Incidental Mutation 'IGL02011:Taar9'
ID 183362
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Taar9
Ensembl Gene ENSMUSG00000037424
Gene Name trace amine-associated receptor 9
Synonyms Tar3, Trar3, Ta3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # IGL02011
Quality Score
Status
Chromosome 10
Chromosomal Location 23984386-23985432 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 23984477 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Histidine at position 319 (R319H)
Ref Sequence ENSEMBL: ENSMUSP00000043552 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041180]
AlphaFold Q5QD04
Predicted Effect possibly damaging
Transcript: ENSMUST00000041180
AA Change: R319H

PolyPhen 2 Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000043552
Gene: ENSMUSG00000037424
AA Change: R319H

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 43 326 7.3e-13 PFAM
Pfam:7tm_1 49 311 8.4e-61 PFAM
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] TAAR9 is a member of a large family of rhodopsin G protein-coupled receptors (GPCRs, or GPRs). GPCRs contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins.[supplied by OMIM, Jul 2005]
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap5m1 T A 14: 49,318,592 (GRCm39) probably benign Het
Arg1 T C 10: 24,792,275 (GRCm39) T215A probably benign Het
Arhgap15 A T 2: 43,670,767 (GRCm39) K50N probably damaging Het
Ctdsp1 C T 1: 74,433,175 (GRCm39) probably benign Het
Cwc22 A T 2: 77,751,366 (GRCm39) D363E possibly damaging Het
Drd2 G T 9: 49,318,258 (GRCm39) C400F probably damaging Het
Eef1akmt1 A T 14: 57,795,555 (GRCm39) Y65N probably damaging Het
Gbp10 C A 5: 105,368,967 (GRCm39) G291W probably damaging Het
Lrit1 T A 14: 36,784,280 (GRCm39) V536E probably damaging Het
Or4d1 C A 11: 87,805,708 (GRCm39) W8L probably benign Het
Or52ab4 G T 7: 102,988,056 (GRCm39) R265L probably damaging Het
Or9s15 T A 1: 92,524,621 (GRCm39) Y127N probably damaging Het
Pcdh12 C T 18: 38,414,473 (GRCm39) G884D probably damaging Het
Pih1d1 G T 7: 44,806,156 (GRCm39) A31S probably damaging Het
Plcxd2 T C 16: 45,785,454 (GRCm39) D317G probably damaging Het
Prkaca T C 8: 84,717,565 (GRCm39) F231S probably damaging Het
Raet1d T A 10: 22,247,473 (GRCm39) I183K probably damaging Het
Scaper A G 9: 55,487,606 (GRCm39) F752S probably damaging Het
Shisa9 C T 16: 12,062,502 (GRCm39) T241I possibly damaging Het
Unkl T A 17: 25,437,565 (GRCm39) V365E probably damaging Het
Usp34 C T 11: 23,421,554 (GRCm39) S3077F probably damaging Het
Vps16 A G 2: 130,283,399 (GRCm39) I566V probably benign Het
Vrk2 T A 11: 26,421,717 (GRCm39) T414S probably benign Het
Xpnpep1 A T 19: 52,990,896 (GRCm39) probably benign Het
Zfp804a A G 2: 82,087,035 (GRCm39) Q288R probably damaging Het
Other mutations in Taar9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00955:Taar9 APN 10 23,985,429 (GRCm39) missense probably benign
IGL02883:Taar9 APN 10 23,985,378 (GRCm39) missense probably benign 0.08
R1468:Taar9 UTSW 10 23,985,382 (GRCm39) missense possibly damaging 0.47
R1468:Taar9 UTSW 10 23,985,382 (GRCm39) missense possibly damaging 0.47
R1598:Taar9 UTSW 10 23,985,305 (GRCm39) missense possibly damaging 0.90
R2072:Taar9 UTSW 10 23,984,877 (GRCm39) missense probably damaging 1.00
R2471:Taar9 UTSW 10 23,985,289 (GRCm39) missense probably benign 0.00
R2519:Taar9 UTSW 10 23,985,152 (GRCm39) missense probably damaging 1.00
R4205:Taar9 UTSW 10 23,984,477 (GRCm39) missense possibly damaging 0.93
R4793:Taar9 UTSW 10 23,985,408 (GRCm39) missense probably benign
R4801:Taar9 UTSW 10 23,984,741 (GRCm39) missense probably damaging 0.97
R4802:Taar9 UTSW 10 23,984,741 (GRCm39) missense probably damaging 0.97
R5457:Taar9 UTSW 10 23,985,003 (GRCm39) missense probably damaging 0.98
R6450:Taar9 UTSW 10 23,985,138 (GRCm39) missense probably damaging 1.00
R6601:Taar9 UTSW 10 23,984,945 (GRCm39) missense probably damaging 1.00
R6915:Taar9 UTSW 10 23,984,910 (GRCm39) missense possibly damaging 0.53
R7179:Taar9 UTSW 10 23,984,882 (GRCm39) missense probably damaging 1.00
R7480:Taar9 UTSW 10 23,984,843 (GRCm39) missense possibly damaging 0.61
R8200:Taar9 UTSW 10 23,985,317 (GRCm39) missense probably damaging 0.99
R9311:Taar9 UTSW 10 23,985,152 (GRCm39) missense probably damaging 0.99
Z1088:Taar9 UTSW 10 23,984,863 (GRCm39) missense probably damaging 1.00
Z1177:Taar9 UTSW 10 23,985,039 (GRCm39) missense probably benign 0.01
Posted On 2014-05-07