Incidental Mutation 'IGL00915:Tas2r126'
ID27604
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r126
Ensembl Gene ENSMUSG00000048284
Gene Nametaste receptor, type 2, member 126
SynonymsT2R12, mt2r35, T2R26, mGR26, Tas2r26
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.060) question?
Stock #IGL00915
Quality Score
Status
Chromosome6
Chromosomal Location42434535-42435464 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 42435349 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Lysine at position 272 (I272K)
Ref Sequence ENSEMBL: ENSMUSP00000056581 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059534]
Predicted Effect possibly damaging
Transcript: ENSMUST00000059534
AA Change: I272K

PolyPhen 2 Score 0.670 (Sensitivity: 0.86; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000056581
Gene: ENSMUSG00000048284
AA Change: I272K

DomainStartEndE-ValueType
Pfam:TAS2R 1 303 2.5e-97 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 T A 17: 24,374,246 Y206N probably damaging Het
Aebp2 A G 6: 140,642,254 N350S probably benign Het
Cerkl A G 2: 79,341,499 S367P probably benign Het
Ddx60 T G 8: 61,987,431 V1039G possibly damaging Het
Fstl4 A T 11: 53,176,998 M563L probably benign Het
Fzd9 C T 5: 135,249,469 V521M probably damaging Het
Gorab C T 1: 163,396,857 R125Q probably benign Het
Macc1 G A 12: 119,447,014 D506N probably benign Het
Mettl17 C A 14: 51,887,289 F119L probably benign Het
Nbas C A 12: 13,374,752 C997* probably null Het
Neil1 A G 9: 57,143,977 probably null Het
Olfr458 A G 6: 42,460,950 I23T probably benign Het
Prune2 A G 19: 17,016,253 E185G probably damaging Het
Ralgapa2 A G 2: 146,342,522 S1522P probably damaging Het
Scd1 A G 19: 44,400,357 L218P possibly damaging Het
Setdb1 A T 3: 95,346,788 F234L probably damaging Het
Sos1 A G 17: 80,433,938 S473P probably benign Het
Spata31d1a T C 13: 59,702,185 S710G probably benign Het
Srp72 C A 5: 76,978,613 C87* probably null Het
Trim38 A T 13: 23,791,032 Y318F possibly damaging Het
Trnt1 A G 6: 106,779,426 K433E probably benign Het
Umodl1 A G 17: 31,008,750 probably benign Het
Urb1 A G 16: 90,779,098 F857L possibly damaging Het
Vps45 A G 3: 96,046,350 probably null Het
Zfhx4 A T 3: 5,245,523 I989F probably damaging Het
Other mutations in Tas2r126
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01327:Tas2r126 APN 6 42434750 missense probably benign 0.09
IGL01690:Tas2r126 APN 6 42435307 missense probably benign 0.02
IGL02153:Tas2r126 APN 6 42434664 missense probably benign 0.32
IGL02291:Tas2r126 APN 6 42435287 missense probably benign 0.00
IGL03365:Tas2r126 APN 6 42435457 missense probably benign 0.36
R0091:Tas2r126 UTSW 6 42435102 missense probably benign
R0486:Tas2r126 UTSW 6 42435291 missense probably benign 0.01
R0611:Tas2r126 UTSW 6 42435091 missense probably damaging 0.99
R1527:Tas2r126 UTSW 6 42435136 missense probably benign 0.03
R1529:Tas2r126 UTSW 6 42434568 missense probably benign 0.00
R1883:Tas2r126 UTSW 6 42435027 missense probably benign
R1884:Tas2r126 UTSW 6 42435027 missense probably benign
R2039:Tas2r126 UTSW 6 42434623 missense probably benign 0.22
R4863:Tas2r126 UTSW 6 42435390 missense probably benign 0.02
R5975:Tas2r126 UTSW 6 42435000 missense possibly damaging 0.69
R7127:Tas2r126 UTSW 6 42434805 missense probably damaging 1.00
R7351:Tas2r126 UTSW 6 42435306 missense probably benign 0.02
R7714:Tas2r126 UTSW 6 42435097 missense probably benign 0.12
Posted On2013-04-17