Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
A |
T |
4: 144,344,392 (GRCm39) |
|
probably null |
Het |
Acp4 |
A |
G |
7: 43,904,414 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,659,738 (GRCm39) |
M1997K |
probably benign |
Het |
Arhgdib |
T |
C |
6: 136,910,647 (GRCm39) |
D38G |
probably damaging |
Het |
Bbox1 |
T |
G |
2: 110,135,871 (GRCm39) |
D36A |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,734,457 (GRCm39) |
K104R |
probably damaging |
Het |
Cacna1i |
G |
A |
15: 80,182,839 (GRCm39) |
C75Y |
probably damaging |
Het |
Ccdc14 |
T |
C |
16: 34,517,528 (GRCm39) |
L70S |
probably damaging |
Het |
Ccdc88a |
T |
G |
11: 29,451,051 (GRCm39) |
V1580G |
probably benign |
Het |
Cdadc1 |
C |
A |
14: 59,823,812 (GRCm39) |
D227Y |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,242,976 (GRCm39) |
Y1415C |
probably damaging |
Het |
Cngb3 |
A |
G |
4: 19,428,489 (GRCm39) |
N493S |
probably benign |
Het |
Dock10 |
T |
A |
1: 80,551,840 (GRCm39) |
Y665F |
probably damaging |
Het |
Gm10549 |
C |
A |
18: 33,597,303 (GRCm39) |
|
probably benign |
Het |
Greb1 |
C |
T |
12: 16,758,683 (GRCm39) |
V678M |
probably damaging |
Het |
Gucy2c |
G |
A |
6: 136,706,211 (GRCm39) |
R497* |
probably null |
Het |
Itgad |
T |
C |
7: 127,782,546 (GRCm39) |
|
probably benign |
Het |
Lgr4 |
C |
A |
2: 109,842,718 (GRCm39) |
T877K |
probably damaging |
Het |
Lrig3 |
A |
G |
10: 125,802,463 (GRCm39) |
D40G |
probably benign |
Het |
Myo3b |
T |
C |
2: 69,935,716 (GRCm39) |
|
probably benign |
Het |
Neb |
A |
G |
2: 52,161,093 (GRCm39) |
Y2193H |
possibly damaging |
Het |
Or4b1 |
T |
A |
2: 89,979,697 (GRCm39) |
I218F |
possibly damaging |
Het |
Or8b3b |
T |
C |
9: 38,584,312 (GRCm39) |
M143V |
probably benign |
Het |
Pard6b |
A |
G |
2: 167,940,847 (GRCm39) |
Q278R |
probably benign |
Het |
Pkd2l1 |
T |
C |
19: 44,143,975 (GRCm39) |
Y366C |
possibly damaging |
Het |
Prl2c1 |
A |
G |
13: 28,041,542 (GRCm39) |
D188G |
probably benign |
Het |
Prl3a1 |
G |
T |
13: 27,454,218 (GRCm39) |
M65I |
probably benign |
Het |
Psg26 |
T |
A |
7: 18,216,691 (GRCm39) |
E49D |
probably benign |
Het |
Rapgef3 |
G |
A |
15: 97,656,273 (GRCm39) |
R38W |
probably damaging |
Het |
Rrn3 |
T |
C |
16: 13,629,453 (GRCm39) |
F590L |
probably benign |
Het |
Serpina12 |
T |
C |
12: 104,004,267 (GRCm39) |
K122E |
probably benign |
Het |
Slc39a6 |
T |
C |
18: 24,715,424 (GRCm39) |
I699V |
probably damaging |
Het |
Tmem259 |
G |
A |
10: 79,813,651 (GRCm39) |
P443S |
probably damaging |
Het |
Vmn1r75 |
T |
A |
7: 11,615,091 (GRCm39) |
F274L |
probably benign |
Het |
|
Other mutations in Pate10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02593:Pate10
|
APN |
9 |
35,653,438 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02612:Pate10
|
APN |
9 |
35,653,460 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02698:Pate10
|
APN |
9 |
35,652,416 (GRCm39) |
splice site |
probably benign |
|
R4240:Pate10
|
UTSW |
9 |
35,653,449 (GRCm39) |
nonsense |
probably null |
|
R4983:Pate10
|
UTSW |
9 |
35,653,465 (GRCm39) |
missense |
probably benign |
0.12 |
R5161:Pate10
|
UTSW |
9 |
35,652,884 (GRCm39) |
nonsense |
probably null |
|
R5545:Pate10
|
UTSW |
9 |
35,652,940 (GRCm39) |
missense |
probably benign |
0.10 |
R5980:Pate10
|
UTSW |
9 |
35,652,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R6131:Pate10
|
UTSW |
9 |
35,652,840 (GRCm39) |
nonsense |
probably null |
|
R6147:Pate10
|
UTSW |
9 |
35,653,528 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6147:Pate10
|
UTSW |
9 |
35,653,406 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8850:Pate10
|
UTSW |
9 |
35,652,391 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Pate10
|
UTSW |
9 |
35,653,466 (GRCm39) |
missense |
possibly damaging |
0.90 |
|