ankrd26
|
UTSW |
6 |
118,500,556 (GRCm39) |
missense |
probably damaging |
0.99 |
|