Incidental Mutation 'IGL02192:Taar8b'
ID283900
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Taar8b
Ensembl Gene ENSMUSG00000100186
Gene Nametrace amine-associated receptor 8B
SynonymsLOC382348
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.103) question?
Stock #IGL02192
Quality Score
Status
Chromosome10
Chromosomal Location24091260-24092294 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 24091364 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 311 (I311F)
Ref Sequence ENSEMBL: ENSMUSP00000090324 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092654]
Predicted Effect probably damaging
Transcript: ENSMUST00000092654
AA Change: I311F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000090324
Gene: ENSMUSG00000100186
AA Change: I311F

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 39 244 1.4e-8 PFAM
Pfam:7TM_GPCR_Srsx 42 327 1.1e-14 PFAM
Pfam:7tm_1 48 312 6.4e-57 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn4 A T 7: 28,898,400 M545K possibly damaging Het
Adamtsl1 A G 4: 86,228,016 E303G probably damaging Het
Anxa13 A T 15: 58,348,780 noncoding transcript Het
Ap2b1 C T 11: 83,346,766 T552I possibly damaging Het
Cars T C 7: 143,571,588 S388G probably damaging Het
Cdh18 A T 15: 23,460,316 D544V probably damaging Het
Chat T C 14: 32,423,322 R377G possibly damaging Het
Col14a1 A G 15: 55,362,402 T154A unknown Het
Col9a1 C T 1: 24,221,987 P311S probably damaging Het
Cpsf3 G T 12: 21,310,193 probably benign Het
Cpsf3 G T 12: 21,310,196 probably null Het
Dock8 T C 19: 25,078,205 probably null Het
Eml6 A G 11: 29,805,743 I837T probably benign Het
Epb41 T C 4: 131,929,717 T792A probably damaging Het
Exph5 A T 9: 53,376,325 R1569* probably null Het
F13b A T 1: 139,517,333 T574S probably damaging Het
Fam160a1 A G 3: 85,673,326 L524P possibly damaging Het
Fam184b G T 5: 45,537,720 D727E probably benign Het
Fhod3 T C 18: 25,056,358 L619P probably damaging Het
Fsd1l A G 4: 53,647,754 I66V probably benign Het
Fv1 A G 4: 147,870,255 D426G possibly damaging Het
Gm3371 A T 14: 44,403,778 probably benign Het
Hnf1a A T 5: 114,960,118 S142T probably damaging Het
Itgb3 A G 11: 104,643,939 I541V probably benign Het
Itgbl1 G T 14: 123,843,926 C239F probably damaging Het
Krt26 C T 11: 99,333,645 R349Q probably benign Het
Larp1b G T 3: 40,967,494 S116I probably benign Het
Lmtk3 A G 7: 45,794,509 probably benign Het
Mapk10 T C 5: 102,989,647 I235V probably damaging Het
Mctp1 C T 13: 76,731,768 probably benign Het
Megf8 G A 7: 25,353,860 D1819N probably damaging Het
Muc6 T C 7: 141,637,804 T2254A possibly damaging Het
Nbr1 T A 11: 101,569,591 S444T probably damaging Het
Ncor2 A T 5: 125,024,237 D1956E probably damaging Het
Ndufaf5 T C 2: 140,188,743 V183A probably benign Het
Nfasc G A 1: 132,570,481 T1155M probably damaging Het
Nol12 A G 15: 78,937,174 E78G probably damaging Het
Npy5r T A 8: 66,681,346 H265L probably benign Het
Olfr1008 G A 2: 85,690,128 G233D possibly damaging Het
Olfr418 T A 1: 173,270,850 L225H probably damaging Het
Pop1 A G 15: 34,529,071 E749G probably benign Het
Ppil3 T C 1: 58,438,388 I66V probably damaging Het
Prl4a1 C A 13: 28,018,571 T43K possibly damaging Het
Prop1 A G 11: 50,953,286 probably benign Het
Qrsl1 A T 10: 43,885,014 I218N probably damaging Het
Rbm22 T A 18: 60,564,412 M63K possibly damaging Het
Rictor T C 15: 6,786,414 S1056P probably benign Het
Rps6kb2 T C 19: 4,157,588 T388A probably damaging Het
Slc7a5 A G 8: 121,886,390 probably benign Het
Sp100 A T 1: 85,708,001 D509V probably damaging Het
Spata18 G T 5: 73,672,518 probably null Het
Sspo C A 6: 48,459,568 T1254K possibly damaging Het
Stk19 A G 17: 34,832,158 probably benign Het
Themis2 C A 4: 132,783,347 probably null Het
Tll2 T C 19: 41,086,263 Y937C possibly damaging Het
Trim34a T A 7: 104,247,732 M1K probably null Het
Usp50 G A 2: 126,778,038 T118I possibly damaging Het
Vps13d G A 4: 145,148,858 S1693F probably benign Het
Vps16 T A 2: 130,440,932 I467N probably damaging Het
Zfp318 C T 17: 46,396,810 R265* probably null Het
Other mutations in Taar8b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Taar8b APN 10 24091756 missense possibly damaging 0.69
IGL01380:Taar8b APN 10 24092107 missense probably damaging 1.00
IGL01536:Taar8b APN 10 24091595 missense probably benign
IGL02282:Taar8b APN 10 24091555 missense possibly damaging 0.83
R0730:Taar8b UTSW 10 24092026 missense probably damaging 1.00
R1871:Taar8b UTSW 10 24092002 missense probably damaging 1.00
R2051:Taar8b UTSW 10 24091314 missense probably benign 0.38
R2265:Taar8b UTSW 10 24091372 missense probably damaging 0.99
R2267:Taar8b UTSW 10 24091372 missense probably damaging 0.99
R2268:Taar8b UTSW 10 24091372 missense probably damaging 0.99
R2269:Taar8b UTSW 10 24091372 missense probably damaging 0.99
R4598:Taar8b UTSW 10 24091838 missense probably benign
R4633:Taar8b UTSW 10 24092252 nonsense probably null
R4833:Taar8b UTSW 10 24092132 missense possibly damaging 0.77
R4949:Taar8b UTSW 10 24091927 missense probably damaging 1.00
R6104:Taar8b UTSW 10 24092237 missense probably damaging 1.00
R6178:Taar8b UTSW 10 24091813 missense probably benign 0.01
R6495:Taar8b UTSW 10 24091262 makesense probably null
R6816:Taar8b UTSW 10 24092181 missense probably benign 0.00
R6913:Taar8b UTSW 10 24092065 missense possibly damaging 0.95
R7072:Taar8b UTSW 10 24091978 missense possibly damaging 0.95
Posted On2015-04-16