Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
A |
T |
14: 118,738,213 (GRCm39) |
V1104D |
probably damaging |
Het |
Adgrl2 |
A |
T |
3: 148,532,161 (GRCm39) |
V1024E |
probably damaging |
Het |
Agbl2 |
A |
G |
2: 90,631,686 (GRCm39) |
H348R |
probably benign |
Het |
Aifm2 |
T |
C |
10: 61,574,354 (GRCm39) |
|
probably benign |
Het |
Avpr1b |
A |
G |
1: 131,528,389 (GRCm39) |
D304G |
probably damaging |
Het |
Duox1 |
A |
G |
2: 122,156,498 (GRCm39) |
D475G |
possibly damaging |
Het |
E2f8 |
T |
C |
7: 48,516,982 (GRCm39) |
|
probably null |
Het |
Fat2 |
T |
A |
11: 55,173,211 (GRCm39) |
I2501F |
probably damaging |
Het |
Gm4181 |
A |
G |
14: 51,870,689 (GRCm39) |
C91R |
probably benign |
Het |
Gm5424 |
T |
A |
10: 61,907,390 (GRCm39) |
|
noncoding transcript |
Het |
Gnai3 |
A |
G |
3: 108,025,660 (GRCm39) |
F140L |
probably benign |
Het |
Htra1 |
A |
T |
7: 130,563,765 (GRCm39) |
D212V |
probably damaging |
Het |
Irgm2 |
T |
C |
11: 58,111,350 (GRCm39) |
V347A |
probably benign |
Het |
Itch |
A |
G |
2: 155,015,964 (GRCm39) |
T150A |
probably benign |
Het |
Itgb3 |
A |
C |
11: 104,528,655 (GRCm39) |
I261L |
possibly damaging |
Het |
Kalrn |
C |
T |
16: 34,212,420 (GRCm39) |
V31M |
probably damaging |
Het |
Klra7 |
C |
T |
6: 130,203,463 (GRCm39) |
C181Y |
probably damaging |
Het |
Klrb1 |
A |
G |
6: 128,690,548 (GRCm39) |
L58S |
probably benign |
Het |
Kndc1 |
A |
G |
7: 139,481,097 (GRCm39) |
E61G |
probably damaging |
Het |
Krt78 |
T |
A |
15: 101,861,842 (GRCm39) |
T135S |
possibly damaging |
Het |
Mpdz |
A |
G |
4: 81,202,808 (GRCm39) |
|
probably null |
Het |
Mphosph6 |
A |
G |
8: 118,519,525 (GRCm39) |
|
probably benign |
Het |
Myo19 |
T |
C |
11: 84,790,222 (GRCm39) |
S393P |
possibly damaging |
Het |
Or51a5 |
A |
G |
7: 102,771,027 (GRCm39) |
|
probably benign |
Het |
Or8g53 |
T |
C |
9: 39,683,214 (GRCm39) |
N294S |
probably damaging |
Het |
Pkdrej |
T |
C |
15: 85,704,988 (GRCm39) |
Y316C |
probably damaging |
Het |
Pkp3 |
A |
T |
7: 140,669,681 (GRCm39) |
|
probably benign |
Het |
Pramel31 |
T |
A |
4: 144,089,983 (GRCm39) |
L341H |
probably damaging |
Het |
Psmb8 |
A |
G |
17: 34,420,217 (GRCm39) |
K270E |
probably benign |
Het |
Ptprq |
T |
C |
10: 107,488,561 (GRCm39) |
N959D |
probably damaging |
Het |
Rab6b |
T |
G |
9: 103,038,074 (GRCm39) |
|
probably null |
Het |
Rhobtb3 |
T |
C |
13: 76,065,843 (GRCm39) |
D180G |
probably damaging |
Het |
Sccpdh |
G |
A |
1: 179,508,074 (GRCm39) |
C238Y |
probably benign |
Het |
Srm |
C |
T |
4: 148,677,803 (GRCm39) |
S147L |
probably benign |
Het |
Synj1 |
A |
T |
16: 90,788,350 (GRCm39) |
S173T |
probably damaging |
Het |
Tas1r1 |
T |
C |
4: 152,112,797 (GRCm39) |
E752G |
possibly damaging |
Het |
Tmem151a |
G |
T |
19: 5,132,875 (GRCm39) |
Y110* |
probably null |
Het |
Ttn |
A |
G |
2: 76,556,957 (GRCm39) |
V30016A |
probably damaging |
Het |
Txnrd2 |
A |
G |
16: 18,287,590 (GRCm39) |
E331G |
probably benign |
Het |
Vldlr |
T |
C |
19: 27,215,485 (GRCm39) |
C161R |
possibly damaging |
Het |
Vmn1r91 |
T |
A |
7: 19,835,415 (GRCm39) |
S111R |
probably damaging |
Het |
Vmn2r66 |
T |
A |
7: 84,655,796 (GRCm39) |
I407F |
probably benign |
Het |
Vps13d |
T |
C |
4: 144,854,850 (GRCm39) |
M2258V |
probably benign |
Het |
Ypel1 |
A |
T |
16: 16,923,872 (GRCm39) |
V59D |
probably benign |
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 |
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 |
R4230:Ankrd26
|
UTSW |
6 |
118,536,349 (GRCm39) |
splice site |
probably null |
|
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 |
|