Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
G |
A |
7: 40,642,603 (GRCm39) |
G91S |
probably damaging |
Het |
Adam21 |
T |
G |
12: 81,607,330 (GRCm39) |
N144T |
probably damaging |
Het |
Adgrg7 |
T |
C |
16: 56,597,515 (GRCm39) |
|
probably null |
Het |
Angpt4 |
T |
C |
2: 151,771,460 (GRCm39) |
S259P |
possibly damaging |
Het |
Aqr |
A |
C |
2: 113,936,363 (GRCm39) |
L1320R |
probably damaging |
Het |
Arhgef10 |
G |
A |
8: 14,990,323 (GRCm39) |
G266D |
probably benign |
Het |
Bop1 |
A |
G |
15: 76,337,546 (GRCm39) |
V693A |
probably damaging |
Het |
Cd86 |
CA |
CAA |
16: 36,426,917 (GRCm39) |
|
probably null |
Het |
Cdc5l |
A |
G |
17: 45,738,863 (GRCm39) |
|
probably null |
Het |
Cfap46 |
C |
A |
7: 139,197,493 (GRCm39) |
R2126L |
unknown |
Het |
Chek2 |
T |
C |
5: 111,008,781 (GRCm39) |
V304A |
probably damaging |
Het |
Cntnap4 |
T |
A |
8: 113,391,731 (GRCm39) |
|
probably null |
Het |
Ctps1 |
C |
A |
4: 120,405,321 (GRCm39) |
G374C |
probably damaging |
Het |
Defa27 |
A |
T |
8: 21,805,625 (GRCm39) |
I22F |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,584,928 (GRCm39) |
S3220P |
probably damaging |
Het |
Dop1b |
T |
G |
16: 93,557,373 (GRCm39) |
|
probably null |
Het |
Dpysl5 |
G |
A |
5: 30,949,642 (GRCm39) |
V471I |
probably benign |
Het |
Duoxa1 |
T |
A |
2: 122,135,728 (GRCm39) |
I124F |
probably damaging |
Het |
Eogt |
T |
A |
6: 97,096,944 (GRCm39) |
I355F |
probably damaging |
Het |
Epha7 |
T |
A |
4: 28,951,279 (GRCm39) |
V800E |
probably damaging |
Het |
Evi5l |
A |
G |
8: 4,255,906 (GRCm39) |
Q633R |
possibly damaging |
Het |
Fam170a |
T |
C |
18: 50,414,728 (GRCm39) |
Y125H |
probably damaging |
Het |
Fbxo15 |
T |
C |
18: 84,980,747 (GRCm39) |
Y241H |
probably damaging |
Het |
Gbe1 |
T |
C |
16: 70,233,828 (GRCm39) |
I235T |
possibly damaging |
Het |
Gfra3 |
C |
T |
18: 34,844,234 (GRCm39) |
R102Q |
probably damaging |
Het |
Gjd4 |
C |
T |
18: 9,280,380 (GRCm39) |
G233S |
probably damaging |
Het |
Gm29106 |
C |
T |
1: 118,127,291 (GRCm39) |
P328S |
probably damaging |
Het |
Hgfac |
G |
T |
5: 35,204,258 (GRCm39) |
R507L |
probably damaging |
Het |
Jakmip3 |
A |
G |
7: 138,609,355 (GRCm39) |
K153R |
probably benign |
Het |
Kcnc1 |
T |
A |
7: 46,077,383 (GRCm39) |
V395E |
probably damaging |
Het |
Krt6b |
T |
C |
15: 101,586,577 (GRCm39) |
D304G |
probably damaging |
Het |
Ldha |
T |
C |
7: 46,500,323 (GRCm39) |
Y174H |
probably benign |
Het |
Lgi4 |
G |
A |
7: 30,766,776 (GRCm39) |
V268M |
possibly damaging |
Het |
Lpar3 |
T |
G |
3: 145,947,061 (GRCm39) |
|
probably null |
Het |
Lrp3 |
T |
C |
7: 34,905,477 (GRCm39) |
D103G |
probably damaging |
Het |
Marchf5 |
G |
A |
19: 37,194,713 (GRCm39) |
|
probably null |
Het |
Muc5b |
A |
T |
7: 141,419,866 (GRCm39) |
H4115L |
possibly damaging |
Het |
Myh13 |
G |
A |
11: 67,239,672 (GRCm39) |
D741N |
probably damaging |
Het |
Naglu |
A |
T |
11: 100,967,252 (GRCm39) |
I401F |
probably damaging |
Het |
Ncam2 |
T |
A |
16: 81,309,759 (GRCm39) |
N416K |
probably damaging |
Het |
Ncan |
A |
G |
8: 70,564,738 (GRCm39) |
L292S |
probably damaging |
Het |
Nkiras1 |
T |
C |
14: 18,276,732 (GRCm38) |
V7A |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,068,708 (GRCm39) |
L203* |
probably null |
Het |
Nscme3l |
A |
T |
19: 5,553,659 (GRCm39) |
S41T |
possibly damaging |
Het |
Onecut2 |
T |
A |
18: 64,474,633 (GRCm39) |
W395R |
probably damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,062 (GRCm39) |
I9K |
probably benign |
Het |
Pak6 |
T |
A |
2: 118,524,003 (GRCm39) |
V386E |
probably damaging |
Het |
Pias2 |
A |
G |
18: 77,220,931 (GRCm39) |
S396G |
probably benign |
Het |
Plxna2 |
T |
A |
1: 194,394,568 (GRCm39) |
L483H |
probably damaging |
Het |
Prss36 |
G |
T |
7: 127,534,763 (GRCm39) |
R484S |
probably benign |
Het |
Ptpn21 |
A |
T |
12: 98,654,996 (GRCm39) |
V657E |
probably benign |
Het |
Rassf2 |
T |
C |
2: 131,838,332 (GRCm39) |
E318G |
probably damaging |
Het |
Rp1 |
A |
C |
1: 4,298,824 (GRCm39) |
S623A |
unknown |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Scn11a |
T |
A |
9: 119,588,982 (GRCm39) |
E1308V |
probably damaging |
Het |
Serpina3c |
A |
T |
12: 104,115,771 (GRCm39) |
S258T |
possibly damaging |
Het |
Slit3 |
A |
G |
11: 35,501,516 (GRCm39) |
T417A |
possibly damaging |
Het |
Sostdc1 |
C |
A |
12: 36,367,310 (GRCm39) |
A162E |
possibly damaging |
Het |
Sox13 |
A |
T |
1: 133,312,129 (GRCm39) |
|
probably null |
Het |
Sox8 |
G |
T |
17: 25,786,514 (GRCm39) |
S396R |
probably benign |
Het |
Sult2a3 |
A |
T |
7: 13,816,685 (GRCm39) |
F164L |
possibly damaging |
Het |
Susd2 |
T |
C |
10: 75,475,685 (GRCm39) |
Y438C |
probably damaging |
Het |
Tas2r106 |
T |
G |
6: 131,655,810 (GRCm39) |
T14P |
probably damaging |
Het |
Tcf25 |
T |
A |
8: 124,127,800 (GRCm39) |
|
probably null |
Het |
Tenm3 |
G |
A |
8: 48,688,970 (GRCm39) |
R2206W |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,081,789 (GRCm39) |
L471P |
unknown |
Het |
Ticrr |
A |
T |
7: 79,343,490 (GRCm39) |
K1118N |
probably damaging |
Het |
Tlr5 |
G |
A |
1: 182,801,064 (GRCm39) |
E123K |
probably benign |
Het |
Ttn |
ATATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTG |
ATATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTG |
2: 76,746,150 (GRCm39) |
|
probably benign |
Het |
U2surp |
A |
G |
9: 95,375,770 (GRCm39) |
V141A |
probably benign |
Het |
Unc79 |
T |
A |
12: 103,100,734 (GRCm39) |
S2050T |
possibly damaging |
Het |
Usp13 |
A |
G |
3: 32,920,020 (GRCm39) |
D235G |
probably benign |
Het |
Vcam1 |
T |
C |
3: 115,919,628 (GRCm39) |
T213A |
possibly damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,786,166 (GRCm39) |
I323N |
possibly damaging |
Het |
Vps13b |
A |
G |
15: 35,877,703 (GRCm39) |
I2892M |
probably damaging |
Het |
Wnt5a |
T |
A |
14: 28,240,329 (GRCm39) |
S160T |
probably benign |
Het |
Zar1 |
G |
A |
5: 72,738,294 (GRCm39) |
P36L |
possibly damaging |
Het |
Zfp773 |
A |
T |
7: 7,135,984 (GRCm39) |
M204K |
probably benign |
Het |
Zhx1 |
T |
C |
15: 57,916,465 (GRCm39) |
T594A |
probably benign |
Het |
|
Other mutations in Eif4enif1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01139:Eif4enif1
|
APN |
11 |
3,171,143 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02237:Eif4enif1
|
APN |
11 |
3,177,876 (GRCm39) |
nonsense |
probably null |
|
IGL02372:Eif4enif1
|
APN |
11 |
3,179,986 (GRCm39) |
missense |
probably benign |
0.09 |
PIT4283001:Eif4enif1
|
UTSW |
11 |
3,184,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0079:Eif4enif1
|
UTSW |
11 |
3,192,676 (GRCm39) |
nonsense |
probably null |
|
R1177:Eif4enif1
|
UTSW |
11 |
3,179,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R1220:Eif4enif1
|
UTSW |
11 |
3,189,493 (GRCm39) |
splice site |
probably benign |
|
R1511:Eif4enif1
|
UTSW |
11 |
3,186,278 (GRCm39) |
missense |
probably benign |
0.00 |
R1675:Eif4enif1
|
UTSW |
11 |
3,165,686 (GRCm39) |
missense |
probably benign |
0.02 |
R1908:Eif4enif1
|
UTSW |
11 |
3,177,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Eif4enif1
|
UTSW |
11 |
3,193,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R2173:Eif4enif1
|
UTSW |
11 |
3,192,367 (GRCm39) |
splice site |
probably null |
|
R2215:Eif4enif1
|
UTSW |
11 |
3,177,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R2517:Eif4enif1
|
UTSW |
11 |
3,171,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Eif4enif1
|
UTSW |
11 |
3,192,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Eif4enif1
|
UTSW |
11 |
3,192,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Eif4enif1
|
UTSW |
11 |
3,192,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Eif4enif1
|
UTSW |
11 |
3,192,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2871:Eif4enif1
|
UTSW |
11 |
3,192,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2871:Eif4enif1
|
UTSW |
11 |
3,192,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2873:Eif4enif1
|
UTSW |
11 |
3,192,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R3147:Eif4enif1
|
UTSW |
11 |
3,194,003 (GRCm39) |
splice site |
probably null |
|
R4195:Eif4enif1
|
UTSW |
11 |
3,193,186 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4196:Eif4enif1
|
UTSW |
11 |
3,193,186 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4708:Eif4enif1
|
UTSW |
11 |
3,170,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Eif4enif1
|
UTSW |
11 |
3,194,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Eif4enif1
|
UTSW |
11 |
3,192,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Eif4enif1
|
UTSW |
11 |
3,193,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R5816:Eif4enif1
|
UTSW |
11 |
3,192,401 (GRCm39) |
missense |
probably benign |
0.13 |
R6018:Eif4enif1
|
UTSW |
11 |
3,192,481 (GRCm39) |
missense |
probably damaging |
0.97 |
R6036:Eif4enif1
|
UTSW |
11 |
3,189,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Eif4enif1
|
UTSW |
11 |
3,189,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6267:Eif4enif1
|
UTSW |
11 |
3,177,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R6514:Eif4enif1
|
UTSW |
11 |
3,190,996 (GRCm39) |
missense |
probably null |
0.01 |
R6638:Eif4enif1
|
UTSW |
11 |
3,192,463 (GRCm39) |
missense |
probably damaging |
0.96 |
R7040:Eif4enif1
|
UTSW |
11 |
3,184,040 (GRCm39) |
missense |
probably benign |
0.33 |
R7385:Eif4enif1
|
UTSW |
11 |
3,170,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7478:Eif4enif1
|
UTSW |
11 |
3,177,709 (GRCm39) |
nonsense |
probably null |
|
R7749:Eif4enif1
|
UTSW |
11 |
3,192,608 (GRCm39) |
missense |
probably damaging |
0.99 |
R8381:Eif4enif1
|
UTSW |
11 |
3,177,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R9029:Eif4enif1
|
UTSW |
11 |
3,174,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R9622:Eif4enif1
|
UTSW |
11 |
3,165,714 (GRCm39) |
missense |
probably benign |
0.26 |
R9646:Eif4enif1
|
UTSW |
11 |
3,170,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Eif4enif1
|
UTSW |
11 |
3,170,384 (GRCm39) |
missense |
probably damaging |
0.98 |
R9747:Eif4enif1
|
UTSW |
11 |
3,163,267 (GRCm39) |
missense |
probably damaging |
0.99 |
|