Incidental Mutation 'IGL01956:Tas2r102'
ID 181101
Institutional Source Australian Phenomics Network (link to record)
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 # IGL01956
Quality Score
Chromosome 6
Chromosomal Location 132739094-132740137 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 132739416 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Stop codon at position 108 (W108*)
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: W108*
SMART Domains Protein: ENSMUSP00000068332
Gene: ENSMUSG00000056901
AA Change: W108*

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: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts3 C T 5: 89,825,770 (GRCm39) G1022D probably damaging Het
Adgrv1 T C 13: 81,594,549 (GRCm39) H4155R possibly damaging Het
Akna A T 4: 63,297,527 (GRCm39) D842E probably benign Het
Cacng5 T C 11: 107,773,735 (GRCm39) E88G possibly damaging Het
Fbxw18 G A 9: 109,522,425 (GRCm39) P148L probably damaging Het
Gzf1 G A 2: 148,525,981 (GRCm39) A151T probably benign Het
Iho1 T C 9: 108,294,518 (GRCm39) probably benign Het
Myo5c A G 9: 75,150,158 (GRCm39) probably null Het
Nudcd1 A G 15: 44,263,612 (GRCm39) Y277H probably damaging Het
Nvl A G 1: 180,962,509 (GRCm39) S154P probably benign Het
Or6c206 T A 10: 129,096,911 (GRCm39) I27N possibly damaging Het
Pah G A 10: 87,374,061 (GRCm39) E76K probably benign Het
Peli1 T A 11: 21,098,501 (GRCm39) I412N probably damaging Het
Rmc1 A G 18: 12,322,407 (GRCm39) N620S probably damaging Het
Slc18a2 T C 19: 59,275,608 (GRCm39) probably benign Het
Stx1a T C 5: 135,066,323 (GRCm39) probably benign Het
Syne2 G A 12: 76,144,748 (GRCm39) D1566N probably damaging Het
Syt7 G T 19: 10,420,755 (GRCm39) E433D probably benign Het
Trappc11 A G 8: 47,981,036 (GRCm39) V135A possibly damaging Het
Unk T C 11: 115,947,160 (GRCm39) S598P probably damaging Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Zfp729a A T 13: 67,769,805 (GRCm39) H141Q probably damaging 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
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
R3615:Tas2r102 UTSW 6 132,739,781 (GRCm39) nonsense probably null
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
Posted On 2014-05-07