Incidental Mutation 'IGL02982:Tas2r135'
ID 406573
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r135
Ensembl Gene ENSMUSG00000056203
Gene Name taste receptor, type 2, member 135
Synonyms mt2r38, Tas2r35
Accession Numbers
Essential gene? Probably non essential (E-score: 0.051) question?
Stock # IGL02982
Quality Score
Status
Chromosome 6
Chromosomal Location 42382463-42383428 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 42383187 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 242 (E242G)
Ref Sequence ENSEMBL: ENSMUSP00000070247 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070178]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000070178
AA Change: E242G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000070247
Gene: ENSMUSG00000056203
AA Change: E242G

DomainStartEndE-ValueType
Pfam:TAS2R 22 320 1.3e-63 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam5 G T 8: 25,294,447 (GRCm39) A384D probably benign Het
Adamts19 T A 18: 59,157,590 (GRCm39) C961S probably damaging Het
Agbl2 G A 2: 90,636,159 (GRCm39) C565Y probably damaging Het
Aox3 G A 1: 58,166,846 (GRCm39) E190K probably benign Het
Arf2 T G 11: 103,872,602 (GRCm39) D74E probably damaging Het
Bptf T G 11: 106,967,500 (GRCm39) D960A probably damaging Het
Ccdc180 G T 4: 45,903,840 (GRCm39) probably benign Het
Ces1a A G 8: 93,771,603 (GRCm39) F65L probably damaging Het
Def8 T C 8: 124,183,278 (GRCm39) probably benign Het
Fat4 T C 3: 38,944,992 (GRCm39) L1295P probably damaging Het
Filip1l A G 16: 57,392,595 (GRCm39) H1061R probably damaging Het
Fut2 C T 7: 45,300,193 (GRCm39) G193E possibly damaging Het
Gldc A G 19: 30,122,545 (GRCm39) probably null Het
Golgb1 A C 16: 36,746,172 (GRCm39) D2917A probably damaging Het
Gpc5 G A 14: 115,607,400 (GRCm39) C334Y probably damaging Het
Gpsm1 T A 2: 26,214,871 (GRCm39) L252Q probably damaging Het
Iars1 C T 13: 49,863,185 (GRCm39) R546C probably benign Het
Kbtbd8 G T 6: 95,103,547 (GRCm39) V399L probably benign Het
Kcnd2 A T 6: 21,217,148 (GRCm39) D284V probably damaging Het
Kcnj6 T C 16: 94,633,376 (GRCm39) K227R possibly damaging Het
Lhx9 A T 1: 138,766,349 (GRCm39) H155Q probably damaging Het
Mcm9 A G 10: 53,501,922 (GRCm39) V221A probably damaging Het
Myo9a A T 9: 59,815,491 (GRCm39) K2237* probably null Het
Ntf3 A T 6: 126,079,340 (GRCm39) D55E probably damaging Het
Or13a28 A T 7: 140,217,865 (GRCm39) I84F probably benign Het
Or4c15b G T 2: 89,113,453 (GRCm39) T29K probably damaging Het
Plek T A 11: 16,931,826 (GRCm39) I342F probably damaging Het
Polrmt A G 10: 79,574,182 (GRCm39) Y853H probably damaging Het
Psg29 A G 7: 16,945,632 (GRCm39) T401A probably damaging Het
Ptprb A G 10: 116,158,533 (GRCm39) T822A probably benign Het
Ptprq A C 10: 107,422,545 (GRCm39) F1616V probably damaging Het
Rpe65 T A 3: 159,305,998 (GRCm39) V19E probably damaging Het
Scamp2 G A 9: 57,488,832 (GRCm39) A178T probably benign Het
Spata31e5 T C 1: 28,817,135 (GRCm39) H299R probably damaging Het
Spta1 A G 1: 174,014,854 (GRCm39) I445V probably benign Het
Ttc22 T C 4: 106,495,783 (GRCm39) V379A probably damaging Het
Unc5d C T 8: 29,142,881 (GRCm39) G857E probably damaging Het
Usp28 A G 9: 48,929,739 (GRCm39) I43V probably benign Het
Vmn2r68 A T 7: 84,883,649 (GRCm39) M152K probably benign Het
Wrn C T 8: 33,833,094 (GRCm39) G133R probably damaging Het
Zfyve26 G A 12: 79,310,644 (GRCm39) T187M probably damaging Het
Zic2 A G 14: 122,715,979 (GRCm39) E367G probably damaging Het
Other mutations in Tas2r135
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01357:Tas2r135 APN 6 42,383,078 (GRCm39) missense probably benign 0.00
IGL01395:Tas2r135 APN 6 42,382,846 (GRCm39) nonsense probably null
IGL02479:Tas2r135 APN 6 42,382,685 (GRCm39) nonsense probably null
IGL02526:Tas2r135 APN 6 42,383,214 (GRCm39) missense probably damaging 1.00
IGL02806:Tas2r135 APN 6 42,383,382 (GRCm39) missense probably benign 0.00
IGL03057:Tas2r135 APN 6 42,378,061 (GRCm39) unclassified probably benign
R0057:Tas2r135 UTSW 6 42,383,354 (GRCm39) missense probably benign 0.07
R0104:Tas2r135 UTSW 6 42,383,258 (GRCm39) missense possibly damaging 0.79
R1412:Tas2r135 UTSW 6 42,382,768 (GRCm39) missense probably benign 0.00
R4517:Tas2r135 UTSW 6 42,383,013 (GRCm39) missense probably benign
R4629:Tas2r135 UTSW 6 42,383,160 (GRCm39) missense probably benign 0.03
R5788:Tas2r135 UTSW 6 42,382,531 (GRCm39) missense probably damaging 1.00
R6021:Tas2r135 UTSW 6 42,383,321 (GRCm39) missense probably damaging 1.00
R6586:Tas2r135 UTSW 6 42,382,952 (GRCm39) missense probably benign 0.18
R7180:Tas2r135 UTSW 6 42,382,685 (GRCm39) nonsense probably null
R7458:Tas2r135 UTSW 6 42,382,881 (GRCm39) missense possibly damaging 0.95
R7850:Tas2r135 UTSW 6 42,383,072 (GRCm39) missense probably benign
R9113:Tas2r135 UTSW 6 42,383,315 (GRCm39) missense probably benign 0.00
Z1176:Tas2r135 UTSW 6 42,383,168 (GRCm39) missense probably benign 0.03
Posted On 2016-08-02