Incidental Mutation 'IGL02816:Tas2r144'
ID 360798
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tas2r144
Ensembl Gene ENSMUSG00000051917
Gene Name taste receptor, type 2, member 144
Synonyms mt2r33, Tas2r44
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # IGL02816
Quality Score
Status
Chromosome 6
Chromosomal Location 42192262-42193221 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 42192539 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 93 (Y93F)
Ref Sequence ENSEMBL: ENSMUSP00000067734 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063489]
AlphaFold Q7TQB8
Predicted Effect probably benign
Transcript: ENSMUST00000063489
AA Change: Y93F

PolyPhen 2 Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000067734
Gene: ENSMUSG00000051917
AA Change: Y93F

DomainStartEndE-ValueType
Pfam:TAS2R 12 314 9.6e-63 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Caskin1 C A 17: 24,721,144 (GRCm39) P495T probably benign Het
Clcn4 A G 7: 7,298,087 (GRCm39) C41R probably damaging Het
Etfdh G A 3: 79,530,112 (GRCm39) T52M probably damaging Het
Fam227a T C 15: 79,510,497 (GRCm39) T386A possibly damaging Het
Gabrr3 T C 16: 59,260,830 (GRCm39) probably benign Het
Krt25 G T 11: 99,208,977 (GRCm39) D284E probably benign Het
Map1b T C 13: 99,578,263 (GRCm39) D130G probably damaging Het
Nlrp3 T A 11: 59,446,608 (GRCm39) F785I probably benign Het
Nrn1 C A 13: 36,914,080 (GRCm39) probably null Het
Numa1 T A 7: 101,645,307 (GRCm39) I311N probably damaging Het
Pkd1 T C 17: 24,813,489 (GRCm39) C4010R probably benign Het
Prph A G 15: 98,955,301 (GRCm39) M423V probably damaging Het
Rb1cc1 T A 1: 6,333,052 (GRCm39) probably benign Het
Ribc2 T G 15: 85,017,106 (GRCm39) V48G probably damaging Het
Scyl1 A T 19: 5,820,410 (GRCm39) N141K probably damaging Het
Sec23a T A 12: 59,025,331 (GRCm39) M497L probably benign Het
Strada C T 11: 106,055,251 (GRCm39) probably benign Het
Tmem94 T A 11: 115,679,530 (GRCm39) probably null Het
Trpc3 A G 3: 36,705,851 (GRCm39) F448S probably damaging Het
Ttc13 A G 8: 125,439,415 (GRCm39) I113T possibly damaging Het
Ttc27 T A 17: 75,054,769 (GRCm39) probably benign Het
Ttll13 G T 7: 79,902,842 (GRCm39) C170F possibly damaging Het
Yes1 C T 5: 32,802,451 (GRCm39) T122M probably damaging Het
Other mutations in Tas2r144
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02349:Tas2r144 APN 6 42,193,010 (GRCm39) missense probably benign 0.26
IGL02644:Tas2r144 APN 6 42,192,787 (GRCm39) missense possibly damaging 0.89
R0375:Tas2r144 UTSW 6 42,193,058 (GRCm39) missense possibly damaging 0.92
R1526:Tas2r144 UTSW 6 42,192,674 (GRCm39) missense probably benign
R1543:Tas2r144 UTSW 6 42,192,537 (GRCm39) missense probably benign 0.00
R1678:Tas2r144 UTSW 6 42,192,490 (GRCm39) missense probably benign 0.44
R1868:Tas2r144 UTSW 6 42,192,936 (GRCm39) missense probably benign 0.01
R1880:Tas2r144 UTSW 6 42,193,004 (GRCm39) missense probably benign 0.02
R4060:Tas2r144 UTSW 6 42,192,563 (GRCm39) missense possibly damaging 0.82
R5173:Tas2r144 UTSW 6 42,193,048 (GRCm39) missense probably benign 0.40
R6108:Tas2r144 UTSW 6 42,192,691 (GRCm39) missense possibly damaging 0.88
R6249:Tas2r144 UTSW 6 42,192,291 (GRCm39) nonsense probably null
R6533:Tas2r144 UTSW 6 42,192,280 (GRCm39) missense probably benign
R6850:Tas2r144 UTSW 6 42,192,857 (GRCm39) missense possibly damaging 0.71
R7237:Tas2r144 UTSW 6 42,192,800 (GRCm39) missense probably damaging 0.99
R7296:Tas2r144 UTSW 6 42,192,373 (GRCm39) missense probably damaging 1.00
R7431:Tas2r144 UTSW 6 42,192,908 (GRCm39) missense probably damaging 1.00
R8206:Tas2r144 UTSW 6 42,192,325 (GRCm39) missense probably damaging 0.98
R9341:Tas2r144 UTSW 6 42,193,066 (GRCm39) missense probably benign 0.03
R9343:Tas2r144 UTSW 6 42,193,066 (GRCm39) missense probably benign 0.03
R9640:Tas2r144 UTSW 6 42,192,428 (GRCm39) missense probably benign 0.00
X0067:Tas2r144 UTSW 6 42,193,099 (GRCm39) missense probably damaging 1.00
Posted On 2015-12-18