Incidental Mutation 'IGL02576:Tas2r123'
ID 299177
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r123
Ensembl Gene ENSMUSG00000057381
Gene Name taste receptor, type 2, member 123
Synonyms mt2r55, mGR23, STC 9-2, T2R23, Tas2r23
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL02576
Quality Score
Status
Chromosome 6
Chromosomal Location 132824105-132825106 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 132824703 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 200 (F200S)
Ref Sequence ENSEMBL: ENSMUSP00000071615 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071696]
AlphaFold P59528
Predicted Effect possibly damaging
Transcript: ENSMUST00000071696
AA Change: F200S

PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000071615
Gene: ENSMUSG00000057381
AA Change: F200S

DomainStartEndE-ValueType
Pfam:TAS2R 7 322 4.6e-79 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 A G 7: 120,032,678 (GRCm39) I232M probably benign Het
Ace G A 11: 105,864,937 (GRCm39) V537M probably damaging Het
Alg1 A G 16: 5,062,393 (GRCm39) E425G possibly damaging Het
Cacng3 G A 7: 122,271,133 (GRCm39) S46N probably benign Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cfap65 A G 1: 74,942,617 (GRCm39) S1646P probably damaging Het
Cimap2 T C 4: 106,448,825 (GRCm39) D411G possibly damaging Het
Col20a1 C T 2: 180,655,198 (GRCm39) Q1152* probably null Het
D130043K22Rik A C 13: 25,040,853 (GRCm39) T92P possibly damaging Het
Drc3 T C 11: 60,261,377 (GRCm39) M176T probably benign Het
Esyt3 T C 9: 99,197,278 (GRCm39) R851G probably benign Het
Fbxo43 A G 15: 36,152,321 (GRCm39) V496A probably benign Het
Fut4 T A 9: 14,662,701 (GRCm39) M198L probably damaging Het
Galt C T 4: 41,755,953 (GRCm39) probably benign Het
Glipr1l1 A G 10: 111,896,224 (GRCm39) K4E possibly damaging Het
Gm9945 A G 11: 53,371,178 (GRCm39) probably benign Het
Hspa12a A C 19: 58,787,842 (GRCm39) I660R possibly damaging Het
Htr3b T C 9: 48,856,804 (GRCm39) I225V possibly damaging Het
Igf2r T C 17: 12,967,650 (GRCm39) D23G possibly damaging Het
Igsf5 A G 16: 96,187,781 (GRCm39) I158V probably benign Het
Itgae A G 11: 73,009,331 (GRCm39) Y505C possibly damaging Het
Kif16b A G 2: 142,704,465 (GRCm39) probably benign Het
Kif26b T C 1: 178,743,912 (GRCm39) V1336A probably benign Het
Kmt2d A G 15: 98,762,001 (GRCm39) S450P unknown Het
Lhfpl2 G A 13: 94,310,734 (GRCm39) M1I probably null Het
Lig4 A G 8: 10,021,116 (GRCm39) I888T probably damaging Het
Msh4 G A 3: 153,573,383 (GRCm39) T563M probably damaging Het
Muc5ac C T 7: 141,370,781 (GRCm39) A3238V probably benign Het
Myo15b A G 11: 115,780,879 (GRCm39) S1246G probably null Het
Or5h25 T C 16: 58,930,134 (GRCm39) I280V probably benign Het
Pecam1 G A 11: 106,562,600 (GRCm39) T599M probably damaging Het
Phf3 G A 1: 30,869,117 (GRCm39) P644S probably benign Het
Pkd1l1 A C 11: 8,794,560 (GRCm39) F2317C possibly damaging Het
Prdm4 A G 10: 85,736,801 (GRCm39) M613T possibly damaging Het
Prim2 A T 1: 33,523,798 (GRCm39) I371N probably damaging Het
Ptprs T C 17: 56,721,958 (GRCm39) D1316G probably damaging Het
Rnf19b C T 4: 128,967,315 (GRCm39) R285* probably null Het
Secisbp2 A G 13: 51,824,894 (GRCm39) N381D possibly damaging Het
Slc28a2 T C 2: 122,288,652 (GRCm39) I586T probably damaging Het
Spef1 T C 2: 131,016,562 (GRCm39) H11R possibly damaging Het
Taar4 T C 10: 23,836,909 (GRCm39) L173S probably damaging Het
Tex16 T A X: 111,028,653 (GRCm39) L384Q probably benign Het
Tox2 A G 2: 163,118,100 (GRCm39) Q168R probably damaging Het
Trim5 T A 7: 103,927,624 (GRCm39) E172V probably damaging Het
Txndc11 G A 16: 10,892,881 (GRCm39) probably benign Het
Vmn1r232 T A 17: 21,134,175 (GRCm39) I142F probably benign Het
Zdhhc25 A T 15: 88,485,472 (GRCm39) H269L probably benign Het
Znrf4 T C 17: 56,819,199 (GRCm39) D36G probably damaging Het
Other mutations in Tas2r123
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01021:Tas2r123 APN 6 132,824,369 (GRCm39) missense probably benign 0.01
IGL01547:Tas2r123 APN 6 132,824,421 (GRCm39) missense probably damaging 1.00
IGL03303:Tas2r123 APN 6 132,824,401 (GRCm39) missense probably damaging 1.00
G1patch:Tas2r123 UTSW 6 132,824,801 (GRCm39) missense probably damaging 0.97
R0068:Tas2r123 UTSW 6 132,824,955 (GRCm39) missense possibly damaging 0.66
R0068:Tas2r123 UTSW 6 132,824,955 (GRCm39) missense possibly damaging 0.66
R0110:Tas2r123 UTSW 6 132,824,295 (GRCm39) missense probably benign 0.01
R0364:Tas2r123 UTSW 6 132,824,644 (GRCm39) missense probably benign
R0415:Tas2r123 UTSW 6 132,824,801 (GRCm39) missense probably damaging 0.97
R0469:Tas2r123 UTSW 6 132,824,295 (GRCm39) missense probably benign 0.01
R1791:Tas2r123 UTSW 6 132,824,528 (GRCm39) missense probably damaging 1.00
R1976:Tas2r123 UTSW 6 132,824,295 (GRCm39) missense probably damaging 0.96
R2328:Tas2r123 UTSW 6 132,824,279 (GRCm39) missense probably benign 0.02
R4282:Tas2r123 UTSW 6 132,825,008 (GRCm39) missense possibly damaging 0.75
R4283:Tas2r123 UTSW 6 132,825,008 (GRCm39) missense possibly damaging 0.75
R4939:Tas2r123 UTSW 6 132,824,808 (GRCm39) missense probably benign 0.32
R5079:Tas2r123 UTSW 6 132,824,681 (GRCm39) missense probably benign 0.01
R5241:Tas2r123 UTSW 6 132,824,181 (GRCm39) missense probably benign 0.06
R5288:Tas2r123 UTSW 6 132,824,190 (GRCm39) missense probably benign 0.17
R5851:Tas2r123 UTSW 6 132,824,271 (GRCm39) missense probably damaging 1.00
R6725:Tas2r123 UTSW 6 132,824,801 (GRCm39) missense probably damaging 0.97
R6895:Tas2r123 UTSW 6 132,824,133 (GRCm39) missense probably benign
R7017:Tas2r123 UTSW 6 132,824,513 (GRCm39) missense probably benign 0.00
R7183:Tas2r123 UTSW 6 132,824,661 (GRCm39) missense possibly damaging 0.95
R8972:Tas2r123 UTSW 6 132,824,333 (GRCm39) missense probably benign 0.30
R9321:Tas2r123 UTSW 6 132,825,095 (GRCm39) missense probably benign
Posted On 2015-04-16