Incidental Mutation 'R6258:Gm4924'
ID 506485
Institutional Source Beutler Lab
Gene Symbol Gm4924
Ensembl Gene ENSMUSG00000073427
Gene Name predicted gene 4924
Synonyms mIF1
MMRRC Submission 044375-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.174) question?
Stock # R6258 (G1)
Quality Score 169.009
Status Not validated
Chromosome 10
Chromosomal Location 82190087-82215477 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to G at 82213307 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147929 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165906] [ENSMUST00000210025] [ENSMUST00000210381] [ENSMUST00000211099]
AlphaFold A0A1B0GR71
Predicted Effect probably benign
Transcript: ENSMUST00000165906
SMART Domains Protein: ENSMUSP00000131819
Gene: ENSMUSG00000073427

DomainStartEndE-ValueType
ZnF_C2H2 34 56 2.4e-3 SMART
ZnF_C2H2 62 84 8.94e-3 SMART
ZnF_C2H2 90 112 9.58e-3 SMART
ZnF_C2H2 146 168 9.08e-4 SMART
ZnF_C2H2 174 196 6.78e-3 SMART
ZnF_C2H2 202 224 8.81e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000210025
Predicted Effect unknown
Transcript: ENSMUST00000210381
AA Change: S368R
Predicted Effect probably benign
Transcript: ENSMUST00000211078
Predicted Effect probably benign
Transcript: ENSMUST00000211099
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 95.7%
Validation Efficiency 99% (74/75)
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl3 T C 7: 82,178,191 (GRCm39) probably null Het
Alms1 A T 6: 85,605,717 (GRCm39) K2456* probably null Het
Alppl2 A T 1: 87,016,184 (GRCm39) M225K probably damaging Het
AU041133 A G 10: 81,986,992 (GRCm39) E215G probably damaging Het
Carmil3 T A 14: 55,737,889 (GRCm39) L815Q probably damaging Het
Casr A G 16: 36,337,971 (GRCm39) C60R probably damaging Het
Cdc7 A G 5: 107,117,093 (GRCm39) K84E probably damaging Het
Cdc73 G A 1: 143,567,211 (GRCm39) T104I probably benign Het
Clcc1 G A 3: 108,580,624 (GRCm39) V313I possibly damaging Het
Cntn3 A G 6: 102,254,178 (GRCm39) probably null Het
Crocc2 A G 1: 93,141,360 (GRCm39) K1171R possibly damaging Het
Ctsa T C 2: 164,676,281 (GRCm39) V86A probably damaging Het
Cyp2s1 ACAGCAGCAGCAGCAGCAGCAGCAG ACAGCAGCAGCAGCAGCAGCAG 7: 25,515,867 (GRCm39) probably benign Het
Dab1 C T 4: 104,588,948 (GRCm39) A524V probably benign Het
Dnah17 C A 11: 118,017,148 (GRCm39) W197C probably damaging Het
Dnah17 A T 11: 118,017,150 (GRCm39) W197R probably damaging Het
Dnah17 C T 11: 118,017,149 (GRCm39) W197* probably null Het
Egflam T A 15: 7,263,773 (GRCm39) T726S probably damaging Het
Eml2 T G 7: 18,913,289 (GRCm39) probably null Het
Ercc6 T A 14: 32,279,813 (GRCm39) D609E probably benign Het
Erg C A 16: 95,181,100 (GRCm39) R147L probably damaging Het
Faiml T C 9: 99,114,513 (GRCm39) I125M possibly damaging Het
Fbxo41 A T 6: 85,455,537 (GRCm39) L549H probably damaging Het
Fbxw2 A T 2: 34,702,825 (GRCm39) probably null Het
Fgd6 T A 10: 93,880,161 (GRCm39) N338K probably benign Het
Gaa C A 11: 119,171,997 (GRCm39) A700D probably benign Het
Gm32742 T A 9: 51,068,862 (GRCm39) I200F probably damaging Het
Gm8369 G A 19: 11,488,973 (GRCm39) A87T possibly damaging Het
H2-M10.1 T A 17: 36,634,994 (GRCm39) I304F unknown Het
Ighv5-8 A G 12: 113,618,611 (GRCm39) T9A possibly damaging Het
Itgb4 C T 11: 115,874,983 (GRCm39) R447W probably benign Het
Jakmip1 G T 5: 37,299,104 (GRCm39) E775* probably null Het
Klhl40 T C 9: 121,607,026 (GRCm39) F62S probably damaging Het
Krtcap3 A T 5: 31,409,572 (GRCm39) R84W probably damaging Het
Lgr6 C T 1: 134,921,748 (GRCm39) A199T probably damaging Het
Lins1 T C 7: 66,360,496 (GRCm39) probably null Het
Magi3 A G 3: 103,996,912 (GRCm39) L211P probably damaging Het
Map2k5 T A 9: 63,124,647 (GRCm39) I359F probably benign Het
Map4k5 C A 12: 69,878,336 (GRCm39) R355L probably benign Het
Mef2c T A 13: 83,801,057 (GRCm39) D252E probably damaging Het
Methig1 T C 15: 100,251,422 (GRCm39) V111A possibly damaging Het
Mical3 A T 6: 120,985,991 (GRCm39) L150Q probably damaging Het
Nf1 A T 11: 79,456,581 (GRCm39) probably null Het
Nisch T A 14: 30,899,085 (GRCm39) probably benign Het
Or4f15 C T 2: 111,814,396 (GRCm39) V8I probably benign Het
Or5p61 T C 7: 107,758,181 (GRCm39) N300D probably damaging Het
Pcdhb12 T C 18: 37,569,892 (GRCm39) V346A probably benign Het
Pde7b T C 10: 20,316,546 (GRCm39) D168G possibly damaging Het
Pdzrn4 A T 15: 92,655,562 (GRCm39) E485V probably damaging Het
Pla2g4a A G 1: 149,733,238 (GRCm39) S504P probably benign Het
Plin2 G T 4: 86,575,526 (GRCm39) A341D probably damaging Het
Psma8 A G 18: 14,854,324 (GRCm39) D68G probably damaging Het
Rcor3 G A 1: 191,808,559 (GRCm39) H207Y probably benign Het
Rptn C G 3: 93,305,437 (GRCm39) H923Q possibly damaging Het
Ryr3 A G 2: 112,490,449 (GRCm39) F3795S probably damaging Het
Samm50 C G 15: 84,084,512 (GRCm39) P150A probably damaging Het
Samm50 C A 15: 84,084,513 (GRCm39) P150H probably damaging Het
Slc28a2b A T 2: 122,353,963 (GRCm39) I530F probably damaging Het
Slc6a18 A T 13: 73,818,164 (GRCm39) C284* probably null Het
Smc3 T A 19: 53,616,162 (GRCm39) probably null Het
Snrnp200 G A 2: 127,060,343 (GRCm39) G529D possibly damaging Het
Sord T A 2: 122,089,613 (GRCm39) probably null Het
Spdl1 T A 11: 34,710,713 (GRCm39) N345I probably damaging Het
Sucnr1 T C 3: 59,993,778 (GRCm39) L102P probably damaging Het
Tbc1d9 T C 8: 83,937,145 (GRCm39) W76R probably damaging Het
Tcerg1 T A 18: 42,686,530 (GRCm39) Y696N probably damaging Het
Thsd7b A G 1: 129,595,655 (GRCm39) T492A probably benign Het
Trdmt1 T A 2: 13,524,870 (GRCm39) Q195L probably benign Het
Ubr3 A G 2: 69,813,208 (GRCm39) probably null Het
Ung A T 5: 114,275,361 (GRCm39) Y250F probably benign Het
Vezf1 A G 11: 87,972,326 (GRCm39) N229S probably damaging Het
Wdfy3 C T 5: 102,020,831 (GRCm39) R2491Q possibly damaging Het
Wdr97 C A 15: 76,239,895 (GRCm39) S277* probably null Het
Zfp1007 T C 5: 109,824,433 (GRCm39) H339R probably benign Het
Zfp709 TCGACG TCG 8: 72,644,552 (GRCm39) probably benign Het
Zscan4-ps1 C A 7: 10,799,829 (GRCm39) E353D probably benign Het
Other mutations in Gm4924
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3431:Gm4924 UTSW 10 82,214,864 (GRCm39) nonsense probably null
R5566:Gm4924 UTSW 10 82,214,475 (GRCm39) missense possibly damaging 0.46
R6170:Gm4924 UTSW 10 82,213,065 (GRCm39) nonsense probably null
R6539:Gm4924 UTSW 10 82,214,358 (GRCm39) intron probably benign
R6861:Gm4924 UTSW 10 82,214,948 (GRCm39) nonsense probably null
R7077:Gm4924 UTSW 10 82,215,057 (GRCm39) missense unknown
R7128:Gm4924 UTSW 10 82,214,533 (GRCm39) missense unknown
R7166:Gm4924 UTSW 10 82,214,035 (GRCm39) missense unknown
R7186:Gm4924 UTSW 10 82,214,778 (GRCm39) missense unknown
R7731:Gm4924 UTSW 10 82,213,361 (GRCm39) missense unknown
R8525:Gm4924 UTSW 10 82,213,701 (GRCm39) intron probably benign
R8555:Gm4924 UTSW 10 82,213,224 (GRCm39) intron probably benign
R9084:Gm4924 UTSW 10 82,213,953 (GRCm39) missense unknown
R9113:Gm4924 UTSW 10 82,214,113 (GRCm39) missense unknown
R9124:Gm4924 UTSW 10 82,214,875 (GRCm39) missense unknown
R9428:Gm4924 UTSW 10 82,213,490 (GRCm39) missense unknown
R9708:Gm4924 UTSW 10 82,214,992 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GTGGTAATACCTTTGCCTGTCTTAG -3'
(R):5'- CAAAGGCTTTACCACATTGACT -3'

Sequencing Primer
(F):5'- AGTTTGGAGAAACCCTTTGAATG -3'
(R):5'- GATGACTATTCTGTGCAAAGGC -3'
Posted On 2018-03-15