Incidental Mutation 'IGL02216:Tas2r143'
ID 284891
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r143
Ensembl Gene ENSMUSG00000046652
Gene Name taste receptor, type 2, member 143
Synonyms Tas2r43, mt2r36
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # IGL02216
Quality Score
Status
Chromosome 6
Chromosomal Location 42377172-42378053 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 42377268 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 33 (R33*)
Ref Sequence ENSEMBL: ENSMUSP00000057910 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057398]
AlphaFold Q7TQB9
Predicted Effect probably null
Transcript: ENSMUST00000057398
AA Change: R33*
SMART Domains Protein: ENSMUSP00000057910
Gene: ENSMUSG00000046652
AA Change: R33*

DomainStartEndE-ValueType
Pfam:TAS2R 1 293 6.7e-68 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930544D05Rik T C 11: 70,507,005 (GRCm39) F48L possibly damaging Het
Adamts12 A G 15: 11,241,571 (GRCm39) N381S possibly damaging Het
Akp3 A T 1: 87,055,372 (GRCm39) Q473L probably damaging Het
Albfm1 T C 5: 90,727,438 (GRCm39) probably benign Het
Ap5s1 T A 2: 131,054,887 (GRCm39) probably benign Het
Atp10b T A 11: 43,150,616 (GRCm39) L1438Q probably damaging Het
B3galt4 G A 17: 34,169,539 (GRCm39) P233L probably damaging Het
Brd8 C T 18: 34,735,780 (GRCm39) S899N probably damaging Het
Cc2d1a C A 8: 84,865,942 (GRCm39) E393* probably null Het
Cd209a G T 8: 3,795,576 (GRCm39) T165N probably damaging Het
Chid1 T C 7: 141,076,506 (GRCm39) probably benign Het
Cln3 A T 7: 126,174,514 (GRCm39) probably null Het
Cped1 A T 6: 22,059,944 (GRCm39) R203S probably damaging Het
Dele1 A T 18: 38,385,913 (GRCm39) I102F probably damaging Het
Dnttip2 G T 3: 122,069,910 (GRCm39) W375L probably benign Het
Dync1h1 T C 12: 110,629,436 (GRCm39) F4280S probably damaging Het
Ephb4 A G 5: 137,370,332 (GRCm39) D844G possibly damaging Het
Fhl2 T A 1: 43,170,879 (GRCm39) E145V probably null Het
Gne T C 4: 44,044,761 (GRCm39) K458E probably benign Het
Grid2 G T 6: 64,322,650 (GRCm39) R550L probably damaging Het
Klhl1 T A 14: 96,360,658 (GRCm39) T731S probably benign Het
Kng1 T A 16: 22,877,283 (GRCm39) D30E probably damaging Het
Kyat1 A G 2: 30,077,264 (GRCm39) V158A probably benign Het
Mcm8 G T 2: 132,681,449 (GRCm39) V642F probably damaging Het
Mdn1 C T 4: 32,739,092 (GRCm39) H3638Y probably benign Het
Neb T G 2: 52,116,502 (GRCm39) T4158P probably benign Het
Neo1 T C 9: 58,824,336 (GRCm39) I697M probably damaging Het
Nfkb1 A T 3: 135,300,724 (GRCm39) V614D probably damaging Het
Or7e169 G A 9: 19,757,861 (GRCm39) S18L probably damaging Het
Otog T C 7: 45,950,892 (GRCm39) S2555P probably damaging Het
Pkd1l1 T A 11: 8,784,897 (GRCm39) R1962S probably damaging Het
Plxnb1 A G 9: 108,929,918 (GRCm39) Y258C probably damaging Het
Pramel12 T A 4: 143,144,298 (GRCm39) probably null Het
Prl3a1 A G 13: 27,454,127 (GRCm39) D35G probably benign Het
Rag1 A T 2: 101,473,726 (GRCm39) V472D possibly damaging Het
Rbpj-ps3 G A 6: 46,506,641 (GRCm39) probably benign Het
Rnf112 C T 11: 61,340,804 (GRCm39) V472M probably damaging Het
Rps18 A G 17: 34,171,015 (GRCm39) probably benign Het
Rptn T C 3: 93,303,080 (GRCm39) S138P possibly damaging Het
Sbpl A C 17: 24,172,690 (GRCm39) N76K probably benign Het
Sh3bp1 A T 15: 78,789,364 (GRCm39) M241L probably benign Het
Slc22a17 T C 14: 55,145,433 (GRCm39) *198W probably null Het
Smc3 C T 19: 53,610,275 (GRCm39) R221C probably damaging Het
Snai1 A G 2: 167,380,768 (GRCm39) E87G probably benign Het
Snx22 C A 9: 65,976,470 (GRCm39) A49S probably benign Het
Try4 A G 6: 41,281,965 (GRCm39) I184V probably benign Het
Ttn T A 2: 76,584,896 (GRCm39) K20355* probably null Het
Ttn A G 2: 76,622,069 (GRCm39) V15491A probably benign Het
Tut7 T C 13: 59,948,237 (GRCm39) T293A probably benign Het
Vmn1r170 A G 7: 23,305,915 (GRCm39) T106A probably damaging Het
Vmn2r59 A T 7: 41,661,817 (GRCm39) V666E probably damaging Het
Vsx1 T C 2: 150,526,495 (GRCm39) N221S possibly damaging Het
Zfp846 A G 9: 20,499,905 (GRCm39) E45G probably damaging Het
Other mutations in Tas2r143
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02832:Tas2r143 APN 6 42,377,259 (GRCm39) missense possibly damaging 0.55
R0125:Tas2r143 UTSW 6 42,377,889 (GRCm39) missense probably benign 0.01
R1035:Tas2r143 UTSW 6 42,377,199 (GRCm39) missense probably benign 0.16
R1073:Tas2r143 UTSW 6 42,377,694 (GRCm39) missense probably benign 0.01
R1400:Tas2r143 UTSW 6 42,377,317 (GRCm39) missense probably benign 0.35
R1774:Tas2r143 UTSW 6 42,377,305 (GRCm39) missense probably damaging 1.00
R2391:Tas2r143 UTSW 6 42,377,810 (GRCm39) missense probably damaging 0.99
R3617:Tas2r143 UTSW 6 42,377,997 (GRCm39) missense probably benign 0.20
R3693:Tas2r143 UTSW 6 42,377,910 (GRCm39) missense probably benign 0.00
R4283:Tas2r143 UTSW 6 42,378,007 (GRCm39) splice site probably null
R4486:Tas2r143 UTSW 6 42,377,628 (GRCm39) missense probably benign 0.15
R5005:Tas2r143 UTSW 6 42,377,658 (GRCm39) missense probably benign 0.02
R6360:Tas2r143 UTSW 6 42,377,769 (GRCm39) missense probably benign 0.40
R7163:Tas2r143 UTSW 6 42,377,202 (GRCm39) missense probably benign
R7827:Tas2r143 UTSW 6 42,377,656 (GRCm39) missense probably damaging 1.00
R8899:Tas2r143 UTSW 6 42,377,888 (GRCm39) nonsense probably null
R8989:Tas2r143 UTSW 6 42,377,828 (GRCm39) missense probably damaging 1.00
R9264:Tas2r143 UTSW 6 42,377,673 (GRCm39) missense probably benign 0.09
Posted On 2015-04-16