Incidental Mutation 'IGL02179:Gm5852'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5852
Ensembl Gene ENSMUSG00000103210
Gene Namepredicted gene 5852
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02179
Quality Score
Chromosomal Location93727026-93728046 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) C to T at 93727716 bp
Amino Acid Change
Predicted Effect noncoding transcript
Transcript: ENSMUST00000193543
Predicted Effect noncoding transcript
Transcript: ENSMUST00000194119
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abl1 C A 2: 31,792,249 A385D probably damaging Het
Ace A G 11: 105,969,789 D174G probably benign Het
Aldh1l2 A G 10: 83,522,837 V98A probably benign Het
AU040320 T A 4: 126,835,612 F522L probably benign Het
Ccdc73 A G 2: 104,907,568 D3G probably damaging Het
Cdk14 A C 5: 5,103,845 L199V probably damaging Het
Cdk15 G T 1: 59,330,941 A381S possibly damaging Het
Cyb5a A G 18: 84,873,155 I68V probably benign Het
Dock5 G A 14: 67,806,496 probably benign Het
Fbxw24 T A 9: 109,609,905 K201* probably null Het
Gsdma3 A G 11: 98,635,271 K274E possibly damaging Het
Hoxa7 T A 6: 52,215,874 Q178L probably damaging Het
Itgae G T 11: 73,134,018 V992L probably benign Het
Klk1b26 A G 7: 44,016,312 N183D probably benign Het
Krt39 A T 11: 99,520,841 S140T probably damaging Het
Lama2 G A 10: 27,070,364 T1953I probably benign Het
Mmp1a G A 9: 7,464,273 R26Q probably benign Het
Myh7b A C 2: 155,614,491 I175L probably benign Het
Nol11 A G 11: 107,189,256 M1T probably null Het
Nrxn1 T A 17: 90,630,083 I641F probably damaging Het
Olfr1047 A T 2: 86,228,247 C241* probably null Het
Olfr1501 T C 19: 13,838,487 T229A probably benign Het
Olfr610 A C 7: 103,506,727 L73R probably damaging Het
Parn G T 16: 13,667,592 H13Q probably benign Het
Pcnx T C 12: 81,933,719 probably benign Het
Pdcd10 T C 3: 75,527,615 D60G probably damaging Het
Phka2 G A X: 160,554,380 probably null Het
Ppargc1a A T 5: 51,473,711 D525E possibly damaging Het
Rad54l2 C A 9: 106,720,390 R139L probably damaging Het
Rnf20 T C 4: 49,638,712 V178A probably benign Het
Ror2 C T 13: 53,110,728 S764N probably damaging Het
Sdccag8 C T 1: 176,878,056 H479Y probably benign Het
Taf8 T C 17: 47,502,233 T13A probably benign Het
Ttc8 T C 12: 98,964,537 L270P possibly damaging Het
Ttn G A 2: 76,887,368 Q365* probably null Het
Uchl1 A G 5: 66,676,294 Q2R probably benign Het
Ufl1 A G 4: 25,254,896 V440A probably damaging Het
Other mutations in Gm5852
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00340:Gm5852 APN 3 93727194 exon noncoding transcript
IGL01432:Gm5852 APN 3 93727779 missense possibly damaging 0.86
IGL02345:Gm5852 APN 3 93727748 exon noncoding transcript
IGL02366:Gm5852 APN 3 93727261 exon noncoding transcript
IGL03279:Gm5852 APN 3 93727277 exon noncoding transcript
Posted On2015-04-16