Incidental Mutation 'R0104:Tas2r135'
ID17082
Institutional Source Beutler Lab
Gene Symbol Tas2r135
Ensembl Gene ENSMUSG00000056203
Gene Nametaste receptor, type 2, member 135
Synonymsmt2r38, Tas2r35
MMRRC Submission 038390-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.063) question?
Stock #R0104 (G1)
Quality Score
Status Validated
Chromosome6
Chromosomal Location42405434-42406526 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 42406324 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 266 (I266F)
Ref Sequence ENSEMBL: ENSMUSP00000070247 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070178]
Predicted Effect possibly damaging
Transcript: ENSMUST00000070178
AA Change: I266F

PolyPhen 2 Score 0.793 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000070247
Gene: ENSMUSG00000056203
AA Change: I266F

DomainStartEndE-ValueType
Pfam:TAS2R 22 320 1.3e-63 PFAM
Meta Mutation Damage Score 0.4938 question?
Coding Region Coverage
  • 1x: 75.5%
  • 3x: 52.6%
  • 10x: 7.5%
  • 20x: 3.0%
Validation Efficiency 100% (37/37)
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3100002H09Rik C A 4: 124,610,676 A28S probably damaging Het
Arhgap5 A T 12: 52,516,717 D157V probably damaging Het
Cfap54 G T 10: 93,028,652 H142N probably damaging Het
Dpp10 A T 1: 123,367,843 M525K probably benign Het
Fsip2 A T 2: 82,978,973 T1879S possibly damaging Het
Gm14129 T C 2: 148,931,573 noncoding transcript Het
Ighv2-7 A T 12: 113,807,468 W66R probably damaging Het
Kif11 T A 19: 37,413,215 V880D probably benign Het
Mcpt1 T A 14: 56,019,431 M142K possibly damaging Het
Mlst8 T C 17: 24,476,117 N264S possibly damaging Het
Nmrk1 T A 19: 18,641,218 S88R probably benign Het
Olfr113 T A 17: 37,574,926 I166F probably damaging Het
Olfr930 A G 9: 38,930,965 S265G possibly damaging Het
Rtn1 A T 12: 72,308,845 I109N probably damaging Het
Slc15a2 T A 16: 36,774,635 L156F possibly damaging Het
Slc22a21 A C 11: 53,951,809 M498R probably null Het
Ssc5d T C 7: 4,936,286 S574P probably benign Het
Taf2 T C 15: 55,038,338 D820G probably benign Het
Tcrg-V4 C T 13: 19,185,310 H75Y probably damaging Het
Vil1 A G 1: 74,418,366 K53E probably benign Het
Zfc3h1 T A 10: 115,415,287 M1261K possibly damaging Het
Zfp655 T C 5: 145,244,015 S228P probably damaging Het
Zfyve9 C A 4: 108,718,163 D574Y probably damaging Het
Other mutations in Tas2r135
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01357:Tas2r135 APN 6 42406144 missense probably benign 0.00
IGL01395:Tas2r135 APN 6 42405912 nonsense probably null
IGL02479:Tas2r135 APN 6 42405751 nonsense probably null
IGL02526:Tas2r135 APN 6 42406280 missense probably damaging 1.00
IGL02806:Tas2r135 APN 6 42406448 missense probably benign 0.00
IGL02982:Tas2r135 APN 6 42406253 missense probably benign
IGL03057:Tas2r135 APN 6 42401127 unclassified probably benign
R0057:Tas2r135 UTSW 6 42406420 missense probably benign 0.07
R1412:Tas2r135 UTSW 6 42405834 missense probably benign 0.00
R4517:Tas2r135 UTSW 6 42406079 missense probably benign
R4629:Tas2r135 UTSW 6 42406226 missense probably benign 0.03
R5788:Tas2r135 UTSW 6 42405597 missense probably damaging 1.00
R6021:Tas2r135 UTSW 6 42406387 missense probably damaging 1.00
R6586:Tas2r135 UTSW 6 42406018 missense probably benign 0.18
R7180:Tas2r135 UTSW 6 42405751 nonsense probably null
R7458:Tas2r135 UTSW 6 42405947 missense possibly damaging 0.95
R7850:Tas2r135 UTSW 6 42406138 missense probably benign
R7933:Tas2r135 UTSW 6 42406138 missense probably benign
Z1176:Tas2r135 UTSW 6 42406234 missense probably benign 0.03
Posted On2013-01-20