Incidental Mutation 'IGL02883:Taar9'
ID 362863
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 # IGL02883
Quality Score
Status
Chromosome 10
Chromosomal Location 23984386-23985432 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 23985378 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Aspartic acid at position 19 (N19D)
Ref Sequence ENSEMBL: ENSMUSP00000043552 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041180]
AlphaFold Q5QD04
Predicted Effect probably benign
Transcript: ENSMUST00000041180
AA Change: N19D

PolyPhen 2 Score 0.084 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000043552
Gene: ENSMUSG00000037424
AA Change: N19D

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 43 326 7.3e-13 PFAM
Pfam:7tm_1 49 311 8.4e-61 PFAM
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810055G02Rik C A 19: 3,766,972 (GRCm39) S186R possibly damaging Het
Acap2 A G 16: 30,915,163 (GRCm39) probably benign Het
Cacna1h G T 17: 25,599,506 (GRCm39) R1726S probably damaging Het
Cdca2 T C 14: 67,944,946 (GRCm39) S133G probably damaging Het
Cep295nl A T 11: 118,224,735 (GRCm39) S36R probably benign Het
Crispld1 A G 1: 17,817,013 (GRCm39) N190S possibly damaging Het
Crtam A G 9: 40,905,797 (GRCm39) V44A probably benign Het
Crtc1 C T 8: 70,858,775 (GRCm39) G112S probably benign Het
Cyp17a1 T C 19: 46,657,790 (GRCm39) N254S probably benign Het
Dmrta1 T C 4: 89,577,011 (GRCm39) S156P probably benign Het
Eno2 A C 6: 124,743,172 (GRCm39) V188G probably damaging Het
Fam20a A T 11: 109,565,953 (GRCm39) I427N probably damaging Het
Fat2 T C 11: 55,147,444 (GRCm39) K3933E probably benign Het
Igkv8-30 T C 6: 70,094,601 (GRCm39) M1V probably null Het
Ist1 G A 8: 110,410,300 (GRCm39) probably benign Het
Kank4 T C 4: 98,661,690 (GRCm39) E765G possibly damaging Het
Kat14 T C 2: 144,235,449 (GRCm39) L92S probably damaging Het
Kcnu1 G A 8: 26,339,855 (GRCm39) V58I probably benign Het
Lrba T A 3: 86,261,513 (GRCm39) V1489E probably damaging Het
Lrba T A 3: 86,352,720 (GRCm39) I1956N probably damaging Het
Mdn1 G A 4: 32,763,199 (GRCm39) V5100I probably benign Het
Mkrn2os C A 6: 115,563,670 (GRCm39) G122* probably null Het
Nme3 T C 17: 25,115,880 (GRCm39) Y78H probably benign Het
Pira13 A G 7: 3,825,179 (GRCm39) S488P possibly damaging Het
Pkd1l2 G A 8: 117,792,484 (GRCm39) T436I probably benign Het
Ppp2r5c T G 12: 110,488,997 (GRCm39) V56G possibly damaging Het
Pramel16 T C 4: 143,676,418 (GRCm39) T229A possibly damaging Het
Prdm10 G A 9: 31,238,644 (GRCm39) V179M probably damaging Het
Rab11fip2 A G 19: 59,895,430 (GRCm39) V344A probably damaging Het
Selp G A 1: 163,957,671 (GRCm39) A267T probably benign Het
Sf3a1 T A 11: 4,129,192 (GRCm39) W718R probably damaging Het
Tas2r113 T G 6: 132,870,382 (GRCm39) S137A probably damaging Het
Traf4 A T 11: 78,052,447 (GRCm39) I66N possibly damaging Het
Ucp3 A T 7: 100,129,849 (GRCm39) T164S probably benign Het
Uggt1 A T 1: 36,216,696 (GRCm39) N96K probably benign Het
Uqcc1 T A 2: 155,753,749 (GRCm39) Q42L possibly damaging Het
Vmn1r128 A G 7: 21,083,440 (GRCm39) K48R probably benign Het
Other mutations in Taar9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00955:Taar9 APN 10 23,985,429 (GRCm39) missense probably benign
IGL02011:Taar9 APN 10 23,984,477 (GRCm39) missense possibly damaging 0.93
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 2015-12-18