Incidental Mutation 'IGL00562:Tas2r134'
ID 277759
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r134
Ensembl Gene ENSMUSG00000056115
Gene Name taste receptor, type 2, member 134
Synonyms Tas2r34, T2R134
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL00562
Quality Score
Status
Chromosome 2
Chromosomal Location 51517523-51518419 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 51518100 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 193 (I193T)
Ref Sequence ENSEMBL: ENSMUSP00000064657 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070028]
AlphaFold Q7TQB0
Predicted Effect possibly damaging
Transcript: ENSMUST00000070028
AA Change: I193T

PolyPhen 2 Score 0.899 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000064657
Gene: ENSMUSG00000056115
AA Change: I193T

DomainStartEndE-ValueType
Pfam:TAS2R 1 291 1.4e-75 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1500035N22Rik T C 5: 25,202,619 (GRCm39) probably benign Het
AU016765 C A 17: 64,826,877 (GRCm39) noncoding transcript Het
Chaf1b T C 16: 93,697,079 (GRCm39) probably benign Het
Clstn2 A G 9: 97,464,505 (GRCm39) probably benign Het
Crip1 T A 12: 113,117,232 (GRCm39) probably null Het
Cubn A G 2: 13,299,041 (GRCm39) S3211P probably benign Het
Dlx6 C T 6: 6,865,143 (GRCm39) R172W probably damaging Het
Fktn A T 4: 53,747,007 (GRCm39) probably null Het
Focad T A 4: 88,267,046 (GRCm39) M1019K unknown Het
Fuca2 A T 10: 13,381,651 (GRCm39) D188V probably damaging Het
Kcna3 A G 3: 106,944,046 (GRCm39) D103G probably damaging Het
Mrpl19 A G 6: 81,942,853 (GRCm39) V19A probably benign Het
Ndufb3 T A 1: 58,634,958 (GRCm39) H103Q possibly damaging Het
Pkd1l3 T C 8: 110,382,779 (GRCm39) V1675A possibly damaging Het
Ptger4 A T 15: 5,272,614 (GRCm39) S2T probably benign Het
Saxo1 C T 4: 86,363,809 (GRCm39) E225K probably damaging Het
Sftpb G T 6: 72,286,845 (GRCm39) A228S probably benign Het
Slc22a29 T A 19: 8,138,993 (GRCm39) T490S probably benign Het
Slc29a1 T C 17: 45,900,918 (GRCm39) N50S probably damaging Het
Smc6 T A 12: 11,351,532 (GRCm39) S854T probably benign Het
Smim23 T C 11: 32,771,893 (GRCm39) T58A probably benign Het
Thsd7a G T 6: 12,379,658 (GRCm39) probably null Het
Trav13n-4 T G 14: 53,601,423 (GRCm39) V64G possibly damaging Het
Trmt10a G A 3: 137,853,177 (GRCm39) E13K probably damaging Het
Txndc11 T C 16: 10,922,496 (GRCm39) S239G probably damaging Het
Vmn2r96 T A 17: 18,804,077 (GRCm39) N442K probably benign Het
Vps13a C T 19: 16,712,078 (GRCm39) probably null Het
Other mutations in Tas2r134
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00563:Tas2r134 APN 2 51,518,100 (GRCm39) missense possibly damaging 0.90
IGL01121:Tas2r134 APN 2 51,518,001 (GRCm39) missense probably damaging 1.00
IGL01122:Tas2r134 APN 2 51,517,671 (GRCm39) missense probably damaging 1.00
IGL01128:Tas2r134 APN 2 51,517,671 (GRCm39) missense probably damaging 1.00
IGL01132:Tas2r134 APN 2 51,517,671 (GRCm39) missense probably damaging 1.00
IGL01312:Tas2r134 APN 2 51,518,247 (GRCm39) missense probably damaging 1.00
IGL01419:Tas2r134 APN 2 51,517,759 (GRCm39) nonsense probably null
IGL01774:Tas2r134 APN 2 51,518,160 (GRCm39) missense probably benign 0.07
IGL02735:Tas2r134 APN 2 51,517,839 (GRCm39) missense probably damaging 1.00
R0799:Tas2r134 UTSW 2 51,518,385 (GRCm39) missense probably benign 0.00
R1205:Tas2r134 UTSW 2 51,517,998 (GRCm39) missense probably benign 0.00
R2267:Tas2r134 UTSW 2 51,518,249 (GRCm39) missense probably benign 0.01
R3736:Tas2r134 UTSW 2 51,517,786 (GRCm39) missense probably damaging 1.00
R5254:Tas2r134 UTSW 2 51,517,559 (GRCm39) missense probably benign 0.39
R5752:Tas2r134 UTSW 2 51,517,880 (GRCm39) missense probably damaging 1.00
R6162:Tas2r134 UTSW 2 51,517,571 (GRCm39) missense probably damaging 1.00
R6940:Tas2r134 UTSW 2 51,518,148 (GRCm39) missense probably benign 0.00
R6954:Tas2r134 UTSW 2 51,517,782 (GRCm39) missense probably benign 0.00
R6996:Tas2r134 UTSW 2 51,517,601 (GRCm39) missense probably benign 0.00
R7206:Tas2r134 UTSW 2 51,518,120 (GRCm39) missense probably benign 0.02
R7303:Tas2r134 UTSW 2 51,518,145 (GRCm39) missense probably benign 0.01
R7348:Tas2r134 UTSW 2 51,518,414 (GRCm39) missense possibly damaging 0.92
R7479:Tas2r134 UTSW 2 51,517,541 (GRCm39) missense not run
R7575:Tas2r134 UTSW 2 51,518,166 (GRCm39) missense probably damaging 1.00
R7686:Tas2r134 UTSW 2 51,518,255 (GRCm39) missense possibly damaging 0.54
R8721:Tas2r134 UTSW 2 51,517,571 (GRCm39) missense probably damaging 1.00
R9384:Tas2r134 UTSW 2 51,518,034 (GRCm39) missense probably damaging 0.97
R9622:Tas2r134 UTSW 2 51,518,358 (GRCm39) missense possibly damaging 0.89
Posted On 2015-04-16