Incidental Mutation 'R6302:Taar7b'
ID 509288
Institutional Source Beutler Lab
Gene Symbol Taar7b
Ensembl Gene ENSMUSG00000095171
Gene Name trace amine-associated receptor 7B
Synonyms LOC209517
MMRRC Submission 044467-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # R6302 (G1)
Quality Score 225.009
Status Not validated
Chromosome 10
Chromosomal Location 23875837-23876913 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 23876158 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 108 (S108T)
Ref Sequence ENSEMBL: ENSMUSP00000090328 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092658]
AlphaFold Q5QD11
Predicted Effect possibly damaging
Transcript: ENSMUST00000092658
AA Change: S108T

PolyPhen 2 Score 0.572 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000090328
Gene: ENSMUSG00000095171
AA Change: S108T

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 56 261 1.9e-7 PFAM
Pfam:7tm_1 64 326 7.3e-59 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm4 G T 4: 144,396,760 (GRCm39) S324* probably null Het
Actl11 T G 9: 107,806,772 (GRCm39) V365G probably benign Het
Adgrg6 T A 10: 14,317,227 (GRCm39) D531V probably benign Het
Ankrd11 A G 8: 123,616,728 (GRCm39) S2354P probably benign Het
Ano9 A T 7: 140,684,221 (GRCm39) W514R probably damaging Het
Arfgef3 A T 10: 18,528,589 (GRCm39) V266E probably damaging Het
Bahcc1 T C 11: 120,167,634 (GRCm39) I1345T probably damaging Het
Bpifb4 G A 2: 153,801,587 (GRCm39) M355I probably benign Het
Catsperb T C 12: 101,554,402 (GRCm39) S699P possibly damaging Het
Cdh23 T G 10: 60,140,872 (GRCm39) I3161L possibly damaging Het
Chd3 T C 11: 69,244,604 (GRCm39) T1257A probably damaging Het
Cnnm4 C T 1: 36,539,036 (GRCm39) T638I probably benign Het
Cspg4b A G 13: 113,504,646 (GRCm39) D1925G probably damaging Het
Cyp26c1 A G 19: 37,674,936 (GRCm39) T86A probably damaging Het
Cyp3a63-ps A G 5: 145,564,847 (GRCm39) noncoding transcript Het
Dnah14 T A 1: 181,428,771 (GRCm39) I259N possibly damaging Het
Dnah17 T C 11: 118,019,981 (GRCm39) D22G probably benign Het
Epn2 T G 11: 61,437,312 (GRCm39) T87P probably damaging Het
Fbxl18 A G 5: 142,874,578 (GRCm39) L81P probably damaging Het
Gas1 A T 13: 60,323,970 (GRCm39) D221E probably damaging Het
Gm8356 T C 14: 17,691,275 (GRCm39) Y130C probably damaging Het
Gpr151 T G 18: 42,712,459 (GRCm39) K73T probably damaging Het
Helq A C 5: 100,946,305 (GRCm39) V12G probably damaging Het
Inpp4b A G 8: 82,494,806 (GRCm39) T74A probably benign Het
Kirrel3 G A 9: 34,919,045 (GRCm39) V234I probably damaging Het
Kxd1 T A 8: 70,972,713 (GRCm39) probably null Het
Lif T C 11: 4,218,924 (GRCm39) Y68H probably damaging Het
Map6 A G 7: 98,985,314 (GRCm39) Q406R probably damaging Het
Mcoln3 A T 3: 145,830,527 (GRCm39) M86L probably benign Het
Mei1 T A 15: 81,987,439 (GRCm39) Y834* probably null Het
Mroh1 T C 15: 76,320,319 (GRCm39) probably null Het
Myo15b T C 11: 115,777,065 (GRCm39) I2319T possibly damaging Het
Myo7b T G 18: 32,127,439 (GRCm39) D621A probably damaging Het
Naip5 C T 13: 100,359,674 (GRCm39) A521T possibly damaging Het
Nek7 T C 1: 138,426,351 (GRCm39) D254G probably damaging Het
Nsd2 A G 5: 34,024,921 (GRCm39) R560G possibly damaging Het
Or2t46 T C 11: 58,472,464 (GRCm39) F265L probably benign Het
Or52x1 A T 7: 104,852,926 (GRCm39) L208H probably damaging Het
Pbx1 T A 1: 168,018,910 (GRCm39) T312S probably benign Het
Peg10 GAT GATCAT 6: 4,756,449 (GRCm39) probably benign Het
Pitrm1 A G 13: 6,610,097 (GRCm39) S390G probably damaging Het
Plcxd3 C T 15: 4,546,239 (GRCm39) T81M probably damaging Het
Pmf1 C T 3: 88,307,017 (GRCm39) probably null Het
Rabep1 T C 11: 70,825,947 (GRCm39) V739A probably damaging Het
Rex2 A G 4: 147,142,451 (GRCm39) D313G possibly damaging Het
Rpia C T 6: 70,750,485 (GRCm39) V216I probably damaging Het
Rsf1 CG CGACGGCGGTG 7: 97,229,115 (GRCm39) probably benign Het
Sec13 T A 6: 113,712,167 (GRCm39) H56L probably damaging Het
Sec16a A T 2: 26,315,817 (GRCm39) V1733D probably damaging Het
Sim2 G A 16: 93,898,089 (GRCm39) A108T probably damaging Het
Slc27a5 T C 7: 12,722,479 (GRCm39) D665G probably damaging Het
Slc38a6 T A 12: 73,383,849 (GRCm39) V180E probably damaging Het
Smarcad1 T G 6: 65,052,122 (GRCm39) N38K possibly damaging Het
Spem2 T C 11: 69,709,091 (GRCm39) T45A possibly damaging Het
Svil T C 18: 5,057,432 (GRCm39) S714P probably benign Het
Tbl3 T C 17: 24,923,645 (GRCm39) K256E probably benign Het
Tcam1 T G 11: 106,177,276 (GRCm39) C423G probably damaging Het
Trpm4 A T 7: 44,977,143 (GRCm39) probably null Het
Ttyh2 T C 11: 114,592,662 (GRCm39) C231R probably damaging Het
Ugt3a1 C T 15: 9,365,397 (GRCm39) P337S probably damaging Het
Vmn2r83 A C 10: 79,304,837 (GRCm39) T16P possibly damaging Het
Vps52 T C 17: 34,182,189 (GRCm39) F589S probably damaging Het
Xkr4 T C 1: 3,286,961 (GRCm39) T410A probably damaging Het
Xkr9 A G 1: 13,742,726 (GRCm39) T4A probably damaging Het
Yars2 T C 16: 16,122,438 (GRCm39) L268P probably damaging Het
Zbtb41 C A 1: 139,357,027 (GRCm39) N427K possibly damaging Het
Zeb2 T C 2: 44,887,771 (GRCm39) T414A probably benign Het
Other mutations in Taar7b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00330:Taar7b APN 10 23,876,740 (GRCm39) missense probably benign 0.01
IGL00771:Taar7b APN 10 23,876,096 (GRCm39) missense probably benign 0.01
IGL01662:Taar7b APN 10 23,875,874 (GRCm39) missense probably benign 0.02
IGL02186:Taar7b APN 10 23,875,879 (GRCm39) missense probably benign 0.00
IGL02399:Taar7b APN 10 23,876,050 (GRCm39) missense probably damaging 0.99
IGL02514:Taar7b APN 10 23,876,882 (GRCm39) missense probably benign 0.00
IGL02601:Taar7b APN 10 23,876,204 (GRCm39) missense probably damaging 1.00
IGL02717:Taar7b APN 10 23,876,258 (GRCm39) missense probably damaging 1.00
IGL02724:Taar7b APN 10 23,876,581 (GRCm39) missense probably benign
IGL02725:Taar7b APN 10 23,875,961 (GRCm39) missense probably benign 0.03
R0103:Taar7b UTSW 10 23,876,192 (GRCm39) missense probably benign 0.00
R2060:Taar7b UTSW 10 23,876,573 (GRCm39) missense possibly damaging 0.95
R4973:Taar7b UTSW 10 23,876,243 (GRCm39) missense probably benign 0.08
R5055:Taar7b UTSW 10 23,876,845 (GRCm39) missense possibly damaging 0.75
R5068:Taar7b UTSW 10 23,876,359 (GRCm39) missense probably benign 0.00
R5069:Taar7b UTSW 10 23,876,359 (GRCm39) missense probably benign 0.00
R5070:Taar7b UTSW 10 23,876,359 (GRCm39) missense probably benign 0.00
R5205:Taar7b UTSW 10 23,875,916 (GRCm39) missense probably benign 0.05
R5994:Taar7b UTSW 10 23,876,246 (GRCm39) missense probably damaging 1.00
R6131:Taar7b UTSW 10 23,876,615 (GRCm39) missense probably benign 0.20
R6332:Taar7b UTSW 10 23,875,849 (GRCm39) missense probably benign 0.05
R6809:Taar7b UTSW 10 23,876,756 (GRCm39) missense probably benign 0.03
R7126:Taar7b UTSW 10 23,875,960 (GRCm39) missense possibly damaging 0.93
R7520:Taar7b UTSW 10 23,876,381 (GRCm39) missense probably damaging 0.99
R8962:Taar7b UTSW 10 23,876,359 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGTGTCAGGAGCCCATATTCC -3'
(R):5'- AGGTGATGCACTTGCCAGAAAC -3'

Sequencing Primer
(F):5'- AGGAGCCCATATTCCCCAGG -3'
(R):5'- TGATGCACTTGCCAGAAACAAATG -3'
Posted On 2018-04-02