Incidental Mutation 'R6249:Tas2r144'
ID 505842
Institutional Source Beutler Lab
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 # R6249 (G1)
Quality Score 225.009
Status Not validated
Chromosome 6
Chromosomal Location 42192262-42193221 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 42192291 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 10 (Y10*)
Ref Sequence ENSEMBL: ENSMUSP00000067734 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063489]
AlphaFold Q7TQB8
Predicted Effect probably null
Transcript: ENSMUST00000063489
AA Change: Y10*
SMART Domains Protein: ENSMUSP00000067734
Gene: ENSMUSG00000051917
AA Change: Y10*

DomainStartEndE-ValueType
Pfam:TAS2R 12 314 9.6e-63 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110004F10Rik A T 7: 115,702,505 (GRCm39) S90C probably damaging Het
Abca9 T C 11: 110,036,453 (GRCm39) D552G probably benign Het
Adgrb3 A G 1: 25,471,639 (GRCm39) L502P probably damaging Het
Agmo T C 12: 37,293,837 (GRCm39) probably null Het
Ank3 A G 10: 69,658,906 (GRCm39) probably null Het
Apol11b G T 15: 77,519,537 (GRCm39) T181K probably benign Het
Arap2 G T 5: 62,803,536 (GRCm39) H1244N probably damaging Het
Arid1b A T 17: 5,329,636 (GRCm39) M838L possibly damaging Het
Aste1 G A 9: 105,273,816 (GRCm39) V19I probably benign Het
B3gnt3 A T 8: 72,145,306 (GRCm39) M354K probably damaging Het
Calcr A T 6: 3,692,711 (GRCm39) M381K possibly damaging Het
Ccdc63 A C 5: 122,263,062 (GRCm39) L160W probably benign Het
Cerkl A G 2: 79,199,122 (GRCm39) L156P probably damaging Het
Csnk2a1-ps3 A G 1: 156,352,800 (GRCm39) M334V probably benign Het
Dab1 C T 4: 104,588,948 (GRCm39) A524V probably benign Het
Ddb1 C A 19: 10,583,084 (GRCm39) Y5* probably null Het
Fignl2 T C 15: 100,952,060 (GRCm39) E74G possibly damaging Het
Glb1l2 C T 9: 26,676,850 (GRCm39) probably benign Het
Gm16503 A G 4: 147,625,508 (GRCm39) M1V probably null Het
Gm2696 A C 10: 77,630,646 (GRCm39) probably benign Het
Gm45844 A G 7: 7,243,092 (GRCm39) S20P probably benign Het
Gm7579 C T 7: 141,765,743 (GRCm39) P50S unknown Het
Idh1 A G 1: 65,205,378 (GRCm39) S196P probably damaging Het
Il1rap T C 16: 26,511,598 (GRCm39) V214A possibly damaging Het
Kctd17 C G 15: 78,314,239 (GRCm39) probably null Het
Lama1 G T 17: 68,105,599 (GRCm39) V2036L probably benign Het
Lars1 G T 18: 42,390,271 (GRCm39) probably null Het
Mdn1 T A 4: 32,708,484 (GRCm39) V1670E possibly damaging Het
Mtmr7 A T 8: 41,034,524 (GRCm39) I266N probably damaging Het
Ncapd3 GGCTGCTGCTGCTGCTGCTGCTG GGCTGCTGCTGCTGCTGCTG 9: 26,999,349 (GRCm39) probably benign Het
Nckap5 T C 1: 125,952,667 (GRCm39) E1295G probably benign Het
Nrxn3 T A 12: 89,221,448 (GRCm39) V409D probably damaging Het
Or13p3 A G 4: 118,566,910 (GRCm39) Y102C probably damaging Het
Or2a5 G T 6: 42,874,238 (GRCm39) L284F probably damaging Het
Or2aj4 T A 16: 19,384,725 (GRCm39) N303Y probably damaging Het
Or51q1 A T 7: 103,628,818 (GRCm39) S140C possibly damaging Het
Or5h22 T C 16: 58,894,795 (GRCm39) Y216C probably damaging Het
Or8b44 T G 9: 38,410,880 (GRCm39) I305R unknown Het
Pcdha4 T A 18: 37,086,729 (GRCm39) V304E probably damaging Het
Pde6c T C 19: 38,147,008 (GRCm39) probably null Het
Pebp4 A T 14: 70,297,099 (GRCm39) T213S possibly damaging Het
Phf2 C A 13: 48,959,348 (GRCm39) R886L unknown Het
Pik3ca A T 3: 32,515,712 (GRCm39) H795L probably damaging Het
Pisd G T 5: 32,896,188 (GRCm39) T379N probably damaging Het
Pld2 T C 11: 70,446,196 (GRCm39) L732P probably damaging Het
Pskh1 A G 8: 106,639,617 (GRCm39) D99G possibly damaging Het
Rest A G 5: 77,429,071 (GRCm39) T497A probably benign Het
Rps24 C T 14: 24,543,530 (GRCm39) T108M possibly damaging Het
Rtel1 C T 2: 180,993,475 (GRCm39) R566C probably damaging Het
Scyl2 A G 10: 89,493,719 (GRCm39) S350P possibly damaging Het
Slc38a7 G T 8: 96,564,302 (GRCm39) probably null Het
Sox5 A G 6: 143,779,009 (GRCm39) I674T probably benign Het
Spata31f1a A T 4: 42,850,528 (GRCm39) W543R probably benign Het
Surf4 C A 2: 26,816,899 (GRCm39) E39D probably damaging Het
Thbs4 C T 13: 92,911,215 (GRCm39) G323R probably damaging Het
Top2b A G 14: 16,399,006 (GRCm38) Y542C probably damaging Het
Trim61 A G 8: 65,467,108 (GRCm39) V51A probably benign Het
Tyrp1 T A 4: 80,769,009 (GRCm39) I501N possibly damaging Het
U2surp C T 9: 95,382,869 (GRCm39) D32N probably benign Het
Ush1c T C 7: 45,864,383 (GRCm39) Y411C probably damaging Het
Vwa7 G A 17: 35,242,365 (GRCm39) V490I probably benign Het
Xylt1 G T 7: 117,266,528 (GRCm39) A849S probably benign Het
Ythdc1 T A 5: 86,979,815 (GRCm39) N599K possibly damaging Het
Zbtb38 T A 9: 96,568,045 (GRCm39) Y1013F probably damaging Het
Zfp709 TCGACG TCG 8: 72,644,552 (GRCm39) probably benign Het
Zswim9 T C 7: 12,994,903 (GRCm39) S418G 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
IGL02816:Tas2r144 APN 6 42,192,539 (GRCm39) missense probably benign 0.03
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
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
Predicted Primers PCR Primer
(F):5'- TTAGAGCCAGTAACCAAATCCTTTC -3'
(R):5'- TACCATCATCCATATCTGTAGCAAC -3'

Sequencing Primer
(F):5'- ATTGCAGCATCACTGACG -3'
(R):5'- TGTAGCAACAGCCTGGAAAAACTC -3'
Posted On 2018-02-28