Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
A |
G |
8: 87,231,908 (GRCm39) |
V1347A |
possibly damaging |
Het |
Adam32 |
G |
A |
8: 25,327,811 (GRCm39) |
T750I |
unknown |
Het |
Adcy1 |
T |
C |
11: 7,111,328 (GRCm39) |
I873T |
probably damaging |
Het |
Anks1b |
T |
A |
10: 89,885,868 (GRCm39) |
M188K |
probably damaging |
Het |
Aopep |
T |
C |
13: 63,338,373 (GRCm39) |
F583S |
probably damaging |
Het |
Arhgef18 |
A |
G |
8: 3,439,074 (GRCm39) |
Y477C |
unknown |
Het |
Cep112 |
T |
C |
11: 108,316,478 (GRCm39) |
|
probably null |
Het |
Clu |
T |
C |
14: 66,218,406 (GRCm39) |
V422A |
probably damaging |
Het |
Cntrl |
T |
C |
2: 35,038,600 (GRCm39) |
L1050P |
probably damaging |
Het |
Col23a1 |
A |
T |
11: 51,458,756 (GRCm39) |
T298S |
possibly damaging |
Het |
Cyp26c1 |
A |
T |
19: 37,675,065 (GRCm39) |
T129S |
probably damaging |
Het |
Cyp2c38 |
A |
C |
19: 39,390,135 (GRCm39) |
V355G |
possibly damaging |
Het |
Cyp4a30b |
G |
A |
4: 115,314,942 (GRCm39) |
V175M |
possibly damaging |
Het |
Cyp7a1 |
A |
T |
4: 6,271,207 (GRCm39) |
N316K |
probably benign |
Het |
Dcaf17 |
T |
A |
2: 70,886,913 (GRCm39) |
Y67* |
probably null |
Het |
Dll3 |
T |
C |
7: 27,994,270 (GRCm39) |
D389G |
probably damaging |
Het |
Fbxo33 |
A |
G |
12: 59,265,830 (GRCm39) |
F146L |
probably benign |
Het |
Gm10118 |
C |
T |
10: 63,762,756 (GRCm39) |
V61M |
unknown |
Het |
Gm9611 |
T |
C |
14: 42,118,026 (GRCm39) |
D102G |
|
Het |
Grik5 |
G |
A |
7: 24,709,897 (GRCm39) |
A946V |
probably benign |
Het |
Il17c |
A |
G |
8: 123,150,207 (GRCm39) |
D150G |
possibly damaging |
Het |
Ino80e |
A |
G |
7: 126,460,893 (GRCm39) |
L22P |
probably damaging |
Het |
Kcnh2 |
G |
T |
5: 24,536,981 (GRCm39) |
T201K |
probably benign |
Het |
Klrb1 |
A |
C |
6: 128,687,012 (GRCm39) |
N173K |
possibly damaging |
Het |
Kmt2d |
T |
A |
15: 98,743,948 (GRCm39) |
Q3737H |
unknown |
Het |
Lemd3 |
T |
C |
10: 120,767,728 (GRCm39) |
D682G |
possibly damaging |
Het |
Lilra5 |
T |
C |
7: 4,241,216 (GRCm39) |
V51A |
probably benign |
Het |
Lrrc25 |
G |
A |
8: 71,070,314 (GRCm39) |
V32I |
possibly damaging |
Het |
Mdh1b |
T |
A |
1: 63,754,360 (GRCm39) |
M403L |
probably benign |
Het |
Mms19 |
G |
A |
19: 41,937,915 (GRCm39) |
L765F |
probably damaging |
Het |
Msx3 |
T |
A |
7: 139,628,900 (GRCm39) |
T5S |
probably benign |
Het |
Myh13 |
A |
C |
11: 67,242,960 (GRCm39) |
I958L |
possibly damaging |
Het |
Myo18b |
T |
A |
5: 113,021,429 (GRCm39) |
|
probably null |
Het |
Myo9a |
G |
A |
9: 59,775,394 (GRCm39) |
V1002I |
probably benign |
Het |
Neb |
T |
C |
2: 52,127,048 (GRCm39) |
K379R |
probably damaging |
Het |
Nsmce2 |
A |
G |
15: 59,473,208 (GRCm39) |
S216G |
probably benign |
Het |
Odad1 |
A |
G |
7: 45,591,263 (GRCm39) |
E246G |
probably damaging |
Het |
Or11h7 |
A |
T |
14: 50,890,801 (GRCm39) |
M36L |
probably benign |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Pkp2 |
A |
T |
16: 16,048,545 (GRCm39) |
M317L |
probably benign |
Het |
Pogz |
T |
A |
3: 94,768,234 (GRCm39) |
H137Q |
probably damaging |
Het |
Prrx2 |
G |
T |
2: 30,735,519 (GRCm39) |
D25Y |
unknown |
Het |
Ptprf |
T |
C |
4: 118,088,844 (GRCm39) |
D653G |
probably benign |
Het |
Rps6kl1 |
T |
A |
12: 85,194,629 (GRCm39) |
E94V |
probably damaging |
Het |
Slc44a1 |
A |
T |
4: 53,481,510 (GRCm39) |
D27V |
probably damaging |
Het |
Slc44a4 |
A |
G |
17: 35,147,253 (GRCm39) |
I549V |
possibly damaging |
Het |
Slc8a3 |
T |
C |
12: 81,361,914 (GRCm39) |
T302A |
probably benign |
Het |
Spic |
T |
A |
10: 88,511,847 (GRCm39) |
K136N |
possibly damaging |
Het |
Stk36 |
T |
C |
1: 74,661,392 (GRCm39) |
L473P |
probably damaging |
Het |
Syce1 |
G |
A |
7: 140,361,987 (GRCm39) |
T32I |
possibly damaging |
Het |
Tars2 |
G |
A |
3: 95,658,199 (GRCm39) |
Q209* |
probably null |
Het |
Tmem9b |
A |
G |
7: 109,344,527 (GRCm39) |
V100A |
probably benign |
Het |
Vmn1r67 |
A |
G |
7: 10,181,128 (GRCm39) |
I131V |
probably benign |
Het |
Vmn2r26 |
C |
T |
6: 124,001,877 (GRCm39) |
T54I |
probably benign |
Het |
Zfp142 |
T |
C |
1: 74,610,747 (GRCm39) |
E1016G |
probably damaging |
Het |
Zfp773 |
T |
C |
7: 7,139,482 (GRCm39) |
T56A |
possibly damaging |
Het |
|
Other mutations in Aebp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00578:Aebp1
|
APN |
11 |
5,821,787 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01464:Aebp1
|
APN |
11 |
5,819,822 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01561:Aebp1
|
APN |
11 |
5,821,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01648:Aebp1
|
APN |
11 |
5,820,607 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01950:Aebp1
|
APN |
11 |
5,819,108 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02094:Aebp1
|
APN |
11 |
5,818,357 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02585:Aebp1
|
APN |
11 |
5,820,855 (GRCm39) |
splice site |
probably null |
|
R0006:Aebp1
|
UTSW |
11 |
5,813,935 (GRCm39) |
unclassified |
probably benign |
|
R0551:Aebp1
|
UTSW |
11 |
5,817,955 (GRCm39) |
missense |
probably benign |
0.04 |
R1144:Aebp1
|
UTSW |
11 |
5,818,475 (GRCm39) |
missense |
probably benign |
0.17 |
R1265:Aebp1
|
UTSW |
11 |
5,821,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R1297:Aebp1
|
UTSW |
11 |
5,820,834 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1518:Aebp1
|
UTSW |
11 |
5,821,469 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1524:Aebp1
|
UTSW |
11 |
5,820,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R2567:Aebp1
|
UTSW |
11 |
5,820,251 (GRCm39) |
missense |
probably benign |
0.29 |
R3155:Aebp1
|
UTSW |
11 |
5,821,425 (GRCm39) |
missense |
probably benign |
0.16 |
R4415:Aebp1
|
UTSW |
11 |
5,815,451 (GRCm39) |
missense |
probably damaging |
0.96 |
R4507:Aebp1
|
UTSW |
11 |
5,820,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5248:Aebp1
|
UTSW |
11 |
5,818,501 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5597:Aebp1
|
UTSW |
11 |
5,816,487 (GRCm39) |
missense |
probably benign |
0.01 |
R5809:Aebp1
|
UTSW |
11 |
5,820,257 (GRCm39) |
missense |
probably benign |
|
R5919:Aebp1
|
UTSW |
11 |
5,821,421 (GRCm39) |
missense |
probably benign |
0.00 |
R5982:Aebp1
|
UTSW |
11 |
5,817,911 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6139:Aebp1
|
UTSW |
11 |
5,821,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7067:Aebp1
|
UTSW |
11 |
5,816,431 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7289:Aebp1
|
UTSW |
11 |
5,815,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7383:Aebp1
|
UTSW |
11 |
5,818,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R7437:Aebp1
|
UTSW |
11 |
5,819,757 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9292:Aebp1
|
UTSW |
11 |
5,815,260 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9429:Aebp1
|
UTSW |
11 |
5,821,649 (GRCm39) |
missense |
probably benign |
0.01 |
R9740:Aebp1
|
UTSW |
11 |
5,821,721 (GRCm39) |
missense |
probably benign |
0.32 |
Z1088:Aebp1
|
UTSW |
11 |
5,821,460 (GRCm39) |
nonsense |
probably null |
|
|