Incidental Mutation 'R3703:Btnl7-ps'
ID258634
Institutional Source Beutler Lab
Gene Symbol Btnl7-ps
Ensembl Gene ENSMUSG00000061728
Gene Namebutyrophilin-like 7, pseudogene
SynonymsBtnl7
MMRRC Submission 040696-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.071) question?
Stock #R3703 (G1)
Quality Score225
Status Validated
Chromosome17
Chromosomal Location34532877-34547651 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to A at 34533967 bp
ZygosityHeterozygous
Amino Acid Change
Predicted Effect noncoding transcript
Transcript: ENSMUST00000023469
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.9%
  • 20x: 93.7%
Validation Efficiency 100% (50/50)
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik T A 3: 36,987,581 C2703S probably damaging Het
Arhgap10 C T 8: 77,259,056 probably null Het
Asap3 TGAGGAGGAGGAGGAGGA TGAGGAGGAGGAGGAGGAGGA 4: 136,241,241 probably benign Het
Bcap29 T C 12: 31,617,152 H170R probably benign Het
Brf1 T C 12: 112,969,371 probably null Het
Cdh12 C A 15: 21,583,826 T584K probably damaging Het
Col13a1 A G 10: 61,867,829 probably null Het
Col25a1 A G 3: 130,550,033 probably null Het
Csrp2 G A 10: 110,937,874 probably benign Het
Ctla2a T A 13: 60,936,007 D37V probably damaging Het
Cubn T A 2: 13,350,943 H1826L probably damaging Het
Dnajc19 A G 3: 34,080,229 probably null Het
Dxo T C 17: 34,838,769 probably benign Het
Edil3 A T 13: 89,177,298 M269L probably benign Het
Fbxl7 C A 15: 26,543,755 G269C probably damaging Het
Gpnmb T A 6: 49,051,865 I439N possibly damaging Het
Grm7 G T 6: 110,646,348 V161F probably damaging Het
Gtpbp3 T G 8: 71,492,135 S345A probably benign Het
Hnrnpul2 A G 19: 8,824,409 E327G probably damaging Het
Ifi207 A T 1: 173,727,463 Y884* probably null Het
Ifi47 T C 11: 49,095,525 S40P probably benign Het
Kcnq3 A G 15: 66,021,739 probably null Het
Kifc3 G A 8: 95,104,028 probably benign Het
Muc4 G C 16: 32,753,919 R1265P probably benign Het
Mug1 C T 6: 121,888,556 probably benign Het
Myh2 A G 11: 67,189,601 I1214V probably benign Het
Naa30 A G 14: 49,187,602 N337S probably benign Het
Nap1l3 A T X: 122,395,524 I499N possibly damaging Het
Nfat5 T A 8: 107,351,421 probably benign Het
Nisch A G 14: 31,176,745 probably benign Het
Nt5c3 A G 6: 56,883,667 probably benign Het
Pklr C T 3: 89,142,701 R328C probably damaging Het
Prrc2c G A 1: 162,710,691 R457C probably damaging Het
Rab1a T G 11: 20,224,506 probably benign Het
Rasa3 A T 8: 13,588,972 D278E probably benign Het
Rdh8 C T 9: 20,823,333 P99S probably damaging Het
Snx9 T A 17: 5,928,200 probably null Het
Spns3 C T 11: 72,499,530 probably benign Het
Sympk A G 7: 19,040,561 Y421C probably damaging Het
Tas1r2 G A 4: 139,667,418 C495Y probably damaging Het
Tmem63a G A 1: 180,963,114 D446N possibly damaging Het
Tmprss15 T C 16: 79,054,142 probably null Het
Tox3 G T 8: 90,248,905 T366K possibly damaging Het
Trdmt1 T A 2: 13,521,297 Q170L probably benign Het
Ttn A T 2: 76,735,408 V28200D probably damaging Het
Zfp616 G A 11: 74,083,319 W138* probably null Het
Zfr2 T G 10: 81,246,079 V493G probably benign Het
Other mutations in Btnl7-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0562:Btnl7-ps UTSW 17 34533524 exon noncoding transcript
R1507:Btnl7-ps UTSW 17 34541463 exon noncoding transcript
R1915:Btnl7-ps UTSW 17 34541645 critical splice acceptor site noncoding transcript
R3841:Btnl7-ps UTSW 17 34542576 exon noncoding transcript
R3915:Btnl7-ps UTSW 17 34541515 exon noncoding transcript
R4970:Btnl7-ps UTSW 17 34537118 splice site noncoding transcript
R5171:Btnl7-ps UTSW 17 34533529 exon noncoding transcript
R5226:Btnl7-ps UTSW 17 34533287 exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- TCTTGCAAGTAGAGGGAGGG -3'
(R):5'- TGTGTGTTTATGTGTATATCTCTCCC -3'

Sequencing Primer
(F):5'- CTAGAGGTGACAAGATAACAAGGTAC -3'
(R):5'- CCCCTTCTGTGTGTGTGACAAG -3'
Posted On2015-01-23