Incidental Mutation 'RF021:Taar7f'
ID603891
Institutional Source Beutler Lab
Gene Symbol Taar7f
Ensembl Gene ENSMUSG00000100950
Gene Nametrace amine-associated receptor 7F
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.106) question?
Stock #RF021 (G1)
Quality Score225.009
Status Validated
Chromosome10
Chromosomal Location24049510-24050586 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 24050423 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Methionine at position 305 (T305M)
Ref Sequence ENSEMBL: ENSMUSP00000071611 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071691]
Predicted Effect possibly damaging
Transcript: ENSMUST00000071691
AA Change: T305M

PolyPhen 2 Score 0.889 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000071611
Gene: ENSMUSG00000100950
AA Change: T305M

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 56 261 1.6e-7 PFAM
Pfam:7TM_GPCR_Srsx 58 341 2e-10 PFAM
Pfam:7tm_1 64 326 6.6e-58 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000119318
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.7%
  • 10x: 99.3%
  • 20x: 98.3%
Validation Efficiency 91% (50/55)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik TTATTATTATTAT TTATTATTATTATTAATATTATTATTAT 3: 37,050,748 probably benign Het
A030005L19Rik GTGGTGGCTG GTGGTGGCTGTGGTGGCTG 1: 82,913,569 probably benign Het
AI837181 CGG CGGTGG 19: 5,425,234 probably benign Het
Ankrd44 T C 1: 54,778,312 H79R probably damaging Het
Atg9a T A 1: 75,182,629 E826V probably damaging Het
Atrnl1 T C 19: 57,642,473 V224A probably benign Het
Cpn2 G A 16: 30,259,338 A515V probably benign Het
Cyp2a12 T C 7: 27,035,360 F402S possibly damaging Het
Defb22 TGCGGCA TGCGGCAGAGCTGGGCGTTGCGGCA 2: 152,485,832 probably benign Het
Diexf A G 1: 193,120,666 F248L probably benign Het
Dnah10 G T 5: 124,777,907 V2016F probably damaging Het
Dock10 T C 1: 80,564,573 probably null Het
Efhd2 GCC GCCGCCCCC 4: 141,874,773 probably benign Het
Fam131a A C 16: 20,694,940 probably benign Het
Gm6614 A T 6: 142,008,714 V31E probably damaging Het
Gm7247 AGACCAGACC A 14: 51,364,324 probably benign Het
Gna13 T C 11: 109,392,392 V186A probably benign Het
Grk3 T A 5: 112,941,688 I333L probably benign Het
Gstp1 A T 19: 4,035,507 V200E probably benign Het
Gtf2h1 T G 7: 46,803,865 V74G possibly damaging Het
Kcnh8 G A 17: 52,978,239 R1079H probably benign Het
Kiz A G 2: 146,870,830 D138G possibly damaging Het
Kmt2b TTCTCCT TTCTCCTTCTCCT 7: 30,586,357 probably benign Het
Lats1 A G 10: 7,710,608 T912A probably damaging Het
Lce1m GCTGCCACC GCTGCCACCACTTCTGCCACC 3: 93,018,269 probably benign Het
Lce1m TGCC TGCCGCCGCTGCCGCC 3: 93,018,295 probably benign Het
Lrrc2 TTGATTCGGTTCACC T 9: 110,981,676 probably null Het
Med12l T C 3: 59,073,290 F359S probably benign Het
Mut A G 17: 40,951,758 I444V probably benign Het
Ncoa2 CTTAAAA C 1: 13,149,109 probably benign Het
Ngp A G 9: 110,421,756 T114A possibly damaging Het
Nlrc5 A T 8: 94,476,888 T539S probably benign Het
Nxf1 A G 19: 8,772,309 D190G probably damaging Het
Olfr229 A T 9: 39,910,045 M81L probably benign Het
Olfr769 A T 10: 129,112,342 F28I probably damaging Het
Pramef25 C G 4: 143,948,908 Q449H probably damaging Het
Prdm15 G A 16: 97,808,756 H563Y probably damaging Het
Rbm12 CAGG CAGGGATTGCGGGACCTGGTATTGCGGGACCAGG 2: 156,096,106 probably benign Het
Sema3g C T 14: 31,227,841 H660Y probably damaging Het
Smarca2 AGCAGCAGCAGCAGCAGCAGCA AGCAGCAGCAGCAGCAGCAGCAGCAGCA 19: 26,630,997 probably benign Het
Stpg2 A T 3: 139,212,250 probably null Het
Tbcb C T 7: 30,224,346 V208M probably damaging Het
Tenm2 T A 11: 36,024,203 Q2169L possibly damaging Het
Tln1 A G 4: 43,555,890 V108A probably damaging Het
Tmc8 T C 11: 117,783,234 M42T probably benign Het
Trdc T C 14: 54,144,203 V115A Het
Ttbk2 A G 2: 120,748,634 V669A probably benign Het
Tusc1 GCC GCCACCACC 4: 93,335,316 probably benign Het
Vps16 A G 2: 130,438,209 H118R probably benign Het
Wdpcp T A 11: 21,711,587 C286* probably null Het
Zbed4 C A 15: 88,781,236 Y502* probably null Het
Zdbf2 T A 1: 63,302,652 N63K possibly damaging Het
Other mutations in Taar7f
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00936:Taar7f APN 10 24050168 missense probably benign
IGL01618:Taar7f APN 10 24050341 missense possibly damaging 0.56
IGL02567:Taar7f APN 10 24050425 missense probably damaging 0.97
R0096:Taar7f UTSW 10 24050254 missense probably benign 0.00
R0139:Taar7f UTSW 10 24050414 missense probably benign 0.04
R0363:Taar7f UTSW 10 24049941 missense probably damaging 1.00
R1776:Taar7f UTSW 10 24049648 missense probably benign 0.14
R1952:Taar7f UTSW 10 24049849 missense probably damaging 1.00
R2049:Taar7f UTSW 10 24050425 missense possibly damaging 0.65
R2280:Taar7f UTSW 10 24049519 missense probably benign
R3120:Taar7f UTSW 10 24049580 missense probably benign
R4210:Taar7f UTSW 10 24050023 missense probably damaging 1.00
R4211:Taar7f UTSW 10 24050023 missense probably damaging 1.00
R4587:Taar7f UTSW 10 24050575 missense probably damaging 0.97
R5092:Taar7f UTSW 10 24049553 missense probably benign
R5512:Taar7f UTSW 10 24050423 missense possibly damaging 0.89
R7439:Taar7f UTSW 10 24049987 missense possibly damaging 0.88
R7441:Taar7f UTSW 10 24049987 missense possibly damaging 0.88
R7839:Taar7f UTSW 10 24050069 missense possibly damaging 0.90
R8326:Taar7f UTSW 10 24049913 missense possibly damaging 0.81
Predicted Primers PCR Primer
(F):5'- ATGAGCAAGCAGACTGCCAG -3'
(R):5'- AGAAACAGACCTGGGCACTC -3'

Sequencing Primer
(F):5'- CAGGGCATCAGACAGCTAC -3'
(R):5'- AGACCTGGGCACTCAGTCTC -3'
Posted On2019-12-04