Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
A |
G |
12: 118,883,576 (GRCm39) |
V564A |
probably damaging |
Het |
Adamts15 |
A |
T |
9: 30,815,818 (GRCm39) |
N679K |
probably damaging |
Het |
Angpt1 |
T |
G |
15: 42,290,373 (GRCm39) |
D497A |
possibly damaging |
Het |
Asap2 |
A |
G |
12: 21,308,164 (GRCm39) |
K849R |
probably benign |
Het |
Aspm |
T |
C |
1: 139,401,391 (GRCm39) |
V1137A |
probably damaging |
Het |
Atp12a |
A |
G |
14: 56,610,746 (GRCm39) |
I297V |
probably benign |
Het |
Atp2a2 |
A |
G |
5: 122,604,071 (GRCm39) |
V454A |
probably benign |
Het |
Carmil1 |
T |
A |
13: 24,338,651 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
A |
T |
4: 128,215,128 (GRCm39) |
K517* |
probably null |
Het |
Csmd3 |
A |
T |
15: 47,469,492 (GRCm39) |
|
probably benign |
Het |
Cyp2d11 |
T |
A |
15: 82,273,697 (GRCm39) |
Q427L |
possibly damaging |
Het |
Eml5 |
C |
T |
12: 98,825,100 (GRCm39) |
V706M |
probably damaging |
Het |
Entpd8 |
A |
C |
2: 24,975,072 (GRCm39) |
S428R |
probably benign |
Het |
Gm10283 |
T |
C |
8: 60,954,253 (GRCm39) |
|
probably benign |
Het |
Gpatch3 |
T |
A |
4: 133,307,995 (GRCm39) |
V363E |
probably damaging |
Het |
Hoxb5 |
T |
A |
11: 96,194,594 (GRCm39) |
M52K |
probably damaging |
Het |
Ift52 |
T |
C |
2: 162,878,627 (GRCm39) |
V307A |
probably benign |
Het |
Igkv1-115 |
T |
C |
6: 68,138,424 (GRCm39) |
|
noncoding transcript |
Het |
Kdm5a |
T |
C |
6: 120,367,605 (GRCm39) |
|
probably benign |
Het |
Lama1 |
T |
A |
17: 68,057,687 (GRCm39) |
|
probably null |
Het |
Lrp6 |
G |
A |
6: 134,433,077 (GRCm39) |
P1418L |
probably benign |
Het |
Mill2 |
T |
C |
7: 18,590,432 (GRCm39) |
F156L |
probably damaging |
Het |
Mnat1 |
A |
G |
12: 73,217,378 (GRCm39) |
R85G |
probably damaging |
Het |
Myrip |
A |
T |
9: 120,261,740 (GRCm39) |
D451V |
probably damaging |
Het |
Or1e1f |
A |
T |
11: 73,855,539 (GRCm39) |
Y35F |
possibly damaging |
Het |
Pdzph1 |
C |
A |
17: 59,281,064 (GRCm39) |
S406I |
probably benign |
Het |
Ptprb |
A |
G |
10: 116,184,116 (GRCm39) |
|
probably benign |
Het |
Rxfp4 |
T |
A |
3: 88,559,742 (GRCm39) |
R236S |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,722,679 (GRCm39) |
M2604V |
probably benign |
Het |
Setd1a |
G |
A |
7: 127,377,673 (GRCm39) |
|
probably benign |
Het |
Spata33 |
A |
T |
8: 123,948,719 (GRCm39) |
H88L |
probably damaging |
Het |
Spcs3 |
A |
T |
8: 54,979,486 (GRCm39) |
N98K |
probably damaging |
Het |
Srgap3 |
A |
G |
6: 112,748,414 (GRCm39) |
S413P |
probably damaging |
Het |
Stap2 |
T |
C |
17: 56,306,961 (GRCm39) |
R239G |
probably benign |
Het |
Surf6 |
A |
G |
2: 26,782,638 (GRCm39) |
Y230H |
probably damaging |
Het |
Tasp1 |
C |
T |
2: 139,676,283 (GRCm39) |
V382M |
probably benign |
Het |
Tnc |
G |
T |
4: 63,933,338 (GRCm39) |
A642E |
possibly damaging |
Het |
Vmn1r202 |
G |
A |
13: 22,685,640 (GRCm39) |
T259I |
probably benign |
Het |
Vmn2r110 |
T |
A |
17: 20,794,558 (GRCm39) |
T704S |
probably damaging |
Het |
Vtcn1 |
A |
T |
3: 100,791,145 (GRCm39) |
D61V |
probably damaging |
Het |
Zc3h12d |
G |
A |
10: 7,738,364 (GRCm39) |
M223I |
probably damaging |
Het |
Zfp592 |
T |
A |
7: 80,687,875 (GRCm39) |
S934T |
probably benign |
Het |
|
Other mutations in Aadacl4fm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00799:Aadacl4fm2
|
APN |
4 |
144,281,843 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4514001:Aadacl4fm2
|
UTSW |
4 |
144,282,081 (GRCm39) |
missense |
probably damaging |
0.98 |
R0089:Aadacl4fm2
|
UTSW |
4 |
144,282,303 (GRCm39) |
missense |
probably benign |
|
R0325:Aadacl4fm2
|
UTSW |
4 |
144,282,081 (GRCm39) |
missense |
probably damaging |
0.98 |
R0920:Aadacl4fm2
|
UTSW |
4 |
144,287,696 (GRCm39) |
splice site |
probably benign |
|
R1301:Aadacl4fm2
|
UTSW |
4 |
144,291,635 (GRCm39) |
missense |
probably benign |
0.00 |
R1711:Aadacl4fm2
|
UTSW |
4 |
144,281,976 (GRCm39) |
missense |
probably damaging |
0.98 |
R4328:Aadacl4fm2
|
UTSW |
4 |
144,282,164 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4382:Aadacl4fm2
|
UTSW |
4 |
144,281,596 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4655:Aadacl4fm2
|
UTSW |
4 |
144,281,645 (GRCm39) |
missense |
probably benign |
0.24 |
R5194:Aadacl4fm2
|
UTSW |
4 |
144,281,652 (GRCm39) |
missense |
probably benign |
0.00 |
R6301:Aadacl4fm2
|
UTSW |
4 |
144,285,224 (GRCm39) |
missense |
probably damaging |
0.99 |
R6508:Aadacl4fm2
|
UTSW |
4 |
144,291,590 (GRCm39) |
nonsense |
probably null |
|
R7206:Aadacl4fm2
|
UTSW |
4 |
144,285,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R7429:Aadacl4fm2
|
UTSW |
4 |
144,291,626 (GRCm39) |
missense |
probably benign |
|
R7520:Aadacl4fm2
|
UTSW |
4 |
144,281,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Aadacl4fm2
|
UTSW |
4 |
144,291,580 (GRCm39) |
missense |
probably damaging |
0.98 |
R8709:Aadacl4fm2
|
UTSW |
4 |
144,281,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Aadacl4fm2
|
UTSW |
4 |
144,282,000 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9529:Aadacl4fm2
|
UTSW |
4 |
144,282,082 (GRCm39) |
missense |
probably benign |
0.00 |
|