Incidental Mutation 'IGL01019:Taar3'
ID53834
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Taar3
Ensembl Gene ENSMUSG00000069708
Gene Nametrace amine-associated receptor 3
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.159) question?
Stock #IGL01019
Quality Score
Status
Chromosome10
Chromosomal Location23949558-23950589 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 23950432 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Valine at position 292 (D292V)
Ref Sequence ENSEMBL: ENSMUSP00000036817 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045152]
Predicted Effect probably damaging
Transcript: ENSMUST00000045152
AA Change: D292V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000036817
Gene: ENSMUSG00000069708
AA Change: D292V

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 42 320 1.8e-13 PFAM
Pfam:7tm_1 48 309 1.4e-53 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik G T 3: 37,006,984 probably null Het
9930022D16Rik T C 11: 109,417,911 probably benign Het
Aatk T C 11: 120,012,275 S375G probably benign Het
Abcg8 T C 17: 84,691,995 M173T probably benign Het
B3galt2 A C 1: 143,646,757 R210S probably benign Het
Capn5 C T 7: 98,135,764 A168T probably damaging Het
Cbx7 C T 15: 79,930,628 G24D probably damaging Het
Ccdc7a A T 8: 129,061,618 S77T probably benign Het
Cd200r2 T A 16: 44,909,469 probably benign Het
Cdh11 T C 8: 102,679,745 H32R probably benign Het
Chdh A T 14: 30,031,332 N66I probably benign Het
Clca3a2 G A 3: 144,813,627 Q263* probably null Het
Dcc T C 18: 71,809,090 I319V probably benign Het
Depdc5 G T 5: 32,893,401 M170I probably damaging Het
Dopey2 T A 16: 93,810,229 L2140Q probably benign Het
Frem3 G A 8: 80,615,134 G1352E probably benign Het
Fsd1l T A 4: 53,694,742 C389S probably damaging Het
Grin2c C T 11: 115,258,110 A221T possibly damaging Het
Gstz1 C A 12: 87,163,801 P153T probably damaging Het
Itgb2 T C 10: 77,542,403 S22P possibly damaging Het
Krt87 G T 15: 101,438,431 Q114K possibly damaging Het
Krtap5-4 A C 7: 142,303,910 S106R unknown Het
Lats1 T C 10: 7,705,671 V740A probably damaging Het
Mcm9 C A 10: 53,629,945 G78C probably damaging Het
Mn1 G A 5: 111,421,547 E1128K possibly damaging Het
Myo1f G A 17: 33,593,003 R592H possibly damaging Het
Nfat5 G T 8: 107,367,514 A277S probably damaging Het
Nfkbia T A 12: 55,490,542 Y254F probably damaging Het
Nr3c2 A T 8: 76,909,214 N315Y probably damaging Het
Otof T C 5: 30,405,216 M258V probably benign Het
Panx3 C T 9: 37,661,471 C261Y probably damaging Het
Pdia2 C A 17: 26,198,922 G38W probably damaging Het
Psg19 G T 7: 18,794,046 Y257* probably null Het
Ptpre A T 7: 135,678,325 K586* probably null Het
Reps1 A G 10: 18,124,895 R752G probably damaging Het
Rpgrip1 T A 14: 52,131,176 D277E possibly damaging Het
Rpl21-ps6 A G 17: 55,915,671 noncoding transcript Het
Serpinf2 T A 11: 75,436,507 E198V possibly damaging Het
Sh3tc1 A G 5: 35,703,375 L1046P probably damaging Het
Snw1 T C 12: 87,450,941 E426G probably benign Het
Sord T A 2: 122,264,083 N317K probably benign Het
Tdrd3 C A 14: 87,472,182 T94K probably damaging Het
Ttn C A 2: 76,856,821 E736* probably null Het
Usp32 A G 11: 85,039,265 V562A probably damaging Het
Vmn1r169 T G 7: 23,577,186 M1R probably null Het
Vmn2r3 C T 3: 64,259,883 C609Y probably damaging Het
Vmn2r69 T C 7: 85,406,531 T800A probably benign Het
Vmn2r72 G A 7: 85,738,334 T674I probably benign Het
Zfp160 T A 17: 21,020,826 M52K possibly damaging Het
Zfp607a T A 7: 27,878,617 C371S probably damaging Het
Other mutations in Taar3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01777:Taar3 APN 10 23950005 missense probably benign 0.39
IGL01940:Taar3 APN 10 23949957 missense probably damaging 1.00
IGL02120:Taar3 APN 10 23950167 missense probably benign 0.33
PIT4445001:Taar3 UTSW 10 23949688 missense possibly damaging 0.85
R0582:Taar3 UTSW 10 23949817 missense probably damaging 1.00
R1925:Taar3 UTSW 10 23950585 missense probably benign 0.22
R2261:Taar3 UTSW 10 23950155 missense probably benign 0.00
R4088:Taar3 UTSW 10 23949859 missense possibly damaging 0.46
R4504:Taar3 UTSW 10 23949573 missense possibly damaging 0.84
R4505:Taar3 UTSW 10 23949573 missense possibly damaging 0.84
R4507:Taar3 UTSW 10 23949573 missense possibly damaging 0.84
R4925:Taar3 UTSW 10 23950543 missense probably damaging 0.99
R6221:Taar3 UTSW 10 23950072 missense possibly damaging 0.92
R6451:Taar3 UTSW 10 23949807 missense possibly damaging 0.96
R7290:Taar3 UTSW 10 23950400 nonsense probably null
R7414:Taar3 UTSW 10 23949817 missense probably damaging 1.00
R8432:Taar3 UTSW 10 23950155 missense probably benign 0.11
X0057:Taar3 UTSW 10 23949646 missense probably benign 0.13
Posted On2013-06-28