Incidental Mutation 'R9227:Eif3m'
ID 699901
Institutional Source Beutler Lab
Gene Symbol Eif3m
Ensembl Gene ENSMUSG00000027170
Gene Name eukaryotic translation initiation factor 3, subunit M
Synonyms Tango7, Pcid1, Ga17
MMRRC Submission 068984-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R9227 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 104830001-104847372 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 104831705 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 285 (M285K)
Ref Sequence ENSEMBL: ENSMUSP00000028592 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028592] [ENSMUST00000111110] [ENSMUST00000111114] [ENSMUST00000148476]
AlphaFold Q99JX4
Predicted Effect probably damaging
Transcript: ENSMUST00000028592
AA Change: M285K

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000028592
Gene: ENSMUSG00000027170
AA Change: M285K

DomainStartEndE-ValueType
Blast:HDc 119 209 1e-12 BLAST
PINT 268 357 6.42e-26 SMART
low complexity region 358 372 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000111110
AA Change: M153K

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000106739
Gene: ENSMUSG00000027170
AA Change: M153K

DomainStartEndE-ValueType
Blast:HDc 13 77 7e-8 BLAST
PINT 136 225 6.42e-26 SMART
low complexity region 226 240 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000111114
SMART Domains Protein: ENSMUSP00000106743
Gene: ENSMUSG00000045106

DomainStartEndE-ValueType
low complexity region 4 20 N/A INTRINSIC
Pfam:CCDC73 27 1061 N/A PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000144358
SMART Domains Protein: ENSMUSP00000114374
Gene: ENSMUSG00000045106

DomainStartEndE-ValueType
Pfam:CCDC73 1 182 3.1e-77 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000148476
SMART Domains Protein: ENSMUSP00000122339
Gene: ENSMUSG00000027170

DomainStartEndE-ValueType
Blast:PINT 84 126 7e-25 BLAST
low complexity region 127 141 N/A INTRINSIC
Meta Mutation Damage Score 0.6329 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 100% (79/79)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that is part of the eurkaryotic translation initiation factor 3 complete (eIF-3) required for protein synthesis. Elevated levels of the encoded protein are present in cancer cell lines. Inactivation of the encoded protein has been shown to interfere with translation of herpes virus mRNAs by preventing the association of mRNAs with the ribosomes. A pseudogene of this gene is located on the X chromosome. [provided by RefSeq, Dec 2011]
PHENOTYPE: Mice homozygous for a targeted allele exhibit embryonic lethality. Mice heterozygous for this allele exhibit decreased body weight and altered organ weights. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adarb1 A T 10: 77,157,626 (GRCm39) F274I probably damaging Het
Adprhl1 C T 8: 13,271,974 (GRCm39) V1595I probably benign Het
Anxa6 A G 11: 54,898,694 (GRCm39) V160A probably benign Het
Appl1 T C 14: 26,645,692 (GRCm39) E706G unknown Het
Arhgap21 T C 2: 20,860,469 (GRCm39) T1313A possibly damaging Het
Armc2 T C 10: 41,823,935 (GRCm39) Y511C probably damaging Het
Atp1a1 A T 3: 101,499,750 (GRCm39) C111S probably damaging Het
Atp6v0d2 T A 4: 19,878,374 (GRCm39) M300L probably benign Het
C1ra T C 6: 124,493,739 (GRCm39) C164R probably damaging Het
Cacna1h T C 17: 25,599,856 (GRCm39) Y1659C probably damaging Het
Catsperb T C 12: 101,516,053 (GRCm39) I563T probably benign Het
Cblif G A 19: 11,737,748 (GRCm39) W386* probably null Het
Cd180 TA TAA 13: 102,841,514 (GRCm39) probably null Het
Cd55b A T 1: 130,350,619 (GRCm39) L26* probably null Het
Cdc42bpa A G 1: 179,933,638 (GRCm39) N759S probably benign Het
Cenpj C T 14: 56,802,176 (GRCm39) E130K possibly damaging Het
Cep250 C T 2: 155,812,042 (GRCm39) A446V unknown Het
Chd7 C T 4: 8,805,272 (GRCm39) S777L probably benign Het
Chrm3 C A 13: 9,928,479 (GRCm39) V186L probably benign Het
Clrn2 A G 5: 45,621,283 (GRCm39) T226A probably damaging Het
Col3a1 C T 1: 45,383,138 (GRCm39) P1071S unknown Het
Dytn A T 1: 63,686,611 (GRCm39) V353D probably benign Het
Egfem1 G A 3: 29,411,317 (GRCm39) E155K probably benign Het
Fam135b T C 15: 71,335,856 (GRCm39) K446R probably benign Het
Fam186a T C 15: 99,853,384 (GRCm39) T119A unknown Het
Frmd4a T C 2: 4,612,844 (GRCm39) S1025P possibly damaging Het
Fubp3 A G 2: 31,502,564 (GRCm39) H449R probably benign Het
Fyco1 A T 9: 123,648,211 (GRCm39) I1241N probably damaging Het
Gabpb2 A T 3: 95,111,998 (GRCm39) M77K probably damaging Het
Gfpt1 T A 6: 87,027,906 (GRCm39) I4K probably damaging Het
Glis1 T C 4: 107,425,327 (GRCm39) S313P probably benign Het
Golga4 T A 9: 118,385,941 (GRCm39) M1021K possibly damaging Het
Grid2ip G A 5: 143,359,194 (GRCm39) R270Q probably damaging Het
Hps4 G A 5: 112,525,905 (GRCm39) S642N possibly damaging Het
Ifit1 A G 19: 34,625,236 (GRCm39) E124G possibly damaging Het
Ifna14 T C 4: 88,489,752 (GRCm39) D95G probably benign Het
Ilkap A C 1: 91,314,937 (GRCm39) I142S probably benign Het
Inpp5e C T 2: 26,288,616 (GRCm39) R588H probably damaging Het
Kif1b A C 4: 149,322,357 (GRCm39) M854R probably damaging Het
Lcn6 A T 2: 25,570,107 (GRCm39) K91M probably damaging Het
Lpin1 A T 12: 16,588,483 (GRCm39) S902R unknown Het
Lrig1 C A 6: 94,607,113 (GRCm39) C160F probably damaging Het
Mapk13 T C 17: 28,994,532 (GRCm39) I141T probably damaging Het
Mapkapk3 A G 9: 107,137,354 (GRCm39) L175P probably damaging Het
Micall2 A G 5: 139,701,827 (GRCm39) V472A unknown Het
Mmp15 T C 8: 96,092,959 (GRCm39) F113L probably benign Het
Msh2 T G 17: 88,026,717 (GRCm39) S738A probably benign Het
Myb C T 10: 21,030,612 (GRCm39) D62N probably benign Het
Myo1f T C 17: 33,795,424 (GRCm39) V53A probably damaging Het
Ncf1 A T 5: 134,250,718 (GRCm39) N367K probably benign Het
Nim1k C A 13: 120,174,118 (GRCm39) V259F probably damaging Het
Nme8 T G 13: 19,874,384 (GRCm39) I139L probably benign Het
Odam T C 5: 88,034,457 (GRCm39) F46L probably benign Het
Ogfr GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG 2: 180,237,059 (GRCm39) probably benign Het
Or7a42 G A 10: 78,791,929 (GRCm39) D297N possibly damaging Het
Pcare A G 17: 72,057,217 (GRCm39) L820P probably damaging Het
Pcdha9 A G 18: 37,131,954 (GRCm39) E341G probably damaging Het
Pmepa1 T C 2: 173,117,962 (GRCm39) T6A probably benign Het
Poglut1 A T 16: 38,355,168 (GRCm39) D219E possibly damaging Het
Racgap1 A G 15: 99,534,078 (GRCm39) S145P possibly damaging Het
Rasgef1a C T 6: 118,066,110 (GRCm39) T441I possibly damaging Het
Rbm6 T C 9: 107,664,498 (GRCm39) T844A probably benign Het
Rbmyf9 T G Y: 3,774,819 (GRCm39) D5E probably damaging Het
Rell1 T C 5: 64,097,105 (GRCm39) probably benign Het
Ripk3 A G 14: 56,023,303 (GRCm39) F134S probably benign Het
Rnf169 T C 7: 99,574,699 (GRCm39) D632G possibly damaging Het
Sclt1 A T 3: 41,665,631 (GRCm39) W146R probably benign Het
Setd5 T C 6: 113,098,755 (GRCm39) F796S possibly damaging Het
Slc24a5 G T 2: 124,922,568 (GRCm39) G110V probably damaging Het
Slc30a10 T A 1: 185,187,391 (GRCm39) M44K probably damaging Het
Slc38a10 T A 11: 119,996,781 (GRCm39) D772V probably benign Het
Thy1 C T 9: 43,958,004 (GRCm39) T44I probably damaging Het
Tinagl1 G T 4: 130,061,271 (GRCm39) S324Y probably benign Het
Tll2 T A 19: 41,093,436 (GRCm39) Y477F probably benign Het
Tmco1 C T 1: 167,136,132 (GRCm39) probably benign Het
Tmco6 T C 18: 36,874,719 (GRCm39) L402P probably damaging Het
Tnrc18 G T 5: 142,773,392 (GRCm39) A479D Het
Uba7 T C 9: 107,853,001 (GRCm39) V12A possibly damaging Het
Usp5 T C 6: 124,795,599 (GRCm39) D598G probably damaging Het
Vmn1r158 C T 7: 22,489,469 (GRCm39) V247I probably benign Het
Vpreb1b A G 16: 17,798,801 (GRCm39) N96D probably damaging Het
Zcchc17 A T 4: 130,230,928 (GRCm39) M87K probably damaging Het
Other mutations in Eif3m
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02003:Eif3m APN 2 104,843,188 (GRCm39) intron probably benign
IGL02661:Eif3m APN 2 104,835,314 (GRCm39) missense probably damaging 0.98
IGL02932:Eif3m APN 2 104,845,214 (GRCm39) missense probably damaging 1.00
R0039:Eif3m UTSW 2 104,836,217 (GRCm39) missense probably damaging 1.00
R0373:Eif3m UTSW 2 104,835,345 (GRCm39) missense probably benign 0.06
R1452:Eif3m UTSW 2 104,837,122 (GRCm39) missense probably damaging 1.00
R1695:Eif3m UTSW 2 104,847,298 (GRCm39) missense probably damaging 0.98
R1934:Eif3m UTSW 2 104,831,624 (GRCm39) missense probably damaging 1.00
R2115:Eif3m UTSW 2 104,837,141 (GRCm39) missense probably damaging 1.00
R2416:Eif3m UTSW 2 104,844,178 (GRCm39) missense probably benign
R4610:Eif3m UTSW 2 104,843,633 (GRCm39) missense probably benign 0.08
R4713:Eif3m UTSW 2 104,837,184 (GRCm39) splice site probably null
R5373:Eif3m UTSW 2 104,843,277 (GRCm39) missense probably damaging 0.99
R5374:Eif3m UTSW 2 104,843,277 (GRCm39) missense probably damaging 0.99
R5725:Eif3m UTSW 2 104,844,186 (GRCm39) missense probably damaging 0.97
R7996:Eif3m UTSW 2 104,831,694 (GRCm39) missense probably benign 0.22
R8983:Eif3m UTSW 2 104,830,139 (GRCm39) missense possibly damaging 0.70
R9082:Eif3m UTSW 2 104,836,217 (GRCm39) missense probably damaging 1.00
R9230:Eif3m UTSW 2 104,831,705 (GRCm39) missense probably damaging 1.00
Z1088:Eif3m UTSW 2 104,843,601 (GRCm39) missense probably damaging 1.00
Z1177:Eif3m UTSW 2 104,831,619 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AACCCAAAGCCGTTTCATTC -3'
(R):5'- AGCCCATGTGTAACTTTAGACC -3'

Sequencing Primer
(F):5'- AACCCAAAGCCGTTTCATTCTACTTC -3'
(R):5'- AGCCTTGCATTGACACTC -3'
Posted On 2022-02-07