Incidental Mutation 'R3762:Gm826'
ID 473349
Institutional Source Beutler Lab
Gene Symbol Gm826
Ensembl Gene ENSMUSG00000074623
Gene Name predicted gene 826
Synonyms Gm46773, LOC329554
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # R3762 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 160153313-160176082 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) C to A at 160155423 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000096729 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099127] [ENSMUST00000109475]
AlphaFold Q3UQ74
Predicted Effect probably benign
Transcript: ENSMUST00000099127
SMART Domains Protein: ENSMUSP00000096729
Gene: ENSMUSG00000074623

DomainStartEndE-ValueType
low complexity region 72 89 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000109475
AA Change: G14C
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138905
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap35 A T 7: 16,299,000 (GRCm39) S22T probably damaging Het
Atp2b1 T C 10: 98,845,351 (GRCm39) I718T probably damaging Het
Cad T A 5: 31,232,890 (GRCm39) probably null Het
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Defa41 C T 8: 21,691,753 (GRCm39) S45F probably damaging Het
Dhx15 G A 5: 52,324,074 (GRCm39) P406L probably benign Het
Dnah17 T A 11: 117,995,352 (GRCm39) M999L probably benign Het
Dpysl4 A G 7: 138,676,672 (GRCm39) E374G probably damaging Het
Gatad2a T C 8: 70,368,930 (GRCm39) probably null Het
H2-M10.1 T A 17: 36,636,216 (GRCm39) H117L probably damaging Het
Klhl9 A T 4: 88,639,830 (GRCm39) V137D possibly damaging Het
Limch1 A G 5: 67,186,183 (GRCm39) Y828C probably damaging Het
Med1 T C 11: 98,046,341 (GRCm39) probably benign Het
Muc5ac A T 7: 141,361,212 (GRCm39) T1507S possibly damaging Het
Pak6 A T 2: 118,526,958 (GRCm39) Q651L probably damaging Het
Plscr2 T A 9: 92,173,133 (GRCm39) V90D probably damaging Het
Rbbp4 G A 4: 129,228,344 (GRCm39) T2I probably damaging Het
Rnf121 G A 7: 101,673,244 (GRCm39) T223M probably damaging Het
Rsph6a A G 7: 18,789,256 (GRCm39) K196R probably damaging Het
Tex47 A T 5: 7,355,529 (GRCm39) I237L probably benign Het
Ulk1 C T 5: 110,937,223 (GRCm39) R691Q probably benign Het
Vmn1r30 C A 6: 58,412,278 (GRCm39) V185L probably benign Het
Vmn2r103 A T 17: 20,032,411 (GRCm39) E728D probably damaging Het
Vmn2r14 A T 5: 109,368,033 (GRCm39) Y320N probably benign Het
Zc3h14 T A 12: 98,724,902 (GRCm39) F188Y probably damaging Het
Other mutations in Gm826
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03182:Gm826 APN 2 160,169,035 (GRCm39) missense unknown
R2365:Gm826 UTSW 2 160,169,130 (GRCm39) missense unknown
R3769:Gm826 UTSW 2 160,169,165 (GRCm39) missense unknown
R4564:Gm826 UTSW 2 160,153,913 (GRCm39) utr 3 prime probably benign
R6125:Gm826 UTSW 2 160,169,034 (GRCm39) missense unknown
R6442:Gm826 UTSW 2 160,169,328 (GRCm39) start gained probably benign
R7048:Gm826 UTSW 2 160,169,026 (GRCm39) nonsense probably null
R7074:Gm826 UTSW 2 160,153,810 (GRCm39) missense unknown
R7491:Gm826 UTSW 2 160,153,942 (GRCm39) missense unknown
R7883:Gm826 UTSW 2 160,169,213 (GRCm39) missense unknown
Predicted Primers
Posted On 2017-04-14