Incidental Mutation 'IGL00467:Tas2r109'
ID 45054
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r109
Ensembl Gene ENSMUSG00000062528
Gene Name taste receptor, type 2, member 109
Synonyms mt2r62, T2R09, mGR09, Tas2r9
Accession Numbers
Essential gene? Probably non essential (E-score: 0.048) question?
Stock # IGL00467
Quality Score
Status
Chromosome 6
Chromosomal Location 132956978-132957928 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 132956986 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Leucine at position 315 (V315L)
Ref Sequence ENSEMBL: ENSMUSP00000069300 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067539]
AlphaFold Q7M707
Predicted Effect probably benign
Transcript: ENSMUST00000067539
AA Change: V315L

PolyPhen 2 Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000069300
Gene: ENSMUSG00000062528
AA Change: V315L

DomainStartEndE-ValueType
Pfam:TAS2R 9 309 4.3e-81 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca9 T C 11: 110,036,496 (GRCm39) probably benign Het
Acvrl1 C A 15: 101,041,221 (GRCm39) probably null Het
Ahnak T A 19: 8,984,587 (GRCm39) M1957K probably damaging Het
Brinp3 A G 1: 146,777,512 (GRCm39) D653G probably damaging Het
Dcstamp T A 15: 39,617,812 (GRCm39) C74S probably benign Het
Esrrg A G 1: 187,943,107 (GRCm39) E360G probably damaging Het
Fam13a C T 6: 58,917,098 (GRCm39) probably benign Het
Glipr1l1 A G 10: 111,914,286 (GRCm39) T216A probably benign Het
Lama2 T A 10: 27,343,193 (GRCm39) probably benign Het
Men1 G A 19: 6,387,237 (GRCm39) probably null Het
Mta3 T A 17: 84,063,113 (GRCm39) probably benign Het
Nfu1 A G 6: 86,997,755 (GRCm39) M213V possibly damaging Het
Pam A T 1: 97,852,152 (GRCm39) probably benign Het
Pcca A T 14: 122,820,041 (GRCm39) M62L probably benign Het
Phf6 A G X: 52,020,523 (GRCm39) Y25C probably damaging Het
Phlpp2 C T 8: 110,652,422 (GRCm39) H589Y probably benign Het
Ppp1r13b A G 12: 111,795,804 (GRCm39) I956T probably damaging Het
Prkcd G A 14: 30,324,379 (GRCm39) probably benign Het
Rapgef4 A T 2: 72,086,656 (GRCm39) N973I possibly damaging Het
Rnf20 G T 4: 49,655,480 (GRCm39) E905* probably null Het
Slc26a6 T A 9: 108,733,088 (GRCm39) D22E probably benign Het
Sp2 C T 11: 96,845,387 (GRCm39) R578H probably damaging Het
Taf6l A T 19: 8,760,752 (GRCm39) N57K probably benign Het
Tasor A G 14: 27,170,121 (GRCm39) N350S probably benign Het
Tex9 T C 9: 72,385,117 (GRCm39) T240A probably benign Het
Trank1 G A 9: 111,193,734 (GRCm39) probably benign Het
Trim30c A T 7: 104,031,389 (GRCm39) Y475* probably null Het
Trim60 T C 8: 65,453,371 (GRCm39) T293A possibly damaging Het
Ttc21b T C 2: 66,018,708 (GRCm39) Y1233C probably damaging Het
Wdr75 A G 1: 45,841,235 (GRCm39) I106V probably benign Het
Zkscan16 T C 4: 58,957,709 (GRCm39) S664P possibly damaging Het
Other mutations in Tas2r109
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01837:Tas2r109 APN 6 132,957,477 (GRCm39) missense probably benign 0.27
IGL02094:Tas2r109 APN 6 132,957,202 (GRCm39) missense possibly damaging 0.78
R0788:Tas2r109 UTSW 6 132,957,264 (GRCm39) missense probably benign 0.01
R0849:Tas2r109 UTSW 6 132,957,856 (GRCm39) missense probably benign 0.00
R1542:Tas2r109 UTSW 6 132,957,873 (GRCm39) missense possibly damaging 0.93
R1583:Tas2r109 UTSW 6 132,957,389 (GRCm39) missense probably benign 0.01
R2035:Tas2r109 UTSW 6 132,957,423 (GRCm39) missense probably benign
R3845:Tas2r109 UTSW 6 132,957,766 (GRCm39) missense probably damaging 0.99
R4060:Tas2r109 UTSW 6 132,957,148 (GRCm39) missense probably damaging 1.00
R4355:Tas2r109 UTSW 6 132,957,144 (GRCm39) missense probably benign
R5353:Tas2r109 UTSW 6 132,957,594 (GRCm39) missense possibly damaging 0.61
R5860:Tas2r109 UTSW 6 132,957,664 (GRCm39) missense probably benign 0.06
R6211:Tas2r109 UTSW 6 132,957,587 (GRCm39) nonsense probably null
R6378:Tas2r109 UTSW 6 132,957,844 (GRCm39) missense probably benign 0.00
R6861:Tas2r109 UTSW 6 132,957,048 (GRCm39) missense probably benign 0.43
R7319:Tas2r109 UTSW 6 132,957,663 (GRCm39) missense probably benign 0.33
R8553:Tas2r109 UTSW 6 132,957,171 (GRCm39) missense probably benign 0.33
R9447:Tas2r109 UTSW 6 132,957,270 (GRCm39) missense probably damaging 1.00
Z1088:Tas2r109 UTSW 6 132,957,264 (GRCm39) missense probably benign 0.07
Posted On 2013-06-11