Incidental Mutation 'R5495:Taar4'
ID 432298
Institutional Source Beutler Lab
Gene Symbol Taar4
Ensembl Gene ENSMUSG00000069707
Gene Name trace amine-associated receptor 4
Synonyms
MMRRC Submission 043056-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.122) question?
Stock # R5495 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 23836392-23837435 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 23837181 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 264 (I264F)
Ref Sequence ENSEMBL: ENSMUSP00000090330 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092660]
AlphaFold Q5QD15
Predicted Effect possibly damaging
Transcript: ENSMUST00000092660
AA Change: I264F

PolyPhen 2 Score 0.951 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000090330
Gene: ENSMUSG00000069707
AA Change: I264F

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 44 328 9.2e-11 PFAM
Pfam:7tm_1 50 313 4.6e-63 PFAM
Coding Region Coverage
  • 1x: 98.4%
  • 3x: 97.3%
  • 10x: 95.3%
  • 20x: 91.4%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired olfactory response and aversion to PEA and puma urine. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akt2 T C 7: 27,335,594 (GRCm39) probably null Het
Arhgap29 T G 3: 121,808,578 (GRCm39) M844R probably damaging Het
Atp1a1 T G 3: 101,498,741 (GRCm39) D184A probably benign Het
Bcl11a T A 11: 24,115,042 (GRCm39) V795E possibly damaging Het
Casp12 T A 9: 5,353,797 (GRCm39) I277N possibly damaging Het
Ccdc59 A G 10: 105,681,239 (GRCm39) K164E probably damaging Het
D630003M21Rik C T 2: 158,062,431 (GRCm39) G30S possibly damaging Het
Dgkd A G 1: 87,854,594 (GRCm39) D632G probably damaging Het
Efr3a A G 15: 65,687,258 (GRCm39) K56E possibly damaging Het
Egflam T A 15: 7,280,722 (GRCm39) R434S probably damaging Het
Fancl C G 11: 26,347,801 (GRCm39) A51G probably damaging Het
Fkbp7 T C 2: 76,493,638 (GRCm39) Y185C probably damaging Het
Galc A G 12: 98,197,673 (GRCm39) probably null Het
Galnt15 A G 14: 31,751,774 (GRCm39) S109G probably damaging Het
Gramd2b T C 18: 56,615,694 (GRCm39) I163T probably damaging Het
Impa1 A G 3: 10,391,230 (GRCm39) V80A probably benign Het
Itga10 T C 3: 96,554,687 (GRCm39) M56T possibly damaging Het
Larp1b G T 3: 40,990,257 (GRCm39) R135I probably damaging Het
Lgals12 C T 19: 7,581,495 (GRCm39) A71T probably damaging Het
Lmbr1 A T 5: 29,551,851 (GRCm39) L78* probably null Het
Lrat C A 3: 82,804,289 (GRCm39) M229I probably benign Het
Mug2 A T 6: 122,056,609 (GRCm39) M1185L probably damaging Het
Naprt T C 15: 75,765,696 (GRCm39) probably null Het
Nfat5 A G 8: 108,095,079 (GRCm39) I1107V probably benign Het
Nr4a2 T C 2: 57,002,387 (GRCm39) Y22C probably damaging Het
Ogfod1 C A 8: 94,790,906 (GRCm39) Q526K probably benign Het
Or2d4 C A 7: 106,543,699 (GRCm39) G170* probably null Het
Or3a10 G A 11: 73,935,611 (GRCm39) T163I probably damaging Het
Or4p21 T C 2: 88,276,401 (GRCm39) T294A probably benign Het
Or8g36 T C 9: 39,422,441 (GRCm39) T192A probably benign Het
Parp10 T G 15: 76,127,366 (GRCm39) I24L probably benign Het
Pcdha11 A G 18: 37,144,079 (GRCm39) T57A probably benign Het
Prdm8 A G 5: 98,333,165 (GRCm39) E244G possibly damaging Het
Prl6a1 T C 13: 27,496,654 (GRCm39) S3P possibly damaging Het
Rab11fip3 T A 17: 26,235,117 (GRCm39) T18S probably damaging Het
Rfc4 T C 16: 22,941,004 (GRCm39) probably benign Het
Rubcnl G T 14: 75,279,777 (GRCm39) V387F possibly damaging Het
S100a7l2 A T 3: 90,997,602 (GRCm39) L38M possibly damaging Het
Serpinb12 T C 1: 106,884,151 (GRCm39) L299P probably damaging Het
Sptbn5 G A 2: 119,876,965 (GRCm39) probably benign Het
Tdpoz4 A T 3: 93,704,806 (GRCm39) T368S probably benign Het
Thsd7b T A 1: 129,523,570 (GRCm39) H124Q probably damaging Het
Ugt1a6a A T 1: 88,066,746 (GRCm39) Q184L probably benign Het
Vnn1 T A 10: 23,774,462 (GRCm39) F168L probably damaging Het
Zan A G 5: 137,468,670 (GRCm39) L267P probably damaging Het
Zswim8 A G 14: 20,772,354 (GRCm39) S1621G probably damaging Het
Other mutations in Taar4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02576:Taar4 APN 10 23,836,909 (GRCm39) missense probably damaging 1.00
IGL03202:Taar4 APN 10 23,836,692 (GRCm39) missense probably damaging 1.00
I2288:Taar4 UTSW 10 23,836,818 (GRCm39) missense probably benign 0.03
R0103:Taar4 UTSW 10 23,837,304 (GRCm39) missense probably damaging 1.00
R0103:Taar4 UTSW 10 23,837,304 (GRCm39) missense probably damaging 1.00
R0514:Taar4 UTSW 10 23,836,780 (GRCm39) missense probably damaging 1.00
R1222:Taar4 UTSW 10 23,837,230 (GRCm39) missense probably benign 0.05
R1248:Taar4 UTSW 10 23,836,936 (GRCm39) missense possibly damaging 0.95
R1514:Taar4 UTSW 10 23,836,510 (GRCm39) missense possibly damaging 0.71
R1921:Taar4 UTSW 10 23,837,239 (GRCm39) missense probably damaging 1.00
R2074:Taar4 UTSW 10 23,837,071 (GRCm39) missense probably benign 0.18
R2354:Taar4 UTSW 10 23,836,912 (GRCm39) missense probably damaging 1.00
R2392:Taar4 UTSW 10 23,837,172 (GRCm39) missense possibly damaging 0.94
R2698:Taar4 UTSW 10 23,837,328 (GRCm39) missense probably damaging 1.00
R3902:Taar4 UTSW 10 23,836,913 (GRCm39) missense probably damaging 1.00
R4688:Taar4 UTSW 10 23,836,731 (GRCm39) missense probably damaging 1.00
R5595:Taar4 UTSW 10 23,836,639 (GRCm39) missense probably damaging 1.00
R5773:Taar4 UTSW 10 23,837,056 (GRCm39) missense probably damaging 1.00
R7403:Taar4 UTSW 10 23,836,957 (GRCm39) missense probably damaging 1.00
R7581:Taar4 UTSW 10 23,837,052 (GRCm39) missense probably damaging 0.97
R7736:Taar4 UTSW 10 23,836,897 (GRCm39) missense probably damaging 1.00
R7859:Taar4 UTSW 10 23,837,032 (GRCm39) missense probably benign 0.35
R8676:Taar4 UTSW 10 23,836,801 (GRCm39) missense possibly damaging 0.56
Predicted Primers PCR Primer
(F):5'- ACAAGCTCTGGGGAGTTCTG -3'
(R):5'- TCCTGTGACTATCATCCTCAGGG -3'

Sequencing Primer
(F):5'- GGAGTTCTGGCTTCCTTCATAGC -3'
(R):5'- TCAGGGCCTTTCGAAACCAG -3'
Posted On 2016-10-05