Incidental Mutation 'IGL01777:Tas2r102'
ID154125
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r102
Ensembl Gene ENSMUSG00000056901
Gene Nametaste receptor, type 2, member 102
SynonymsTas2r2, mt2r51, mGR02, STC 9-7
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.036) question?
Stock #IGL01777
Quality Score
Status
Chromosome6
Chromosomal Location132762131-132763174 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 132762852 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Isoleucine at position 241 (T241I)
Ref Sequence ENSEMBL: ENSMUSP00000068332 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000069268]
Predicted Effect probably damaging
Transcript: ENSMUST00000069268
AA Change: T241I

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000068332
Gene: ENSMUSG00000056901
AA Change: T241I

DomainStartEndE-ValueType
Pfam:TAS2R 21 317 3.6e-100 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204939
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl2 T C 3: 60,024,784 V240A possibly damaging Het
Aftph A T 11: 20,726,554 C352S possibly damaging Het
Cand2 T C 6: 115,792,857 V876A probably damaging Het
Ccar1 T C 10: 62,780,577 I125V possibly damaging Het
Celsr3 A T 9: 108,835,942 M1858L probably benign Het
Csmd3 A T 15: 47,698,198 N2134K probably benign Het
Dhx29 A G 13: 112,930,872 I96V probably benign Het
Dst A G 1: 34,199,397 T3727A probably benign Het
Elavl4 T A 4: 110,206,661 probably null Het
Eno2 C T 6: 124,766,637 G113D probably damaging Het
Esf1 A C 2: 140,157,172 probably null Het
Frmd4b T C 6: 97,295,944 D783G probably benign Het
Gm13023 T G 4: 143,795,118 C435G possibly damaging Het
Grin2a C T 16: 9,644,130 V713I probably benign Het
Impa1 C T 3: 10,322,948 G138D probably damaging Het
Kcnt2 A G 1: 140,595,998 T1079A probably benign Het
Kmt2a A G 9: 44,849,005 S549P probably damaging Het
Magoh C A 4: 107,883,176 Q86K probably benign Het
Moxd1 C A 10: 24,252,596 T182K probably benign Het
Olfr476 A G 7: 107,967,502 Y35C probably damaging Het
Rab3b A T 4: 108,929,410 Q119L probably damaging Het
Snap47 T A 11: 59,421,651 probably null Het
Taar3 A G 10: 23,950,005 R150G probably benign Het
Tas2r114 C T 6: 131,689,701 W121* probably null Het
Trak1 G A 9: 121,431,560 probably null Het
Ubn1 T C 16: 5,072,149 V426A possibly damaging Het
Vmn1r40 T C 6: 89,714,222 L7P probably benign Het
Vmn2r43 T C 7: 8,255,273 I314V probably damaging Het
Vrtn T G 12: 84,648,922 S149A probably benign Het
Other mutations in Tas2r102
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00685:Tas2r102 APN 6 132762525 missense possibly damaging 0.58
IGL01956:Tas2r102 APN 6 132762453 nonsense probably null
IGL02126:Tas2r102 APN 6 132762644 missense probably damaging 1.00
IGL02650:Tas2r102 APN 6 132762210 missense probably null 0.00
R0483:Tas2r102 UTSW 6 132762365 missense probably damaging 1.00
R0573:Tas2r102 UTSW 6 132762673 missense probably damaging 0.98
R0726:Tas2r102 UTSW 6 132762452 missense probably damaging 1.00
R1777:Tas2r102 UTSW 6 132762291 missense probably benign 0.08
R3615:Tas2r102 UTSW 6 132762818 nonsense probably null
R3616:Tas2r102 UTSW 6 132762818 nonsense probably null
R4556:Tas2r102 UTSW 6 132762915 missense probably damaging 1.00
R4633:Tas2r102 UTSW 6 132762679 missense possibly damaging 0.87
R4724:Tas2r102 UTSW 6 132762557 missense probably damaging 0.97
R5268:Tas2r102 UTSW 6 132762397 missense probably damaging 0.98
R5494:Tas2r102 UTSW 6 132763143 missense probably benign 0.12
Posted On2014-02-04