Incidental Mutation 'IGL01346:Taar2'
ID 75048
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Taar2
Ensembl Gene ENSMUSG00000059763
Gene Name trace amine-associated receptor 2
Synonyms Gpr58
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01346
Quality Score
Status
Chromosome 10
Chromosomal Location 23814470-23817481 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 23816997 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 179 (Y179C)
Ref Sequence ENSEMBL: ENSMUSP00000078137 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079134]
AlphaFold Q5QD17
Predicted Effect probably damaging
Transcript: ENSMUST00000079134
AA Change: Y179C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000078137
Gene: ENSMUSG00000059763
AA Change: Y179C

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 42 318 2.4e-10 PFAM
Pfam:7tm_1 48 303 2.9e-54 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3300002I08Rik A G 2: 150,152,980 (GRCm39) V135A unknown Het
Cnot4 A T 6: 35,047,183 (GRCm39) I143N probably damaging Het
Cnot6l A T 5: 96,234,105 (GRCm39) M302K probably damaging Het
Dmxl2 T C 9: 54,322,759 (GRCm39) T1542A probably damaging Het
Dnaaf9 A G 2: 130,633,766 (GRCm39) probably benign Het
Dnhd1 T C 7: 105,363,116 (GRCm39) S3893P probably benign Het
Duox2 A T 2: 122,117,683 (GRCm39) probably benign Het
Dusp1 T C 17: 26,725,295 (GRCm39) N355D probably benign Het
Fam76b T C 9: 13,741,046 (GRCm39) C60R probably damaging Het
Gnptab G A 10: 88,272,041 (GRCm39) V944I possibly damaging Het
Gys1 A G 7: 45,091,961 (GRCm39) Y249C probably damaging Het
Ift88 A T 14: 57,681,862 (GRCm39) E215D probably damaging Het
Kcnu1 T C 8: 26,424,551 (GRCm39) probably benign Het
Lmln C A 16: 32,937,490 (GRCm39) N618K probably benign Het
Lrrc75a T C 11: 62,496,813 (GRCm39) T250A probably damaging Het
Mpp4 A G 1: 59,164,719 (GRCm39) S435P probably damaging Het
Myo1c T A 11: 75,563,076 (GRCm39) V1036E probably damaging Het
Nlrp12 T G 7: 3,289,316 (GRCm39) T399P probably damaging Het
Or2y16 A G 11: 49,335,595 (GRCm39) R306G probably benign Het
Or4c118 A G 2: 88,974,575 (GRCm39) F264S possibly damaging Het
Parp8 A T 13: 117,031,600 (GRCm39) C332S possibly damaging Het
Pdcd11 G A 19: 47,098,053 (GRCm39) V780I probably benign Het
Plekha5 A G 6: 140,480,292 (GRCm39) probably benign Het
Ppt1 T A 4: 122,737,848 (GRCm39) I62K probably damaging Het
Proser3 T C 7: 30,249,071 (GRCm39) N7S probably benign Het
Ptk2b A G 14: 66,414,567 (GRCm39) L311P possibly damaging Het
Rasal2 T C 1: 156,988,786 (GRCm39) N706S probably benign Het
Ripk2 A G 4: 16,132,775 (GRCm39) probably null Het
Setx T A 2: 29,034,821 (GRCm39) H435Q probably damaging Het
Smurf2 T A 11: 106,721,741 (GRCm39) probably benign Het
Snx32 A G 19: 5,547,764 (GRCm39) L182P possibly damaging Het
Stpg2 A G 3: 139,125,635 (GRCm39) probably benign Het
Tenm2 G A 11: 35,918,232 (GRCm39) R1843* probably null Het
Tmco4 T C 4: 138,748,260 (GRCm39) I280T probably damaging Het
Tuba4a C A 1: 75,193,921 (GRCm39) C46F probably damaging Het
Ubr1 A G 2: 120,703,603 (GRCm39) probably null Het
Vldlr A T 19: 27,217,081 (GRCm39) I45L possibly damaging Het
Vmn2r120 C A 17: 57,852,232 (GRCm39) G28V probably benign Het
Vmn2r37 C A 7: 9,209,680 (GRCm39) V611L probably benign Het
Vmn2r67 A G 7: 84,786,127 (GRCm39) L626P probably damaging Het
Wdr19 C T 5: 65,379,082 (GRCm39) probably benign Het
Zfp595 T A 13: 67,464,749 (GRCm39) K505* probably null Het
Other mutations in Taar2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00229:Taar2 APN 10 23,817,266 (GRCm39) missense possibly damaging 0.50
IGL00807:Taar2 APN 10 23,816,573 (GRCm39) missense probably benign 0.00
IGL01433:Taar2 APN 10 23,816,657 (GRCm39) missense probably benign 0.02
IGL01782:Taar2 APN 10 23,817,042 (GRCm39) missense probably damaging 1.00
IGL03106:Taar2 APN 10 23,817,195 (GRCm39) missense probably damaging 0.99
IGL03372:Taar2 APN 10 23,817,069 (GRCm39) missense probably benign 0.03
R0046:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0046:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0090:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0101:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0101:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0103:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0157:Taar2 UTSW 10 23,817,389 (GRCm39) missense probably damaging 1.00
R0189:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0190:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0226:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0226:Taar2 UTSW 10 23,816,961 (GRCm39) missense probably damaging 1.00
R0265:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0267:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0349:Taar2 UTSW 10 23,817,407 (GRCm39) missense probably benign 0.01
R0349:Taar2 UTSW 10 23,817,327 (GRCm39) missense possibly damaging 0.79
R0426:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R0556:Taar2 UTSW 10 23,816,793 (GRCm39) missense probably damaging 1.00
R0698:Taar2 UTSW 10 23,817,393 (GRCm39) missense probably benign 0.00
R1191:Taar2 UTSW 10 23,816,927 (GRCm39) missense probably damaging 1.00
R2919:Taar2 UTSW 10 23,817,454 (GRCm39) missense probably benign 0.00
R4615:Taar2 UTSW 10 23,817,263 (GRCm39) missense probably benign 0.43
R4658:Taar2 UTSW 10 23,817,401 (GRCm39) missense probably benign 0.04
R4766:Taar2 UTSW 10 23,816,669 (GRCm39) missense probably damaging 0.98
R4872:Taar2 UTSW 10 23,816,591 (GRCm39) missense probably benign 0.02
R5205:Taar2 UTSW 10 23,816,874 (GRCm39) missense probably benign 0.42
R5271:Taar2 UTSW 10 23,816,930 (GRCm39) missense probably damaging 0.97
R5517:Taar2 UTSW 10 23,816,627 (GRCm39) missense possibly damaging 0.92
R6033:Taar2 UTSW 10 23,816,874 (GRCm39) missense probably benign
R6033:Taar2 UTSW 10 23,816,874 (GRCm39) missense probably benign
R6325:Taar2 UTSW 10 23,816,615 (GRCm39) missense probably benign 0.05
R6398:Taar2 UTSW 10 23,817,177 (GRCm39) missense probably benign 0.00
R6762:Taar2 UTSW 10 23,817,300 (GRCm39) missense probably damaging 0.98
R7121:Taar2 UTSW 10 23,816,725 (GRCm39) missense probably damaging 1.00
R7209:Taar2 UTSW 10 23,816,597 (GRCm39) missense possibly damaging 0.57
R7709:Taar2 UTSW 10 23,816,621 (GRCm39) missense probably benign 0.00
R8045:Taar2 UTSW 10 23,817,386 (GRCm39) missense probably damaging 1.00
R8223:Taar2 UTSW 10 23,817,248 (GRCm39) missense probably damaging 1.00
R8743:Taar2 UTSW 10 23,817,369 (GRCm39) missense probably damaging 1.00
R9307:Taar2 UTSW 10 23,817,237 (GRCm39) missense probably damaging 1.00
R9350:Taar2 UTSW 10 23,817,345 (GRCm39) missense probably damaging 1.00
R9351:Taar2 UTSW 10 23,816,900 (GRCm39) missense probably benign 0.14
R9755:Taar2 UTSW 10 23,817,038 (GRCm39) missense probably damaging 1.00
Z1176:Taar2 UTSW 10 23,817,084 (GRCm39) missense possibly damaging 0.94
Posted On 2013-10-07