Incidental Mutation 'IGL02821:Eif3f'
ID 361017
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Eif3f
Ensembl Gene ENSMUSG00000031029
Gene Name eukaryotic translation initiation factor 3, subunit F
Synonyms Eif3s5, 0610037M02Rik
Accession Numbers
Essential gene? Probably essential (E-score: 0.965) question?
Stock # IGL02821
Quality Score
Status
Chromosome 7
Chromosomal Location 108533622-108541149 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to T at 108533881 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000050252 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033342] [ENSMUST00000055745]
AlphaFold Q9DCH4
PDB Structure Solution structure of the Pyrin/PAAD-DAPIN domain in mouse NALP10 (NACHT, leucine rich repeat and PYD containing 10) [SOLUTION NMR]
Predicted Effect unknown
Transcript: ENSMUST00000033342
AA Change: Q81H
SMART Domains Protein: ENSMUSP00000033342
Gene: ENSMUSG00000031029
AA Change: Q81H

DomainStartEndE-ValueType
low complexity region 2 93 N/A INTRINSIC
JAB_MPN 95 225 3.11e-42 SMART
Pfam:MitMem_reg 247 359 7e-27 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000055745
SMART Domains Protein: ENSMUSP00000050252
Gene: ENSMUSG00000049709

DomainStartEndE-ValueType
PYRIN 9 88 4.13e-18 SMART
low complexity region 126 137 N/A INTRINSIC
AAA 161 302 1.07e-2 SMART
low complexity region 576 597 N/A INTRINSIC
low complexity region 646 659 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153596
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930474N05Rik T C 14: 35,818,473 (GRCm39) L157S probably benign Het
Adam15 A G 3: 89,252,663 (GRCm39) S309P probably damaging Het
Agtpbp1 A T 13: 59,630,415 (GRCm39) M772K possibly damaging Het
Ankfn1 T C 11: 89,282,442 (GRCm39) M402V probably benign Het
Anln G A 9: 22,269,418 (GRCm39) T822I possibly damaging Het
Atp13a4 A G 16: 29,260,125 (GRCm39) V589A probably benign Het
Ccm2l C T 2: 152,909,779 (GRCm39) L44F probably damaging Het
Cd177 A T 7: 24,443,818 (GRCm39) L760Q probably damaging Het
Cd177 G T 7: 24,443,819 (GRCm39) L760M probably damaging Het
Cfap69 T C 5: 5,714,017 (GRCm39) E5G probably benign Het
Col4a1 G A 8: 11,271,375 (GRCm39) T753I probably benign Het
Col6a3 T A 1: 90,731,600 (GRCm39) D1551V probably damaging Het
Ddx20 A G 3: 105,586,593 (GRCm39) V584A probably benign Het
Dop1a C A 9: 86,402,209 (GRCm39) H1136Q probably benign Het
Egf T C 3: 129,496,128 (GRCm39) E329G probably damaging Het
Eif3c A G 7: 126,157,831 (GRCm39) V337A probably benign Het
Evc T A 5: 37,483,740 (GRCm39) I187F probably benign Het
Fam117a T G 11: 95,254,815 (GRCm39) probably benign Het
H2-M10.4 A T 17: 36,771,323 (GRCm39) V285E probably damaging Het
Hps4 G T 5: 112,523,307 (GRCm39) M608I probably benign Het
Idh3b T A 2: 130,126,321 (GRCm39) N6I probably benign Het
Itgam A T 7: 127,675,281 (GRCm39) M169L probably damaging Het
Kcnn3 G A 3: 89,570,029 (GRCm39) G614D possibly damaging Het
Kcnn3 A G 3: 89,428,281 (GRCm39) N169S possibly damaging Het
Mn1 A T 5: 111,569,717 (GRCm39) K1229M probably damaging Het
Ms4a19 A G 19: 11,118,897 (GRCm39) *71Q probably null Het
Nckap5 A G 1: 125,955,553 (GRCm39) M401T probably damaging Het
Or1af1 T C 2: 37,110,112 (GRCm39) S204P probably damaging Het
Or8c13 T C 9: 38,091,964 (GRCm39) N52D possibly damaging Het
Or8d4 T G 9: 40,038,561 (GRCm39) E232A probably benign Het
Pttg1ip2 G A 5: 5,502,039 (GRCm39) Q138* probably null Het
Sim2 G A 16: 93,898,047 (GRCm39) V94M probably damaging Het
Slc46a3 G A 5: 147,822,822 (GRCm39) T340M probably benign Het
Ssc4d A G 5: 135,994,923 (GRCm39) probably benign Het
Trav12-1 A G 14: 53,775,916 (GRCm39) D22G probably damaging Het
Trgv4 T A 13: 19,369,422 (GRCm39) D55E possibly damaging Het
Trps1 G A 15: 50,524,273 (GRCm39) T969M probably damaging Het
Ttn T A 2: 76,719,894 (GRCm39) probably benign Het
Ubqln4 A G 3: 88,470,458 (GRCm39) N310S probably benign Het
Vapa T C 17: 65,889,756 (GRCm39) probably benign Het
Vmn1r65 T C 7: 6,011,893 (GRCm39) T114A possibly damaging Het
Vps13d T C 4: 144,875,332 (GRCm39) E1725G probably damaging Het
Vps53 A G 11: 76,027,143 (GRCm39) probably benign Het
Xkr9 T C 1: 13,742,799 (GRCm39) L28P probably damaging Het
Other mutations in Eif3f
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02690:Eif3f APN 7 108,533,925 (GRCm39) missense probably damaging 1.00
IGL02821:Eif3f APN 7 108,533,882 (GRCm39) unclassified probably benign
R0010:Eif3f UTSW 7 108,540,212 (GRCm39) missense possibly damaging 0.93
R1054:Eif3f UTSW 7 108,537,024 (GRCm39) critical splice donor site probably null
R1886:Eif3f UTSW 7 108,539,958 (GRCm39) missense probably benign 0.08
R2877:Eif3f UTSW 7 108,534,019 (GRCm39) splice site probably null
R3700:Eif3f UTSW 7 108,539,482 (GRCm39) missense probably benign 0.23
R3882:Eif3f UTSW 7 108,540,162 (GRCm39) missense possibly damaging 0.88
R4471:Eif3f UTSW 7 108,540,153 (GRCm39) missense possibly damaging 0.79
R4472:Eif3f UTSW 7 108,540,153 (GRCm39) missense possibly damaging 0.79
R4817:Eif3f UTSW 7 108,536,982 (GRCm39) missense probably damaging 0.99
R4953:Eif3f UTSW 7 108,533,847 (GRCm39) unclassified probably benign
R5744:Eif3f UTSW 7 108,537,624 (GRCm39) missense probably damaging 0.99
R7162:Eif3f UTSW 7 108,539,938 (GRCm39) missense probably benign 0.02
R7235:Eif3f UTSW 7 108,537,295 (GRCm39) missense possibly damaging 0.78
R7445:Eif3f UTSW 7 108,533,865 (GRCm39) missense unknown
R9077:Eif3f UTSW 7 108,539,425 (GRCm39) missense probably benign 0.00
Posted On 2015-12-18