Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
A |
2: 69,158,344 (GRCm39) |
|
probably null |
Het |
Ap3b1 |
T |
C |
13: 94,598,911 (GRCm39) |
V495A |
probably benign |
Het |
Astn1 |
T |
C |
1: 158,338,724 (GRCm39) |
|
probably benign |
Het |
Bora |
A |
G |
14: 99,290,974 (GRCm39) |
D94G |
probably damaging |
Het |
Bpifb9b |
G |
T |
2: 154,155,544 (GRCm39) |
V348L |
possibly damaging |
Het |
Cd160 |
A |
T |
3: 96,716,139 (GRCm39) |
I17N |
possibly damaging |
Het |
Cyp2d11 |
A |
C |
15: 82,274,265 (GRCm39) |
I372S |
probably damaging |
Het |
Dennd2c |
T |
A |
3: 103,044,559 (GRCm39) |
V380D |
probably damaging |
Het |
Fat4 |
C |
T |
3: 39,037,088 (GRCm39) |
A3580V |
probably benign |
Het |
Filip1 |
A |
G |
9: 79,725,548 (GRCm39) |
S1024P |
probably benign |
Het |
Flnc |
G |
A |
6: 29,447,511 (GRCm39) |
E1105K |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,268,908 (GRCm39) |
E415V |
probably benign |
Het |
Gdap1l1 |
T |
A |
2: 163,295,588 (GRCm39) |
F224Y |
probably damaging |
Het |
Gm11146 |
A |
T |
16: 77,385,498 (GRCm39) |
|
probably null |
Het |
Gsn |
G |
T |
2: 35,192,507 (GRCm39) |
R485L |
probably damaging |
Het |
Havcr1 |
A |
G |
11: 46,666,320 (GRCm39) |
Y261C |
probably damaging |
Het |
Maneal |
A |
T |
4: 124,752,960 (GRCm39) |
I229N |
probably benign |
Het |
Med24 |
A |
T |
11: 98,619,661 (GRCm39) |
M27K |
probably benign |
Het |
Nipsnap2 |
T |
A |
5: 129,825,056 (GRCm39) |
|
probably benign |
Het |
Noa1 |
T |
A |
5: 77,455,426 (GRCm39) |
Q430L |
probably benign |
Het |
Or1l4 |
C |
A |
2: 37,091,281 (GRCm39) |
S9R |
possibly damaging |
Het |
Or5d47 |
T |
A |
2: 87,804,754 (GRCm39) |
N85I |
probably benign |
Het |
Or7g12 |
T |
C |
9: 18,899,908 (GRCm39) |
V208A |
probably benign |
Het |
Or8h9 |
T |
C |
2: 86,789,527 (GRCm39) |
I92V |
probably benign |
Het |
Pde3a |
T |
A |
6: 141,405,529 (GRCm39) |
S460R |
probably damaging |
Het |
Pdzd8 |
T |
C |
19: 59,288,922 (GRCm39) |
Q826R |
possibly damaging |
Het |
Pfkfb4 |
C |
T |
9: 108,854,178 (GRCm39) |
R351W |
probably damaging |
Het |
Pikfyve |
T |
A |
1: 65,311,730 (GRCm39) |
I1989N |
probably damaging |
Het |
Poldip2 |
T |
A |
11: 78,408,734 (GRCm39) |
F200I |
probably damaging |
Het |
Prodh2 |
T |
C |
7: 30,205,929 (GRCm39) |
V208A |
probably damaging |
Het |
Ranbp10 |
T |
C |
8: 106,553,635 (GRCm39) |
D89G |
probably damaging |
Het |
Rbm33 |
T |
A |
5: 28,544,015 (GRCm39) |
S90R |
probably damaging |
Het |
Slc44a4 |
A |
C |
17: 35,147,637 (GRCm39) |
D441A |
probably damaging |
Het |
Slc4a10 |
A |
T |
2: 62,059,014 (GRCm39) |
I174F |
probably damaging |
Het |
Smim17 |
T |
C |
7: 6,430,160 (GRCm39) |
|
probably benign |
Het |
Tln1 |
T |
C |
4: 43,546,760 (GRCm39) |
E872G |
probably damaging |
Het |
Tmem214 |
G |
A |
5: 31,030,090 (GRCm39) |
A296T |
probably benign |
Het |
Top2b |
T |
C |
14: 16,406,733 (GRCm38) |
L625S |
probably damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,695,593 (GRCm39) |
V273A |
probably benign |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Whrn |
T |
G |
4: 63,353,724 (GRCm39) |
K348Q |
probably damaging |
Het |
Zc3h14 |
T |
C |
12: 98,730,154 (GRCm39) |
V399A |
probably benign |
Het |
|
Other mutations in Acsbg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01474:Acsbg2
|
APN |
17 |
57,168,621 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02418:Acsbg2
|
APN |
17 |
57,156,730 (GRCm39) |
missense |
probably benign |
|
R0023:Acsbg2
|
UTSW |
17 |
57,154,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R0023:Acsbg2
|
UTSW |
17 |
57,154,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R0149:Acsbg2
|
UTSW |
17 |
57,160,924 (GRCm39) |
splice site |
probably benign |
|
R1542:Acsbg2
|
UTSW |
17 |
57,156,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Acsbg2
|
UTSW |
17 |
57,160,855 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4170:Acsbg2
|
UTSW |
17 |
57,160,846 (GRCm39) |
missense |
probably benign |
0.00 |
R4465:Acsbg2
|
UTSW |
17 |
57,168,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R4867:Acsbg2
|
UTSW |
17 |
57,169,914 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5169:Acsbg2
|
UTSW |
17 |
57,156,913 (GRCm39) |
missense |
probably benign |
0.07 |
R5524:Acsbg2
|
UTSW |
17 |
57,157,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6521:Acsbg2
|
UTSW |
17 |
57,168,565 (GRCm39) |
missense |
probably benign |
0.00 |
R6531:Acsbg2
|
UTSW |
17 |
57,153,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Acsbg2
|
UTSW |
17 |
57,153,633 (GRCm39) |
missense |
probably damaging |
0.99 |
R7167:Acsbg2
|
UTSW |
17 |
57,164,000 (GRCm39) |
missense |
probably benign |
0.44 |
R7423:Acsbg2
|
UTSW |
17 |
57,175,257 (GRCm39) |
missense |
probably benign |
|
R7970:Acsbg2
|
UTSW |
17 |
57,156,728 (GRCm39) |
missense |
probably benign |
0.43 |
R8023:Acsbg2
|
UTSW |
17 |
57,152,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R8104:Acsbg2
|
UTSW |
17 |
57,152,443 (GRCm39) |
missense |
probably benign |
0.27 |
R8887:Acsbg2
|
UTSW |
17 |
57,175,285 (GRCm39) |
missense |
probably benign |
0.25 |
Z1177:Acsbg2
|
UTSW |
17 |
57,160,898 (GRCm39) |
missense |
probably benign |
0.02 |
|