Incidental Mutation 'IGL02126:Tas2r102'
ID 280858
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 # IGL02126
Quality Score
Status
Chromosome 6
Chromosomal Location 132739094-132740137 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 132739607 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 172 (R172G)
Ref Sequence ENSEMBL: ENSMUSP00000068332 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000069268]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000069268
AA Change: R172G

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000068332
Gene: ENSMUSG00000056901
AA Change: R172G

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: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh16a1 G A 7: 44,795,459 (GRCm39) P400L probably damaging Het
Angptl3 T C 4: 98,919,738 (GRCm39) probably null Het
Atoh1 T C 6: 64,706,334 (GRCm39) W10R probably damaging Het
Brd8 C T 18: 34,735,780 (GRCm39) S899N probably damaging Het
Ccm2 A G 11: 6,544,154 (GRCm39) T317A probably damaging Het
Ccnt1 A T 15: 98,465,484 (GRCm39) W12R probably damaging Het
Celf1 T A 2: 90,831,408 (GRCm39) L79H probably damaging Het
Cmip T C 8: 118,175,770 (GRCm39) V423A probably damaging Het
Ddr1 T A 17: 35,999,481 (GRCm39) I431F probably damaging Het
Dnah6 A G 6: 73,080,149 (GRCm39) L2343P probably benign Het
Duox1 A G 2: 122,176,817 (GRCm39) D1446G probably benign Het
Erich3 A G 3: 154,419,599 (GRCm39) H231R possibly damaging Het
Fam221b T A 4: 43,666,450 (GRCm39) I54F probably benign Het
Fcgbpl1 G A 7: 27,839,281 (GRCm39) V365M probably damaging Het
Galntl5 T C 5: 25,394,839 (GRCm39) F69L possibly damaging Het
Gba2 T G 4: 43,567,918 (GRCm39) probably null Het
Gbf1 C A 19: 46,240,556 (GRCm39) P46Q probably damaging Het
Gimap6 T G 6: 48,679,635 (GRCm39) S134R probably damaging Het
Gm5424 A C 10: 61,907,377 (GRCm39) noncoding transcript Het
Hexb T C 13: 97,314,532 (GRCm39) K404E possibly damaging Het
Hs3st3a1 G A 11: 64,327,331 (GRCm39) V147M probably damaging Het
Hsd17b4 T C 18: 50,315,063 (GRCm39) V610A probably benign Het
Loxl3 T A 6: 83,025,628 (GRCm39) W329R probably damaging Het
Lrrc52 A G 1: 167,273,575 (GRCm39) F247S probably damaging Het
Naa38 C T 11: 69,287,045 (GRCm39) R42W probably damaging Het
Nadsyn1 G A 7: 143,357,753 (GRCm39) Q485* probably null Het
Nid1 A G 13: 13,663,743 (GRCm39) probably null Het
Ofcc1 T C 13: 40,362,251 (GRCm39) T224A probably benign Het
Or5m11b T G 2: 85,806,517 (GRCm39) I310S probably benign Het
Palld A G 8: 62,330,476 (GRCm39) Y134H possibly damaging Het
Pfkfb4 C T 9: 108,854,178 (GRCm39) R351W probably damaging Het
Pfn3 T C 13: 55,562,699 (GRCm39) D94G possibly damaging Het
Pkhd1 G A 1: 20,187,419 (GRCm39) R3630C probably damaging Het
Por T A 5: 135,744,829 (GRCm39) F31I probably benign Het
Ppp1r12c T C 7: 4,492,858 (GRCm39) E127G probably benign Het
Ppp1r9a T A 6: 5,156,229 (GRCm39) S1162T probably damaging Het
Psen2 C A 1: 180,057,488 (GRCm39) A297S probably benign Het
Rpusd2 G A 2: 118,869,119 (GRCm39) R514Q probably damaging Het
Rxrg A G 1: 167,462,029 (GRCm39) M235V probably damaging Het
Sash1 T C 10: 8,615,229 (GRCm39) M644V probably damaging Het
Sf3b3 T C 8: 111,550,075 (GRCm39) T648A probably benign Het
Slco1a7 T A 6: 141,684,739 (GRCm39) T239S probably benign Het
Ssu72 T C 4: 155,816,483 (GRCm39) I155T probably benign Het
Tmem214 G A 5: 31,030,090 (GRCm39) A296T probably benign Het
Trav12-2 C A 14: 53,853,859 (GRCm39) N2K probably damaging Het
Tyrp1 C T 4: 80,755,845 (GRCm39) Q205* probably null Het
Ubr4 T A 4: 139,180,052 (GRCm39) probably null Het
Ush2a A G 1: 187,995,588 (GRCm39) S120G probably benign Het
Vmn2r100 T C 17: 19,741,504 (GRCm39) probably benign Het
Zer1 G T 2: 29,994,928 (GRCm39) T489K probably benign Het
Zfp955b G T 17: 33,521,238 (GRCm39) G236* probably null 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
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 2015-04-16