Incidental Mutation 'IGL00816:Taar8c'
ID 14345
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Taar8c
Ensembl Gene ENSMUSG00000100004
Gene Name trace amine-associated receptor 8C
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.098) question?
Stock # IGL00816
Quality Score
Status
Chromosome 10
Chromosomal Location 23976776-23977810 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 23977173 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 213 (I213N)
Ref Sequence ENSEMBL: ENSMUSP00000133193 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170267]
AlphaFold Q5QD05
Predicted Effect probably damaging
Transcript: ENSMUST00000170267
AA Change: I213N

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000133193
Gene: ENSMUSG00000100004
AA Change: I213N

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 40 244 2.7e-8 PFAM
Pfam:7TM_GPCR_Srsx 42 327 4.9e-15 PFAM
Pfam:7tm_1 48 312 2.3e-57 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrv1 A T 13: 81,545,322 (GRCm39) D5654E probably benign Het
Alg6 A G 4: 99,630,598 (GRCm39) S146G probably null Het
Anks1 T C 17: 28,278,367 (GRCm39) probably null Het
Bcor T C X: 11,904,059 (GRCm39) I1662V probably damaging Het
Bzw1 T C 1: 58,438,213 (GRCm39) F98L probably damaging Het
Cdc14b A G 13: 64,353,217 (GRCm39) V453A probably benign Het
Copg1 G T 6: 87,870,880 (GRCm39) A228S possibly damaging Het
D1Pas1 A G 1: 186,701,609 (GRCm39) I513V possibly damaging Het
Efemp1 G A 11: 28,876,223 (GRCm39) V463M probably benign Het
Ep400 T A 5: 110,883,356 (GRCm39) probably benign Het
Faim G A 9: 98,874,218 (GRCm39) G15R probably damaging Het
Fgd3 A G 13: 49,418,262 (GRCm39) probably benign Het
Furin C A 7: 80,042,315 (GRCm39) G427W probably damaging Het
Glycam1 T G 15: 103,472,659 (GRCm39) D25A probably damaging Het
Gpr119 A G X: 47,763,047 (GRCm39) L30P probably damaging Het
Gria1 T A 11: 57,208,568 (GRCm39) M752K possibly damaging Het
Mcph1 C T 8: 18,682,413 (GRCm39) P517S possibly damaging Het
Mug1 T A 6: 121,859,597 (GRCm39) Y1199N probably damaging Het
Myt1 A G 2: 181,449,308 (GRCm39) D663G probably damaging Het
Ppp1r1c A T 2: 79,540,241 (GRCm39) probably null Het
Rab1a C T 11: 20,174,727 (GRCm39) T100M possibly damaging Het
Rfx6 A G 10: 51,554,501 (GRCm39) K114R probably benign Het
Rmdn1 T C 4: 19,595,119 (GRCm39) V177A probably benign Het
Setd5 T G 6: 113,088,375 (GRCm39) L168V probably damaging Het
Slc25a10 A T 11: 120,385,976 (GRCm39) probably benign Het
Slc38a7 A T 8: 96,570,748 (GRCm39) I252N probably damaging Het
Slit2 G A 5: 48,146,493 (GRCm39) E95K possibly damaging Het
Tagln3 A T 16: 45,544,556 (GRCm39) C38* probably null Het
Tmcc2 C A 1: 132,308,436 (GRCm39) A153S probably benign Het
Tuft1 A T 3: 94,523,138 (GRCm39) I291N probably damaging Het
Vmn2r10 T A 5: 109,150,451 (GRCm39) M198L possibly damaging Het
Vps13d T A 4: 144,882,564 (GRCm39) M1004L probably benign Het
Wfdc3 T C 2: 164,584,945 (GRCm39) probably benign Het
Wfikkn2 G A 11: 94,128,921 (GRCm39) Q407* probably null Het
Zfp106 T C 2: 120,357,329 (GRCm39) I1189V probably benign Het
Zic2 T A 14: 122,715,971 (GRCm39) C364* probably null Het
Other mutations in Taar8c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01733:Taar8c APN 10 23,977,155 (GRCm39) missense possibly damaging 0.86
R0669:Taar8c UTSW 10 23,977,401 (GRCm39) missense probably damaging 1.00
R1186:Taar8c UTSW 10 23,977,463 (GRCm39) nonsense probably null
R1452:Taar8c UTSW 10 23,977,508 (GRCm39) missense probably benign 0.00
R2256:Taar8c UTSW 10 23,976,969 (GRCm39) missense probably benign 0.01
R4364:Taar8c UTSW 10 23,977,477 (GRCm39) missense probably benign 0.02
R4904:Taar8c UTSW 10 23,977,147 (GRCm39) missense probably benign 0.01
R5314:Taar8c UTSW 10 23,977,246 (GRCm39) missense probably damaging 1.00
R6163:Taar8c UTSW 10 23,977,116 (GRCm39) missense probably benign 0.00
R6631:Taar8c UTSW 10 23,977,701 (GRCm39) missense probably benign 0.01
R7428:Taar8c UTSW 10 23,977,446 (GRCm39) missense probably damaging 1.00
R7497:Taar8c UTSW 10 23,977,116 (GRCm39) missense probably benign 0.00
R7525:Taar8c UTSW 10 23,977,764 (GRCm39) missense probably benign 0.03
R8122:Taar8c UTSW 10 23,977,107 (GRCm39) missense probably benign 0.14
R8280:Taar8c UTSW 10 23,976,835 (GRCm39) missense probably benign 0.37
R8293:Taar8c UTSW 10 23,977,015 (GRCm39) missense probably benign 0.00
R8772:Taar8c UTSW 10 23,977,705 (GRCm39) missense probably benign
R9165:Taar8c UTSW 10 23,977,500 (GRCm39) missense probably damaging 1.00
Z1177:Taar8c UTSW 10 23,977,305 (GRCm39) missense probably benign 0.37
Z1177:Taar8c UTSW 10 23,977,148 (GRCm39) missense probably benign 0.15
Posted On 2012-12-06