Incidental Mutation 'R2156:Tas1r2'
ID 234801
Institutional Source Beutler Lab
Gene Symbol Tas1r2
Ensembl Gene ENSMUSG00000028738
Gene Name taste receptor, type 1, member 2
Synonyms TR2, Gpr71, T1r2
MMRRC Submission 040159-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.108) question?
Stock # R2156 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 139380849-139397591 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 139396352 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 564 (R564G)
Ref Sequence ENSEMBL: ENSMUSP00000127737 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030510] [ENSMUST00000166773]
AlphaFold Q925I4
Predicted Effect possibly damaging
Transcript: ENSMUST00000030510
AA Change: R593G

PolyPhen 2 Score 0.645 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000030510
Gene: ENSMUSG00000028738
AA Change: R593G

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:ANF_receptor 73 459 2e-90 PFAM
Pfam:NCD3G 495 548 2.4e-17 PFAM
Pfam:7tm_3 581 818 2.8e-33 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000166773
AA Change: R564G

PolyPhen 2 Score 0.792 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000127737
Gene: ENSMUSG00000028738
AA Change: R564G

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:ANF_receptor 73 213 5.3e-38 PFAM
Pfam:ANF_receptor 217 429 8.4e-31 PFAM
Pfam:NCD3G 466 519 7.4e-19 PFAM
Pfam:7tm_3 550 790 3e-47 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.6%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous mutant mice show diminished behavioral and nervous responses to sweet tastants. Response to umami tastants is unimpaired. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810065E05Rik T A 11: 58,313,134 (GRCm39) probably null Het
Acaa2 T C 18: 74,926,476 (GRCm39) probably null Het
Adam7 T C 14: 68,748,792 (GRCm39) Q485R probably benign Het
Adcy4 T G 14: 56,006,627 (GRCm39) T1069P probably benign Het
Arsj T C 3: 126,232,337 (GRCm39) L361P probably damaging Het
Birc2 A C 9: 7,826,939 (GRCm39) L349R probably damaging Het
C1qa T C 4: 136,623,727 (GRCm39) Y159C probably damaging Het
Cdh13 A G 8: 119,963,703 (GRCm39) K428E probably damaging Het
Cenpe T C 3: 134,953,235 (GRCm39) M1563T probably benign Het
Col10a1 T C 10: 34,271,696 (GRCm39) V556A probably benign Het
Creg2 G A 1: 39,662,338 (GRCm39) L265F probably damaging Het
Cyp1a2 T A 9: 57,589,433 (GRCm39) D127V probably damaging Het
Cyp3a44 A T 5: 145,740,480 (GRCm39) Y53* probably null Het
Cyth1 C T 11: 118,073,634 (GRCm39) R233Q probably damaging Het
Dnmbp G A 19: 43,890,346 (GRCm39) H474Y possibly damaging Het
Dvl1 G A 4: 155,932,273 (GRCm39) V28I possibly damaging Het
Ercc2 G A 7: 19,120,717 (GRCm39) R206H possibly damaging Het
Evx2 T A 2: 74,486,360 (GRCm39) H343L probably damaging Het
Fcrl2 T A 3: 87,164,648 (GRCm39) I293F probably benign Het
Gcnt4 A G 13: 97,082,974 (GRCm39) E90G probably damaging Het
Gid8 T G 2: 180,358,751 (GRCm39) C139G probably benign Het
Gm11938 C A 11: 99,493,933 (GRCm39) C54F probably damaging Het
Gm3336 G A 8: 71,174,509 (GRCm39) V158I probably benign Het
Gucy1b1 T C 3: 81,968,327 (GRCm39) N60D probably benign Het
Hdac7 T C 15: 97,691,944 (GRCm39) K810E probably benign Het
Hsp90ab1 A G 17: 45,880,629 (GRCm39) F361L possibly damaging Het
Igf2bp3 A T 6: 49,085,858 (GRCm39) probably null Het
Inpp4b T A 8: 82,775,118 (GRCm39) I772N probably damaging Het
Iqca1 A G 1: 90,017,238 (GRCm39) L390P possibly damaging Het
Itgb2 C T 10: 77,396,082 (GRCm39) R586W probably benign Het
Itih1 A G 14: 30,655,432 (GRCm39) S588P possibly damaging Het
Iyd T A 10: 3,497,166 (GRCm39) probably null Het
Kl A G 5: 150,912,425 (GRCm39) K725E probably benign Het
Layn T A 9: 50,968,697 (GRCm39) M349L probably benign Het
Map3k5 T C 10: 19,900,683 (GRCm39) Y286H probably damaging Het
Med4 C T 14: 73,755,472 (GRCm39) probably benign Het
Mfn1 T A 3: 32,588,400 (GRCm39) N42K possibly damaging Het
Mindy2 T C 9: 70,563,874 (GRCm39) D152G probably benign Het
Mrc2 A G 11: 105,238,682 (GRCm39) probably null Het
Mrpl11 C A 19: 5,012,497 (GRCm39) A26E probably damaging Het
Msh6 G A 17: 88,293,568 (GRCm39) W774* probably null Het
Mtch1 A T 17: 29,561,841 (GRCm39) V121E probably damaging Het
Mtg2 G T 2: 179,725,923 (GRCm39) E178* probably null Het
Nbas A T 12: 13,491,510 (GRCm39) N1461Y probably damaging Het
Ndfip2 A G 14: 105,525,204 (GRCm39) T65A probably benign Het
Ninl G T 2: 150,786,503 (GRCm39) Q1146K probably damaging Het
Notch1 T C 2: 26,350,873 (GRCm39) D2089G possibly damaging Het
Notch3 C T 17: 32,366,818 (GRCm39) V906M probably damaging Het
Or51l14 A G 7: 103,101,371 (GRCm39) I276V probably benign Het
Or6b6 A G 7: 106,570,775 (GRCm39) Y259H probably damaging Het
Osmr A T 15: 6,873,891 (GRCm39) Y169N probably benign Het
Ovgp1 T C 3: 105,885,033 (GRCm39) V124A possibly damaging Het
P2rx1 T C 11: 72,904,939 (GRCm39) M369T probably benign Het
Pde4dip T C 3: 97,631,534 (GRCm39) Q1125R probably damaging Het
Podn A T 4: 107,878,892 (GRCm39) V180E probably damaging Het
Pold1 A T 7: 44,188,542 (GRCm39) V475E probably damaging Het
Polg A G 7: 79,111,468 (GRCm39) I261T possibly damaging Het
Satb1 G T 17: 52,047,438 (GRCm39) Q595K probably benign Het
Scaf8 T A 17: 3,214,407 (GRCm39) probably null Het
Semp2l1 T A 1: 32,585,128 (GRCm39) M261L probably benign Het
Serpinb3a C T 1: 106,975,202 (GRCm39) probably null Het
Slc22a26 T C 19: 7,779,480 (GRCm39) D112G probably damaging Het
Slc25a23 A G 17: 57,352,562 (GRCm39) F441L probably benign Het
Slc25a53 T C X: 135,884,216 (GRCm39) T42A probably damaging Het
Slc6a15 T C 10: 103,229,269 (GRCm39) Y103H probably damaging Het
Slx4 A G 16: 3,804,223 (GRCm39) S864P probably benign Het
Snap91 T C 9: 86,707,130 (GRCm39) E220G probably damaging Het
Spam1 T C 6: 24,796,267 (GRCm39) F73L probably damaging Het
Sphkap C T 1: 83,255,710 (GRCm39) V393M probably benign Het
Spred2 T C 11: 19,971,241 (GRCm39) Y370H probably damaging Het
Sqle T C 15: 59,195,578 (GRCm39) probably null Het
Srrm2 A G 17: 24,037,237 (GRCm39) T1390A probably benign Het
Tbl2 G T 5: 135,185,374 (GRCm39) probably null Het
Tcof1 T C 18: 60,964,901 (GRCm39) D606G possibly damaging Het
Tdpoz3 T A 3: 93,734,087 (GRCm39) L254H probably damaging Het
Trpm1 A T 7: 63,884,736 (GRCm39) I806F probably damaging Het
Ttc22 A G 4: 106,496,237 (GRCm39) D429G probably benign Het
Ube2o C A 11: 116,471,972 (GRCm39) G90C probably damaging Het
Usp34 T A 11: 23,332,602 (GRCm39) F1110I probably damaging Het
Vmn2r82 T C 10: 79,214,722 (GRCm39) L235P probably damaging Het
Vps35 A G 8: 86,013,129 (GRCm39) V116A probably benign Het
Wdfy3 A G 5: 102,046,291 (GRCm39) probably null Het
Zeb2 T C 2: 44,878,821 (GRCm39) K1138E probably benign Het
Zfp513 G A 5: 31,357,866 (GRCm39) T169I probably benign Het
Zfp629 T C 7: 127,211,551 (GRCm39) D86G probably benign Het
Other mutations in Tas1r2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00911:Tas1r2 APN 4 139,387,602 (GRCm39) missense probably benign 0.03
IGL00952:Tas1r2 APN 4 139,382,563 (GRCm39) missense probably benign 0.00
IGL00972:Tas1r2 APN 4 139,387,347 (GRCm39) missense probably damaging 0.99
IGL01939:Tas1r2 APN 4 139,396,488 (GRCm39) missense probably damaging 1.00
IGL02247:Tas1r2 APN 4 139,396,827 (GRCm39) missense probably damaging 1.00
IGL02663:Tas1r2 APN 4 139,387,593 (GRCm39) missense probably benign
IGL03155:Tas1r2 APN 4 139,396,467 (GRCm39) missense possibly damaging 0.95
R0395:Tas1r2 UTSW 4 139,382,665 (GRCm39) missense possibly damaging 0.86
R0798:Tas1r2 UTSW 4 139,397,024 (GRCm39) missense probably damaging 1.00
R1221:Tas1r2 UTSW 4 139,396,436 (GRCm39) missense probably benign 0.00
R1223:Tas1r2 UTSW 4 139,387,515 (GRCm39) missense probably damaging 1.00
R1261:Tas1r2 UTSW 4 139,382,599 (GRCm39) missense probably damaging 0.99
R1262:Tas1r2 UTSW 4 139,382,599 (GRCm39) missense probably damaging 0.99
R1330:Tas1r2 UTSW 4 139,396,640 (GRCm39) missense probably benign 0.05
R1466:Tas1r2 UTSW 4 139,396,722 (GRCm39) missense probably damaging 1.00
R1466:Tas1r2 UTSW 4 139,396,722 (GRCm39) missense probably damaging 1.00
R1879:Tas1r2 UTSW 4 139,397,006 (GRCm39) missense probably damaging 1.00
R2112:Tas1r2 UTSW 4 139,382,666 (GRCm39) missense probably benign 0.00
R2509:Tas1r2 UTSW 4 139,387,162 (GRCm39) missense probably damaging 1.00
R2510:Tas1r2 UTSW 4 139,387,162 (GRCm39) missense probably damaging 1.00
R2511:Tas1r2 UTSW 4 139,387,162 (GRCm39) missense probably damaging 1.00
R3429:Tas1r2 UTSW 4 139,396,886 (GRCm39) missense probably damaging 1.00
R3430:Tas1r2 UTSW 4 139,396,886 (GRCm39) missense probably damaging 1.00
R3703:Tas1r2 UTSW 4 139,394,729 (GRCm39) missense probably damaging 1.00
R4105:Tas1r2 UTSW 4 139,387,363 (GRCm39) missense probably benign 0.06
R4106:Tas1r2 UTSW 4 139,387,363 (GRCm39) missense probably benign 0.06
R4107:Tas1r2 UTSW 4 139,387,363 (GRCm39) missense probably benign 0.06
R4614:Tas1r2 UTSW 4 139,387,098 (GRCm39) missense probably damaging 1.00
R4811:Tas1r2 UTSW 4 139,396,311 (GRCm39) missense probably damaging 1.00
R5314:Tas1r2 UTSW 4 139,382,672 (GRCm39) missense probably damaging 1.00
R5461:Tas1r2 UTSW 4 139,387,320 (GRCm39) missense probably benign 0.01
R5639:Tas1r2 UTSW 4 139,387,107 (GRCm39) missense probably damaging 1.00
R5703:Tas1r2 UTSW 4 139,394,647 (GRCm39) missense probably damaging 1.00
R6176:Tas1r2 UTSW 4 139,396,199 (GRCm39) missense probably damaging 1.00
R6297:Tas1r2 UTSW 4 139,389,361 (GRCm39) missense possibly damaging 0.47
R6441:Tas1r2 UTSW 4 139,396,467 (GRCm39) missense probably damaging 0.99
R6748:Tas1r2 UTSW 4 139,396,922 (GRCm39) missense probably damaging 0.98
R6863:Tas1r2 UTSW 4 139,397,030 (GRCm39) missense probably damaging 1.00
R6975:Tas1r2 UTSW 4 139,397,031 (GRCm39) missense probably damaging 1.00
R7106:Tas1r2 UTSW 4 139,389,360 (GRCm39) missense probably benign
R7265:Tas1r2 UTSW 4 139,396,963 (GRCm39) missense probably benign 0.01
R7580:Tas1r2 UTSW 4 139,387,056 (GRCm39) missense probably benign 0.05
R7651:Tas1r2 UTSW 4 139,396,938 (GRCm39) missense probably benign 0.14
R8041:Tas1r2 UTSW 4 139,387,290 (GRCm39) missense possibly damaging 0.65
R8530:Tas1r2 UTSW 4 139,389,460 (GRCm39) missense probably benign
R8747:Tas1r2 UTSW 4 139,387,318 (GRCm39) missense probably benign
R8824:Tas1r2 UTSW 4 139,381,074 (GRCm39) splice site probably benign
R8904:Tas1r2 UTSW 4 139,394,714 (GRCm39) missense probably damaging 1.00
R8906:Tas1r2 UTSW 4 139,397,046 (GRCm39) missense probably damaging 1.00
R9315:Tas1r2 UTSW 4 139,381,046 (GRCm39) missense possibly damaging 0.91
R9336:Tas1r2 UTSW 4 139,389,316 (GRCm39) missense probably damaging 1.00
R9419:Tas1r2 UTSW 4 139,387,036 (GRCm39) missense possibly damaging 0.65
R9776:Tas1r2 UTSW 4 139,396,208 (GRCm39) missense possibly damaging 0.68
Z1088:Tas1r2 UTSW 4 139,387,735 (GRCm39) missense possibly damaging 0.90
Predicted Primers PCR Primer
(F):5'- CTACTGACAGGAGTTGCTGTG -3'
(R):5'- ACACAATCTGGAAGGAGCGC -3'

Sequencing Primer
(F):5'- GCTCTTGTAGATGAGTTTAACTGTC -3'
(R):5'- AGGAGCGCACCGTGATG -3'
Posted On 2014-10-01