Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921513I03Rik |
G |
A |
10: 120,614,635 (GRCm39) |
|
probably benign |
Het |
4930432E11Rik |
C |
T |
7: 29,262,704 (GRCm39) |
|
noncoding transcript |
Het |
Adcy10 |
T |
C |
1: 165,400,112 (GRCm39) |
V1507A |
probably damaging |
Het |
Ap3b2 |
T |
A |
7: 81,110,746 (GRCm39) |
M1010L |
unknown |
Het |
Bmp10 |
T |
C |
6: 87,411,130 (GRCm39) |
S308P |
probably benign |
Het |
Cnih3 |
C |
A |
1: 181,282,274 (GRCm39) |
Y169* |
probably null |
Het |
Cpsf4l |
A |
G |
11: 113,590,685 (GRCm39) |
S222P |
possibly damaging |
Het |
Cyp2d10 |
G |
A |
15: 82,288,808 (GRCm39) |
|
probably benign |
Het |
Dcstamp |
A |
T |
15: 39,617,928 (GRCm39) |
E112D |
probably damaging |
Het |
Fras1 |
C |
T |
5: 96,929,496 (GRCm39) |
Q3967* |
probably null |
Het |
Gcm1 |
C |
A |
9: 77,972,121 (GRCm39) |
P354H |
possibly damaging |
Het |
Gen1 |
A |
G |
12: 11,291,867 (GRCm39) |
S706P |
probably benign |
Het |
Glb1l3 |
G |
T |
9: 26,736,466 (GRCm39) |
T532N |
probably benign |
Het |
Gm5069 |
T |
A |
1: 180,154,872 (GRCm39) |
|
probably benign |
Het |
Itgb2 |
G |
T |
10: 77,385,895 (GRCm39) |
C286F |
probably damaging |
Het |
Jak3 |
A |
G |
8: 72,131,124 (GRCm39) |
Y48C |
probably damaging |
Het |
Lrp2 |
G |
A |
2: 69,367,960 (GRCm39) |
S184L |
probably benign |
Het |
Myo1f |
T |
A |
17: 33,798,945 (GRCm39) |
N203K |
probably benign |
Het |
Nrxn2 |
G |
A |
19: 6,522,306 (GRCm39) |
G182R |
probably damaging |
Het |
Or4k15c |
T |
C |
14: 50,321,943 (GRCm39) |
N65S |
probably damaging |
Het |
Or4p8 |
A |
G |
2: 88,727,503 (GRCm39) |
V146A |
probably benign |
Het |
Or5g23 |
A |
C |
2: 85,438,664 (GRCm39) |
L197V |
probably benign |
Het |
Otog |
C |
T |
7: 45,954,903 (GRCm39) |
S2692L |
probably damaging |
Het |
Pde9a |
C |
T |
17: 31,672,444 (GRCm39) |
T34I |
probably benign |
Het |
Phip |
T |
C |
9: 82,763,394 (GRCm39) |
T1295A |
possibly damaging |
Het |
Pik3cb |
A |
G |
9: 98,953,430 (GRCm39) |
V451A |
probably benign |
Het |
Psd2 |
T |
G |
18: 36,137,809 (GRCm39) |
|
probably benign |
Het |
Pycr2 |
T |
C |
1: 180,733,762 (GRCm39) |
I118T |
probably damaging |
Het |
Rnf17 |
T |
G |
14: 56,658,623 (GRCm39) |
M104R |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,266,259 (GRCm39) |
V615A |
probably benign |
Het |
Sel1l3 |
T |
A |
5: 53,327,747 (GRCm39) |
R511W |
possibly damaging |
Het |
Sis |
T |
C |
3: 72,854,804 (GRCm39) |
N478D |
probably benign |
Het |
Trps1 |
T |
A |
15: 50,685,674 (GRCm39) |
S584C |
probably damaging |
Het |
Vmn2r124 |
T |
C |
17: 18,284,491 (GRCm39) |
|
probably benign |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,567,787 (GRCm39) |
S1027P |
probably benign |
Het |
Zfp644 |
A |
T |
5: 106,783,760 (GRCm39) |
I929K |
probably benign |
Het |
|
Other mutations in Gzmc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02552:Gzmc
|
APN |
14 |
56,472,039 (GRCm39) |
start codon destroyed |
probably null |
|
IGL02974:Gzmc
|
APN |
14 |
56,471,451 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03408:Gzmc
|
APN |
14 |
56,471,473 (GRCm39) |
missense |
probably damaging |
0.98 |
R0133:Gzmc
|
UTSW |
14 |
56,469,754 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0366:Gzmc
|
UTSW |
14 |
56,470,193 (GRCm39) |
nonsense |
probably null |
|
R1533:Gzmc
|
UTSW |
14 |
56,471,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1551:Gzmc
|
UTSW |
14 |
56,470,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Gzmc
|
UTSW |
14 |
56,469,737 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1686:Gzmc
|
UTSW |
14 |
56,471,341 (GRCm39) |
missense |
probably benign |
0.00 |
R2398:Gzmc
|
UTSW |
14 |
56,470,228 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4730:Gzmc
|
UTSW |
14 |
56,469,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Gzmc
|
UTSW |
14 |
56,469,826 (GRCm39) |
missense |
probably damaging |
0.97 |
R4987:Gzmc
|
UTSW |
14 |
56,468,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R5166:Gzmc
|
UTSW |
14 |
56,471,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R6237:Gzmc
|
UTSW |
14 |
56,471,486 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7494:Gzmc
|
UTSW |
14 |
56,469,785 (GRCm39) |
nonsense |
probably null |
|
R7846:Gzmc
|
UTSW |
14 |
56,469,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Gzmc
|
UTSW |
14 |
56,469,829 (GRCm39) |
missense |
probably benign |
|
R8183:Gzmc
|
UTSW |
14 |
56,470,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Gzmc
|
UTSW |
14 |
56,469,042 (GRCm39) |
missense |
probably benign |
0.01 |
|