Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm3 |
T |
C |
3: 59,784,463 (GRCm39) |
L312P |
probably damaging |
Het |
Acap2 |
A |
C |
16: 30,946,146 (GRCm39) |
W284G |
probably damaging |
Het |
Acsf3 |
T |
C |
8: 123,506,986 (GRCm39) |
L93P |
possibly damaging |
Het |
Agbl2 |
G |
T |
2: 90,614,368 (GRCm39) |
|
probably benign |
Het |
Arap3 |
C |
T |
18: 38,124,754 (GRCm39) |
G242D |
probably damaging |
Het |
Asxl3 |
G |
A |
18: 22,657,401 (GRCm39) |
V1804I |
possibly damaging |
Het |
Bnc1 |
C |
A |
7: 81,623,251 (GRCm39) |
V659L |
probably benign |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Car9 |
A |
G |
4: 43,507,363 (GRCm39) |
E103G |
probably benign |
Het |
Chrm4 |
A |
G |
2: 91,758,176 (GRCm39) |
T195A |
probably damaging |
Het |
Cldn10 |
T |
C |
14: 119,092,424 (GRCm39) |
I8T |
probably damaging |
Het |
Col12a1 |
G |
A |
9: 79,599,654 (GRCm39) |
S833F |
probably benign |
Het |
Cryba2 |
T |
A |
1: 74,929,720 (GRCm39) |
D139V |
possibly damaging |
Het |
Emp1 |
T |
A |
6: 135,354,210 (GRCm39) |
M1K |
probably null |
Het |
Entrep3 |
C |
T |
3: 89,095,903 (GRCm39) |
R545* |
probably null |
Het |
Exosc4 |
C |
A |
15: 76,213,836 (GRCm39) |
A220E |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,282,112 (GRCm39) |
|
probably benign |
Het |
Grid2 |
C |
T |
6: 64,040,919 (GRCm39) |
T287I |
probably benign |
Het |
Grifin |
C |
T |
5: 140,550,494 (GRCm39) |
A7T |
probably damaging |
Het |
Kcnq2 |
A |
T |
2: 180,750,819 (GRCm39) |
I340N |
probably damaging |
Het |
Klrb1 |
T |
A |
6: 128,687,600 (GRCm39) |
H98L |
probably benign |
Het |
Krt90 |
T |
C |
15: 101,471,088 (GRCm39) |
H58R |
possibly damaging |
Het |
Krtap5-2 |
C |
A |
7: 141,729,468 (GRCm39) |
G71C |
unknown |
Het |
Krtap7-1 |
A |
T |
16: 89,305,011 (GRCm39) |
M47K |
probably benign |
Het |
Lmntd1 |
T |
A |
6: 145,373,002 (GRCm39) |
|
probably null |
Het |
Ly6g2 |
A |
G |
15: 75,093,505 (GRCm39) |
|
probably benign |
Het |
Musk |
A |
G |
4: 58,286,128 (GRCm39) |
N6S |
possibly damaging |
Het |
Or2aj4 |
A |
G |
16: 19,385,298 (GRCm39) |
C112R |
probably damaging |
Het |
Or51a39 |
A |
G |
7: 102,362,808 (GRCm39) |
F271L |
probably damaging |
Het |
Or56a42-ps1 |
A |
T |
7: 104,776,241 (GRCm39) |
F89Y |
possibly damaging |
Het |
Or5p58 |
T |
G |
7: 107,694,454 (GRCm39) |
T108P |
probably benign |
Het |
Or8c15 |
T |
A |
9: 38,120,874 (GRCm39) |
I122N |
probably damaging |
Het |
Pcdh19 |
A |
G |
X: 132,586,719 (GRCm39) |
M432T |
probably benign |
Het |
Prdm1 |
A |
G |
10: 44,317,338 (GRCm39) |
F495S |
probably damaging |
Het |
Prkar2a |
T |
C |
9: 108,610,403 (GRCm39) |
Y211H |
possibly damaging |
Het |
Ralgapa1 |
C |
A |
12: 55,754,862 (GRCm39) |
G1143V |
probably damaging |
Het |
Rbbp7 |
A |
G |
X: 161,552,783 (GRCm39) |
|
probably null |
Het |
Scel |
C |
A |
14: 103,770,762 (GRCm39) |
H65Q |
probably damaging |
Het |
Sec24d |
T |
C |
3: 123,137,463 (GRCm39) |
|
probably benign |
Het |
Sfswap |
C |
A |
5: 129,637,860 (GRCm39) |
T839N |
probably benign |
Het |
Slc15a1 |
T |
C |
14: 121,699,911 (GRCm39) |
I636V |
possibly damaging |
Het |
Slc15a1 |
G |
T |
14: 121,699,886 (GRCm39) |
P644H |
probably benign |
Het |
Slc6a21 |
T |
A |
7: 44,935,883 (GRCm39) |
I38N |
possibly damaging |
Het |
Sucla2 |
C |
T |
14: 73,816,913 (GRCm39) |
Q218* |
probably null |
Het |
Tbc1d14 |
A |
T |
5: 36,665,019 (GRCm39) |
L237* |
probably null |
Het |
Trpm7 |
C |
T |
2: 126,639,863 (GRCm39) |
E1578K |
probably damaging |
Het |
Ttc17 |
G |
A |
2: 94,161,012 (GRCm39) |
T896I |
probably damaging |
Het |
Virma |
A |
G |
4: 11,513,163 (GRCm39) |
D339G |
possibly damaging |
Het |
Vmn2r54 |
T |
A |
7: 12,349,533 (GRCm39) |
Y683F |
probably benign |
Het |
Xrra1 |
T |
A |
7: 99,563,411 (GRCm39) |
L466Q |
probably damaging |
Het |
|
Other mutations in Gzmg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02323:Gzmg
|
APN |
14 |
56,394,729 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02633:Gzmg
|
APN |
14 |
56,394,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R0456:Gzmg
|
UTSW |
14 |
56,395,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R1368:Gzmg
|
UTSW |
14 |
56,395,263 (GRCm39) |
missense |
probably benign |
0.41 |
R1663:Gzmg
|
UTSW |
14 |
56,394,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Gzmg
|
UTSW |
14 |
56,395,832 (GRCm39) |
missense |
probably benign |
0.00 |
R3691:Gzmg
|
UTSW |
14 |
56,395,134 (GRCm39) |
splice site |
probably benign |
|
R4509:Gzmg
|
UTSW |
14 |
56,394,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Gzmg
|
UTSW |
14 |
56,394,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Gzmg
|
UTSW |
14 |
56,396,979 (GRCm39) |
start codon destroyed |
probably null |
|
R7502:Gzmg
|
UTSW |
14 |
56,394,284 (GRCm39) |
missense |
not run |
|
R8022:Gzmg
|
UTSW |
14 |
56,394,903 (GRCm39) |
missense |
probably benign |
0.15 |
R8255:Gzmg
|
UTSW |
14 |
56,395,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Gzmg
|
UTSW |
14 |
56,394,193 (GRCm39) |
missense |
probably benign |
0.01 |
R8774-TAIL:Gzmg
|
UTSW |
14 |
56,394,193 (GRCm39) |
missense |
probably benign |
0.01 |
R8949:Gzmg
|
UTSW |
14 |
56,396,926 (GRCm39) |
critical splice donor site |
probably null |
|
R9187:Gzmg
|
UTSW |
14 |
56,394,714 (GRCm39) |
missense |
probably benign |
0.00 |
R9422:Gzmg
|
UTSW |
14 |
56,395,812 (GRCm39) |
missense |
probably benign |
|
|