Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atg7 |
T |
C |
6: 114,679,014 (GRCm39) |
V366A |
probably damaging |
Het |
Cadm2 |
A |
T |
16: 66,581,702 (GRCm39) |
V192E |
probably damaging |
Het |
Chil6 |
C |
T |
3: 106,297,268 (GRCm39) |
S291N |
possibly damaging |
Het |
D7Ertd443e |
T |
C |
7: 133,951,320 (GRCm39) |
T118A |
probably benign |
Het |
Dennd4b |
G |
A |
3: 90,175,675 (GRCm39) |
R148Q |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 31,012,776 (GRCm39) |
T1837S |
probably damaging |
Het |
Elapor2 |
T |
A |
5: 9,472,296 (GRCm39) |
|
probably null |
Het |
Ext1 |
A |
G |
15: 52,951,539 (GRCm39) |
V515A |
probably damaging |
Het |
Fer1l4 |
T |
C |
2: 155,890,109 (GRCm39) |
E272G |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,825,236 (GRCm39) |
H1475Q |
probably benign |
Het |
Grid1 |
T |
C |
14: 35,242,662 (GRCm39) |
S672P |
possibly damaging |
Het |
Gtpbp4 |
A |
G |
13: 9,029,463 (GRCm39) |
|
probably null |
Het |
Hsp90aa1 |
A |
T |
12: 110,659,168 (GRCm39) |
V543E |
probably damaging |
Het |
Irf5 |
T |
C |
6: 29,531,145 (GRCm39) |
S4P |
probably benign |
Het |
Kif2b |
G |
T |
11: 91,466,286 (GRCm39) |
Q666K |
probably benign |
Het |
Macc1 |
A |
T |
12: 119,414,110 (GRCm39) |
H762L |
probably benign |
Het |
Map1s |
C |
T |
8: 71,369,751 (GRCm39) |
T941M |
probably damaging |
Het |
Mrgprb1 |
T |
A |
7: 48,097,523 (GRCm39) |
I130F |
probably benign |
Het |
Nbeal1 |
T |
G |
1: 60,276,311 (GRCm39) |
V684G |
possibly damaging |
Het |
Ngly1 |
C |
T |
14: 16,270,508 (GRCm38) |
Q173* |
probably null |
Het |
Plcb3 |
A |
T |
19: 6,943,587 (GRCm39) |
M104K |
probably benign |
Het |
Ptprf |
T |
C |
4: 118,082,121 (GRCm39) |
Y1039C |
probably damaging |
Het |
Rab38 |
A |
G |
7: 88,079,695 (GRCm39) |
Y29C |
probably damaging |
Het |
Rcan2 |
T |
A |
17: 44,347,921 (GRCm39) |
V210E |
probably damaging |
Het |
Rptn |
A |
T |
3: 93,304,008 (GRCm39) |
Q447L |
probably benign |
Het |
Scel |
G |
A |
14: 103,839,642 (GRCm39) |
R495K |
probably benign |
Het |
Scn11a |
G |
T |
9: 119,584,304 (GRCm39) |
P1437Q |
probably damaging |
Het |
Sim2 |
A |
G |
16: 93,910,315 (GRCm39) |
D239G |
probably damaging |
Het |
Skap2 |
A |
G |
6: 51,836,998 (GRCm39) |
Y356H |
probably damaging |
Het |
Skint11 |
A |
G |
4: 114,051,798 (GRCm39) |
T49A |
probably benign |
Het |
Snx33 |
G |
A |
9: 56,832,681 (GRCm39) |
H463Y |
probably benign |
Het |
Steap2 |
T |
C |
5: 5,727,544 (GRCm39) |
T264A |
possibly damaging |
Het |
Stk40 |
T |
A |
4: 126,028,852 (GRCm39) |
V238E |
probably damaging |
Het |
Sun2 |
T |
C |
15: 79,618,328 (GRCm39) |
D277G |
probably benign |
Het |
Ttll9 |
T |
C |
2: 152,832,020 (GRCm39) |
|
probably null |
Het |
Vmn1r54 |
G |
A |
6: 90,246,347 (GRCm39) |
C87Y |
probably benign |
Het |
|
Other mutations in Plcg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00594:Plcg2
|
APN |
8 |
118,282,810 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00911:Plcg2
|
APN |
8 |
118,313,254 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00952:Plcg2
|
APN |
8 |
118,333,956 (GRCm39) |
missense |
probably benign |
|
IGL01115:Plcg2
|
APN |
8 |
118,284,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01326:Plcg2
|
APN |
8 |
118,300,738 (GRCm39) |
splice site |
probably benign |
|
IGL01357:Plcg2
|
APN |
8 |
118,340,900 (GRCm39) |
splice site |
probably benign |
|
IGL01705:Plcg2
|
APN |
8 |
118,308,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01755:Plcg2
|
APN |
8 |
118,347,980 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01828:Plcg2
|
APN |
8 |
118,316,972 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Plcg2
|
APN |
8 |
118,306,635 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02345:Plcg2
|
APN |
8 |
118,311,919 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02448:Plcg2
|
APN |
8 |
118,333,960 (GRCm39) |
missense |
probably benign |
|
IGL02587:Plcg2
|
APN |
8 |
118,284,852 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02646:Plcg2
|
APN |
8 |
118,330,622 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03409:Plcg2
|
APN |
8 |
118,310,234 (GRCm39) |
missense |
probably damaging |
0.96 |
Ctenophore
|
UTSW |
8 |
118,284,057 (GRCm39) |
missense |
probably damaging |
0.98 |
Porifera
|
UTSW |
8 |
118,306,585 (GRCm39) |
missense |
possibly damaging |
0.79 |
Poseidon
|
UTSW |
8 |
118,341,977 (GRCm39) |
missense |
probably damaging |
1.00 |
Poseidon2
|
UTSW |
8 |
118,304,613 (GRCm39) |
missense |
possibly damaging |
0.80 |
queen
|
UTSW |
8 |
118,308,446 (GRCm39) |
missense |
probably benign |
0.00 |
Seahorse
|
UTSW |
8 |
118,316,574 (GRCm39) |
splice site |
probably null |
|
Teleost
|
UTSW |
8 |
118,310,288 (GRCm39) |
missense |
probably damaging |
1.00 |
Theseus
|
UTSW |
8 |
118,323,071 (GRCm39) |
missense |
probably damaging |
0.99 |
trident
|
UTSW |
8 |
118,339,717 (GRCm39) |
missense |
probably benign |
0.00 |
R0172:Plcg2
|
UTSW |
8 |
118,306,521 (GRCm39) |
missense |
probably benign |
0.00 |
R0194:Plcg2
|
UTSW |
8 |
118,300,136 (GRCm39) |
splice site |
probably benign |
|
R0410:Plcg2
|
UTSW |
8 |
118,342,112 (GRCm39) |
missense |
probably damaging |
0.98 |
R0462:Plcg2
|
UTSW |
8 |
118,312,044 (GRCm39) |
missense |
probably benign |
0.06 |
R0494:Plcg2
|
UTSW |
8 |
118,282,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R0522:Plcg2
|
UTSW |
8 |
118,341,027 (GRCm39) |
splice site |
probably null |
|
R0612:Plcg2
|
UTSW |
8 |
118,300,104 (GRCm39) |
missense |
probably benign |
0.01 |
R1239:Plcg2
|
UTSW |
8 |
118,282,783 (GRCm39) |
missense |
probably benign |
|
R1367:Plcg2
|
UTSW |
8 |
118,341,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Plcg2
|
UTSW |
8 |
118,340,974 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1756:Plcg2
|
UTSW |
8 |
118,319,447 (GRCm39) |
missense |
probably benign |
0.02 |
R2176:Plcg2
|
UTSW |
8 |
118,339,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R3500:Plcg2
|
UTSW |
8 |
118,339,717 (GRCm39) |
missense |
probably benign |
0.00 |
R4043:Plcg2
|
UTSW |
8 |
118,339,717 (GRCm39) |
missense |
probably benign |
0.00 |
R4654:Plcg2
|
UTSW |
8 |
118,231,054 (GRCm39) |
missense |
probably benign |
|
R4883:Plcg2
|
UTSW |
8 |
118,333,872 (GRCm39) |
nonsense |
probably null |
|
R4932:Plcg2
|
UTSW |
8 |
118,333,822 (GRCm39) |
missense |
probably benign |
0.05 |
R5080:Plcg2
|
UTSW |
8 |
118,316,742 (GRCm39) |
missense |
probably benign |
0.10 |
R5226:Plcg2
|
UTSW |
8 |
118,304,613 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5264:Plcg2
|
UTSW |
8 |
118,361,532 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5298:Plcg2
|
UTSW |
8 |
118,331,988 (GRCm39) |
missense |
probably benign |
|
R5473:Plcg2
|
UTSW |
8 |
118,361,140 (GRCm39) |
missense |
probably benign |
|
R5557:Plcg2
|
UTSW |
8 |
118,313,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R5805:Plcg2
|
UTSW |
8 |
118,325,234 (GRCm39) |
critical splice donor site |
probably null |
|
R5826:Plcg2
|
UTSW |
8 |
118,337,583 (GRCm39) |
missense |
probably benign |
0.19 |
R5871:Plcg2
|
UTSW |
8 |
118,230,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Plcg2
|
UTSW |
8 |
118,231,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R6142:Plcg2
|
UTSW |
8 |
118,312,010 (GRCm39) |
missense |
probably benign |
|
R6609:Plcg2
|
UTSW |
8 |
118,294,909 (GRCm39) |
missense |
probably benign |
0.31 |
R6684:Plcg2
|
UTSW |
8 |
118,323,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R6710:Plcg2
|
UTSW |
8 |
118,284,086 (GRCm39) |
missense |
probably benign |
0.05 |
R6931:Plcg2
|
UTSW |
8 |
118,284,058 (GRCm39) |
missense |
probably benign |
0.24 |
R6946:Plcg2
|
UTSW |
8 |
118,230,929 (GRCm39) |
missense |
probably benign |
|
R7036:Plcg2
|
UTSW |
8 |
118,323,045 (GRCm39) |
missense |
probably benign |
|
R7070:Plcg2
|
UTSW |
8 |
118,323,045 (GRCm39) |
missense |
probably benign |
|
R7072:Plcg2
|
UTSW |
8 |
118,316,574 (GRCm39) |
splice site |
probably null |
|
R7214:Plcg2
|
UTSW |
8 |
118,310,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7351:Plcg2
|
UTSW |
8 |
118,317,049 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7393:Plcg2
|
UTSW |
8 |
118,306,564 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7443:Plcg2
|
UTSW |
8 |
118,231,028 (GRCm39) |
missense |
probably benign |
0.00 |
R7513:Plcg2
|
UTSW |
8 |
118,306,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R7609:Plcg2
|
UTSW |
8 |
118,284,852 (GRCm39) |
missense |
probably benign |
0.01 |
R8134:Plcg2
|
UTSW |
8 |
118,284,057 (GRCm39) |
missense |
probably damaging |
0.98 |
R8399:Plcg2
|
UTSW |
8 |
118,323,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8701:Plcg2
|
UTSW |
8 |
118,308,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Plcg2
|
UTSW |
8 |
118,306,585 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8774-TAIL:Plcg2
|
UTSW |
8 |
118,306,585 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8938:Plcg2
|
UTSW |
8 |
118,231,114 (GRCm39) |
critical splice donor site |
probably null |
|
R9003:Plcg2
|
UTSW |
8 |
118,342,002 (GRCm39) |
missense |
|
|
R9286:Plcg2
|
UTSW |
8 |
118,331,976 (GRCm39) |
missense |
probably benign |
0.19 |
R9318:Plcg2
|
UTSW |
8 |
118,323,107 (GRCm39) |
missense |
probably benign |
|
RF008:Plcg2
|
UTSW |
8 |
118,300,263 (GRCm39) |
splice site |
probably null |
|
X0027:Plcg2
|
UTSW |
8 |
118,282,722 (GRCm39) |
missense |
probably benign |
0.03 |
|