Incidental Mutation 'R1270:Taar1'
ID 151282
Institutional Source Beutler Lab
Gene Symbol Taar1
Ensembl Gene ENSMUSG00000056379
Gene Name trace amine-associated receptor 1
Synonyms Trar1, Tar1
MMRRC Submission 039336-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.114) question?
Stock # R1270 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 23920356-23921469 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 23920533 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 43 (V43A)
Ref Sequence ENSEMBL: ENSMUSP00000049527 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051532]
AlphaFold Q923Y8
Predicted Effect probably damaging
Transcript: ENSMUST00000051532
AA Change: V43A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000049527
Gene: ENSMUSG00000056379
AA Change: V43A

Pfam:7TM_GPCR_Srsx 33 316 1.4e-11 PFAM
Pfam:7tm_1 39 301 2.4e-62 PFAM
Meta Mutation Damage Score 0.7276 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.1%
  • 10x: 95.5%
  • 20x: 89.7%
Validation Efficiency 97% (36/37)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a G-protein coupled receptor activated by trace amines. The encoded protein responds little or not at all to dopamine, serotonin, epinephrine, or histamine, but responds well to beta-phenylethylamine, p-tyramine, octopamine, and tryptamine. While primarily functioning in neurologic systems, there is evidence that this gene is involved in blood cell and immunologic functions as well. This gene is thought to be intronless. [provided by RefSeq, Nov 2015]
PHENOTYPE: Mice homozygous for a null mutation display decreased prepulse inhibition and increased sensitivity to amphetamines. Mice homozygous for another knock-out allele exhibit increased sensitivity to MDMA-induced hyperthermia, brain dopamine and serotonin levels, and induced hyperactivity. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc3 C T 11: 94,357,384 (GRCm38) R1129Q probably damaging Het
Adam7 T A 14: 68,527,669 (GRCm38) K93M probably damaging Het
Aldh1a2 T G 9: 71,281,706 (GRCm38) L301V probably benign Het
Alg9 A G 9: 50,787,572 (GRCm38) probably benign Het
Aspg C T 12: 112,116,447 (GRCm38) T187I probably damaging Het
Bltp1 T A 3: 36,952,184 (GRCm38) H1662Q probably damaging Het
C4a A G 17: 34,814,528 (GRCm38) noncoding transcript Het
Cdh2 T G 18: 16,627,557 (GRCm38) probably benign Het
Ceacam1 T C 7: 25,466,314 (GRCm38) probably null Het
Cep250 G A 2: 155,990,681 (GRCm38) V1509I probably benign Het
D130043K22Rik T C 13: 24,857,338 (GRCm38) S248P probably benign Het
Dgkd A T 1: 87,934,125 (GRCm38) M801L probably damaging Het
Edc4 A G 8: 105,891,264 (GRCm38) E1152G possibly damaging Het
Enkd1 A G 8: 105,703,901 (GRCm38) I334T probably damaging Het
Gli3 C T 13: 15,723,744 (GRCm38) A803V probably benign Het
Glrx3 A G 7: 137,453,414 (GRCm38) N95S probably benign Het
Ints2 C T 11: 86,233,085 (GRCm38) G626R probably damaging Het
Kank2 A T 9: 21,772,760 (GRCm38) N724K probably damaging Het
Kctd20 A G 17: 28,966,931 (GRCm38) D416G possibly damaging Het
Lmtk3 A G 7: 45,793,828 (GRCm38) E645G probably damaging Het
Mrgpra9 A T 7: 47,252,783 (GRCm38) probably null Het
Muc1 T A 3: 89,232,107 (GRCm38) Y605N probably damaging Het
Or4a47 C T 2: 89,835,322 (GRCm38) V208M possibly damaging Het
Or8g17 A C 9: 39,019,247 (GRCm38) I98R possibly damaging Het
Prx T A 7: 27,518,930 (GRCm38) I952N probably damaging Het
Shf G A 2: 122,368,682 (GRCm38) P51S probably damaging Het
Skint5 A T 4: 113,942,659 (GRCm38) Y90* probably null Het
Swt1 A T 1: 151,384,391 (GRCm38) N752K probably benign Het
Tenm2 T C 11: 36,041,659 (GRCm38) N1702D probably damaging Het
Tff2 C T 17: 31,144,169 (GRCm38) probably null Het
Trim2 G A 3: 84,167,677 (GRCm38) A686V probably damaging Het
Ube2q2l A T 6: 136,401,787 (GRCm38) I15N probably damaging Het
Other mutations in Taar1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00782:Taar1 APN 10 23,920,446 (GRCm38) missense probably benign 0.00
R0022:Taar1 UTSW 10 23,920,727 (GRCm38) missense probably benign 0.45
R0126:Taar1 UTSW 10 23,920,547 (GRCm38) missense probably benign 0.00
R0442:Taar1 UTSW 10 23,920,482 (GRCm38) missense possibly damaging 0.80
R0720:Taar1 UTSW 10 23,921,073 (GRCm38) missense probably damaging 1.00
R0931:Taar1 UTSW 10 23,921,283 (GRCm38) missense probably damaging 1.00
R1834:Taar1 UTSW 10 23,921,189 (GRCm38) missense probably benign 0.04
R2137:Taar1 UTSW 10 23,921,270 (GRCm38) missense probably benign
R3765:Taar1 UTSW 10 23,921,307 (GRCm38) missense probably damaging 1.00
R3873:Taar1 UTSW 10 23,920,584 (GRCm38) missense probably damaging 1.00
R5334:Taar1 UTSW 10 23,920,545 (GRCm38) missense probably damaging 1.00
R5418:Taar1 UTSW 10 23,921,316 (GRCm38) missense possibly damaging 0.91
R5578:Taar1 UTSW 10 23,920,820 (GRCm38) missense possibly damaging 0.71
R7048:Taar1 UTSW 10 23,920,824 (GRCm38) missense probably benign 0.40
R7096:Taar1 UTSW 10 23,920,911 (GRCm38) missense possibly damaging 0.48
R7163:Taar1 UTSW 10 23,921,020 (GRCm38) missense probably benign 0.38
R7707:Taar1 UTSW 10 23,921,237 (GRCm38) missense possibly damaging 0.69
R7854:Taar1 UTSW 10 23,920,782 (GRCm38) missense probably benign 0.00
R8036:Taar1 UTSW 10 23,921,135 (GRCm38) missense probably benign 0.01
R8442:Taar1 UTSW 10 23,920,624 (GRCm38) nonsense probably null
R8855:Taar1 UTSW 10 23,921,078 (GRCm38) missense possibly damaging 0.50
R9777:Taar1 UTSW 10 23,920,778 (GRCm38) missense probably damaging 0.99
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2014-01-29