Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago2 |
T |
C |
15: 72,985,601 (GRCm39) |
I665V |
probably benign |
Het |
Aoc1l3 |
T |
G |
6: 48,964,508 (GRCm39) |
F172C |
probably damaging |
Het |
Arhgap32 |
A |
T |
9: 32,063,983 (GRCm39) |
M74L |
possibly damaging |
Het |
Asb4 |
T |
C |
6: 5,398,304 (GRCm39) |
C90R |
possibly damaging |
Het |
B3galt4 |
T |
A |
17: 34,169,821 (GRCm39) |
D139V |
probably damaging |
Het |
Camta2 |
A |
C |
11: 70,564,964 (GRCm39) |
I852S |
probably benign |
Het |
Cd200l1 |
A |
T |
16: 45,264,294 (GRCm39) |
M88K |
probably benign |
Het |
Cox4i2 |
G |
T |
2: 152,599,015 (GRCm39) |
E57D |
probably benign |
Het |
Dip2b |
T |
C |
15: 100,091,724 (GRCm39) |
I1055T |
probably benign |
Het |
Eif1ad18 |
T |
A |
12: 88,050,602 (GRCm39) |
W46R |
probably benign |
Het |
Ephb1 |
C |
A |
9: 101,806,463 (GRCm39) |
|
probably null |
Het |
Fbxw7 |
A |
T |
3: 84,879,723 (GRCm39) |
|
probably null |
Het |
Frem1 |
C |
A |
4: 82,840,506 (GRCm39) |
D1789Y |
probably damaging |
Het |
Gm29106 |
A |
T |
1: 118,127,524 (GRCm39) |
R405S |
probably damaging |
Het |
Greb1l |
G |
A |
18: 10,547,482 (GRCm39) |
V1567M |
possibly damaging |
Het |
Hapstr1 |
A |
G |
16: 8,648,553 (GRCm39) |
|
probably null |
Het |
Heatr1 |
C |
A |
13: 12,449,956 (GRCm39) |
D1983E |
probably benign |
Het |
Lhfpl2 |
G |
T |
13: 94,311,029 (GRCm39) |
A100S |
probably damaging |
Het |
Lrp5 |
A |
T |
19: 3,655,301 (GRCm39) |
V1073D |
probably damaging |
Het |
Naip6 |
G |
A |
13: 100,438,706 (GRCm39) |
L364F |
possibly damaging |
Het |
Nek9 |
A |
G |
12: 85,350,311 (GRCm39) |
L921P |
probably damaging |
Het |
Nim1k |
C |
T |
13: 120,189,263 (GRCm39) |
E49K |
probably damaging |
Het |
Nsun5 |
A |
C |
5: 135,399,046 (GRCm39) |
N32T |
probably damaging |
Het |
Nuggc |
T |
C |
14: 65,855,092 (GRCm39) |
S325P |
probably damaging |
Het |
Or2d36 |
A |
G |
7: 106,747,290 (GRCm39) |
I256V |
probably damaging |
Het |
Or5w12 |
T |
A |
2: 87,501,797 (GRCm39) |
K305* |
probably null |
Het |
Pcdhga7 |
A |
G |
18: 37,848,710 (GRCm39) |
D239G |
probably damaging |
Het |
Pld2 |
A |
G |
11: 70,444,273 (GRCm39) |
D523G |
probably benign |
Het |
Prokr1 |
C |
A |
6: 87,565,455 (GRCm39) |
W130L |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,381,562 (GRCm39) |
N266S |
probably damaging |
Het |
Rdh10 |
T |
C |
1: 16,176,255 (GRCm39) |
V5A |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,267,834 (GRCm39) |
L1140P |
possibly damaging |
Het |
Sacs |
A |
G |
14: 61,448,874 (GRCm39) |
D3640G |
probably damaging |
Het |
Smarca2 |
A |
G |
19: 26,668,749 (GRCm39) |
E916G |
probably damaging |
Het |
Steap3 |
A |
T |
1: 120,171,624 (GRCm39) |
H160Q |
probably damaging |
Het |
Tlk2 |
T |
C |
11: 105,147,779 (GRCm39) |
|
probably null |
Het |
Tmprss4 |
A |
G |
9: 45,097,220 (GRCm39) |
V15A |
probably benign |
Het |
Togaram2 |
T |
C |
17: 72,014,129 (GRCm39) |
L559P |
probably damaging |
Het |
Topbp1 |
T |
A |
9: 103,213,045 (GRCm39) |
L990H |
probably damaging |
Het |
Ttll7 |
A |
G |
3: 146,615,369 (GRCm39) |
T278A |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,604,780 (GRCm39) |
L18385F |
probably damaging |
Het |
Upf3a |
G |
T |
8: 13,841,911 (GRCm39) |
A149S |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Zfp316 |
A |
T |
5: 143,239,280 (GRCm39) |
F913Y |
probably damaging |
Het |
|
Other mutations in Eif4g3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01817:Eif4g3
|
APN |
4 |
137,847,673 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02171:Eif4g3
|
APN |
4 |
137,853,900 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02487:Eif4g3
|
APN |
4 |
137,930,689 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02514:Eif4g3
|
APN |
4 |
137,853,505 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02622:Eif4g3
|
APN |
4 |
137,824,677 (GRCm39) |
splice site |
probably benign |
|
IGL02725:Eif4g3
|
APN |
4 |
137,897,782 (GRCm39) |
splice site |
probably benign |
|
IGL02735:Eif4g3
|
APN |
4 |
137,853,522 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03008:Eif4g3
|
APN |
4 |
137,847,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03077:Eif4g3
|
APN |
4 |
137,853,166 (GRCm39) |
missense |
probably damaging |
1.00 |
N/A - 535:Eif4g3
|
UTSW |
4 |
137,847,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R0013:Eif4g3
|
UTSW |
4 |
137,903,159 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0193:Eif4g3
|
UTSW |
4 |
137,873,687 (GRCm39) |
splice site |
probably benign |
|
R0240:Eif4g3
|
UTSW |
4 |
137,897,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R0240:Eif4g3
|
UTSW |
4 |
137,897,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R0563:Eif4g3
|
UTSW |
4 |
137,903,151 (GRCm39) |
splice site |
probably benign |
|
R0841:Eif4g3
|
UTSW |
4 |
137,893,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0884:Eif4g3
|
UTSW |
4 |
137,879,087 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1116:Eif4g3
|
UTSW |
4 |
137,819,086 (GRCm39) |
critical splice donor site |
probably null |
|
R1145:Eif4g3
|
UTSW |
4 |
137,893,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Eif4g3
|
UTSW |
4 |
137,893,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R1192:Eif4g3
|
UTSW |
4 |
137,898,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Eif4g3
|
UTSW |
4 |
137,933,395 (GRCm39) |
missense |
probably damaging |
0.99 |
R1535:Eif4g3
|
UTSW |
4 |
137,824,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1571:Eif4g3
|
UTSW |
4 |
137,847,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1576:Eif4g3
|
UTSW |
4 |
137,824,181 (GRCm39) |
missense |
probably damaging |
0.99 |
R1607:Eif4g3
|
UTSW |
4 |
137,853,874 (GRCm39) |
missense |
probably benign |
0.00 |
R1618:Eif4g3
|
UTSW |
4 |
137,933,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Eif4g3
|
UTSW |
4 |
137,898,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Eif4g3
|
UTSW |
4 |
137,907,802 (GRCm39) |
missense |
probably benign |
0.37 |
R1857:Eif4g3
|
UTSW |
4 |
137,903,187 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1907:Eif4g3
|
UTSW |
4 |
137,885,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Eif4g3
|
UTSW |
4 |
137,832,617 (GRCm39) |
splice site |
probably benign |
|
R2106:Eif4g3
|
UTSW |
4 |
137,810,230 (GRCm39) |
start gained |
probably benign |
|
R2124:Eif4g3
|
UTSW |
4 |
137,912,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R2301:Eif4g3
|
UTSW |
4 |
137,899,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R2519:Eif4g3
|
UTSW |
4 |
137,824,629 (GRCm39) |
missense |
probably benign |
0.37 |
R3033:Eif4g3
|
UTSW |
4 |
137,830,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R3870:Eif4g3
|
UTSW |
4 |
137,824,211 (GRCm39) |
missense |
probably damaging |
0.98 |
R4542:Eif4g3
|
UTSW |
4 |
137,930,728 (GRCm39) |
missense |
probably damaging |
0.99 |
R4582:Eif4g3
|
UTSW |
4 |
137,898,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R4607:Eif4g3
|
UTSW |
4 |
137,853,769 (GRCm39) |
missense |
probably benign |
0.03 |
R4608:Eif4g3
|
UTSW |
4 |
137,853,769 (GRCm39) |
missense |
probably benign |
0.03 |
R4658:Eif4g3
|
UTSW |
4 |
137,933,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Eif4g3
|
UTSW |
4 |
137,925,408 (GRCm39) |
missense |
probably benign |
0.01 |
R4739:Eif4g3
|
UTSW |
4 |
137,925,408 (GRCm39) |
missense |
probably benign |
0.01 |
R4739:Eif4g3
|
UTSW |
4 |
137,910,510 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4740:Eif4g3
|
UTSW |
4 |
137,925,408 (GRCm39) |
missense |
probably benign |
0.01 |
R4760:Eif4g3
|
UTSW |
4 |
137,811,629 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4825:Eif4g3
|
UTSW |
4 |
137,921,392 (GRCm39) |
missense |
probably benign |
|
R4826:Eif4g3
|
UTSW |
4 |
137,905,256 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4941:Eif4g3
|
UTSW |
4 |
137,897,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R5040:Eif4g3
|
UTSW |
4 |
137,824,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Eif4g3
|
UTSW |
4 |
137,873,610 (GRCm39) |
missense |
probably benign |
0.00 |
R5155:Eif4g3
|
UTSW |
4 |
137,854,054 (GRCm39) |
missense |
probably benign |
0.36 |
R5226:Eif4g3
|
UTSW |
4 |
137,824,105 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5229:Eif4g3
|
UTSW |
4 |
137,824,105 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5303:Eif4g3
|
UTSW |
4 |
137,853,873 (GRCm39) |
missense |
probably benign |
0.04 |
R5369:Eif4g3
|
UTSW |
4 |
137,910,645 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5394:Eif4g3
|
UTSW |
4 |
137,830,709 (GRCm39) |
splice site |
probably null |
|
R5665:Eif4g3
|
UTSW |
4 |
137,853,900 (GRCm39) |
missense |
probably benign |
0.03 |
R5678:Eif4g3
|
UTSW |
4 |
137,879,053 (GRCm39) |
missense |
probably damaging |
0.99 |
R5695:Eif4g3
|
UTSW |
4 |
137,890,744 (GRCm39) |
splice site |
probably null |
|
R5704:Eif4g3
|
UTSW |
4 |
137,918,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R5924:Eif4g3
|
UTSW |
4 |
137,929,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R6214:Eif4g3
|
UTSW |
4 |
137,785,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R6278:Eif4g3
|
UTSW |
4 |
137,915,394 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6519:Eif4g3
|
UTSW |
4 |
137,721,319 (GRCm39) |
missense |
probably benign |
|
R6659:Eif4g3
|
UTSW |
4 |
137,905,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6720:Eif4g3
|
UTSW |
4 |
137,903,143 (GRCm39) |
splice site |
probably null |
|
R6812:Eif4g3
|
UTSW |
4 |
137,830,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Eif4g3
|
UTSW |
4 |
137,853,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R7176:Eif4g3
|
UTSW |
4 |
137,898,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Eif4g3
|
UTSW |
4 |
137,921,435 (GRCm39) |
missense |
probably benign |
0.02 |
R7618:Eif4g3
|
UTSW |
4 |
137,898,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R7805:Eif4g3
|
UTSW |
4 |
137,873,665 (GRCm39) |
missense |
probably benign |
0.00 |
R7935:Eif4g3
|
UTSW |
4 |
137,824,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R7983:Eif4g3
|
UTSW |
4 |
137,878,904 (GRCm39) |
missense |
probably benign |
0.00 |
R8261:Eif4g3
|
UTSW |
4 |
137,898,429 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8371:Eif4g3
|
UTSW |
4 |
137,824,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R8499:Eif4g3
|
UTSW |
4 |
137,893,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R8670:Eif4g3
|
UTSW |
4 |
137,885,823 (GRCm39) |
critical splice donor site |
probably null |
|
R8672:Eif4g3
|
UTSW |
4 |
137,853,823 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8744:Eif4g3
|
UTSW |
4 |
137,721,372 (GRCm39) |
small deletion |
probably benign |
|
R8767:Eif4g3
|
UTSW |
4 |
137,930,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R8771:Eif4g3
|
UTSW |
4 |
137,907,848 (GRCm39) |
nonsense |
probably null |
|
R8989:Eif4g3
|
UTSW |
4 |
137,912,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R9292:Eif4g3
|
UTSW |
4 |
137,921,382 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9294:Eif4g3
|
UTSW |
4 |
137,917,968 (GRCm39) |
missense |
probably damaging |
0.98 |
R9607:Eif4g3
|
UTSW |
4 |
137,893,045 (GRCm39) |
missense |
probably benign |
0.28 |
R9617:Eif4g3
|
UTSW |
4 |
137,824,190 (GRCm39) |
missense |
probably damaging |
0.99 |
RF008:Eif4g3
|
UTSW |
4 |
137,903,235 (GRCm39) |
missense |
probably damaging |
0.98 |
X0067:Eif4g3
|
UTSW |
4 |
137,890,930 (GRCm39) |
critical splice donor site |
probably null |
|
|