Incidental Mutation 'IGL03383:Gm10654'
ID 420775
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10654
Ensembl Gene ENSMUSG00000074252
Gene Name predicted gene 10654
Synonyms EG665828
Accession Numbers
Essential gene? Probably essential (E-score: 0.913) question?
Stock # IGL03383
Quality Score
Status
Chromosome 8
Chromosomal Location 71384049-71385681 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 71384775 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000098653
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agbl4 C T 4: 111,514,620 (GRCm39) probably benign Het
Cit T C 5: 116,011,904 (GRCm39) probably benign Het
Clmp A G 9: 40,685,737 (GRCm39) N211S probably damaging Het
Cnot2 A G 10: 116,330,722 (GRCm39) probably benign Het
Cntn6 A G 6: 104,753,418 (GRCm39) probably benign Het
Dnajb9 C T 12: 44,255,096 (GRCm39) probably benign Het
Ece2 T A 16: 20,451,847 (GRCm39) N411K possibly damaging Het
Fshr A G 17: 89,354,127 (GRCm39) I77T possibly damaging Het
Fshr A G 17: 89,293,121 (GRCm39) M519T probably damaging Het
Gm5093 A G 17: 46,750,517 (GRCm39) I170T probably benign Het
Meis3 A G 7: 15,917,744 (GRCm39) K299R probably damaging Het
Nxf1 T C 19: 8,741,061 (GRCm39) F15L probably damaging Het
Nxpe3 T C 16: 55,670,076 (GRCm39) D343G probably benign Het
Or4a73 A T 2: 89,420,656 (GRCm39) Y268N probably benign Het
Polr3k A G 2: 181,507,820 (GRCm39) T65A probably damaging Het
Preb A T 5: 31,115,665 (GRCm39) W222R probably damaging Het
Psmd11 T C 11: 80,360,671 (GRCm39) I56T probably damaging Het
Rtkn2 A G 10: 67,853,667 (GRCm39) T232A probably damaging Het
Scaf11 T C 15: 96,318,064 (GRCm39) probably null Het
Slc4a10 A T 2: 62,097,780 (GRCm39) K493M probably damaging Het
Stard10 A G 7: 100,991,777 (GRCm39) K112E probably damaging Het
Sugp1 A T 8: 70,522,217 (GRCm39) probably benign Het
Tasor A G 14: 27,163,918 (GRCm39) I235V possibly damaging Het
Tmem156 T C 5: 65,233,040 (GRCm39) E139G probably damaging Het
Tubd1 C T 11: 86,439,834 (GRCm39) probably benign Het
Uap1 G A 1: 169,986,460 (GRCm39) T174M probably damaging Het
Vmn2r13 T C 5: 109,304,398 (GRCm39) T678A probably damaging Het
Vmn2r84 A T 10: 130,222,556 (GRCm39) C555S probably damaging Het
Vps13d T C 4: 144,894,889 (GRCm39) probably null Het
Vps8 T C 16: 21,254,573 (GRCm39) probably null Het
Wee1 A G 7: 109,738,899 (GRCm39) N590S probably damaging Het
Zfp112 C A 7: 23,825,103 (GRCm39) S357Y probably damaging Het
Zfp423 T A 8: 88,586,080 (GRCm39) K48* probably null Het
Zscan4d A G 7: 10,896,692 (GRCm39) V226A probably benign Het
Other mutations in Gm10654
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02559:Gm10654 APN 8 71,384,774 (GRCm39) exon noncoding transcript
R4911:Gm10654 UTSW 8 71,384,496 (GRCm39) exon noncoding transcript
Posted On 2016-08-02