Incidental Mutation 'R1952:Taar7f'
ID 217392
Institutional Source Beutler Lab
Gene Symbol Taar7f
Ensembl Gene ENSMUSG00000100950
Gene Name trace amine-associated receptor 7F
Synonyms
MMRRC Submission 039966-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.089) question?
Stock # R1952 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 23925408-23926484 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 23925747 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 114 (Y114N)
Ref Sequence ENSEMBL: ENSMUSP00000071611 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071691]
AlphaFold Q5QD08
Predicted Effect probably damaging
Transcript: ENSMUST00000071691
AA Change: Y114N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000071611
Gene: ENSMUSG00000100950
AA Change: Y114N

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: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 75 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700024G13Rik A G 14: 32,110,293 (GRCm39) V6A possibly damaging Het
Accsl G T 2: 93,689,778 (GRCm39) H376Q probably damaging Het
Adgrg1 T C 8: 95,735,119 (GRCm39) probably null Het
Alyref C G 11: 120,486,758 (GRCm39) V168L probably damaging Het
Ankrd12 T C 17: 66,338,566 (GRCm39) D128G probably damaging Het
Bcl2l14 A G 6: 134,409,329 (GRCm39) Y301C probably damaging Het
Camsap3 A G 8: 3,654,789 (GRCm39) T804A probably damaging Het
Capn11 A T 17: 45,953,885 (GRCm39) W154R probably damaging Het
Cd44 T A 2: 102,683,432 (GRCm39) T201S probably damaging Het
Cers4 G A 8: 4,573,461 (GRCm39) W319* probably null Het
Col27a1 T A 4: 63,202,130 (GRCm39) probably null Het
Crnkl1 G A 2: 145,770,120 (GRCm39) A241V probably damaging Het
Cyp2c68 T C 19: 39,700,972 (GRCm39) Y282C probably benign Het
Dmd T A X: 82,874,123 (GRCm39) I1342N probably damaging Het
Dusp7 T A 9: 106,248,028 (GRCm39) C219S probably benign Het
Epha7 A G 4: 28,950,474 (GRCm39) N759S probably damaging Het
Fat1 T C 8: 45,486,963 (GRCm39) V3413A probably benign Het
Gls2 A G 10: 128,045,231 (GRCm39) H576R probably benign Het
Gm4884 G A 7: 40,693,671 (GRCm39) V547M probably benign Het
Hap1 A G 11: 100,243,105 (GRCm39) V174A probably damaging Het
Il12rb2 A G 6: 67,269,300 (GRCm39) S838P probably damaging Het
Ints8 T C 4: 11,221,150 (GRCm39) I742V probably benign Het
Katnal2 G T 18: 77,067,707 (GRCm39) S411R probably benign Het
Lrp1 A C 10: 127,403,300 (GRCm39) V2091G probably damaging Het
Mettl21c A T 1: 44,056,368 (GRCm39) D20E probably damaging Het
Mib1 A T 18: 10,812,077 (GRCm39) E991D possibly damaging Het
Mip T C 10: 128,061,772 (GRCm39) S8P possibly damaging Het
Mllt6 T C 11: 97,568,048 (GRCm39) S826P probably damaging Het
Mlst8 AT ATT 17: 24,696,987 (GRCm39) probably null Het
Myrfl C T 10: 116,658,716 (GRCm39) V414I probably benign Het
Nbeal1 T C 1: 60,273,999 (GRCm39) V409A probably damaging Het
Nin T A 12: 70,077,700 (GRCm39) Q1035L probably damaging Het
Nlgn1 T A 3: 25,490,464 (GRCm39) D421V probably damaging Het
Nlrp10 A G 7: 108,523,770 (GRCm39) V570A probably benign Het
Olfm3 A T 3: 114,895,589 (GRCm39) E157V probably null Het
Or8g24 T A 9: 38,989,580 (GRCm39) I154F probably benign Het
Or8g37 T C 9: 39,731,363 (GRCm39) S143P probably benign Het
Otud7a A G 7: 63,300,624 (GRCm39) D21G probably damaging Het
Pax2 A G 19: 44,777,271 (GRCm39) T155A probably benign Het
Pcf11 A T 7: 92,310,546 (GRCm39) S481T probably damaging Het
Prkab2 T C 3: 97,573,943 (GRCm39) V194A probably benign Het
Prl3a1 G A 13: 27,454,136 (GRCm39) G38E possibly damaging Het
Psmb8 T C 17: 34,419,884 (GRCm39) V246A probably damaging Het
Ptpn12 A T 5: 21,203,308 (GRCm39) V490E probably benign Het
Ptprm A T 17: 67,247,575 (GRCm39) S587T probably benign Het
Qars1 G A 9: 108,390,380 (GRCm39) R427H probably benign Het
R3hdml T C 2: 163,340,216 (GRCm39) F128L probably benign Het
Rapgef4 A G 2: 72,038,471 (GRCm39) M541V probably benign Het
Rhbdf1 G A 11: 32,164,277 (GRCm39) R234* probably null Het
Rufy1 A T 11: 50,297,233 (GRCm39) D406E probably benign Het
Satb1 A T 17: 52,047,173 (GRCm39) L683Q probably damaging Het
Satb2 T C 1: 56,938,229 (GRCm39) T132A probably damaging Het
Sbspon A G 1: 15,930,519 (GRCm39) S156P probably damaging Het
Shb A T 4: 45,458,347 (GRCm39) probably null Het
She A G 3: 89,756,792 (GRCm39) K282R possibly damaging Het
Slc25a13 A G 6: 6,152,482 (GRCm39) L85P probably damaging Het
Slc7a13 A T 4: 19,841,578 (GRCm39) H475L probably benign Het
Sorl1 C T 9: 41,957,920 (GRCm39) V575I probably benign Het
Spag9 T A 11: 93,988,184 (GRCm39) C833S possibly damaging Het
Speer2 A C 16: 69,654,052 (GRCm39) N232K probably damaging Het
Syncrip A T 9: 88,358,927 (GRCm39) M194K probably damaging Het
Sytl3 A C 17: 6,995,732 (GRCm39) T171P probably damaging Het
Tamalin T C 15: 101,122,381 (GRCm39) Y67H probably benign Het
Tap1 C G 17: 34,412,481 (GRCm39) P506R probably damaging Het
Tle6 T C 10: 81,431,319 (GRCm39) D212G possibly damaging Het
Trim80 G T 11: 115,332,155 (GRCm39) E116* probably null Het
Ttll4 A G 1: 74,726,718 (GRCm39) R745G probably damaging Het
Vdac2 A T 14: 21,887,947 (GRCm39) I85F possibly damaging Het
Vmn1r188 A G 13: 22,272,309 (GRCm39) R88G probably damaging Het
Washc2 T C 6: 116,232,052 (GRCm39) S821P possibly damaging Het
Wdhd1 T C 14: 47,507,647 (GRCm39) Y213C probably damaging Het
Wdr55 C A 18: 36,893,437 (GRCm39) P33Q probably damaging Het
Yrdc C T 4: 124,745,739 (GRCm39) A32V probably benign Het
Zfp608 T A 18: 55,030,851 (GRCm39) K1030* probably null Het
Zfp618 T A 4: 63,050,555 (GRCm39) probably null Het
Other mutations in Taar7f
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00936:Taar7f APN 10 23,926,066 (GRCm39) missense probably benign
IGL01618:Taar7f APN 10 23,926,239 (GRCm39) missense possibly damaging 0.56
IGL02567:Taar7f APN 10 23,926,323 (GRCm39) missense probably damaging 0.97
R0096:Taar7f UTSW 10 23,926,152 (GRCm39) missense probably benign 0.00
R0139:Taar7f UTSW 10 23,926,312 (GRCm39) missense probably benign 0.04
R0363:Taar7f UTSW 10 23,925,839 (GRCm39) missense probably damaging 1.00
R1776:Taar7f UTSW 10 23,925,546 (GRCm39) missense probably benign 0.14
R2049:Taar7f UTSW 10 23,926,323 (GRCm39) missense possibly damaging 0.65
R2280:Taar7f UTSW 10 23,925,417 (GRCm39) missense probably benign
R3120:Taar7f UTSW 10 23,925,478 (GRCm39) missense probably benign
R4210:Taar7f UTSW 10 23,925,921 (GRCm39) missense probably damaging 1.00
R4211:Taar7f UTSW 10 23,925,921 (GRCm39) missense probably damaging 1.00
R4587:Taar7f UTSW 10 23,926,473 (GRCm39) missense probably damaging 0.97
R5092:Taar7f UTSW 10 23,925,451 (GRCm39) missense probably benign
R5512:Taar7f UTSW 10 23,926,321 (GRCm39) missense possibly damaging 0.89
R7439:Taar7f UTSW 10 23,925,885 (GRCm39) missense possibly damaging 0.88
R7441:Taar7f UTSW 10 23,925,885 (GRCm39) missense possibly damaging 0.88
R7839:Taar7f UTSW 10 23,925,967 (GRCm39) missense possibly damaging 0.90
R8326:Taar7f UTSW 10 23,925,811 (GRCm39) missense possibly damaging 0.81
R9443:Taar7f UTSW 10 23,926,311 (GRCm39) missense probably benign 0.00
R9687:Taar7f UTSW 10 23,925,727 (GRCm39) missense probably benign 0.19
RF021:Taar7f UTSW 10 23,926,321 (GRCm39) missense possibly damaging 0.89
Predicted Primers PCR Primer
(F):5'- GTGTCAGAAGCCCATACTCC -3'
(R):5'- AGAAGGTGATGCACTTGCC -3'

Sequencing Primer
(F):5'- ATACTCCCCAGGCCCTCG -3'
(R):5'- GTGATGCACTTGCCAGAAAC -3'
Posted On 2014-08-01