Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
T |
C |
1: 159,902,978 (GRCm39) |
S83P |
possibly damaging |
Het |
Actr10 |
A |
T |
12: 70,999,733 (GRCm39) |
E176D |
probably benign |
Het |
Adcy3 |
G |
A |
12: 4,258,662 (GRCm39) |
|
probably null |
Het |
AI429214 |
T |
A |
8: 37,461,278 (GRCm39) |
I142N |
probably damaging |
Het |
Alox12 |
A |
G |
11: 70,143,936 (GRCm39) |
L148S |
probably damaging |
Het |
Ank3 |
A |
G |
10: 69,809,680 (GRCm39) |
I1147V |
probably benign |
Het |
Apoc2 |
C |
T |
7: 19,407,493 (GRCm39) |
V12I |
probably benign |
Het |
Arap3 |
T |
C |
18: 38,124,407 (GRCm39) |
S311G |
probably benign |
Het |
Arih2 |
G |
T |
9: 108,488,841 (GRCm39) |
H292Q |
probably damaging |
Het |
Cdc14a |
A |
T |
3: 116,101,843 (GRCm39) |
D312E |
probably benign |
Het |
Cdh12 |
T |
G |
15: 21,237,800 (GRCm39) |
W12G |
possibly damaging |
Het |
Cisd2 |
A |
T |
3: 135,114,616 (GRCm39) |
N118K |
probably damaging |
Het |
Cntnap5b |
A |
G |
1: 99,999,827 (GRCm39) |
Q195R |
probably benign |
Het |
Cyp2r1 |
A |
G |
7: 114,161,966 (GRCm39) |
|
probably null |
Het |
Cyp4f37 |
A |
G |
17: 32,848,864 (GRCm39) |
D244G |
possibly damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dido1 |
T |
A |
2: 180,302,048 (GRCm39) |
H1952L |
probably damaging |
Het |
Dnah10 |
T |
A |
5: 124,871,283 (GRCm39) |
|
probably null |
Het |
Dnal4 |
T |
A |
15: 79,646,714 (GRCm39) |
M56L |
probably damaging |
Het |
Emilin2 |
A |
G |
17: 71,581,112 (GRCm39) |
V538A |
probably benign |
Het |
Eps8l2 |
A |
G |
7: 140,922,015 (GRCm39) |
D31G |
probably damaging |
Het |
Erp44 |
A |
T |
4: 48,219,479 (GRCm39) |
L112* |
probably null |
Het |
Etl4 |
C |
T |
2: 20,813,900 (GRCm39) |
T1907I |
possibly damaging |
Het |
Exoc3 |
A |
G |
13: 74,330,400 (GRCm39) |
F510L |
probably benign |
Het |
Fam114a2 |
G |
T |
11: 57,383,942 (GRCm39) |
T324K |
possibly damaging |
Het |
Fer1l4 |
G |
A |
2: 155,888,091 (GRCm39) |
R465C |
probably damaging |
Het |
Frmd4b |
A |
C |
6: 97,436,173 (GRCm39) |
S2R |
probably benign |
Het |
Fscn1 |
A |
T |
5: 142,946,778 (GRCm39) |
D192V |
possibly damaging |
Het |
Gm3486 |
T |
A |
14: 41,206,472 (GRCm39) |
*200C |
probably null |
Het |
Gusb |
A |
T |
5: 130,029,366 (GRCm39) |
H138Q |
probably benign |
Het |
Hdac9 |
A |
T |
12: 34,578,293 (GRCm39) |
M4K |
possibly damaging |
Het |
Hhipl1 |
G |
T |
12: 108,284,964 (GRCm39) |
R439L |
probably benign |
Het |
Hoxd9 |
A |
G |
2: 74,528,980 (GRCm39) |
E194G |
probably benign |
Het |
Itgb1 |
A |
G |
8: 129,448,902 (GRCm39) |
S503G |
possibly damaging |
Het |
Kcnt2 |
T |
A |
1: 140,437,216 (GRCm39) |
C500S |
probably damaging |
Het |
Kdm7a |
G |
A |
6: 39,123,983 (GRCm39) |
S727L |
possibly damaging |
Het |
Klhdc4 |
A |
G |
8: 122,540,507 (GRCm39) |
F92L |
probably damaging |
Het |
Klrb1a |
A |
G |
6: 128,596,137 (GRCm39) |
V62A |
probably damaging |
Het |
Krit1 |
A |
G |
5: 3,863,032 (GRCm39) |
|
probably null |
Het |
Krt40 |
A |
G |
11: 99,432,566 (GRCm39) |
I150T |
possibly damaging |
Het |
Larp4b |
A |
G |
13: 9,208,738 (GRCm39) |
T464A |
probably benign |
Het |
Lrrc52 |
T |
G |
1: 167,293,964 (GRCm39) |
D107A |
probably damaging |
Het |
Mapkap1 |
G |
T |
2: 34,408,692 (GRCm39) |
V35F |
probably damaging |
Het |
Mccc1 |
A |
G |
3: 36,044,313 (GRCm39) |
V171A |
probably damaging |
Het |
Metap1d |
A |
T |
2: 71,346,104 (GRCm39) |
R222* |
probably null |
Het |
Mrgpre |
G |
A |
7: 143,334,603 (GRCm39) |
A300V |
probably benign |
Het |
Mterf1b |
C |
A |
5: 4,246,606 (GRCm39) |
N82K |
probably benign |
Het |
Myh9 |
C |
T |
15: 77,669,422 (GRCm39) |
W533* |
probably null |
Het |
Myom2 |
A |
G |
8: 15,148,472 (GRCm39) |
|
probably null |
Het |
Ncor1 |
G |
A |
11: 62,257,808 (GRCm39) |
P329S |
probably damaging |
Het |
Nr2f1 |
T |
C |
13: 78,344,611 (GRCm39) |
|
probably benign |
Het |
Or10x1 |
T |
G |
1: 174,197,236 (GRCm39) |
V251G |
probably benign |
Het |
Or11a4 |
T |
A |
17: 37,536,451 (GRCm39) |
L145* |
probably null |
Het |
Or2a57 |
C |
T |
6: 43,212,838 (GRCm39) |
Q99* |
probably null |
Het |
Or2w6 |
A |
T |
13: 21,843,244 (GRCm39) |
I83N |
possibly damaging |
Het |
Or52p2 |
T |
C |
7: 102,237,237 (GRCm39) |
T238A |
probably benign |
Het |
Or6c210 |
A |
G |
10: 129,496,532 (GRCm39) |
I286V |
probably benign |
Het |
Or6z1 |
A |
T |
7: 6,504,675 (GRCm39) |
C183* |
probably null |
Het |
Pcdha11 |
T |
C |
18: 37,138,950 (GRCm39) |
L193P |
probably benign |
Het |
Pcdhb20 |
T |
A |
18: 37,639,285 (GRCm39) |
F604I |
probably damaging |
Het |
Pde1a |
T |
C |
2: 79,708,545 (GRCm39) |
H291R |
probably damaging |
Het |
Pfkm |
G |
A |
15: 98,024,260 (GRCm39) |
V423M |
probably damaging |
Het |
Pira1 |
C |
A |
7: 3,739,337 (GRCm39) |
E510D |
probably benign |
Het |
Pkd2l1 |
G |
T |
19: 44,146,108 (GRCm39) |
Q149K |
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,392,955 (GRCm39) |
N1763K |
probably benign |
Het |
Prpf39 |
A |
C |
12: 65,089,528 (GRCm39) |
N89H |
probably damaging |
Het |
Rad54l2 |
A |
G |
9: 106,587,537 (GRCm39) |
F743L |
probably damaging |
Het |
Raver2 |
A |
G |
4: 100,991,320 (GRCm39) |
|
probably null |
Het |
Ric8b |
T |
C |
10: 84,783,709 (GRCm39) |
L189P |
probably damaging |
Het |
Sccpdh |
T |
C |
1: 179,495,957 (GRCm39) |
F13L |
probably benign |
Het |
Scd2 |
T |
C |
19: 44,291,448 (GRCm39) |
F296L |
probably damaging |
Het |
Scg2 |
G |
T |
1: 79,414,023 (GRCm39) |
D233E |
probably benign |
Het |
Sema5b |
C |
A |
16: 35,448,377 (GRCm39) |
|
probably null |
Het |
Skint5 |
A |
T |
4: 113,636,286 (GRCm39) |
V644E |
unknown |
Het |
Slc44a5 |
G |
T |
3: 153,969,678 (GRCm39) |
V612F |
possibly damaging |
Het |
Snd1 |
C |
T |
6: 28,520,234 (GRCm39) |
R107* |
probably null |
Het |
Sun5 |
G |
T |
2: 153,702,589 (GRCm39) |
T189K |
probably damaging |
Het |
Tap1 |
A |
T |
17: 34,412,151 (GRCm39) |
E452V |
probably damaging |
Het |
Tcam1 |
A |
G |
11: 106,173,652 (GRCm39) |
N32S |
probably benign |
Het |
Tep1 |
T |
C |
14: 51,067,715 (GRCm39) |
E2167G |
probably damaging |
Het |
Tm9sf1 |
C |
T |
14: 55,873,827 (GRCm39) |
R557H |
probably damaging |
Het |
Tmem175 |
T |
C |
5: 108,793,821 (GRCm39) |
V317A |
probably damaging |
Het |
Tsga13 |
A |
G |
6: 30,874,139 (GRCm39) |
V231A |
probably benign |
Het |
Tspan12 |
A |
G |
6: 21,799,970 (GRCm39) |
S126P |
probably damaging |
Het |
Uvrag |
G |
T |
7: 98,637,398 (GRCm39) |
D143E |
probably damaging |
Het |
Vmn1r230 |
T |
A |
17: 21,067,036 (GRCm39) |
M75K |
possibly damaging |
Het |
Vmn2r120 |
A |
T |
17: 57,852,287 (GRCm39) |
F10I |
probably benign |
Het |
Vmn2r57 |
T |
C |
7: 41,049,284 (GRCm39) |
T822A |
probably benign |
Het |
Vmn2r67 |
T |
C |
7: 84,799,768 (GRCm39) |
Y490C |
probably damaging |
Het |
Zc3h7b |
T |
A |
15: 81,667,386 (GRCm39) |
W644R |
probably damaging |
Het |
Zeb1 |
A |
G |
18: 5,766,962 (GRCm39) |
D491G |
probably damaging |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
A |
T |
2: 174,486,308 (GRCm39) |
T328S |
possibly damaging |
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 |
R0110:Pla2g4a
|
UTSW |
1 |
149,716,398 (GRCm39) |
missense |
possibly damaging |
0.67 |
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 |
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 |
|