Incidental Mutation 'R3615:Tas2r102'
ID 268429
Institutional Source Beutler Lab
Gene Symbol Tas2r102
Ensembl Gene ENSMUSG00000056901
Gene Name taste receptor, type 2, member 102
Synonyms STC 9-7, mt2r51, mGR02, Tas2r2
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R3615 (G1)
Quality Score 225
Status Validated
Chromosome 6
Chromosomal Location 132739094-132740137 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 132739781 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 230 (Q230*)
Ref Sequence ENSEMBL: ENSMUSP00000068332 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000069268]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000069268
AA Change: Q230*
SMART Domains Protein: ENSMUSP00000068332
Gene: ENSMUSG00000056901
AA Change: Q230*

DomainStartEndE-ValueType
Pfam:TAS2R 21 317 3.6e-100 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204939
Meta Mutation Damage Score 0.9711 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.3%
Validation Efficiency 98% (40/41)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 T C 6: 128,535,257 (GRCm39) T818A probably benign Het
Aasdh A G 5: 77,036,629 (GRCm39) V304A probably benign Het
Angptl3 G A 4: 98,922,702 (GRCm39) A248T probably benign Het
Ap2b1 T A 11: 83,215,391 (GRCm39) C112S possibly damaging Het
Aqr A T 2: 113,967,368 (GRCm39) I549N probably damaging Het
Barhl1 C T 2: 28,801,562 (GRCm39) D161N possibly damaging Het
Col28a1 A G 6: 8,014,942 (GRCm39) V821A probably damaging Het
Dclk2 G A 3: 86,827,342 (GRCm39) P46S probably damaging Het
Dnah1 A G 14: 31,037,105 (GRCm39) L247P possibly damaging Het
Dpysl2 T A 14: 67,071,819 (GRCm39) H107L probably damaging Het
Dzip3 A G 16: 48,757,426 (GRCm39) L869S probably damaging Het
Efs T C 14: 55,157,552 (GRCm39) Y160C probably damaging Het
Enam A T 5: 88,652,306 (GRCm39) N1197Y possibly damaging Het
Espl1 A G 15: 102,221,424 (GRCm39) I944V probably damaging Het
Fam184b A G 5: 45,740,157 (GRCm39) V343A possibly damaging Het
Fbxw26 A T 9: 109,572,828 (GRCm39) Y105* probably null Het
Fiz1 A G 7: 5,011,171 (GRCm39) L449P probably benign Het
Foxi2 T A 7: 135,012,180 (GRCm39) C23S possibly damaging Het
Gdf2 G A 14: 33,666,914 (GRCm39) R212Q probably damaging Het
Gm5105 C A 3: 137,755,449 (GRCm39) A46S unknown Het
Grik5 C T 7: 24,721,996 (GRCm39) A581T probably benign Het
Gse1 C G 8: 121,299,481 (GRCm39) probably benign Het
Hsp90aa1 T A 12: 110,662,114 (GRCm39) M1L possibly damaging Het
Hsp90aa1 C A 12: 110,662,115 (GRCm39) probably null Het
Krt25 A C 11: 99,208,124 (GRCm39) V368G possibly damaging Het
Lacc1 A G 14: 77,270,727 (GRCm39) V269A probably benign Het
Lamc1 T C 1: 153,126,896 (GRCm39) K417E probably damaging Het
Miip A G 4: 147,950,371 (GRCm39) M75T probably benign Het
Nlrp10 A G 7: 108,523,683 (GRCm39) F599S probably benign Het
Nlrp12 T A 7: 3,289,205 (GRCm39) M436L probably benign Het
Or4b13 T C 2: 90,082,753 (GRCm39) E193G possibly damaging Het
Pafah1b1 G A 11: 74,581,058 (GRCm39) S57F probably damaging Het
Pla2g2e G A 4: 138,607,685 (GRCm39) V22I probably benign Het
Plekhd1 A G 12: 80,764,044 (GRCm39) E202G probably damaging Het
Prss21 A G 17: 24,091,805 (GRCm39) T258A probably benign Het
Prss34 A G 17: 25,517,820 (GRCm39) E65G probably benign Het
Psap A G 10: 60,130,383 (GRCm39) N149S probably benign Het
Ptprf C T 4: 118,095,080 (GRCm39) A275T probably benign Het
Sem1 A G 6: 6,578,520 (GRCm39) L12P probably damaging Het
Sf3b3 A G 8: 111,571,155 (GRCm39) Y4H probably damaging Het
Sh3bp4 G T 1: 89,065,427 (GRCm39) R7L probably damaging Het
Slc16a1 T A 3: 104,560,886 (GRCm39) L397Q probably damaging Het
Smg5 A G 3: 88,243,758 (GRCm39) S10G possibly damaging Het
Spata31e5 T C 1: 28,815,656 (GRCm39) D792G probably benign Het
Spata31g1 A G 4: 42,971,864 (GRCm39) N399S probably benign Het
Tdo2 A G 3: 81,882,735 (GRCm39) Y13H possibly damaging Het
Tmem231 C T 8: 112,644,945 (GRCm39) R187H possibly damaging Het
Tmem30b A G 12: 73,592,353 (GRCm39) M254T probably damaging Het
Trpm1 G A 7: 63,893,318 (GRCm39) G1057R probably damaging Het
Tusc3 A T 8: 39,617,879 (GRCm39) K347N probably damaging Het
Usp36 C T 11: 118,167,585 (GRCm39) probably null Het
Vash2 T C 1: 190,702,616 (GRCm39) Y117C probably damaging Het
Vrk2 A G 11: 26,439,866 (GRCm39) I235T possibly damaging Het
Wdr20 A G 12: 110,760,373 (GRCm39) T420A probably benign Het
Other mutations in Tas2r102
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00685:Tas2r102 APN 6 132,739,488 (GRCm39) missense possibly damaging 0.58
IGL01777:Tas2r102 APN 6 132,739,815 (GRCm39) missense probably damaging 0.98
IGL01956:Tas2r102 APN 6 132,739,416 (GRCm39) nonsense probably null
IGL02126:Tas2r102 APN 6 132,739,607 (GRCm39) missense probably damaging 1.00
IGL02650:Tas2r102 APN 6 132,739,173 (GRCm39) missense probably null 0.00
R0483:Tas2r102 UTSW 6 132,739,328 (GRCm39) missense probably damaging 1.00
R0573:Tas2r102 UTSW 6 132,739,636 (GRCm39) missense probably damaging 0.98
R0726:Tas2r102 UTSW 6 132,739,415 (GRCm39) missense probably damaging 1.00
R1777:Tas2r102 UTSW 6 132,739,254 (GRCm39) missense probably benign 0.08
R3616:Tas2r102 UTSW 6 132,739,781 (GRCm39) nonsense probably null
R4556:Tas2r102 UTSW 6 132,739,878 (GRCm39) missense probably damaging 1.00
R4633:Tas2r102 UTSW 6 132,739,642 (GRCm39) missense possibly damaging 0.87
R4724:Tas2r102 UTSW 6 132,739,520 (GRCm39) missense probably damaging 0.97
R5268:Tas2r102 UTSW 6 132,739,360 (GRCm39) missense probably damaging 0.98
R5494:Tas2r102 UTSW 6 132,740,106 (GRCm39) missense probably benign 0.12
Predicted Primers PCR Primer
(F):5'- GCTTGGAAATCTGATGCAAAGC -3'
(R):5'- TGGACTGAAGGATACATGAGTTC -3'

Sequencing Primer
(F):5'- AGCATGCTTGAAGAGAGGTTCTATC -3'
(R):5'- CTGAAGGATACATGAGTTCAGTTATC -3'
Posted On 2015-02-19