Incidental Mutation 'R1855:Eif4g1'
ID |
206057 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Eif4g1
|
Ensembl Gene |
ENSMUSG00000045983 |
Gene Name |
eukaryotic translation initiation factor 4, gamma 1 |
Synonyms |
E030015G23Rik |
MMRRC Submission |
039879-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.970)
|
Stock # |
R1855 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
20491457-20511633 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 20505911 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Lysine
at position 1025
(T1025K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144320
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044783]
[ENSMUST00000073840]
[ENSMUST00000115457]
[ENSMUST00000115460]
[ENSMUST00000115461]
[ENSMUST00000143939]
[ENSMUST00000115463]
[ENSMUST00000128594]
[ENSMUST00000156226]
[ENSMUST00000142344]
[ENSMUST00000150333]
|
AlphaFold |
Q6NZJ6 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000044783
AA Change: T1322K
PolyPhen 2
Score 0.775 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000047678 Gene: ENSMUSG00000045983 AA Change: T1322K
Domain | Start | End | E-Value | Type |
low complexity region
|
60 |
81 |
N/A |
INTRINSIC |
PDB:1LJ2|D
|
179 |
206 |
1e-10 |
PDB |
low complexity region
|
260 |
286 |
N/A |
INTRINSIC |
low complexity region
|
436 |
457 |
N/A |
INTRINSIC |
low complexity region
|
464 |
487 |
N/A |
INTRINSIC |
Blast:MIF4G
|
638 |
683 |
7e-9 |
BLAST |
low complexity region
|
685 |
707 |
N/A |
INTRINSIC |
MIF4G
|
765 |
993 |
5.14e-72 |
SMART |
low complexity region
|
1035 |
1047 |
N/A |
INTRINSIC |
low complexity region
|
1092 |
1106 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1178 |
N/A |
INTRINSIC |
low complexity region
|
1186 |
1201 |
N/A |
INTRINSIC |
MA3
|
1242 |
1354 |
3.83e-39 |
SMART |
low complexity region
|
1441 |
1452 |
N/A |
INTRINSIC |
eIF5C
|
1508 |
1595 |
3.78e-33 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000073840
AA Change: T1315K
PolyPhen 2
Score 0.775 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000073506 Gene: ENSMUSG00000045983 AA Change: T1315K
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
74 |
N/A |
INTRINSIC |
PDB:1LJ2|D
|
172 |
199 |
1e-10 |
PDB |
low complexity region
|
253 |
279 |
N/A |
INTRINSIC |
low complexity region
|
429 |
450 |
N/A |
INTRINSIC |
low complexity region
|
457 |
480 |
N/A |
INTRINSIC |
Blast:MIF4G
|
631 |
676 |
7e-9 |
BLAST |
low complexity region
|
678 |
700 |
N/A |
INTRINSIC |
MIF4G
|
758 |
986 |
5.14e-72 |
SMART |
low complexity region
|
1028 |
1040 |
N/A |
INTRINSIC |
low complexity region
|
1085 |
1099 |
N/A |
INTRINSIC |
low complexity region
|
1150 |
1171 |
N/A |
INTRINSIC |
low complexity region
|
1179 |
1194 |
N/A |
INTRINSIC |
MA3
|
1235 |
1347 |
3.83e-39 |
SMART |
low complexity region
|
1434 |
1445 |
N/A |
INTRINSIC |
eIF5C
|
1501 |
1588 |
3.78e-33 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000104051
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000115457
AA Change: T1275K
PolyPhen 2
Score 0.775 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000111117 Gene: ENSMUSG00000045983 AA Change: T1275K
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
34 |
N/A |
INTRINSIC |
PDB:1LJ2|D
|
132 |
159 |
9e-11 |
PDB |
low complexity region
|
213 |
239 |
N/A |
INTRINSIC |
low complexity region
|
389 |
410 |
N/A |
INTRINSIC |
low complexity region
|
417 |
440 |
N/A |
INTRINSIC |
Blast:MIF4G
|
591 |
636 |
7e-9 |
BLAST |
low complexity region
|
638 |
660 |
N/A |
INTRINSIC |
MIF4G
|
718 |
946 |
5.14e-72 |
SMART |
low complexity region
|
988 |
1000 |
N/A |
INTRINSIC |
low complexity region
|
1045 |
1059 |
N/A |
INTRINSIC |
low complexity region
|
1110 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1139 |
1154 |
N/A |
INTRINSIC |
MA3
|
1195 |
1307 |
3.83e-39 |
SMART |
low complexity region
|
1394 |
1405 |
N/A |
INTRINSIC |
eIF5C
|
1461 |
1548 |
3.78e-33 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000115460
AA Change: T1322K
PolyPhen 2
Score 0.775 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000111120 Gene: ENSMUSG00000045983 AA Change: T1322K
Domain | Start | End | E-Value | Type |
low complexity region
|
60 |
81 |
N/A |
INTRINSIC |
PDB:1LJ2|D
|
179 |
206 |
1e-10 |
PDB |
low complexity region
|
260 |
286 |
N/A |
INTRINSIC |
low complexity region
|
436 |
457 |
N/A |
INTRINSIC |
low complexity region
|
464 |
487 |
N/A |
INTRINSIC |
Blast:MIF4G
|
638 |
683 |
7e-9 |
BLAST |
low complexity region
|
685 |
707 |
N/A |
INTRINSIC |
MIF4G
|
765 |
993 |
5.14e-72 |
SMART |
low complexity region
|
1035 |
1047 |
N/A |
INTRINSIC |
low complexity region
|
1092 |
1106 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1178 |
N/A |
INTRINSIC |
low complexity region
|
1186 |
1201 |
N/A |
INTRINSIC |
MA3
|
1242 |
1354 |
3.83e-39 |
SMART |
low complexity region
|
1441 |
1452 |
N/A |
INTRINSIC |
eIF5C
|
1508 |
1595 |
3.78e-33 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000115461
AA Change: T1316K
PolyPhen 2
Score 0.775 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000111121 Gene: ENSMUSG00000045983 AA Change: T1316K
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
74 |
N/A |
INTRINSIC |
PDB:1LJ2|D
|
172 |
199 |
1e-10 |
PDB |
low complexity region
|
253 |
279 |
N/A |
INTRINSIC |
low complexity region
|
429 |
450 |
N/A |
INTRINSIC |
low complexity region
|
457 |
480 |
N/A |
INTRINSIC |
Blast:MIF4G
|
631 |
676 |
8e-9 |
BLAST |
low complexity region
|
678 |
693 |
N/A |
INTRINSIC |
MIF4G
|
759 |
987 |
5.14e-72 |
SMART |
low complexity region
|
1029 |
1041 |
N/A |
INTRINSIC |
low complexity region
|
1086 |
1100 |
N/A |
INTRINSIC |
low complexity region
|
1151 |
1172 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1195 |
N/A |
INTRINSIC |
MA3
|
1236 |
1348 |
3.83e-39 |
SMART |
low complexity region
|
1435 |
1446 |
N/A |
INTRINSIC |
eIF5C
|
1502 |
1589 |
3.78e-33 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000143939
AA Change: T1025K
PolyPhen 2
Score 0.775 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000144320 Gene: ENSMUSG00000045983 AA Change: T1025K
Domain | Start | End | E-Value | Type |
low complexity region
|
139 |
160 |
N/A |
INTRINSIC |
low complexity region
|
167 |
190 |
N/A |
INTRINSIC |
Blast:MIF4G
|
341 |
386 |
6e-9 |
BLAST |
low complexity region
|
388 |
410 |
N/A |
INTRINSIC |
MIF4G
|
468 |
696 |
2.2e-74 |
SMART |
low complexity region
|
738 |
750 |
N/A |
INTRINSIC |
low complexity region
|
795 |
809 |
N/A |
INTRINSIC |
low complexity region
|
860 |
881 |
N/A |
INTRINSIC |
low complexity region
|
889 |
904 |
N/A |
INTRINSIC |
MA3
|
945 |
1057 |
1.7e-41 |
SMART |
low complexity region
|
1144 |
1155 |
N/A |
INTRINSIC |
eIF5C
|
1211 |
1298 |
1.8e-35 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000115463
AA Change: T1308K
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000111123 Gene: ENSMUSG00000045983 AA Change: T1308K
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
74 |
N/A |
INTRINSIC |
PDB:1LJ2|D
|
172 |
199 |
1e-10 |
PDB |
low complexity region
|
253 |
279 |
N/A |
INTRINSIC |
low complexity region
|
429 |
450 |
N/A |
INTRINSIC |
low complexity region
|
457 |
480 |
N/A |
INTRINSIC |
Blast:MIF4G
|
631 |
676 |
7e-9 |
BLAST |
low complexity region
|
678 |
700 |
N/A |
INTRINSIC |
MIF4G
|
758 |
986 |
5.14e-72 |
SMART |
low complexity region
|
1030 |
1036 |
N/A |
INTRINSIC |
low complexity region
|
1078 |
1092 |
N/A |
INTRINSIC |
low complexity region
|
1143 |
1164 |
N/A |
INTRINSIC |
low complexity region
|
1172 |
1187 |
N/A |
INTRINSIC |
MA3
|
1228 |
1340 |
3.83e-39 |
SMART |
low complexity region
|
1427 |
1438 |
N/A |
INTRINSIC |
eIF5C
|
1494 |
1581 |
3.78e-33 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132320
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000129958
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000128594
|
SMART Domains |
Protein: ENSMUSP00000144594 Gene: ENSMUSG00000045983
Domain | Start | End | E-Value | Type |
PDB:1LJ2|D
|
8 |
35 |
5e-11 |
PDB |
low complexity region
|
89 |
115 |
N/A |
INTRINSIC |
low complexity region
|
265 |
286 |
N/A |
INTRINSIC |
low complexity region
|
293 |
316 |
N/A |
INTRINSIC |
Blast:MIF4G
|
467 |
512 |
4e-9 |
BLAST |
low complexity region
|
514 |
536 |
N/A |
INTRINSIC |
MIF4G
|
594 |
795 |
1.1e-52 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000156226
|
SMART Domains |
Protein: ENSMUSP00000119215 Gene: ENSMUSG00000045983
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
74 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000142344
|
SMART Domains |
Protein: ENSMUSP00000116029 Gene: ENSMUSG00000045983
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
74 |
N/A |
INTRINSIC |
PDB:1LJ2|D
|
172 |
199 |
5e-11 |
PDB |
low complexity region
|
253 |
279 |
N/A |
INTRINSIC |
low complexity region
|
429 |
450 |
N/A |
INTRINSIC |
low complexity region
|
457 |
480 |
N/A |
INTRINSIC |
Blast:MIF4G
|
631 |
672 |
6e-8 |
BLAST |
low complexity region
|
678 |
693 |
N/A |
INTRINSIC |
MIF4G
|
759 |
958 |
5.49e-49 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150333
|
SMART Domains |
Protein: ENSMUSP00000144107 Gene: ENSMUSG00000045983
Domain | Start | End | E-Value | Type |
PDB:1LJ2|D
|
113 |
140 |
5e-11 |
PDB |
low complexity region
|
194 |
220 |
N/A |
INTRINSIC |
low complexity region
|
370 |
391 |
N/A |
INTRINSIC |
low complexity region
|
398 |
421 |
N/A |
INTRINSIC |
Blast:MIF4G
|
572 |
613 |
9e-8 |
BLAST |
low complexity region
|
619 |
641 |
N/A |
INTRINSIC |
MIF4G
|
699 |
900 |
1.1e-52 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000231598
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000231477
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.4%
|
Validation Efficiency |
97% (72/74) |
MGI Phenotype |
FUNCTION: This gene encodes a member of the eukaryotic translation initiation factors (eIF) that play important roles in translation initiation by mediating recruitment of additional initiation factors and providing a scaffold for ribosome/mRNA-bridging. Along with eIF4A and eIF4E, the encoded protein forms the eIF4F complex that bridges the 5' UTR with the polyadenylated 3' UTR resulting in mRNA circularization, enhanced translation initiation and mRNA stability. Through its association with eIF3, the encoded protein mediates recruitment of the 43S pre-initiation complex to mRNA. Alternative splicing of this gene results in multiple transcript variants. Pseudogenes for this gene have been identified on chromosomes 2 and 13. [provided by RefSeq, Jan 2015] PHENOTYPE: Mice homozygous for an amino acid substitution (R1207H) are viable and fertile. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
T |
A |
1: 11,818,195 (GRCm39) |
L285Q |
probably damaging |
Het |
Acaca |
T |
C |
11: 84,262,380 (GRCm39) |
L1994P |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,878,350 (GRCm39) |
|
probably benign |
Het |
Aff3 |
T |
C |
1: 38,249,385 (GRCm39) |
E574G |
probably benign |
Het |
Ankrd1 |
T |
C |
19: 36,096,635 (GRCm39) |
K64R |
probably damaging |
Het |
Arhgap23 |
T |
C |
11: 97,339,523 (GRCm39) |
I163T |
probably damaging |
Het |
Ascc3 |
A |
T |
10: 50,494,018 (GRCm39) |
Q151L |
probably benign |
Het |
Atad2 |
G |
A |
15: 57,960,685 (GRCm39) |
P971L |
possibly damaging |
Het |
C1s1 |
A |
C |
6: 124,511,315 (GRCm39) |
|
probably null |
Het |
Ccdc150 |
T |
C |
1: 54,407,069 (GRCm39) |
|
probably benign |
Het |
Cdhr3 |
A |
T |
12: 33,110,351 (GRCm39) |
I311N |
probably damaging |
Het |
Chad |
T |
A |
11: 94,456,303 (GRCm39) |
L127H |
probably damaging |
Het |
Clasp1 |
G |
A |
1: 118,436,624 (GRCm39) |
A303T |
probably damaging |
Het |
Clptm1 |
A |
G |
7: 19,372,134 (GRCm39) |
V234A |
probably benign |
Het |
Cnih3 |
C |
A |
1: 181,282,186 (GRCm39) |
S140* |
probably null |
Het |
Col24a1 |
G |
A |
3: 145,164,895 (GRCm39) |
G1033D |
probably damaging |
Het |
Csnk1a1 |
T |
A |
18: 61,708,498 (GRCm39) |
|
probably null |
Het |
Cttnbp2 |
T |
A |
6: 18,378,412 (GRCm39) |
I1475L |
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,411,815 (GRCm39) |
V3728A |
possibly damaging |
Het |
Dock9 |
C |
A |
14: 121,877,571 (GRCm39) |
V391F |
probably damaging |
Het |
Ehmt2 |
A |
T |
17: 35,129,752 (GRCm39) |
I949F |
probably damaging |
Het |
Enpp2 |
C |
T |
15: 54,709,219 (GRCm39) |
E803K |
probably damaging |
Het |
Esrrg |
A |
T |
1: 187,943,295 (GRCm39) |
M423L |
probably damaging |
Het |
Etnppl |
A |
T |
3: 130,414,371 (GRCm39) |
I89F |
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fbln7 |
A |
G |
2: 128,735,755 (GRCm39) |
T248A |
possibly damaging |
Het |
Galnt9 |
C |
T |
5: 110,763,390 (GRCm39) |
T465M |
probably damaging |
Het |
Grcc10 |
A |
G |
6: 124,717,541 (GRCm39) |
V57A |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,298,708 (GRCm39) |
M614K |
possibly damaging |
Het |
Itch |
C |
T |
2: 155,014,374 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
C |
A |
11: 69,298,112 (GRCm39) |
A167S |
probably damaging |
Het |
Kidins220 |
C |
T |
12: 25,106,590 (GRCm39) |
R1348C |
probably damaging |
Het |
Kif17 |
T |
C |
4: 138,015,582 (GRCm39) |
L577P |
probably benign |
Het |
Krt25 |
A |
T |
11: 99,209,141 (GRCm39) |
L258Q |
probably damaging |
Het |
Marchf10 |
T |
C |
11: 105,281,218 (GRCm39) |
T356A |
probably benign |
Het |
Mical2 |
G |
A |
7: 111,944,489 (GRCm39) |
A940T |
probably benign |
Het |
Mrpl4 |
A |
G |
9: 20,914,667 (GRCm39) |
E81G |
possibly damaging |
Het |
Mtcl1 |
A |
G |
17: 66,686,509 (GRCm39) |
V447A |
probably benign |
Het |
Mtor |
C |
A |
4: 148,637,546 (GRCm39) |
N2502K |
probably benign |
Het |
Notch4 |
G |
A |
17: 34,799,936 (GRCm39) |
D966N |
probably benign |
Het |
Oip5 |
C |
A |
2: 119,442,271 (GRCm39) |
K214N |
probably benign |
Het |
Or8a1b |
A |
T |
9: 37,623,266 (GRCm39) |
F103Y |
possibly damaging |
Het |
Pabir2 |
T |
A |
X: 52,342,933 (GRCm39) |
Q201H |
probably benign |
Het |
Pak5 |
A |
T |
2: 135,929,429 (GRCm39) |
S585T |
probably benign |
Het |
Pard3 |
T |
A |
8: 128,174,293 (GRCm39) |
|
probably null |
Het |
Pcnx2 |
A |
T |
8: 126,534,735 (GRCm39) |
|
probably benign |
Het |
Pcsk5 |
T |
C |
19: 17,492,556 (GRCm39) |
Y939C |
possibly damaging |
Het |
Pde1a |
A |
G |
2: 79,728,408 (GRCm39) |
|
probably null |
Het |
Pde9a |
C |
T |
17: 31,674,094 (GRCm39) |
P60S |
probably damaging |
Het |
Pikfyve |
C |
A |
1: 65,297,957 (GRCm39) |
T1562K |
probably benign |
Het |
Plekhg6 |
A |
T |
6: 125,352,802 (GRCm39) |
M115K |
probably damaging |
Het |
Pogz |
C |
T |
3: 94,786,160 (GRCm39) |
T863I |
probably benign |
Het |
Ppp1r3a |
A |
T |
6: 14,754,993 (GRCm39) |
W85R |
probably damaging |
Het |
Rnf123 |
C |
A |
9: 107,938,990 (GRCm39) |
R826L |
probably damaging |
Het |
Slc1a6 |
T |
A |
10: 78,648,758 (GRCm39) |
V493E |
probably damaging |
Het |
Slc22a2 |
A |
G |
17: 12,805,699 (GRCm39) |
D150G |
probably damaging |
Het |
Snap47 |
C |
T |
11: 59,319,159 (GRCm39) |
|
probably benign |
Het |
Spata22 |
A |
G |
11: 73,231,385 (GRCm39) |
D213G |
probably benign |
Het |
St6galnac2 |
T |
A |
11: 116,581,141 (GRCm39) |
R60S |
probably benign |
Het |
Stk32c |
A |
G |
7: 138,701,363 (GRCm39) |
F263S |
probably damaging |
Het |
Supt6 |
T |
C |
11: 78,123,366 (GRCm39) |
I104V |
possibly damaging |
Het |
Tex2 |
T |
C |
11: 106,437,702 (GRCm39) |
E158G |
possibly damaging |
Het |
Tiam2 |
C |
T |
17: 3,465,410 (GRCm39) |
R380C |
probably damaging |
Het |
Trim25 |
C |
T |
11: 88,906,407 (GRCm39) |
T410I |
probably benign |
Het |
Usp18 |
T |
A |
6: 121,239,076 (GRCm39) |
C212S |
probably benign |
Het |
Vmn1r2 |
A |
G |
4: 3,172,588 (GRCm39) |
Y169C |
probably damaging |
Het |
Wdr33 |
A |
T |
18: 32,039,909 (GRCm39) |
|
probably benign |
Het |
Xpr1 |
A |
G |
1: 155,159,002 (GRCm39) |
Y597H |
probably benign |
Het |
Yy1 |
CGGG |
CGGGGGGGGG |
12: 108,759,916 (GRCm39) |
|
probably benign |
Het |
Zfp54 |
T |
A |
17: 21,654,404 (GRCm39) |
Y299* |
probably null |
Het |
Zfp566 |
T |
G |
7: 29,777,927 (GRCm39) |
S85R |
probably benign |
Het |
|
Other mutations in Eif4g1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00584:Eif4g1
|
APN |
16 |
20,505,504 (GRCm39) |
intron |
probably benign |
|
IGL00707:Eif4g1
|
APN |
16 |
20,507,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00950:Eif4g1
|
APN |
16 |
20,502,378 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01397:Eif4g1
|
APN |
16 |
20,498,425 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01657:Eif4g1
|
APN |
16 |
20,500,966 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01875:Eif4g1
|
APN |
16 |
20,499,790 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02728:Eif4g1
|
APN |
16 |
20,505,502 (GRCm39) |
intron |
probably benign |
|
IGL03155:Eif4g1
|
APN |
16 |
20,511,167 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03339:Eif4g1
|
APN |
16 |
20,499,734 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0032:Eif4g1
|
UTSW |
16 |
20,504,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:Eif4g1
|
UTSW |
16 |
20,504,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Eif4g1
|
UTSW |
16 |
20,494,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R0556:Eif4g1
|
UTSW |
16 |
20,494,544 (GRCm39) |
missense |
probably damaging |
0.99 |
R0576:Eif4g1
|
UTSW |
16 |
20,502,818 (GRCm39) |
missense |
probably damaging |
0.98 |
R1424:Eif4g1
|
UTSW |
16 |
20,497,692 (GRCm39) |
missense |
probably benign |
0.03 |
R1469:Eif4g1
|
UTSW |
16 |
20,498,758 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1469:Eif4g1
|
UTSW |
16 |
20,498,758 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1487:Eif4g1
|
UTSW |
16 |
20,497,623 (GRCm39) |
unclassified |
probably benign |
|
R1659:Eif4g1
|
UTSW |
16 |
20,499,811 (GRCm39) |
missense |
probably damaging |
0.99 |
R1697:Eif4g1
|
UTSW |
16 |
20,498,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R1848:Eif4g1
|
UTSW |
16 |
20,500,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Eif4g1
|
UTSW |
16 |
20,497,398 (GRCm39) |
missense |
probably damaging |
0.99 |
R3001:Eif4g1
|
UTSW |
16 |
20,511,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R3002:Eif4g1
|
UTSW |
16 |
20,511,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R4402:Eif4g1
|
UTSW |
16 |
20,497,593 (GRCm39) |
unclassified |
probably benign |
|
R4477:Eif4g1
|
UTSW |
16 |
20,497,593 (GRCm39) |
unclassified |
probably benign |
|
R4478:Eif4g1
|
UTSW |
16 |
20,497,593 (GRCm39) |
unclassified |
probably benign |
|
R4479:Eif4g1
|
UTSW |
16 |
20,497,593 (GRCm39) |
unclassified |
probably benign |
|
R4480:Eif4g1
|
UTSW |
16 |
20,497,593 (GRCm39) |
unclassified |
probably benign |
|
R4623:Eif4g1
|
UTSW |
16 |
20,500,095 (GRCm39) |
unclassified |
probably benign |
|
R4658:Eif4g1
|
UTSW |
16 |
20,504,684 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4751:Eif4g1
|
UTSW |
16 |
20,505,265 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4859:Eif4g1
|
UTSW |
16 |
20,500,923 (GRCm39) |
missense |
probably benign |
0.44 |
R5267:Eif4g1
|
UTSW |
16 |
20,504,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R5376:Eif4g1
|
UTSW |
16 |
20,502,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Eif4g1
|
UTSW |
16 |
20,505,645 (GRCm39) |
missense |
probably benign |
|
R5719:Eif4g1
|
UTSW |
16 |
20,507,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R6632:Eif4g1
|
UTSW |
16 |
20,504,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R6849:Eif4g1
|
UTSW |
16 |
20,499,495 (GRCm39) |
missense |
probably benign |
0.08 |
R7134:Eif4g1
|
UTSW |
16 |
20,500,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R7793:Eif4g1
|
UTSW |
16 |
20,507,364 (GRCm39) |
missense |
probably benign |
0.00 |
R7861:Eif4g1
|
UTSW |
16 |
20,498,452 (GRCm39) |
missense |
probably benign |
|
R8309:Eif4g1
|
UTSW |
16 |
20,507,578 (GRCm39) |
missense |
probably benign |
0.19 |
R8365:Eif4g1
|
UTSW |
16 |
20,502,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R8726:Eif4g1
|
UTSW |
16 |
20,494,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R8778:Eif4g1
|
UTSW |
16 |
20,492,196 (GRCm39) |
intron |
probably benign |
|
R9604:Eif4g1
|
UTSW |
16 |
20,500,255 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9658:Eif4g1
|
UTSW |
16 |
20,502,863 (GRCm39) |
missense |
probably benign |
0.01 |
R9779:Eif4g1
|
UTSW |
16 |
20,498,251 (GRCm39) |
missense |
probably damaging |
0.97 |
X0062:Eif4g1
|
UTSW |
16 |
20,503,251 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Eif4g1
|
UTSW |
16 |
20,501,476 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Eif4g1
|
UTSW |
16 |
20,492,158 (GRCm39) |
intron |
probably benign |
|
Z1177:Eif4g1
|
UTSW |
16 |
20,505,116 (GRCm39) |
frame shift |
probably null |
|
Z1177:Eif4g1
|
UTSW |
16 |
20,502,655 (GRCm39) |
missense |
probably benign |
0.06 |
|
Predicted Primers |
PCR Primer
(F):5'- TCCGCATAGCTCACCAATTC -3'
(R):5'- TCATCAATCCCGATGGCCTC -3'
Sequencing Primer
(F):5'- CCTTTGTGGGATTCCTGAAATC -3'
(R):5'- TGGCCTCCAAACCCAAGTCTG -3'
|
Posted On |
2014-06-23 |