Incidental Mutation 'IGL01760:Gm2016'
ID153257
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm2016
Ensembl Gene ENSMUSG00000072905
Gene Namepredicted gene 2016
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.463) question?
Stock #IGL01760
Quality Score
Status
Chromosome12
Chromosomal Location87874072-87877859 bp(+) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) A to T at 87877021 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000105774 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000110147]
Predicted Effect probably benign
Transcript: ENSMUST00000110147
SMART Domains Protein: ENSMUSP00000105774
Gene: ENSMUSG00000072905

DomainStartEndE-ValueType
low complexity region 3 25 N/A INTRINSIC
eIF1a 28 110 2.58e-46 SMART
low complexity region 125 144 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre5 T A 8: 83,731,957 T147S probably benign Het
BC030867 T C 11: 102,255,596 C233R probably benign Het
Chst3 A T 10: 60,186,470 V185D probably damaging Het
Col14a1 A C 15: 55,423,459 D892A unknown Het
Dopey1 A G 9: 86,519,923 T1059A probably benign Het
Erlec1 A C 11: 30,934,731 S441A probably benign Het
Frmd4b G T 6: 97,308,702 T289N probably damaging Het
Gm6133 G A 18: 78,350,175 R128Q probably benign Het
Gnai2 A G 9: 107,616,518 S155P probably damaging Het
Hspg2 T C 4: 137,512,671 S517P possibly damaging Het
Ighv9-1 C A 12: 114,094,194 E29* probably null Het
Lrp1 T C 10: 127,573,501 K1583R probably benign Het
Ltbp1 C T 17: 75,227,150 T211M probably damaging Het
Mttp A G 3: 138,111,736 S418P probably benign Het
Napa A G 7: 16,098,744 N23S possibly damaging Het
Odf2 C A 2: 29,914,460 Q347K probably damaging Het
Ogdhl A G 14: 32,339,937 D504G probably damaging Het
Olfr433 T C 1: 174,042,625 L225P probably damaging Het
Pdxdc1 A T 16: 13,859,152 N273K probably damaging Het
Rslcan18 T C 13: 67,113,951 I11V probably benign Het
Spidr G T 16: 15,912,560 R664S possibly damaging Het
Tead3 T C 17: 28,333,081 N385S probably benign Het
Trim13 T A 14: 61,605,723 N396K probably benign Het
Trp53bp2 C T 1: 182,448,428 A160V possibly damaging Het
Vmn2r69 A G 7: 85,406,864 S689P possibly damaging Het
Vmn2r79 A T 7: 87,002,158 Q255L probably benign Het
Wsb1 T C 11: 79,242,041 Y276C probably damaging Het
Zfp236 G T 18: 82,621,422 N1233K probably damaging Het
Other mutations in Gm2016
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1567:Gm2016 UTSW 12 87876984 missense unknown
R4077:Gm2016 UTSW 12 87876631 missense unknown
R4077:Gm2016 UTSW 12 87876940 missense possibly damaging 0.94
R4078:Gm2016 UTSW 12 87876631 missense unknown
R4641:Gm2016 UTSW 12 87876676 missense probably damaging 0.97
R6358:Gm2016 UTSW 12 87877000 missense unknown
Z1088:Gm2016 UTSW 12 87876934 missense possibly damaging 0.49
Posted On2014-02-04