Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adh1 |
G |
A |
3: 137,992,672 (GRCm39) |
V263M |
probably damaging |
Het |
Akap13 |
T |
A |
7: 75,375,096 (GRCm39) |
H1909Q |
probably benign |
Het |
Atg2b |
C |
T |
12: 105,588,403 (GRCm39) |
A1936T |
probably damaging |
Het |
Atp8b3 |
G |
T |
10: 80,360,210 (GRCm39) |
L954M |
probably damaging |
Het |
C8a |
T |
C |
4: 104,713,617 (GRCm39) |
Y171C |
probably damaging |
Het |
Cd6 |
A |
G |
19: 10,768,466 (GRCm39) |
S508P |
probably benign |
Het |
Cdk4 |
A |
G |
10: 126,900,492 (GRCm39) |
D86G |
possibly damaging |
Het |
Cdr2l |
G |
T |
11: 115,281,796 (GRCm39) |
R100S |
probably benign |
Het |
Cndp1 |
T |
A |
18: 84,640,357 (GRCm39) |
T283S |
probably benign |
Het |
Cr2 |
T |
C |
1: 194,823,529 (GRCm39) |
Y1023C |
probably null |
Het |
Csmd3 |
A |
G |
15: 47,713,181 (GRCm39) |
F1494L |
probably benign |
Het |
Eeig2 |
A |
G |
3: 108,887,101 (GRCm39) |
V299A |
possibly damaging |
Het |
Eng |
G |
T |
2: 32,562,394 (GRCm39) |
G231W |
probably benign |
Het |
Erp44 |
A |
G |
4: 48,218,126 (GRCm39) |
V181A |
probably benign |
Het |
Fkbp15 |
A |
G |
4: 62,241,487 (GRCm39) |
S553P |
probably damaging |
Het |
Glg1 |
A |
G |
8: 111,909,205 (GRCm39) |
V495A |
probably damaging |
Het |
Gm9631 |
A |
T |
11: 121,836,454 (GRCm39) |
D28E |
possibly damaging |
Het |
Gnptab |
G |
T |
10: 88,268,927 (GRCm39) |
L543F |
probably damaging |
Het |
H4c3 |
A |
T |
13: 23,882,353 (GRCm39) |
I27N |
probably damaging |
Het |
Khdrbs2 |
T |
G |
1: 32,696,558 (GRCm39) |
L329R |
possibly damaging |
Het |
Kidins220 |
C |
A |
12: 25,088,498 (GRCm39) |
H1080Q |
probably damaging |
Het |
Maml1 |
G |
A |
11: 50,156,715 (GRCm39) |
P487S |
probably benign |
Het |
Me1 |
C |
T |
9: 86,480,771 (GRCm39) |
|
probably null |
Het |
Morc2a |
C |
T |
11: 3,631,775 (GRCm39) |
R569C |
probably benign |
Het |
Mrc1 |
A |
G |
2: 14,271,335 (GRCm39) |
Q413R |
probably damaging |
Het |
Mrgprx1 |
A |
T |
7: 47,671,517 (GRCm39) |
C77S |
probably benign |
Het |
Mtarc2 |
T |
C |
1: 184,566,048 (GRCm39) |
|
probably benign |
Het |
Myo1d |
A |
T |
11: 80,575,147 (GRCm39) |
|
probably benign |
Het |
Nr4a1 |
T |
G |
15: 101,171,940 (GRCm39) |
L538R |
probably damaging |
Het |
Olfm1 |
T |
C |
2: 28,119,564 (GRCm39) |
Y385H |
probably damaging |
Het |
Or4a39 |
A |
T |
2: 89,236,675 (GRCm39) |
F249L |
possibly damaging |
Het |
Or5m9 |
A |
G |
2: 85,877,627 (GRCm39) |
E267G |
probably damaging |
Het |
Pkd1 |
T |
A |
17: 24,795,148 (GRCm39) |
Y2278* |
probably null |
Het |
Prkdc |
G |
T |
16: 15,647,556 (GRCm39) |
C3660F |
probably benign |
Het |
Ptpn11 |
T |
C |
5: 121,281,199 (GRCm39) |
D493G |
probably damaging |
Het |
Rad23b |
T |
A |
4: 55,383,601 (GRCm39) |
F278I |
possibly damaging |
Het |
Saxo2 |
T |
C |
7: 82,297,613 (GRCm39) |
I9V |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,582,604 (GRCm39) |
I98V |
probably benign |
Het |
Serac1 |
T |
A |
17: 6,124,528 (GRCm39) |
|
probably benign |
Het |
Simc1 |
T |
C |
13: 54,672,473 (GRCm39) |
C274R |
probably benign |
Het |
Sirt3 |
A |
G |
7: 140,444,006 (GRCm39) |
|
probably benign |
Het |
Tctn3 |
A |
G |
19: 40,585,880 (GRCm39) |
L555P |
probably damaging |
Het |
Ttc14 |
A |
G |
3: 33,855,507 (GRCm39) |
I151V |
probably benign |
Het |
Ush2a |
T |
A |
1: 187,995,518 (GRCm39) |
Y96* |
probably null |
Het |
Usp42 |
T |
C |
5: 143,706,970 (GRCm39) |
T270A |
possibly damaging |
Het |
Vmn1r31 |
A |
G |
6: 58,449,784 (GRCm39) |
I27T |
probably benign |
Het |
Vmn2r93 |
G |
A |
17: 18,536,906 (GRCm39) |
A530T |
possibly 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 |
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 |
|
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 |
|