Incidental Mutation 'R5719:Eif4g1'
| ID |
451381 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Eif4g1
|
| Ensembl Gene |
ENSMUSG00000045983 |
| Gene Name |
eukaryotic translation initiation factor 4, gamma 1 |
| Synonyms |
E030015G23Rik |
| MMRRC Submission |
043339-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.970)
|
| Stock # |
R5719 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
20491457-20511633 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 20507761 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Aspartic acid
at position 1182
(V1182D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000144320
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044783]
[ENSMUST00000073840]
[ENSMUST00000115457]
[ENSMUST00000115460]
[ENSMUST00000115461]
[ENSMUST00000115463]
[ENSMUST00000143939]
[ENSMUST00000232207]
[ENSMUST00000118919]
[ENSMUST00000149543]
[ENSMUST00000156226]
|
| AlphaFold |
Q6NZJ6 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000044783
AA Change: V1479D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000047678
Gene: ENSMUSG00000045983
AA Change: V1479D
| 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 |
probably damaging
Transcript: ENSMUST00000073840
AA Change: V1472D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000073506
Gene: ENSMUSG00000045983
AA Change: V1472D
| 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 |
probably damaging
Transcript: ENSMUST00000115457
AA Change: V1432D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000111117
Gene: ENSMUSG00000045983
AA Change: V1432D
| 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 |
probably damaging
Transcript: ENSMUST00000115460
AA Change: V1479D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000111120
Gene: ENSMUSG00000045983
AA Change: V1479D
| 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 |
probably damaging
Transcript: ENSMUST00000115461
AA Change: V1473D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000111121
Gene: ENSMUSG00000045983
AA Change: V1473D
| 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 |
probably benign
Transcript: ENSMUST00000115463
AA Change: V1465D
PolyPhen 2
Score 0.040 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000111123
Gene: ENSMUSG00000045983
AA Change: V1465D
| 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: ENSMUST00000129958
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132320
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000143939
AA Change: V1182D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000144320
Gene: ENSMUSG00000045983
AA Change: V1182D
| 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 |
probably benign
Transcript: ENSMUST00000232207
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231598
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000118919
|
| SMART Domains |
Protein: ENSMUSP00000113719
Gene: ENSMUSG00000050821
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:FAM131
|
1 |
271 |
4e-119 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000149543
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000231477
|
| 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 |
|
| Meta Mutation Damage Score |
0.9491 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.3%
|
| Validation Efficiency |
98% (79/81) |
| 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: 69 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A130051J06Rik |
C |
T |
15: 95,688,641 (GRCm39) |
|
probably benign |
Het |
| A630001G21Rik |
T |
A |
1: 85,651,106 (GRCm39) |
R110W |
probably benign |
Het |
| Abca4 |
T |
C |
3: 121,928,915 (GRCm39) |
|
probably null |
Het |
| Abcc3 |
T |
C |
11: 94,241,894 (GRCm39) |
N1379S |
probably damaging |
Het |
| Actrt3 |
A |
C |
3: 30,652,276 (GRCm39) |
F273V |
probably benign |
Het |
| Adam22 |
T |
C |
5: 8,417,217 (GRCm39) |
D75G |
probably benign |
Het |
| Ash1l |
C |
A |
3: 88,961,805 (GRCm39) |
D2392E |
possibly damaging |
Het |
| Ash1l |
T |
C |
3: 88,965,933 (GRCm39) |
I2445T |
probably damaging |
Het |
| Bltp2 |
T |
A |
11: 78,164,071 (GRCm39) |
H1137Q |
probably damaging |
Het |
| Cacna2d2 |
A |
G |
9: 107,401,851 (GRCm39) |
I762V |
probably benign |
Het |
| Ccdc127 |
T |
A |
13: 74,505,187 (GRCm39) |
|
probably benign |
Het |
| Ccdc91 |
C |
G |
6: 147,477,001 (GRCm39) |
L230V |
unknown |
Het |
| Cdk13 |
A |
G |
13: 17,894,240 (GRCm39) |
I1129T |
probably damaging |
Het |
| Cnot1 |
C |
T |
8: 96,470,924 (GRCm39) |
R1308H |
possibly damaging |
Het |
| Crhr2 |
T |
C |
6: 55,080,207 (GRCm39) |
H144R |
probably damaging |
Het |
| Dnmt1 |
T |
C |
9: 20,823,891 (GRCm39) |
N993S |
possibly damaging |
Het |
| Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
| Fam234a |
T |
A |
17: 26,433,627 (GRCm39) |
Q399L |
possibly damaging |
Het |
| Fyb1 |
A |
T |
15: 6,610,350 (GRCm39) |
K308* |
probably null |
Het |
| Gfral |
C |
T |
9: 76,104,328 (GRCm39) |
R228Q |
probably benign |
Het |
| Gm10309 |
A |
T |
17: 86,806,421 (GRCm39) |
|
probably benign |
Het |
| Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
| Gm5501 |
G |
A |
18: 9,917,417 (GRCm39) |
|
noncoding transcript |
Het |
| Gm6309 |
A |
T |
5: 146,104,992 (GRCm39) |
V307D |
probably benign |
Het |
| Gm9871 |
T |
A |
6: 101,773,148 (GRCm39) |
|
noncoding transcript |
Het |
| Greb1l |
G |
A |
18: 10,542,427 (GRCm39) |
E1341K |
probably damaging |
Het |
| Herc3 |
T |
A |
6: 58,871,528 (GRCm39) |
V70E |
possibly damaging |
Het |
| Hes7 |
A |
G |
11: 69,012,415 (GRCm39) |
E41G |
probably damaging |
Het |
| Ifi27l2b |
T |
C |
12: 103,422,046 (GRCm39) |
D106G |
unknown |
Het |
| Igfbp6 |
A |
T |
15: 102,056,616 (GRCm39) |
Y184F |
probably damaging |
Het |
| Isyna1 |
A |
G |
8: 71,047,352 (GRCm39) |
Y25C |
probably damaging |
Het |
| Kcng3 |
G |
T |
17: 83,938,563 (GRCm39) |
T162K |
possibly damaging |
Het |
| Krt36 |
T |
C |
11: 99,994,987 (GRCm39) |
D195G |
possibly damaging |
Het |
| Lrwd1 |
A |
T |
5: 136,161,093 (GRCm39) |
|
probably null |
Het |
| Lsg1 |
C |
T |
16: 30,380,593 (GRCm39) |
A615T |
probably benign |
Het |
| Myo5a |
A |
T |
9: 75,059,213 (GRCm39) |
E480D |
probably damaging |
Het |
| Myrf |
T |
A |
19: 10,194,087 (GRCm39) |
D690V |
probably damaging |
Het |
| N4bp1 |
T |
C |
8: 87,578,312 (GRCm39) |
I684M |
probably damaging |
Het |
| Nlrc3 |
C |
T |
16: 3,781,589 (GRCm39) |
A607T |
probably damaging |
Het |
| Nuak1 |
A |
T |
10: 84,245,584 (GRCm39) |
I87N |
probably damaging |
Het |
| Odad2 |
G |
T |
18: 7,211,496 (GRCm39) |
Q793K |
probably benign |
Het |
| Or5p66 |
T |
G |
7: 107,885,599 (GRCm39) |
T245P |
probably damaging |
Het |
| Or5w11 |
T |
C |
2: 87,459,475 (GRCm39) |
|
probably null |
Het |
| Or8b4 |
A |
T |
9: 37,830,647 (GRCm39) |
E236D |
probably damaging |
Het |
| Osbpl9 |
T |
A |
4: 108,919,763 (GRCm39) |
R689* |
probably null |
Het |
| Ppargc1b |
T |
A |
18: 61,440,639 (GRCm39) |
M744L |
probably benign |
Het |
| Prss40 |
A |
T |
1: 34,591,598 (GRCm39) |
|
probably benign |
Het |
| Ptprd |
T |
A |
4: 75,972,839 (GRCm39) |
|
probably null |
Het |
| Rft1 |
T |
C |
14: 30,385,183 (GRCm39) |
|
probably benign |
Het |
| Rftn2 |
C |
T |
1: 55,253,445 (GRCm39) |
V53I |
probably damaging |
Het |
| Rnaset2a |
T |
C |
17: 8,350,879 (GRCm39) |
Y167C |
probably damaging |
Het |
| Schip1 |
T |
C |
3: 68,315,560 (GRCm39) |
|
probably benign |
Het |
| Scn5a |
A |
C |
9: 119,359,118 (GRCm39) |
L643R |
possibly damaging |
Het |
| Shroom3 |
T |
A |
5: 93,090,877 (GRCm39) |
M1128K |
probably benign |
Het |
| Skint8 |
C |
A |
4: 111,807,390 (GRCm39) |
L359M |
probably damaging |
Het |
| Slc14a2 |
A |
G |
18: 78,252,257 (GRCm39) |
L18P |
probably benign |
Het |
| Slc22a3 |
C |
T |
17: 12,642,691 (GRCm39) |
V509M |
probably damaging |
Het |
| Slc7a5 |
A |
C |
8: 122,610,381 (GRCm39) |
F478V |
probably benign |
Het |
| Smc1b |
T |
A |
15: 84,980,859 (GRCm39) |
N803I |
probably benign |
Het |
| Snf8 |
T |
A |
11: 95,932,551 (GRCm39) |
N115K |
probably damaging |
Het |
| Stox2 |
T |
A |
8: 47,866,172 (GRCm39) |
K57* |
probably null |
Het |
| Tmem248 |
T |
A |
5: 130,258,429 (GRCm39) |
F41I |
probably damaging |
Het |
| Tmprss7 |
T |
C |
16: 45,506,793 (GRCm39) |
S90G |
probably damaging |
Het |
| Top3b |
T |
C |
16: 16,703,700 (GRCm39) |
V285A |
probably damaging |
Het |
| Tsen15 |
T |
C |
1: 152,247,534 (GRCm39) |
T153A |
probably damaging |
Het |
| Usp34 |
T |
G |
11: 23,304,846 (GRCm39) |
S360A |
probably benign |
Het |
| Wdr24 |
T |
C |
17: 26,047,314 (GRCm39) |
|
probably null |
Het |
| Zbtb2 |
G |
A |
10: 4,319,456 (GRCm39) |
T190I |
probably benign |
Het |
| Zranb3 |
T |
C |
1: 127,891,613 (GRCm39) |
S788G |
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 |
|
R1855:Eif4g1
|
UTSW |
16 |
20,505,911 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
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 |
|
|
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'- ATCAGCGTGTGTTCGACTGG -3'
(R):5'- CACAGGTATTTCTGCAGCAGTC -3'
Sequencing Primer
(F):5'- AGCGTGTGTTCGACTGGATAGAC -3'
(R):5'- CCATTAGATTGCCTGGCT -3'
|
| Posted On |
2017-01-03 |
Incidental Mutation