Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
T |
13: 61,001,320 (GRCm39) |
|
probably benign |
Het |
Abcg3 |
A |
G |
5: 105,125,482 (GRCm39) |
I67T |
probably damaging |
Het |
Adam10 |
T |
A |
9: 70,655,530 (GRCm39) |
W333R |
probably damaging |
Het |
Ahnak |
C |
T |
19: 8,995,596 (GRCm39) |
R5627* |
probably null |
Het |
AI606181 |
A |
C |
19: 41,582,170 (GRCm39) |
K113N |
unknown |
Het |
Alms1 |
A |
T |
6: 85,597,351 (GRCm39) |
R1195* |
probably null |
Het |
Ankrd11 |
T |
C |
8: 123,618,914 (GRCm39) |
D1646G |
possibly damaging |
Het |
Ap2m1 |
T |
A |
16: 20,360,990 (GRCm39) |
I334N |
possibly damaging |
Het |
Arpc1b |
T |
A |
5: 145,064,525 (GRCm39) |
W361R |
probably damaging |
Het |
Baiap2l1 |
T |
C |
5: 144,212,701 (GRCm39) |
Y438C |
probably damaging |
Het |
Brd8dc |
A |
T |
18: 34,729,204 (GRCm39) |
D42E |
probably damaging |
Het |
Ccdc110 |
T |
A |
8: 46,388,194 (GRCm39) |
N50K |
probably benign |
Het |
Ccdc168 |
C |
A |
1: 44,098,384 (GRCm39) |
V905F |
probably benign |
Het |
Cdhr1 |
T |
C |
14: 36,802,633 (GRCm39) |
Y610C |
probably damaging |
Het |
Celsr3 |
G |
A |
9: 108,704,204 (GRCm39) |
C229Y |
possibly damaging |
Het |
Clca4b |
A |
T |
3: 144,619,112 (GRCm39) |
Y676N |
probably damaging |
Het |
Cntln |
C |
T |
4: 85,014,994 (GRCm39) |
T1095I |
probably damaging |
Het |
Cog2 |
T |
C |
8: 125,255,797 (GRCm39) |
|
probably null |
Het |
Col11a1 |
A |
T |
3: 113,899,105 (GRCm39) |
|
probably benign |
Het |
Cpe |
T |
A |
8: 65,064,501 (GRCm39) |
I233F |
probably damaging |
Het |
Dcaf11 |
T |
C |
14: 55,806,537 (GRCm39) |
V446A |
probably damaging |
Het |
Defa34 |
A |
G |
8: 22,155,988 (GRCm39) |
|
probably null |
Het |
Dnah12 |
A |
G |
14: 26,520,856 (GRCm39) |
R1892G |
probably damaging |
Het |
Dock4 |
A |
G |
12: 40,671,311 (GRCm39) |
|
probably benign |
Het |
Dync1h1 |
C |
A |
12: 110,606,378 (GRCm39) |
Q2483K |
probably benign |
Het |
Enpp3 |
A |
T |
10: 24,652,679 (GRCm39) |
D759E |
probably damaging |
Het |
Epyc |
A |
G |
10: 97,485,625 (GRCm39) |
T22A |
probably benign |
Het |
Fam227b |
T |
A |
2: 125,942,841 (GRCm39) |
S319C |
probably damaging |
Het |
Fam83a |
C |
A |
15: 57,873,322 (GRCm39) |
Q384K |
probably benign |
Het |
Fam83b |
G |
T |
9: 76,400,108 (GRCm39) |
L332I |
possibly damaging |
Het |
Gal3st2c |
C |
T |
1: 93,937,219 (GRCm39) |
P388L |
probably benign |
Het |
Ggn |
C |
T |
7: 28,870,721 (GRCm39) |
P47S |
probably damaging |
Het |
Gli3 |
T |
G |
13: 15,899,370 (GRCm39) |
L919R |
probably damaging |
Het |
Gm5134 |
C |
A |
10: 75,810,079 (GRCm39) |
T120N |
probably benign |
Het |
Gmip |
C |
T |
8: 70,268,259 (GRCm39) |
|
probably benign |
Het |
Gpr39 |
C |
T |
1: 125,605,237 (GRCm39) |
T55M |
probably damaging |
Het |
Grk4 |
A |
G |
5: 34,873,557 (GRCm39) |
T208A |
probably damaging |
Het |
Gsdme |
C |
A |
6: 50,223,107 (GRCm39) |
|
probably benign |
Het |
Gucy2e |
T |
C |
11: 69,126,402 (GRCm39) |
D326G |
probably benign |
Het |
Hadhb |
T |
C |
5: 30,374,483 (GRCm39) |
|
probably benign |
Het |
Hectd4 |
T |
A |
5: 121,419,959 (GRCm39) |
Y635N |
possibly damaging |
Het |
Hectd4 |
G |
A |
5: 121,443,736 (GRCm39) |
E1319K |
possibly damaging |
Het |
Ikbkb |
A |
T |
8: 23,161,651 (GRCm39) |
C412* |
probably null |
Het |
Itpa |
A |
T |
2: 130,521,338 (GRCm39) |
|
probably benign |
Het |
Klhl10 |
A |
G |
11: 100,347,758 (GRCm39) |
T605A |
probably benign |
Het |
Krt74 |
T |
C |
15: 101,671,751 (GRCm39) |
|
noncoding transcript |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Lap3 |
T |
C |
5: 45,652,632 (GRCm39) |
|
probably benign |
Het |
Lrrc10 |
T |
A |
10: 116,881,695 (GRCm39) |
L123Q |
probably damaging |
Het |
Map3k6 |
T |
C |
4: 132,971,105 (GRCm39) |
L273P |
probably damaging |
Het |
Mbl1 |
A |
G |
14: 40,880,706 (GRCm39) |
N198S |
probably damaging |
Het |
Mcf2l |
A |
G |
8: 13,047,337 (GRCm39) |
D233G |
probably damaging |
Het |
Mdga2 |
T |
C |
12: 66,517,700 (GRCm39) |
K45E |
possibly damaging |
Het |
Mdn1 |
A |
G |
4: 32,738,619 (GRCm39) |
N3524S |
probably benign |
Het |
Mrc1 |
T |
A |
2: 14,243,353 (GRCm39) |
|
probably benign |
Het |
Msto1 |
A |
G |
3: 88,818,848 (GRCm39) |
L269P |
probably benign |
Het |
Mtcl1 |
C |
T |
17: 66,665,109 (GRCm39) |
E1149K |
possibly damaging |
Het |
Naca |
C |
T |
10: 127,880,659 (GRCm39) |
A1897V |
probably benign |
Het |
Ncapg |
T |
C |
5: 45,850,489 (GRCm39) |
|
probably benign |
Het |
Neb |
A |
T |
2: 52,180,755 (GRCm39) |
|
probably benign |
Het |
Or5p5 |
T |
C |
7: 107,413,895 (GRCm39) |
Y35H |
probably damaging |
Het |
Or8b12i |
T |
C |
9: 20,082,561 (GRCm39) |
Y102C |
probably benign |
Het |
Or8g27 |
G |
A |
9: 39,129,024 (GRCm39) |
V124I |
possibly damaging |
Het |
Parp2 |
T |
A |
14: 51,057,130 (GRCm39) |
Y361N |
probably damaging |
Het |
Parp3 |
A |
G |
9: 106,348,995 (GRCm39) |
F466L |
possibly damaging |
Het |
Pcdh15 |
A |
T |
10: 74,126,808 (GRCm39) |
N296Y |
probably damaging |
Het |
Pcf11 |
G |
A |
7: 92,307,039 (GRCm39) |
P1043L |
probably damaging |
Het |
Pdzrn3 |
A |
T |
6: 101,128,014 (GRCm39) |
I884N |
probably damaging |
Het |
Phf24 |
G |
T |
4: 42,933,761 (GRCm39) |
V48L |
possibly damaging |
Het |
Plcl2 |
T |
C |
17: 50,915,010 (GRCm39) |
L673P |
probably damaging |
Het |
Ppp1r3c |
A |
T |
19: 36,711,617 (GRCm39) |
F51Y |
possibly damaging |
Het |
Prmt1 |
A |
G |
7: 44,628,225 (GRCm39) |
|
probably benign |
Het |
Proc |
G |
A |
18: 32,258,171 (GRCm39) |
T258I |
probably benign |
Het |
Prom2 |
T |
G |
2: 127,373,033 (GRCm39) |
S679R |
possibly damaging |
Het |
Psen2 |
T |
C |
1: 180,066,479 (GRCm39) |
T153A |
probably damaging |
Het |
Rem2 |
T |
C |
14: 54,713,754 (GRCm39) |
|
probably benign |
Het |
Rin2 |
A |
G |
2: 145,702,953 (GRCm39) |
K550E |
probably benign |
Het |
Rtn4 |
T |
A |
11: 29,683,849 (GRCm39) |
|
probably benign |
Het |
Semp2l1 |
T |
A |
1: 32,584,956 (GRCm39) |
N318I |
possibly damaging |
Het |
Ssh1 |
A |
T |
5: 114,084,766 (GRCm39) |
D448E |
probably benign |
Het |
Ssmem1 |
A |
T |
6: 30,519,547 (GRCm39) |
|
probably null |
Het |
Stam2 |
A |
T |
2: 52,609,998 (GRCm39) |
|
probably benign |
Het |
Syne1 |
A |
G |
10: 5,317,600 (GRCm39) |
L498P |
probably damaging |
Het |
Syne2 |
AGAGTGAG |
AGAGTGAGTGAG |
12: 76,144,734 (GRCm39) |
|
probably null |
Het |
Taf6l |
G |
T |
19: 8,755,885 (GRCm39) |
H254Q |
probably benign |
Het |
Tas2r123 |
T |
C |
6: 132,824,295 (GRCm39) |
V64A |
probably benign |
Het |
Tnnc1 |
A |
G |
14: 30,933,365 (GRCm39) |
D149G |
probably damaging |
Het |
Tpp2 |
A |
G |
1: 44,038,853 (GRCm39) |
D1133G |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 44,017,664 (GRCm39) |
V756E |
probably benign |
Het |
Traf3ip3 |
T |
A |
1: 192,860,539 (GRCm39) |
|
probably null |
Het |
Tsen15 |
A |
G |
1: 152,247,548 (GRCm39) |
V148A |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,694,672 (GRCm39) |
|
probably benign |
Het |
Ube2u |
A |
G |
4: 100,343,870 (GRCm39) |
I90V |
probably benign |
Het |
Unc79 |
T |
A |
12: 103,045,329 (GRCm39) |
|
probably null |
Het |
Usp47 |
T |
C |
7: 111,655,787 (GRCm39) |
S155P |
possibly damaging |
Het |
Wdr41 |
T |
C |
13: 95,154,619 (GRCm39) |
|
probably benign |
Het |
Zfp217 |
C |
T |
2: 169,957,382 (GRCm39) |
A539T |
probably benign |
Het |
Zfp423 |
A |
G |
8: 88,508,887 (GRCm39) |
S486P |
possibly damaging |
Het |
Zfp628 |
A |
T |
7: 4,922,732 (GRCm39) |
Q318L |
probably benign |
Het |
|
Other mutations in Pla2g4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00660:Pla2g4a
|
APN |
1 |
149,761,954 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00763:Pla2g4a
|
APN |
1 |
149,727,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01548:Pla2g4a
|
APN |
1 |
149,808,407 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01683:Pla2g4a
|
APN |
1 |
149,733,405 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01903:Pla2g4a
|
APN |
1 |
149,716,370 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02049:Pla2g4a
|
APN |
1 |
149,736,847 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02103:Pla2g4a
|
APN |
1 |
149,776,950 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03132:Pla2g4a
|
APN |
1 |
149,778,035 (GRCm39) |
splice site |
probably benign |
|
IGL03299:Pla2g4a
|
APN |
1 |
149,727,118 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03302:Pla2g4a
|
APN |
1 |
149,740,698 (GRCm39) |
missense |
probably benign |
0.00 |
R0469:Pla2g4a
|
UTSW |
1 |
149,716,398 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0488:Pla2g4a
|
UTSW |
1 |
149,747,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Pla2g4a
|
UTSW |
1 |
149,716,455 (GRCm39) |
missense |
probably benign |
0.44 |
R1468:Pla2g4a
|
UTSW |
1 |
149,763,344 (GRCm39) |
splice site |
probably benign |
|
R1470:Pla2g4a
|
UTSW |
1 |
149,716,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Pla2g4a
|
UTSW |
1 |
149,716,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R1521:Pla2g4a
|
UTSW |
1 |
149,733,437 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1718:Pla2g4a
|
UTSW |
1 |
149,747,274 (GRCm39) |
splice site |
probably benign |
|
R1778:Pla2g4a
|
UTSW |
1 |
149,778,196 (GRCm39) |
splice site |
probably benign |
|
R1967:Pla2g4a
|
UTSW |
1 |
149,797,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R2063:Pla2g4a
|
UTSW |
1 |
149,716,427 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2291:Pla2g4a
|
UTSW |
1 |
149,776,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R3855:Pla2g4a
|
UTSW |
1 |
149,705,928 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4512:Pla2g4a
|
UTSW |
1 |
149,736,802 (GRCm39) |
splice site |
probably null |
|
R4568:Pla2g4a
|
UTSW |
1 |
149,717,977 (GRCm39) |
missense |
probably benign |
0.43 |
R5266:Pla2g4a
|
UTSW |
1 |
149,740,918 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5855:Pla2g4a
|
UTSW |
1 |
149,755,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R5897:Pla2g4a
|
UTSW |
1 |
149,740,899 (GRCm39) |
missense |
probably damaging |
0.99 |
R6012:Pla2g4a
|
UTSW |
1 |
149,808,428 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6193:Pla2g4a
|
UTSW |
1 |
149,778,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6246:Pla2g4a
|
UTSW |
1 |
149,748,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6248:Pla2g4a
|
UTSW |
1 |
149,748,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Pla2g4a
|
UTSW |
1 |
149,733,238 (GRCm39) |
missense |
probably benign |
0.00 |
R6260:Pla2g4a
|
UTSW |
1 |
149,733,238 (GRCm39) |
missense |
probably benign |
0.00 |
R6293:Pla2g4a
|
UTSW |
1 |
149,755,798 (GRCm39) |
missense |
probably damaging |
0.98 |
R6310:Pla2g4a
|
UTSW |
1 |
149,717,977 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6490:Pla2g4a
|
UTSW |
1 |
149,727,086 (GRCm39) |
nonsense |
probably null |
|
R6502:Pla2g4a
|
UTSW |
1 |
149,748,367 (GRCm39) |
nonsense |
probably null |
|
R6614:Pla2g4a
|
UTSW |
1 |
149,717,986 (GRCm39) |
missense |
probably benign |
0.07 |
R6671:Pla2g4a
|
UTSW |
1 |
149,763,382 (GRCm39) |
missense |
probably benign |
|
R6745:Pla2g4a
|
UTSW |
1 |
149,761,981 (GRCm39) |
missense |
probably benign |
0.07 |
R6880:Pla2g4a
|
UTSW |
1 |
149,727,202 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7058:Pla2g4a
|
UTSW |
1 |
149,727,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7163:Pla2g4a
|
UTSW |
1 |
149,716,416 (GRCm39) |
nonsense |
probably null |
|
R7422:Pla2g4a
|
UTSW |
1 |
149,808,438 (GRCm39) |
missense |
probably benign |
0.32 |
R7454:Pla2g4a
|
UTSW |
1 |
149,748,441 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7474:Pla2g4a
|
UTSW |
1 |
149,740,951 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7514:Pla2g4a
|
UTSW |
1 |
149,727,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7536:Pla2g4a
|
UTSW |
1 |
149,755,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Pla2g4a
|
UTSW |
1 |
149,762,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R7744:Pla2g4a
|
UTSW |
1 |
149,736,853 (GRCm39) |
missense |
probably benign |
0.06 |
R7766:Pla2g4a
|
UTSW |
1 |
149,736,809 (GRCm39) |
missense |
probably benign |
0.00 |
R7783:Pla2g4a
|
UTSW |
1 |
149,748,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8031:Pla2g4a
|
UTSW |
1 |
149,776,964 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8145:Pla2g4a
|
UTSW |
1 |
149,716,394 (GRCm39) |
missense |
probably benign |
0.42 |
R8189:Pla2g4a
|
UTSW |
1 |
149,733,337 (GRCm39) |
missense |
probably benign |
0.04 |
R8252:Pla2g4a
|
UTSW |
1 |
149,727,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8315:Pla2g4a
|
UTSW |
1 |
149,761,965 (GRCm39) |
missense |
probably benign |
0.02 |
R8762:Pla2g4a
|
UTSW |
1 |
149,761,935 (GRCm39) |
missense |
probably benign |
0.00 |
R8783:Pla2g4a
|
UTSW |
1 |
149,740,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8838:Pla2g4a
|
UTSW |
1 |
149,747,256 (GRCm39) |
missense |
probably benign |
0.00 |
R9132:Pla2g4a
|
UTSW |
1 |
149,747,230 (GRCm39) |
missense |
probably benign |
0.01 |
R9282:Pla2g4a
|
UTSW |
1 |
149,747,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R9412:Pla2g4a
|
UTSW |
1 |
149,755,772 (GRCm39) |
missense |
probably damaging |
0.99 |
X0021:Pla2g4a
|
UTSW |
1 |
149,740,677 (GRCm39) |
missense |
possibly damaging |
0.66 |
Z1177:Pla2g4a
|
UTSW |
1 |
149,747,185 (GRCm39) |
missense |
probably damaging |
1.00 |
|