Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AAdacl4fm3 |
G |
A |
4: 144,429,969 (GRCm39) |
T340I |
possibly damaging |
Het |
Acot10 |
A |
T |
15: 20,665,883 (GRCm39) |
V286E |
possibly damaging |
Het |
Bpifa6 |
T |
C |
2: 153,831,130 (GRCm39) |
L232P |
probably damaging |
Het |
Calr4 |
A |
G |
4: 109,096,134 (GRCm39) |
N104S |
possibly damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,921,510 (GRCm39) |
E550G |
possibly damaging |
Het |
Cfhr4 |
G |
A |
1: 139,629,668 (GRCm39) |
T712I |
probably damaging |
Het |
D3Ertd751e |
T |
A |
3: 41,708,287 (GRCm39) |
N141K |
probably benign |
Het |
Emilin2 |
A |
G |
17: 71,587,851 (GRCm39) |
|
probably benign |
Het |
Eml6 |
T |
C |
11: 29,734,236 (GRCm39) |
E1168G |
possibly damaging |
Het |
Fbxo48 |
T |
C |
11: 16,903,659 (GRCm39) |
I95T |
probably benign |
Het |
Fpr3 |
A |
T |
17: 18,190,953 (GRCm39) |
T75S |
probably benign |
Het |
Gm5145 |
A |
G |
17: 20,791,452 (GRCm39) |
K277E |
probably damaging |
Het |
Gnao1 |
A |
G |
8: 94,677,067 (GRCm39) |
|
probably benign |
Het |
Krt8 |
G |
A |
15: 101,907,367 (GRCm39) |
R239C |
probably benign |
Het |
Lrrc17 |
A |
T |
5: 21,766,078 (GRCm39) |
N187Y |
probably damaging |
Het |
Neil1 |
C |
T |
9: 57,052,263 (GRCm39) |
R195H |
probably damaging |
Het |
Nr2f1 |
C |
A |
13: 78,343,275 (GRCm39) |
|
probably benign |
Het |
Pi4ka |
C |
A |
16: 17,135,217 (GRCm39) |
G946W |
probably damaging |
Het |
Rad54l |
A |
G |
4: 115,962,994 (GRCm39) |
Y335H |
probably damaging |
Het |
Rgsl1 |
C |
T |
1: 153,675,684 (GRCm39) |
R159H |
probably damaging |
Het |
Scn11a |
T |
C |
9: 119,634,750 (GRCm39) |
D357G |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Timeless |
A |
G |
10: 128,075,785 (GRCm39) |
M6V |
probably damaging |
Het |
Vps16 |
T |
C |
2: 130,281,636 (GRCm39) |
|
probably null |
Het |
Zfp955b |
C |
A |
17: 33,519,624 (GRCm39) |
Q31K |
probably damaging |
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 |
|
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 |
|
R5555:Plcg2
|
UTSW |
8 |
118,339,734 (GRCm39) |
nonsense |
probably null |
|
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 |
|