Incidental Mutation 'IGL02345:Gm5852'
ID289232
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5852
Ensembl Gene ENSMUSG00000103210
Gene Namepredicted gene 5852
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02345
Quality Score
Status
Chromosome3
Chromosomal Location93727026-93728046 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to A at 93727748 bp
ZygosityHeterozygous
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