Incidental Mutation 'IGL02345: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 #IGL02345
Quality Score
Chromosomal Location93727026-93728046 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to A at 93727748 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: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc1 G T 16: 14,396,351 D177Y possibly damaging Het
Casc3 T C 11: 98,827,564 probably benign Het
Cnga1 C T 5: 72,605,272 V300I probably benign Het
Dcun1d4 A G 5: 73,511,152 D41G probably damaging Het
Dnm1l T C 16: 16,329,894 S181G possibly damaging Het
Dyrk1a T G 16: 94,671,362 S242A possibly damaging Het
Fcgbp T A 7: 28,071,643 probably benign Het
Fibcd1 T C 2: 31,816,592 Y409C probably damaging Het
Fig4 A T 10: 41,267,774 W230R probably null Het
Flt1 T C 5: 147,582,626 S960G probably benign Het
Fyb A G 15: 6,619,662 S390G possibly damaging Het
Gbx2 T C 1: 89,928,976 T231A probably benign Het
Gm16432 G A 1: 178,015,188 V60I possibly damaging Het
Lmo7 T C 14: 101,887,473 V456A probably damaging Het
Mark3 A G 12: 111,627,107 N191S probably damaging Het
Olfr871 C A 9: 20,213,018 S223Y possibly damaging Het
Pik3c2a C T 7: 116,405,891 E381K probably damaging Het
Pik3r5 A G 11: 68,492,726 D457G probably benign Het
Plcg2 T C 8: 117,585,180 S404P probably damaging Het
Prr16 T C 18: 51,303,229 F260S probably damaging Het
Psd4 T C 2: 24,401,823 probably null Het
Ptgs1 A G 2: 36,242,971 D327G probably null Het
Rgsl1 C T 1: 153,804,009 probably null Het
Spg20 T A 3: 55,117,726 probably null Het
Sugp1 A G 8: 70,043,084 probably benign Het
Tubgcp3 A T 8: 12,625,056 I713N probably damaging Het
Usp19 A G 9: 108,493,858 T240A probably benign Het
Vash2 A G 1: 190,978,215 V81A probably benign Het
Vmn2r41 T G 7: 8,138,768 N566H probably damaging Het
Wdr31 A G 4: 62,458,846 I42T possibly damaging Het
Zfp292 C T 4: 34,809,244 V1272I possibly damaging Het
Zfp638 C T 6: 83,984,875 R1899C 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
IGL02179:Gm5852 APN 3 93727716 exon noncoding transcript
IGL02366:Gm5852 APN 3 93727261 exon noncoding transcript
IGL03279:Gm5852 APN 3 93727277 exon noncoding transcript
Posted On2015-04-16