Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
A |
T |
6: 23,092,561 (GRCm39) |
Y146* |
probably null |
Het |
Adcy2 |
A |
G |
13: 68,944,722 (GRCm39) |
L220P |
probably damaging |
Het |
Agl |
T |
C |
3: 116,574,914 (GRCm39) |
Y660C |
probably damaging |
Het |
Ak1 |
A |
G |
2: 32,519,622 (GRCm39) |
T17A |
probably benign |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Ankrd11 |
A |
T |
8: 123,629,161 (GRCm39) |
|
probably null |
Het |
Ap5b1 |
T |
C |
19: 5,620,502 (GRCm39) |
S641P |
possibly damaging |
Het |
Apoc4 |
A |
G |
7: 19,415,304 (GRCm39) |
M1T |
probably null |
Het |
Arhgap5 |
T |
C |
12: 52,564,817 (GRCm39) |
V596A |
probably benign |
Het |
Ascc3 |
A |
G |
10: 50,493,838 (GRCm39) |
E91G |
probably damaging |
Het |
Bach2 |
T |
A |
4: 32,580,055 (GRCm39) |
V637E |
probably benign |
Het |
Bicd2 |
T |
G |
13: 49,532,881 (GRCm39) |
L489R |
possibly damaging |
Het |
Bltp1 |
C |
T |
3: 36,949,527 (GRCm39) |
T2I |
possibly damaging |
Het |
Boc |
A |
T |
16: 44,322,007 (GRCm39) |
|
probably null |
Het |
Cbln2 |
T |
A |
18: 86,734,791 (GRCm39) |
V188D |
probably damaging |
Het |
Ccl11 |
A |
C |
11: 81,953,123 (GRCm39) |
T94P |
probably damaging |
Het |
Cd109 |
A |
T |
9: 78,611,044 (GRCm39) |
H1220L |
probably benign |
Het |
Cd226 |
A |
G |
18: 89,265,435 (GRCm39) |
I125V |
probably benign |
Het |
Cep135 |
T |
A |
5: 76,780,176 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
T |
G |
9: 71,537,821 (GRCm39) |
E1233A |
probably damaging |
Het |
Ckap5 |
T |
A |
2: 91,437,891 (GRCm39) |
D1597E |
possibly damaging |
Het |
Clptm1 |
A |
G |
7: 19,380,762 (GRCm39) |
I63T |
possibly damaging |
Het |
Cpsf7 |
C |
T |
19: 10,518,073 (GRCm39) |
P428S |
probably damaging |
Het |
Cuedc1 |
C |
T |
11: 88,068,216 (GRCm39) |
P155S |
probably damaging |
Het |
Dgkb |
T |
C |
12: 38,134,228 (GRCm39) |
Y45H |
probably damaging |
Het |
Dglucy |
T |
C |
12: 100,823,181 (GRCm39) |
F459L |
probably damaging |
Het |
Dmp1 |
T |
A |
5: 104,359,790 (GRCm39) |
D155E |
possibly damaging |
Het |
Dnah1 |
T |
A |
14: 31,023,813 (GRCm39) |
I960F |
possibly damaging |
Het |
Drosha |
G |
T |
15: 12,915,467 (GRCm39) |
M795I |
probably damaging |
Het |
Dsg1b |
A |
G |
18: 20,529,532 (GRCm39) |
T326A |
probably damaging |
Het |
Dusp16 |
T |
G |
6: 134,695,802 (GRCm39) |
N343T |
probably benign |
Het |
Faim2 |
T |
C |
15: 99,398,127 (GRCm39) |
S274G |
possibly damaging |
Het |
Fhip2a |
G |
T |
19: 57,370,324 (GRCm39) |
V523L |
probably benign |
Het |
Fndc1 |
T |
C |
17: 8,023,761 (GRCm39) |
R65G |
probably damaging |
Het |
Fnip2 |
A |
T |
3: 79,419,632 (GRCm39) |
|
probably benign |
Het |
Grm3 |
T |
C |
5: 9,639,793 (GRCm39) |
Y84C |
possibly damaging |
Het |
Herc2 |
T |
C |
7: 55,787,607 (GRCm39) |
F1755L |
probably damaging |
Het |
Hivep1 |
C |
T |
13: 42,313,625 (GRCm39) |
T1955I |
possibly damaging |
Het |
Ift20 |
T |
C |
11: 78,431,797 (GRCm39) |
I97T |
probably damaging |
Het |
Il36rn |
T |
C |
2: 24,171,376 (GRCm39) |
C155R |
probably damaging |
Het |
Maf1 |
G |
A |
15: 76,237,563 (GRCm39) |
D175N |
probably damaging |
Het |
Mical3 |
T |
C |
6: 120,928,283 (GRCm39) |
K996E |
probably damaging |
Het |
Midn |
A |
G |
10: 79,990,983 (GRCm39) |
N331S |
probably benign |
Het |
Mki67 |
T |
A |
7: 135,300,238 (GRCm39) |
K1599* |
probably null |
Het |
Mlx |
A |
G |
11: 100,979,805 (GRCm39) |
Q162R |
possibly damaging |
Het |
Nalf1 |
A |
G |
8: 9,820,607 (GRCm39) |
S138P |
probably benign |
Het |
Ngp |
T |
C |
9: 110,249,929 (GRCm39) |
C76R |
probably damaging |
Het |
Nin |
C |
T |
12: 70,072,251 (GRCm39) |
G1210D |
probably benign |
Het |
Nlgn1 |
A |
G |
3: 25,488,034 (GRCm39) |
I738T |
probably benign |
Het |
Nop53 |
A |
C |
7: 15,672,153 (GRCm39) |
F465C |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,114,680 (GRCm39) |
D503G |
possibly damaging |
Het |
Npbwr1 |
T |
A |
1: 5,986,570 (GRCm39) |
S315C |
probably damaging |
Het |
Nup42 |
G |
T |
5: 24,386,989 (GRCm39) |
G260* |
probably null |
Het |
Ogdh |
G |
C |
11: 6,284,626 (GRCm39) |
R200P |
possibly damaging |
Het |
Or4b13 |
T |
A |
2: 90,083,036 (GRCm39) |
I99L |
probably benign |
Het |
Or52n20 |
A |
G |
7: 104,320,808 (GRCm39) |
T300A |
possibly damaging |
Het |
Or5m13b |
T |
G |
2: 85,753,939 (GRCm39) |
|
probably null |
Het |
Or6ae1 |
C |
T |
7: 139,742,729 (GRCm39) |
V45I |
probably damaging |
Het |
Or7g16 |
G |
A |
9: 18,726,801 (GRCm39) |
S263L |
probably benign |
Het |
Or7g33 |
A |
T |
9: 19,448,688 (GRCm39) |
C179* |
probably null |
Het |
Ovgp1 |
T |
A |
3: 105,894,309 (GRCm39) |
|
probably benign |
Het |
Papln |
T |
A |
12: 83,819,992 (GRCm39) |
C150S |
probably damaging |
Het |
Pde1c |
A |
T |
6: 56,135,996 (GRCm39) |
L316Q |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Piezo2 |
G |
T |
18: 63,277,997 (GRCm39) |
D302E |
probably damaging |
Het |
Pirb |
A |
T |
7: 3,720,637 (GRCm39) |
L287Q |
probably benign |
Het |
Plin1 |
A |
G |
7: 79,375,378 (GRCm39) |
|
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,688,484 (GRCm39) |
I698T |
probably damaging |
Het |
Ppp1r12c |
G |
T |
7: 4,485,974 (GRCm39) |
C572* |
probably null |
Het |
Ptgis |
T |
C |
2: 167,056,769 (GRCm39) |
M273V |
possibly damaging |
Het |
Samd14 |
C |
A |
11: 94,914,110 (GRCm39) |
T283K |
probably damaging |
Het |
Scnn1g |
A |
T |
7: 121,337,411 (GRCm39) |
K91* |
probably null |
Het |
Slc24a4 |
A |
G |
12: 102,180,166 (GRCm39) |
Q95R |
probably damaging |
Het |
Slfn9 |
T |
G |
11: 82,879,027 (GRCm39) |
D34A |
probably benign |
Het |
Smarca4 |
A |
T |
9: 21,588,776 (GRCm39) |
I1193F |
probably damaging |
Het |
Spata31e5 |
A |
G |
1: 28,816,260 (GRCm39) |
W591R |
probably damaging |
Het |
Sphkap |
T |
C |
1: 83,255,632 (GRCm39) |
M706V |
probably benign |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Stxbp1 |
T |
C |
2: 32,688,201 (GRCm39) |
D488G |
probably damaging |
Het |
Sugp2 |
C |
T |
8: 70,695,306 (GRCm39) |
|
probably null |
Het |
Tekt5 |
T |
C |
16: 10,213,070 (GRCm39) |
I72V |
probably benign |
Het |
Themis |
T |
A |
10: 28,658,720 (GRCm39) |
N582K |
probably benign |
Het |
Tmed11 |
C |
A |
5: 108,934,000 (GRCm39) |
M65I |
possibly damaging |
Het |
Top3a |
G |
T |
11: 60,633,315 (GRCm39) |
P927Q |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,976,207 (GRCm39) |
N165K |
possibly damaging |
Het |
Tsfm |
A |
G |
10: 126,866,663 (GRCm39) |
S2P |
probably damaging |
Het |
Wdr47 |
C |
A |
3: 108,534,758 (GRCm39) |
S559* |
probably null |
Het |
Wnt2b |
T |
C |
3: 104,860,331 (GRCm39) |
Y192C |
probably damaging |
Het |
Zfp280b |
A |
G |
10: 75,874,370 (GRCm39) |
D83G |
probably benign |
Het |
Zfp345 |
T |
C |
2: 150,314,038 (GRCm39) |
T500A |
possibly damaging |
Het |
Zfp78 |
T |
A |
7: 6,382,074 (GRCm39) |
C343S |
probably damaging |
Het |
|
Other mutations in Lca5l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00667:Lca5l
|
APN |
16 |
95,962,612 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02893:Lca5l
|
APN |
16 |
95,980,113 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03056:Lca5l
|
APN |
16 |
95,962,551 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03208:Lca5l
|
APN |
16 |
95,980,046 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03267:Lca5l
|
APN |
16 |
95,960,983 (GRCm39) |
missense |
probably benign |
0.03 |
R0417:Lca5l
|
UTSW |
16 |
95,963,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R0961:Lca5l
|
UTSW |
16 |
95,962,560 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1458:Lca5l
|
UTSW |
16 |
95,961,059 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1650:Lca5l
|
UTSW |
16 |
95,980,140 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1669:Lca5l
|
UTSW |
16 |
95,961,008 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1706:Lca5l
|
UTSW |
16 |
95,977,164 (GRCm39) |
missense |
probably benign |
0.41 |
R2004:Lca5l
|
UTSW |
16 |
95,963,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Lca5l
|
UTSW |
16 |
95,979,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R4307:Lca5l
|
UTSW |
16 |
95,960,756 (GRCm39) |
unclassified |
probably benign |
|
R4824:Lca5l
|
UTSW |
16 |
95,963,229 (GRCm39) |
nonsense |
probably null |
|
R4920:Lca5l
|
UTSW |
16 |
95,980,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R4991:Lca5l
|
UTSW |
16 |
95,960,932 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5591:Lca5l
|
UTSW |
16 |
95,979,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R5774:Lca5l
|
UTSW |
16 |
95,977,261 (GRCm39) |
missense |
probably benign |
0.22 |
R6243:Lca5l
|
UTSW |
16 |
95,980,112 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6403:Lca5l
|
UTSW |
16 |
95,975,045 (GRCm39) |
missense |
probably benign |
0.41 |
R7153:Lca5l
|
UTSW |
16 |
95,975,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R7754:Lca5l
|
UTSW |
16 |
95,960,761 (GRCm39) |
missense |
unknown |
|
R7758:Lca5l
|
UTSW |
16 |
95,980,037 (GRCm39) |
missense |
probably benign |
0.00 |
R7814:Lca5l
|
UTSW |
16 |
95,963,757 (GRCm39) |
critical splice donor site |
probably null |
|
R8357:Lca5l
|
UTSW |
16 |
95,960,908 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8401:Lca5l
|
UTSW |
16 |
95,963,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R8457:Lca5l
|
UTSW |
16 |
95,960,908 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8527:Lca5l
|
UTSW |
16 |
95,960,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8807:Lca5l
|
UTSW |
16 |
95,979,808 (GRCm39) |
missense |
probably benign |
0.01 |
R9105:Lca5l
|
UTSW |
16 |
95,960,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R9146:Lca5l
|
UTSW |
16 |
95,960,998 (GRCm39) |
missense |
probably damaging |
0.98 |
R9165:Lca5l
|
UTSW |
16 |
95,977,218 (GRCm39) |
missense |
probably damaging |
0.99 |
R9378:Lca5l
|
UTSW |
16 |
95,977,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R9657:Lca5l
|
UTSW |
16 |
95,974,953 (GRCm39) |
nonsense |
probably null |
|
RF031:Lca5l
|
UTSW |
16 |
95,960,504 (GRCm39) |
frame shift |
probably null |
|
RF042:Lca5l
|
UTSW |
16 |
95,960,497 (GRCm39) |
frame shift |
probably null |
|
RF050:Lca5l
|
UTSW |
16 |
95,960,501 (GRCm39) |
small deletion |
probably benign |
|
RF059:Lca5l
|
UTSW |
16 |
95,960,501 (GRCm39) |
small deletion |
probably benign |
|
|