Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Adgrl4 |
T |
C |
3: 151,205,947 (GRCm39) |
|
probably benign |
Het |
Ano4 |
C |
T |
10: 88,790,559 (GRCm39) |
A847T |
probably damaging |
Het |
Atp11a |
A |
G |
8: 12,878,434 (GRCm39) |
|
probably benign |
Het |
Cct4 |
T |
A |
11: 22,952,297 (GRCm39) |
S463T |
probably benign |
Het |
Cfap251 |
G |
T |
5: 123,440,495 (GRCm39) |
V1094L |
probably benign |
Het |
Cnmd |
T |
C |
14: 79,894,093 (GRCm39) |
N98S |
probably damaging |
Het |
Copz2 |
A |
T |
11: 96,747,533 (GRCm39) |
Q172L |
possibly damaging |
Het |
Ctdp1 |
C |
A |
18: 80,494,369 (GRCm39) |
|
probably null |
Het |
Cyfip1 |
C |
T |
7: 55,563,199 (GRCm39) |
T865I |
possibly damaging |
Het |
Cyp2c37 |
A |
T |
19: 40,000,276 (GRCm39) |
D466V |
possibly damaging |
Het |
Dytn |
A |
G |
1: 63,682,507 (GRCm39) |
L380P |
possibly damaging |
Het |
Fam124b |
G |
A |
1: 80,191,243 (GRCm39) |
R47C |
probably damaging |
Het |
Foxe3 |
G |
A |
4: 114,782,972 (GRCm39) |
A80V |
probably damaging |
Het |
Kera |
A |
T |
10: 97,448,749 (GRCm39) |
Y323F |
probably damaging |
Het |
Lipf |
A |
T |
19: 33,946,197 (GRCm39) |
Y205F |
probably damaging |
Het |
Lipo2 |
T |
C |
19: 33,698,237 (GRCm39) |
E380G |
probably benign |
Het |
Mcm2 |
A |
T |
6: 88,864,786 (GRCm39) |
H563Q |
possibly damaging |
Het |
Mindy3 |
T |
C |
2: 12,352,974 (GRCm39) |
E409G |
probably benign |
Het |
Mns1 |
A |
G |
9: 72,346,564 (GRCm39) |
K16E |
probably benign |
Het |
Naip5 |
T |
A |
13: 100,356,338 (GRCm39) |
E1092D |
probably benign |
Het |
Nlrp4g |
T |
C |
9: 124,349,153 (GRCm38) |
|
noncoding transcript |
Het |
Nrxn1 |
A |
G |
17: 90,868,196 (GRCm39) |
S1105P |
probably damaging |
Het |
Odf2l |
G |
A |
3: 144,834,706 (GRCm39) |
R186H |
probably damaging |
Het |
Or13g1 |
T |
A |
7: 85,956,274 (GRCm39) |
T16S |
probably benign |
Het |
Or2d3c |
T |
C |
7: 106,525,800 (GRCm39) |
I289V |
possibly damaging |
Het |
Phxr2 |
T |
C |
10: 98,961,931 (GRCm39) |
|
probably benign |
Het |
Plcxd3 |
T |
C |
15: 4,546,725 (GRCm39) |
F243S |
probably damaging |
Het |
Ppp1r27 |
T |
C |
11: 120,441,553 (GRCm39) |
N76D |
possibly damaging |
Het |
Ptprz1 |
A |
G |
6: 22,972,797 (GRCm39) |
T236A |
probably damaging |
Het |
Pyroxd1 |
C |
G |
6: 142,300,467 (GRCm39) |
S199* |
probably null |
Het |
R3hdm1 |
T |
C |
1: 128,102,975 (GRCm39) |
|
probably benign |
Het |
Sall2 |
T |
A |
14: 52,552,616 (GRCm39) |
Q193L |
probably damaging |
Het |
Srpk1 |
T |
C |
17: 28,827,698 (GRCm39) |
S39G |
probably benign |
Het |
Tcaf3 |
A |
G |
6: 42,564,513 (GRCm39) |
V883A |
probably damaging |
Het |
Tmem104 |
T |
A |
11: 115,134,550 (GRCm39) |
V362E |
probably damaging |
Het |
|
Other mutations in Gm5884 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00482:Gm5884
|
APN |
6 |
128,623,166 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01668:Gm5884
|
APN |
6 |
128,622,377 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01730:Gm5884
|
APN |
6 |
128,622,669 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02401:Gm5884
|
APN |
6 |
128,622,377 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02601:Gm5884
|
APN |
6 |
128,622,749 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02812:Gm5884
|
APN |
6 |
128,622,738 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03178:Gm5884
|
APN |
6 |
128,622,690 (GRCm39) |
unclassified |
noncoding transcript |
|
R0488:Gm5884
|
UTSW |
6 |
128,623,031 (GRCm39) |
unclassified |
noncoding transcript |
|
R1633:Gm5884
|
UTSW |
6 |
128,623,028 (GRCm39) |
unclassified |
noncoding transcript |
|
R1925:Gm5884
|
UTSW |
6 |
128,622,050 (GRCm39) |
unclassified |
noncoding transcript |
|
R2919:Gm5884
|
UTSW |
6 |
128,622,021 (GRCm39) |
unclassified |
noncoding transcript |
|
|