Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,858,576 (GRCm39) |
Y542F |
possibly damaging |
Het |
Ccl24 |
T |
C |
5: 135,599,732 (GRCm39) |
K93E |
probably benign |
Het |
Ccr9 |
T |
A |
9: 123,608,601 (GRCm39) |
D94E |
probably damaging |
Het |
Cd79a |
G |
A |
7: 24,598,759 (GRCm39) |
V103M |
probably damaging |
Het |
Ces1e |
A |
G |
8: 93,950,521 (GRCm39) |
|
probably null |
Het |
Cul9 |
T |
C |
17: 46,837,566 (GRCm39) |
E993G |
probably damaging |
Het |
Cyp4a14 |
T |
C |
4: 115,348,575 (GRCm39) |
I330V |
probably benign |
Het |
Cyp7a1 |
T |
C |
4: 6,273,801 (GRCm39) |
D35G |
probably benign |
Het |
Dmpk |
C |
A |
7: 18,820,411 (GRCm39) |
|
probably benign |
Het |
Gcnt1 |
G |
T |
19: 17,306,547 (GRCm39) |
R393S |
probably benign |
Het |
Lctl |
C |
T |
9: 64,042,130 (GRCm39) |
|
probably benign |
Het |
Mttp |
A |
T |
3: 137,810,468 (GRCm39) |
I664N |
possibly damaging |
Het |
Myh1 |
C |
T |
11: 67,102,328 (GRCm39) |
A873V |
probably benign |
Het |
Nedd9 |
A |
G |
13: 41,492,330 (GRCm39) |
V54A |
probably damaging |
Het |
Or3a1b |
T |
G |
11: 74,012,459 (GRCm39) |
C115G |
possibly damaging |
Het |
Or4f14 |
A |
T |
2: 111,743,167 (GRCm39) |
V36E |
possibly damaging |
Het |
Or6b1 |
G |
T |
6: 42,814,937 (GRCm39) |
E41* |
probably null |
Het |
Pak6 |
A |
T |
2: 118,523,784 (GRCm39) |
E313V |
probably benign |
Het |
Pla2g4a |
A |
G |
1: 149,740,698 (GRCm39) |
S402P |
probably benign |
Het |
Polq |
T |
C |
16: 36,892,134 (GRCm39) |
M2012T |
probably damaging |
Het |
Ppp1r12b |
A |
T |
1: 134,765,788 (GRCm39) |
|
probably benign |
Het |
Rbp3 |
A |
G |
14: 33,676,616 (GRCm39) |
H188R |
probably damaging |
Het |
Rps6ka2 |
C |
A |
17: 7,566,787 (GRCm39) |
Q682K |
possibly damaging |
Het |
Scgb2b7 |
A |
T |
7: 31,404,506 (GRCm39) |
C65S |
probably damaging |
Het |
Spag4 |
A |
G |
2: 155,910,340 (GRCm39) |
Q322R |
probably damaging |
Het |
Spef2 |
T |
C |
15: 9,676,466 (GRCm39) |
T702A |
probably benign |
Het |
Spmap2l |
T |
G |
5: 77,202,423 (GRCm39) |
S281R |
probably benign |
Het |
Taf3 |
G |
T |
2: 9,956,942 (GRCm39) |
F408L |
probably damaging |
Het |
Tead2 |
T |
G |
7: 44,882,323 (GRCm39) |
Y121D |
possibly damaging |
Het |
Tmco5 |
A |
T |
2: 116,722,760 (GRCm39) |
T294S |
probably damaging |
Het |
Trim37 |
A |
G |
11: 87,037,827 (GRCm39) |
E187G |
possibly damaging |
Het |
Ubb |
T |
A |
11: 62,443,243 (GRCm39) |
L91Q |
probably damaging |
Het |
Ugt2a3 |
G |
A |
5: 87,484,439 (GRCm39) |
P195L |
probably damaging |
Het |
Zan |
T |
C |
5: 137,466,652 (GRCm39) |
S402G |
possibly damaging |
Het |
Zc3h7a |
T |
A |
16: 10,959,574 (GRCm39) |
H793L |
probably damaging |
Het |
Zfhx4 |
C |
T |
3: 5,468,773 (GRCm39) |
T2977I |
possibly damaging |
Het |
|
Other mutations in Ankrd34b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00500:Ankrd34b
|
APN |
13 |
92,575,295 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02684:Ankrd34b
|
APN |
13 |
92,575,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02695:Ankrd34b
|
APN |
13 |
92,576,120 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0143:Ankrd34b
|
UTSW |
13 |
92,576,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Ankrd34b
|
UTSW |
13 |
92,576,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R2138:Ankrd34b
|
UTSW |
13 |
92,575,914 (GRCm39) |
missense |
probably damaging |
0.97 |
R2504:Ankrd34b
|
UTSW |
13 |
92,575,569 (GRCm39) |
splice site |
probably null |
|
R4782:Ankrd34b
|
UTSW |
13 |
92,574,813 (GRCm39) |
missense |
probably damaging |
0.98 |
R6123:Ankrd34b
|
UTSW |
13 |
92,575,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R7159:Ankrd34b
|
UTSW |
13 |
92,575,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7238:Ankrd34b
|
UTSW |
13 |
92,575,139 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7367:Ankrd34b
|
UTSW |
13 |
92,574,795 (GRCm39) |
missense |
probably benign |
0.00 |
R8005:Ankrd34b
|
UTSW |
13 |
92,575,230 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8297:Ankrd34b
|
UTSW |
13 |
92,576,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:Ankrd34b
|
UTSW |
13 |
92,575,590 (GRCm39) |
missense |
probably benign |
0.22 |
R8991:Ankrd34b
|
UTSW |
13 |
92,575,725 (GRCm39) |
missense |
probably benign |
0.01 |
R9084:Ankrd34b
|
UTSW |
13 |
92,575,720 (GRCm39) |
missense |
probably benign |
0.04 |
R9418:Ankrd34b
|
UTSW |
13 |
92,575,232 (GRCm39) |
missense |
probably damaging |
1.00 |
|