Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
C |
13: 119,606,478 (GRCm39) |
V240A |
probably damaging |
Het |
A930009A15Rik |
C |
T |
10: 115,406,019 (GRCm39) |
|
probably benign |
Het |
Aarsd1 |
A |
G |
11: 101,301,970 (GRCm39) |
I201T |
probably damaging |
Het |
Acaca |
T |
A |
11: 84,152,414 (GRCm39) |
Y854N |
probably benign |
Het |
Adra2c |
T |
C |
5: 35,437,759 (GRCm39) |
L177P |
probably damaging |
Het |
Akr1c12 |
A |
T |
13: 4,329,309 (GRCm39) |
I16N |
probably damaging |
Het |
Aldh8a1 |
A |
T |
10: 21,256,729 (GRCm39) |
I47F |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,886,879 (GRCm39) |
I736V |
probably benign |
Het |
Bmp2 |
A |
T |
2: 133,402,817 (GRCm39) |
M123L |
probably benign |
Het |
C1ql1 |
T |
C |
11: 102,836,812 (GRCm39) |
Y159C |
probably damaging |
Het |
Ccdc148 |
T |
C |
2: 58,713,645 (GRCm39) |
Y502C |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,098,593 (GRCm39) |
V835E |
possibly damaging |
Het |
Cenpf |
A |
T |
1: 189,390,864 (GRCm39) |
N989K |
probably damaging |
Het |
Ciz1 |
A |
G |
2: 32,257,380 (GRCm39) |
M142V |
probably benign |
Het |
Cnot4 |
T |
C |
6: 35,029,939 (GRCm39) |
R320G |
possibly damaging |
Het |
Cyth1 |
G |
T |
11: 118,073,689 (GRCm39) |
H215N |
probably damaging |
Het |
Dapk1 |
G |
A |
13: 60,908,987 (GRCm39) |
G1200D |
probably damaging |
Het |
Dhps |
A |
G |
8: 85,799,181 (GRCm39) |
Y103C |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 31,041,865 (GRCm39) |
E35D |
probably benign |
Het |
Dnajb9 |
A |
T |
12: 44,254,169 (GRCm39) |
D79E |
probably damaging |
Het |
Eif4a2 |
T |
C |
16: 22,928,877 (GRCm39) |
F164S |
probably benign |
Het |
Enpp2 |
T |
C |
15: 54,714,813 (GRCm39) |
T595A |
probably benign |
Het |
Exoc6b |
T |
A |
6: 84,768,366 (GRCm39) |
|
probably null |
Het |
Fam171a1 |
T |
C |
2: 3,221,391 (GRCm39) |
S286P |
probably damaging |
Het |
Fermt2 |
T |
A |
14: 45,706,782 (GRCm39) |
N338I |
probably damaging |
Het |
Fhdc1 |
A |
G |
3: 84,353,438 (GRCm39) |
F596L |
probably benign |
Het |
Fry |
T |
C |
5: 150,304,359 (GRCm39) |
V583A |
probably benign |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Gdap1 |
T |
A |
1: 17,231,665 (GRCm39) |
F337I |
possibly damaging |
Het |
Git2 |
C |
T |
5: 114,904,550 (GRCm39) |
R123H |
probably damaging |
Het |
Gpr6 |
A |
T |
10: 40,946,652 (GRCm39) |
I310N |
possibly damaging |
Het |
Gpsm2 |
G |
A |
3: 108,608,061 (GRCm39) |
A239V |
probably damaging |
Het |
Hexa |
T |
C |
9: 59,471,267 (GRCm39) |
V507A |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,345,531 (GRCm39) |
H4718L |
possibly damaging |
Het |
Hrh4 |
T |
C |
18: 13,154,970 (GRCm39) |
F170L |
possibly damaging |
Het |
Ica1 |
T |
C |
6: 8,658,266 (GRCm39) |
T284A |
probably benign |
Het |
Itga5 |
T |
C |
15: 103,258,876 (GRCm39) |
N774S |
probably damaging |
Het |
Itgb2 |
T |
C |
10: 77,395,992 (GRCm39) |
S556P |
probably benign |
Het |
Kash5 |
A |
T |
7: 44,854,035 (GRCm39) |
H31Q |
possibly damaging |
Het |
Kcnq4 |
A |
G |
4: 120,568,565 (GRCm39) |
F384L |
probably benign |
Het |
Lama2 |
A |
T |
10: 26,882,726 (GRCm39) |
N2612K |
probably benign |
Het |
Lrrc14b |
G |
T |
13: 74,508,892 (GRCm39) |
A505E |
probably damaging |
Het |
Ly6g |
T |
C |
15: 75,030,413 (GRCm39) |
I77T |
probably benign |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mrgpre |
C |
T |
7: 143,335,087 (GRCm39) |
V139M |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,753,411 (GRCm38) |
S1096T |
probably benign |
Het |
Myrfl |
G |
A |
10: 116,667,430 (GRCm39) |
R337* |
probably null |
Het |
Ndufa4 |
C |
T |
6: 11,906,092 (GRCm39) |
V20I |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,299,595 (GRCm39) |
D241G |
probably null |
Het |
Nid1 |
A |
G |
13: 13,643,028 (GRCm39) |
D322G |
probably benign |
Het |
Nova1 |
A |
T |
12: 46,747,544 (GRCm39) |
D244E |
unknown |
Het |
Or11g27 |
T |
A |
14: 50,771,770 (GRCm39) |
D300E |
probably benign |
Het |
Or4a68 |
T |
C |
2: 89,269,745 (GRCm39) |
K293E |
possibly damaging |
Het |
Or5m10b |
A |
G |
2: 85,699,350 (GRCm39) |
K138R |
probably benign |
Het |
Padi2 |
C |
A |
4: 140,676,648 (GRCm39) |
N595K |
possibly damaging |
Het |
Pag1 |
A |
G |
3: 9,758,951 (GRCm39) |
I389T |
probably damaging |
Het |
Pcdh10 |
G |
T |
3: 45,335,810 (GRCm39) |
G708V |
possibly damaging |
Het |
Pecam1 |
A |
G |
11: 106,590,610 (GRCm39) |
S55P |
probably damaging |
Het |
Plin3 |
A |
T |
17: 56,591,192 (GRCm39) |
V196E |
possibly damaging |
Het |
Plxdc1 |
A |
T |
11: 97,847,316 (GRCm39) |
L119Q |
possibly damaging |
Het |
Pnliprp1 |
A |
T |
19: 58,726,681 (GRCm39) |
N346I |
probably damaging |
Het |
Ppp1r27 |
A |
T |
11: 120,441,856 (GRCm39) |
Y8* |
probably null |
Het |
Prg3 |
A |
T |
2: 84,819,746 (GRCm39) |
D80V |
probably damaging |
Het |
Prmt5 |
T |
C |
14: 54,745,347 (GRCm39) |
N607D |
possibly damaging |
Het |
Ptprs |
A |
G |
17: 56,730,538 (GRCm39) |
F1144L |
probably benign |
Het |
Rai14 |
C |
T |
15: 10,593,189 (GRCm39) |
G152R |
probably damaging |
Het |
Rap1gds1 |
T |
A |
3: 138,661,976 (GRCm39) |
R427* |
probably null |
Het |
Recql5 |
A |
G |
11: 115,819,248 (GRCm39) |
V106A |
probably benign |
Het |
Resp18 |
T |
C |
1: 75,250,615 (GRCm39) |
T155A |
probably benign |
Het |
Rfx6 |
A |
G |
10: 51,557,914 (GRCm39) |
D129G |
probably benign |
Het |
Rsf1 |
T |
A |
7: 97,310,374 (GRCm39) |
I368K |
|
Het |
Sema6a |
C |
G |
18: 47,424,231 (GRCm39) |
V226L |
probably damaging |
Het |
Sf1 |
A |
G |
19: 6,422,234 (GRCm39) |
E220G |
probably damaging |
Het |
Shld2 |
C |
T |
14: 33,959,423 (GRCm39) |
S853N |
probably damaging |
Het |
Sidt1 |
T |
A |
16: 44,079,848 (GRCm39) |
Y602F |
probably damaging |
Het |
Slc17a8 |
A |
G |
10: 89,428,008 (GRCm39) |
I273T |
probably benign |
Het |
Slc28a2b |
A |
T |
2: 122,353,325 (GRCm39) |
I502F |
not run |
Het |
Slc41a1 |
A |
T |
1: 131,766,889 (GRCm39) |
I136F |
probably damaging |
Het |
Snrpb |
T |
C |
2: 130,018,939 (GRCm39) |
I51V |
probably benign |
Het |
Sprr2f |
T |
A |
3: 92,273,254 (GRCm39) |
C18S |
unknown |
Het |
Stab1 |
T |
C |
14: 30,876,622 (GRCm39) |
N864S |
probably benign |
Het |
Svil |
C |
A |
18: 5,095,188 (GRCm39) |
T1457K |
probably benign |
Het |
Syt1 |
A |
T |
10: 108,340,262 (GRCm39) |
I352N |
probably damaging |
Het |
Tas2r119 |
A |
G |
15: 32,178,279 (GRCm39) |
K282E |
probably damaging |
Het |
Timeless |
T |
C |
10: 128,080,538 (GRCm39) |
F473S |
probably damaging |
Het |
Tmc3 |
A |
G |
7: 83,247,481 (GRCm39) |
D192G |
probably damaging |
Het |
Trmt1l |
T |
A |
1: 151,316,591 (GRCm39) |
I184N |
possibly damaging |
Het |
Ttll6 |
G |
A |
11: 96,025,701 (GRCm39) |
V61M |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,632,755 (GRCm39) |
E14100K |
probably damaging |
Het |
Txndc2 |
T |
A |
17: 65,945,620 (GRCm39) |
I186F |
possibly damaging |
Het |
Ubr1 |
A |
T |
2: 120,703,672 (GRCm39) |
S1553T |
possibly damaging |
Het |
Vmn1r208 |
T |
C |
13: 22,956,705 (GRCm39) |
N264S |
probably benign |
Het |
Vmn1r87 |
T |
A |
7: 12,865,613 (GRCm39) |
M225L |
probably benign |
Het |
Vmn2r101 |
T |
A |
17: 19,831,899 (GRCm39) |
C632S |
possibly damaging |
Het |
Wdr97 |
T |
A |
15: 76,241,949 (GRCm39) |
Y747* |
probably null |
Het |
Zfp474 |
T |
C |
18: 52,772,261 (GRCm39) |
S305P |
probably benign |
Het |
Zfp59 |
A |
G |
7: 27,552,863 (GRCm39) |
N105S |
probably benign |
Het |
Zfp804b |
T |
A |
5: 6,822,301 (GRCm39) |
Y254F |
possibly damaging |
Het |
|
Other mutations in Lnx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Lnx1
|
APN |
5 |
74,846,378 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01538:Lnx1
|
APN |
5 |
74,780,816 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02351:Lnx1
|
APN |
5 |
74,788,027 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02358:Lnx1
|
APN |
5 |
74,788,027 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03011:Lnx1
|
APN |
5 |
74,846,420 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03188:Lnx1
|
APN |
5 |
74,780,924 (GRCm39) |
missense |
probably damaging |
1.00 |
bobcat
|
UTSW |
5 |
74,846,351 (GRCm39) |
missense |
probably damaging |
1.00 |
Caracal
|
UTSW |
5 |
74,766,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0490:Lnx1
|
UTSW |
5 |
74,781,008 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0714:Lnx1
|
UTSW |
5 |
74,768,570 (GRCm39) |
splice site |
probably benign |
|
R1343:Lnx1
|
UTSW |
5 |
74,758,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R1533:Lnx1
|
UTSW |
5 |
74,780,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Lnx1
|
UTSW |
5 |
74,846,071 (GRCm39) |
missense |
probably benign |
|
R1714:Lnx1
|
UTSW |
5 |
74,768,398 (GRCm39) |
missense |
probably null |
1.00 |
R1727:Lnx1
|
UTSW |
5 |
74,768,577 (GRCm39) |
splice site |
probably null |
|
R1806:Lnx1
|
UTSW |
5 |
74,766,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Lnx1
|
UTSW |
5 |
74,780,727 (GRCm39) |
missense |
probably benign |
0.25 |
R2879:Lnx1
|
UTSW |
5 |
74,780,784 (GRCm39) |
missense |
probably benign |
0.03 |
R2984:Lnx1
|
UTSW |
5 |
74,846,083 (GRCm39) |
nonsense |
probably null |
|
R3790:Lnx1
|
UTSW |
5 |
74,789,027 (GRCm39) |
splice site |
probably benign |
|
R3953:Lnx1
|
UTSW |
5 |
74,766,750 (GRCm39) |
missense |
probably benign |
|
R4509:Lnx1
|
UTSW |
5 |
74,780,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Lnx1
|
UTSW |
5 |
74,780,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R4511:Lnx1
|
UTSW |
5 |
74,780,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Lnx1
|
UTSW |
5 |
74,846,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Lnx1
|
UTSW |
5 |
74,771,457 (GRCm39) |
missense |
probably benign |
0.16 |
R4624:Lnx1
|
UTSW |
5 |
74,821,121 (GRCm39) |
intron |
probably benign |
|
R4647:Lnx1
|
UTSW |
5 |
74,771,457 (GRCm39) |
missense |
probably benign |
0.16 |
R4648:Lnx1
|
UTSW |
5 |
74,771,457 (GRCm39) |
missense |
probably benign |
0.16 |
R4877:Lnx1
|
UTSW |
5 |
74,788,784 (GRCm39) |
missense |
probably benign |
0.01 |
R4883:Lnx1
|
UTSW |
5 |
74,768,530 (GRCm39) |
missense |
probably benign |
|
R5256:Lnx1
|
UTSW |
5 |
74,846,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Lnx1
|
UTSW |
5 |
74,838,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R6185:Lnx1
|
UTSW |
5 |
74,846,269 (GRCm39) |
nonsense |
probably null |
|
R6408:Lnx1
|
UTSW |
5 |
74,846,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Lnx1
|
UTSW |
5 |
74,768,541 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7083:Lnx1
|
UTSW |
5 |
74,788,846 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7085:Lnx1
|
UTSW |
5 |
74,788,846 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7261:Lnx1
|
UTSW |
5 |
74,838,175 (GRCm39) |
nonsense |
probably null |
|
R7511:Lnx1
|
UTSW |
5 |
74,780,972 (GRCm39) |
missense |
probably benign |
0.01 |
R7670:Lnx1
|
UTSW |
5 |
74,846,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R8145:Lnx1
|
UTSW |
5 |
74,846,060 (GRCm39) |
missense |
probably benign |
0.22 |
R9015:Lnx1
|
UTSW |
5 |
74,780,783 (GRCm39) |
missense |
probably benign |
0.00 |
R9224:Lnx1
|
UTSW |
5 |
74,766,810 (GRCm39) |
missense |
probably benign |
0.37 |
R9321:Lnx1
|
UTSW |
5 |
74,780,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R9340:Lnx1
|
UTSW |
5 |
74,758,584 (GRCm39) |
missense |
probably benign |
0.01 |
R9704:Lnx1
|
UTSW |
5 |
74,780,879 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Lnx1
|
UTSW |
5 |
74,788,102 (GRCm39) |
missense |
possibly damaging |
0.80 |
|