Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
T |
3: 121,915,447 (GRCm39) |
T971S |
probably damaging |
Het |
Catsperb |
C |
T |
12: 101,590,994 (GRCm39) |
Q1021* |
probably null |
Het |
Ccdc62 |
A |
G |
5: 124,072,156 (GRCm39) |
T62A |
probably benign |
Het |
Cuzd1 |
A |
G |
7: 130,913,412 (GRCm39) |
S402P |
probably damaging |
Het |
Dcun1d1 |
C |
T |
3: 35,949,819 (GRCm39) |
V244M |
probably damaging |
Het |
Dennd2c |
A |
G |
3: 103,038,977 (GRCm39) |
T42A |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,560,385 (GRCm39) |
|
probably null |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dpp4 |
A |
T |
2: 62,178,893 (GRCm39) |
F607L |
probably benign |
Het |
Ech1 |
C |
T |
7: 28,529,763 (GRCm39) |
|
probably null |
Het |
Fam53a |
A |
G |
5: 33,765,184 (GRCm39) |
L174P |
probably damaging |
Het |
Fh1 |
T |
C |
1: 175,446,690 (GRCm39) |
D62G |
probably null |
Het |
Gpatch11 |
T |
C |
17: 79,147,528 (GRCm39) |
I103T |
probably damaging |
Het |
Hmgcll1 |
A |
T |
9: 75,988,731 (GRCm39) |
T169S |
probably benign |
Het |
Kbtbd3 |
A |
T |
9: 4,330,687 (GRCm39) |
I354F |
probably benign |
Het |
Kdm5b |
T |
C |
1: 134,541,007 (GRCm39) |
F700L |
possibly damaging |
Het |
Mamdc4 |
C |
A |
2: 25,457,756 (GRCm39) |
G439V |
probably damaging |
Het |
Mrps30 |
A |
T |
13: 118,517,134 (GRCm39) |
S362T |
probably damaging |
Het |
Mug1 |
C |
T |
6: 121,815,683 (GRCm39) |
S29L |
possibly damaging |
Het |
Myh2 |
G |
A |
11: 67,069,174 (GRCm39) |
D328N |
probably damaging |
Het |
Or10j3b |
C |
A |
1: 173,043,973 (GRCm39) |
H252N |
probably damaging |
Het |
Or5b98 |
A |
G |
19: 12,931,823 (GRCm39) |
Y290C |
probably damaging |
Het |
Or5j1 |
T |
C |
2: 86,878,942 (GRCm39) |
T213A |
probably benign |
Het |
Or8g54 |
T |
A |
9: 39,706,710 (GRCm39) |
I13N |
probably benign |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pira13 |
T |
A |
7: 3,825,251 (GRCm39) |
M464L |
probably benign |
Het |
Pus7l |
G |
A |
15: 94,425,746 (GRCm39) |
P552S |
probably benign |
Het |
Rest |
A |
G |
5: 77,428,844 (GRCm39) |
K421R |
probably damaging |
Het |
Rttn |
C |
A |
18: 89,032,735 (GRCm39) |
H668N |
probably damaging |
Het |
Scn9a |
T |
C |
2: 66,393,686 (GRCm39) |
I228V |
possibly damaging |
Het |
Scp2 |
G |
T |
4: 107,948,513 (GRCm39) |
Q155K |
probably damaging |
Het |
Sec61a2 |
G |
A |
2: 5,881,219 (GRCm39) |
R18* |
probably null |
Het |
Serpinb8 |
T |
A |
1: 107,525,321 (GRCm39) |
M41K |
probably damaging |
Het |
Sgsm2 |
A |
T |
11: 74,756,204 (GRCm39) |
W382R |
probably damaging |
Het |
Slc26a10 |
G |
T |
10: 127,009,530 (GRCm39) |
T606N |
possibly damaging |
Het |
Slc30a6 |
T |
C |
17: 74,711,027 (GRCm39) |
I40T |
possibly damaging |
Het |
Slfn5 |
G |
A |
11: 82,847,204 (GRCm39) |
E30K |
possibly damaging |
Het |
Sorcs2 |
C |
A |
5: 36,555,154 (GRCm39) |
R79L |
probably benign |
Het |
Tmc5 |
G |
A |
7: 118,268,527 (GRCm39) |
S865N |
probably damaging |
Het |
Tmprss11c |
T |
A |
5: 86,437,119 (GRCm39) |
M1L |
possibly damaging |
Het |
Trpv5 |
C |
G |
6: 41,630,288 (GRCm39) |
E601Q |
probably damaging |
Het |
Ttc39b |
A |
T |
4: 83,158,285 (GRCm39) |
|
probably benign |
Het |
Ttll6 |
T |
A |
11: 96,029,689 (GRCm39) |
C201S |
probably damaging |
Het |
Vezt |
A |
G |
10: 93,832,859 (GRCm39) |
V204A |
probably benign |
Het |
Zfp433 |
A |
T |
10: 81,556,722 (GRCm39) |
H408L |
probably damaging |
Het |
Zfp865 |
T |
C |
7: 5,032,450 (GRCm39) |
I145T |
possibly damaging |
Het |
|
Other mutations in Vmn1r45 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Vmn1r45
|
APN |
6 |
89,910,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02010:Vmn1r45
|
APN |
6 |
89,910,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02124:Vmn1r45
|
APN |
6 |
89,910,035 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02413:Vmn1r45
|
APN |
6 |
89,910,503 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0123:Vmn1r45
|
UTSW |
6 |
89,910,492 (GRCm39) |
nonsense |
probably null |
|
R0225:Vmn1r45
|
UTSW |
6 |
89,910,492 (GRCm39) |
nonsense |
probably null |
|
R1513:Vmn1r45
|
UTSW |
6 |
89,910,058 (GRCm39) |
missense |
probably damaging |
0.97 |
R2154:Vmn1r45
|
UTSW |
6 |
89,910,965 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3082:Vmn1r45
|
UTSW |
6 |
89,910,724 (GRCm39) |
missense |
probably benign |
0.03 |
R3781:Vmn1r45
|
UTSW |
6 |
89,910,799 (GRCm39) |
missense |
probably benign |
|
R4982:Vmn1r45
|
UTSW |
6 |
89,910,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R5086:Vmn1r45
|
UTSW |
6 |
89,910,082 (GRCm39) |
missense |
probably benign |
0.06 |
R5327:Vmn1r45
|
UTSW |
6 |
89,910,123 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5470:Vmn1r45
|
UTSW |
6 |
89,910,698 (GRCm39) |
missense |
probably benign |
0.04 |
R7046:Vmn1r45
|
UTSW |
6 |
89,910,538 (GRCm39) |
missense |
probably benign |
0.00 |
R7050:Vmn1r45
|
UTSW |
6 |
89,910,703 (GRCm39) |
missense |
probably damaging |
0.97 |
R7171:Vmn1r45
|
UTSW |
6 |
89,910,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Vmn1r45
|
UTSW |
6 |
89,910,133 (GRCm39) |
missense |
probably benign |
0.15 |
R7401:Vmn1r45
|
UTSW |
6 |
89,910,416 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7417:Vmn1r45
|
UTSW |
6 |
89,910,035 (GRCm39) |
missense |
probably benign |
0.03 |
R8068:Vmn1r45
|
UTSW |
6 |
89,910,261 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8223:Vmn1r45
|
UTSW |
6 |
89,910,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R8942:Vmn1r45
|
UTSW |
6 |
89,910,876 (GRCm39) |
missense |
probably benign |
0.00 |
RF019:Vmn1r45
|
UTSW |
6 |
89,910,091 (GRCm39) |
missense |
probably damaging |
0.99 |
X0026:Vmn1r45
|
UTSW |
6 |
89,910,724 (GRCm39) |
missense |
probably benign |
0.00 |
|