Incidental Mutation 'IGL02644:Tas2r144'
ID 301858
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 # IGL02644
Quality Score
Status
Chromosome 6
Chromosomal Location 42192262-42193221 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 42192787 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 176 (S176P)
Ref Sequence ENSEMBL: ENSMUSP00000067734 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063489]
AlphaFold Q7TQB8
Predicted Effect possibly damaging
Transcript: ENSMUST00000063489
AA Change: S176P

PolyPhen 2 Score 0.891 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000067734
Gene: ENSMUSG00000051917
AA Change: S176P

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: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl4 A T 3: 151,198,007 (GRCm39) Y89F probably benign Het
Agl A G 3: 116,580,246 (GRCm39) Y406H probably damaging Het
Ankhd1 G A 18: 36,711,828 (GRCm39) probably null Het
Ankmy1 T C 1: 92,812,776 (GRCm39) D511G probably benign Het
Arid2 T C 15: 96,266,589 (GRCm39) Y546H probably damaging Het
Asap1 G T 15: 63,982,911 (GRCm39) P806T probably damaging Het
Aspa T A 11: 73,212,992 (GRCm39) T117S probably damaging Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
Bspry A T 4: 62,414,565 (GRCm39) H386L probably damaging Het
C1qc T C 4: 136,617,629 (GRCm39) T156A possibly damaging Het
Cfhr4 A G 1: 139,708,905 (GRCm39) M1T probably null Het
Copz2 A T 11: 96,744,257 (GRCm39) probably benign Het
Cybb A G X: 9,333,395 (GRCm39) V23A probably benign Het
D630003M21Rik T A 2: 158,058,730 (GRCm39) D390V possibly damaging Het
Dennd10 T A 19: 60,810,741 (GRCm39) S43T possibly damaging Het
Dpy19l2 G T 9: 24,569,888 (GRCm39) P355Q probably damaging Het
Gcn1 A T 5: 115,713,250 (GRCm39) Q71L probably benign Het
Gpd1l T C 9: 114,732,725 (GRCm39) probably null Het
Hydin A G 8: 111,265,100 (GRCm39) D2761G probably damaging Het
Ifi202b T A 1: 173,799,280 (GRCm39) H256L probably benign Het
Igkv8-24 T C 6: 70,193,872 (GRCm39) Y112C probably damaging Het
Lama3 G A 18: 12,658,910 (GRCm39) R2022Q probably benign Het
Mroh4 T A 15: 74,482,224 (GRCm39) R675S possibly damaging Het
Mtf1 T G 4: 124,714,028 (GRCm39) C146G probably damaging Het
Nubpl A G 12: 52,317,841 (GRCm39) D178G probably damaging Het
Or7e165 A C 9: 19,695,010 (GRCm39) I194L probably benign Het
Pam16 A G 16: 4,434,697 (GRCm39) S91P probably damaging Het
Pcdhac2 A G 18: 37,278,232 (GRCm39) E404G probably benign Het
Pde7a C A 3: 19,311,031 (GRCm39) probably benign Het
Perm1 G T 4: 156,303,043 (GRCm39) G529V probably damaging Het
Pik3c2a T C 7: 115,972,049 (GRCm39) T794A probably benign Het
Ppfibp1 A G 6: 146,923,938 (GRCm39) Y722C probably damaging Het
Ppm1m A T 9: 106,074,082 (GRCm39) I241N probably damaging Het
Psd T C 19: 46,311,834 (GRCm39) Y282C probably damaging Het
Rpl27 T A 11: 101,336,317 (GRCm39) probably benign Het
Scaf1 A G 7: 44,655,357 (GRCm39) probably benign Het
Sec14l2 A T 11: 4,053,380 (GRCm39) probably benign Het
Smchd1 T A 17: 71,667,016 (GRCm39) probably benign Het
Sptb A T 12: 76,652,391 (GRCm39) D1615E probably damaging Het
Stt3a A C 9: 36,663,649 (GRCm39) C198G possibly damaging Het
Tlr13 A G X: 105,200,503 (GRCm39) D80G probably benign Het
Tmco4 A G 4: 138,737,920 (GRCm39) probably benign Het
Tnpo2 T A 8: 85,771,109 (GRCm39) C132S possibly damaging Het
Tubgcp3 T C 8: 12,698,733 (GRCm39) D406G probably damaging Het
Vmn2r125 G A 4: 156,703,294 (GRCm39) R224Q probably benign Het
Zfp524 C A 7: 5,020,479 (GRCm39) D2E probably damaging Het
Other mutations in Tas2r144
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02349:Tas2r144 APN 6 42,193,010 (GRCm39) missense probably benign 0.26
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
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 2015-04-16