Incidental Mutation 'R5485:Gm5709'
ID 484447
Institutional Source Beutler Lab
Gene Symbol Gm5709
Ensembl Gene ENSMUSG00000095128
Gene Name predicted gene 5709
Synonyms
MMRRC Submission 043046-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.121) question?
Stock # R5485 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 59509876-59543154 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to T at 59542983 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000177879
SMART Domains Protein: ENSMUSP00000136253
Gene: ENSMUSG00000095128

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:DUF2424 37 208 4.9e-8 PFAM
Pfam:COesterase 90 226 8.7e-9 PFAM
Pfam:Abhydrolase_3 107 287 7.8e-39 PFAM
Pfam:Abhydrolase_3 278 375 2.5e-10 PFAM
Meta Mutation Damage Score 0.0852 question?
Coding Region Coverage
  • 1x: 98.2%
  • 3x: 97.3%
  • 10x: 95.1%
  • 20x: 90.6%
Validation Efficiency 98% (59/60)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700093K21Rik A T 11: 23,467,378 (GRCm39) V85D probably benign Het
Abcb8 A G 5: 24,605,159 (GRCm39) N115S probably benign Het
Appl1 C A 14: 26,684,823 (GRCm39) L75F probably damaging Het
Atp13a5 A G 16: 29,100,760 (GRCm39) probably null Het
Atp2c2 T A 8: 120,479,801 (GRCm39) probably null Het
Cfap54 T A 10: 92,864,979 (GRCm39) I94F probably damaging Het
Clasp1 A G 1: 118,395,643 (GRCm39) I194V possibly damaging Het
Crebbp A C 16: 3,932,777 (GRCm39) D1000E probably benign Het
Ctdnep1 C T 11: 69,872,316 (GRCm39) R3W possibly damaging Het
Dgkb T C 12: 38,177,363 (GRCm39) V230A probably damaging Het
Duoxa2 T C 2: 122,129,633 (GRCm39) F38L possibly damaging Het
Ecd T C 14: 20,388,273 (GRCm39) S172G probably benign Het
Endog G T 2: 30,061,663 (GRCm39) probably benign Het
Eqtn G A 4: 94,813,193 (GRCm39) P131L possibly damaging Het
Gabbr1 T A 17: 37,367,767 (GRCm39) S290T possibly damaging Het
Glt8d2 T A 10: 82,487,282 (GRCm39) R319S possibly damaging Het
Gm16686 A G 4: 88,673,641 (GRCm39) probably benign Het
Gm7381 T C 8: 3,892,161 (GRCm39) noncoding transcript Het
Gorab T G 1: 163,213,871 (GRCm39) D353A possibly damaging Het
Gstm1 A G 3: 107,924,720 (GRCm39) L20P probably damaging Het
Hexim2 A G 11: 103,029,884 (GRCm39) D312G probably benign Het
Hfm1 A G 5: 106,995,528 (GRCm39) probably null Het
Mbd4 C A 6: 115,827,679 (GRCm39) A66S probably benign Het
Mmp27 T A 9: 7,573,363 (GRCm39) W152R probably damaging Het
Mogat1 A G 1: 78,500,307 (GRCm39) T124A probably benign Het
Mrps18b A T 17: 36,225,236 (GRCm39) V102D probably damaging Het
Or10g3b A T 14: 52,586,776 (GRCm39) C242* probably null Het
Peg10 T A 6: 4,755,565 (GRCm39) M47K probably benign Het
Plxnc1 T G 10: 94,758,604 (GRCm39) Q364P probably benign Het
Psd A T 19: 46,304,528 (GRCm39) probably null Het
Rims1 T G 1: 22,522,289 (GRCm39) I470L possibly damaging Het
Sbsn T C 7: 30,452,542 (GRCm39) V519A possibly damaging Het
Senp1 A G 15: 97,964,377 (GRCm39) V279A probably benign Het
Sfxn5 T A 6: 85,309,582 (GRCm39) probably benign Het
Slc6a13 T A 6: 121,313,032 (GRCm39) M483K probably damaging Het
Slc6a21 G A 7: 44,931,966 (GRCm39) probably null Het
Slco6c1 T C 1: 97,053,481 (GRCm39) Y140C probably damaging Het
Spata32 A G 11: 103,100,122 (GRCm39) S128P probably damaging Het
Spty2d1 G T 7: 46,647,633 (GRCm39) T432K possibly damaging Het
Stx8 A G 11: 67,911,792 (GRCm39) Q170R probably benign Het
Sytl3 G A 17: 6,982,879 (GRCm39) V112I probably benign Het
Tdrkh A G 3: 94,336,019 (GRCm39) I420V probably benign Het
Tmem117 T C 15: 94,992,711 (GRCm39) V457A probably benign Het
Tpk1 T C 6: 43,642,746 (GRCm39) probably benign Het
Trpc2 GTGTCCTA GTGTCCTATGTCCTA 7: 101,744,420 (GRCm39) probably null Het
Tsen54 A G 11: 115,706,048 (GRCm39) E90G probably benign Het
Ugt1a2 A T 1: 88,128,968 (GRCm39) M204L probably damaging Het
Vmn2r17 A T 5: 109,567,972 (GRCm39) I32F probably benign Het
Xkr6 T C 14: 64,056,833 (GRCm39) V248A unknown Het
Zfhx4 C A 3: 5,308,067 (GRCm39) S431Y probably damaging Het
Zfp318 T A 17: 46,723,180 (GRCm39) S1728T possibly damaging Het
Zfp563 T C 17: 33,308,540 (GRCm39) probably benign Het
Other mutations in Gm5709
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01720:Gm5709 APN 3 59,513,975 (GRCm39) splice site noncoding transcript
R0090:Gm5709 UTSW 3 59,526,192 (GRCm39) exon noncoding transcript
R0662:Gm5709 UTSW 3 59,514,164 (GRCm39) intron noncoding transcript
R1311:Gm5709 UTSW 3 59,526,100 (GRCm39) exon noncoding transcript
R1540:Gm5709 UTSW 3 59,526,073 (GRCm39) exon noncoding transcript
R2023:Gm5709 UTSW 3 59,543,142 (GRCm39) exon noncoding transcript
R4660:Gm5709 UTSW 3 59,526,124 (GRCm39) exon noncoding transcript
R5256:Gm5709 UTSW 3 59,509,971 (GRCm39) exon noncoding transcript
R5478:Gm5709 UTSW 3 59,543,095 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- GCTGCACAGAGAAACCCTTTC -3'
(R):5'- TCATGGGATACAAGACTCTGTG -3'

Sequencing Primer
(F):5'- GAAACCCTTTCTTGAAAAACCAAAAC -3'
(R):5'- ACAAGACTCTGTGCTTTGGATTC -3'
Posted On 2017-07-18