Incidental Mutation 'R1311:Gm5709'
ID 157923
Institutional Source Beutler Lab
Gene Symbol Gm5709
Ensembl Gene ENSMUSG00000095128
Gene Name predicted gene 5709
Synonyms
MMRRC Submission 039377-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.121) question?
Stock # R1311 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 59509876-59543154 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 59526100 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
Coding Region Coverage
  • 1x: 98.8%
  • 3x: 97.7%
  • 10x: 94.1%
  • 20x: 86.2%
Validation Efficiency 98% (42/43)
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr1c T C 2: 58,170,261 (GRCm39) Q449R probably benign Het
Cap1 A G 4: 122,759,007 (GRCm39) Y195H possibly damaging Het
Casp8ap2 T A 4: 32,648,111 (GRCm39) N1939K probably damaging Het
Cd209c T A 8: 3,995,908 (GRCm39) M1L probably benign Het
Ckb TCCACCACCA TCCACCA 12: 111,636,079 (GRCm39) probably benign Het
Col13a1 A G 10: 61,699,789 (GRCm39) probably benign Het
Dennd4a T C 9: 64,817,286 (GRCm39) V1640A probably benign Het
Eml6 T C 11: 29,781,088 (GRCm39) probably benign Het
Fat3 G A 9: 15,932,706 (GRCm39) T1409I probably damaging Het
Gm4884 G C 7: 40,692,539 (GRCm39) E169D possibly damaging Het
Htr2b C A 1: 86,038,346 (GRCm39) A87S probably damaging Het
Kansl2 G T 15: 98,426,797 (GRCm39) H275N possibly damaging Het
Megf6 G A 4: 154,348,239 (GRCm39) probably null Het
Mtpn A G 6: 35,489,185 (GRCm39) I113T possibly damaging Het
Myh6 G T 14: 55,183,822 (GRCm39) A1704E probably damaging Het
Notum C T 11: 120,546,575 (GRCm39) probably benign Het
Nxpe2 T C 9: 48,237,914 (GRCm39) T114A probably damaging Het
Olfml1 T C 7: 107,167,103 (GRCm39) probably null Het
Or14c41 T A 7: 86,235,161 (GRCm39) V226D probably damaging Het
Ptpn5 A T 7: 46,728,980 (GRCm39) probably benign Het
Rapgef2 A G 3: 78,990,854 (GRCm39) F985L probably benign Het
Slc7a7 A T 14: 54,610,487 (GRCm39) Y386* probably null Het
Snph G T 2: 151,439,122 (GRCm39) P36Q probably damaging Het
St18 T C 1: 6,915,868 (GRCm39) C838R probably damaging Het
Sucla2 C T 14: 73,798,074 (GRCm39) probably benign Het
Supt7l T C 5: 31,677,605 (GRCm39) Y187C probably damaging Het
Sycp2l A T 13: 41,288,661 (GRCm39) K241* probably null Het
Tenm2 G T 11: 35,959,421 (GRCm39) probably benign Het
Tfap4 A G 16: 4,377,290 (GRCm39) probably null Het
Tmem132e T C 11: 82,335,122 (GRCm39) Y643H probably damaging Het
Tmem200c A T 17: 69,147,758 (GRCm39) S114C probably damaging Het
Ush2a T C 1: 188,679,342 (GRCm39) I4850T possibly damaging Het
Zmym6 G T 4: 127,017,151 (GRCm39) L977F probably damaging 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
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
R5485:Gm5709 UTSW 3 59,542,983 (GRCm39) intron noncoding transcript
Predicted Primers PCR Primer
(F):5'- ACTACTTGAGCAAATGTGGAGTGCAG -3'
(R):5'- GATGAACACAGGGAGATACCCATGC -3'

Sequencing Primer
(F):5'- ACTTCCAAGTGTAGGCTATCGAC -3'
(R):5'- GGGAGATACCCATGCTACAAAATAC -3'
Posted On 2014-02-18