Incidental Mutation 'R6442:Gm826'
ID 519044
Institutional Source Beutler Lab
Gene Symbol Gm826
Ensembl Gene ENSMUSG00000074623
Gene Name predicted gene 826
Synonyms Gm46773, LOC329554
MMRRC Submission 044580-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # R6442 (G1)
Quality Score 140.008
Status Not validated
Chromosome 2
Chromosomal Location 160153313-160176082 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to A at 160169328 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000096729 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099127]
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 noncoding transcript
Transcript: ENSMUST00000138905
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 93.9%
Validation Efficiency 100% (36/36)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp9a T C 2: 168,491,481 (GRCm39) T695A probably benign Het
Btla A G 16: 45,044,821 (GRCm39) N36D probably benign Het
Btla T C 16: 45,070,713 (GRCm39) V224A possibly damaging Het
Cep126 T C 9: 8,100,564 (GRCm39) N657D probably benign Het
Cops3 T A 11: 59,718,780 (GRCm39) K171N probably benign Het
Crocc2 A G 1: 93,112,775 (GRCm39) R193G probably benign Het
Dis3l T C 9: 64,214,837 (GRCm39) I911V probably benign Het
Dpp6 G A 5: 27,923,507 (GRCm39) probably null Het
Efcab5 A T 11: 76,996,260 (GRCm39) Y1100* probably null Het
Fcgbpl1 C T 7: 27,843,611 (GRCm39) T833I possibly damaging Het
Galnt10 A G 11: 57,656,448 (GRCm39) T211A probably benign Het
Gdf9 A G 11: 53,324,515 (GRCm39) T95A probably benign Het
Hsd17b6 C T 10: 127,829,636 (GRCm39) probably null Het
Hyal4 A G 6: 24,765,849 (GRCm39) N401S probably benign Het
Itga8 C T 2: 12,234,954 (GRCm39) V435I probably benign Het
Nr1h5 G A 3: 102,848,427 (GRCm39) P418L probably damaging Het
Or3a4 G A 11: 73,945,505 (GRCm39) R27W probably benign Het
Or4f15 G A 2: 111,813,874 (GRCm39) P182S probably damaging Het
Or4n4 T G 14: 50,518,826 (GRCm39) K295Q probably damaging Het
Or6c214 C A 10: 129,591,277 (GRCm39) G14V probably damaging Het
Or9i14 T C 19: 13,792,992 (GRCm39) probably benign Het
Prdm11 G A 2: 92,805,990 (GRCm39) A320V probably benign Het
Ptpn5 T C 7: 46,732,831 (GRCm39) probably null Het
Reln T A 5: 22,137,774 (GRCm39) I2473L probably benign Het
Rmnd5a A T 6: 71,371,659 (GRCm39) C180* probably null Het
Rsrc1 C T 3: 66,901,982 (GRCm39) P44L unknown Het
Sapcd2 T A 2: 25,266,134 (GRCm39) probably benign Het
Sec24b A G 3: 129,790,350 (GRCm39) L462S probably damaging Het
Slc26a9 A T 1: 131,686,555 (GRCm39) Y425F possibly damaging Het
Sult1b1 T C 5: 87,682,912 (GRCm39) D11G probably benign Het
Tgs1 T A 4: 3,604,760 (GRCm39) Y727* probably null Het
Tmem80 T C 7: 140,915,839 (GRCm39) V83A probably benign Het
Ttn T C 2: 76,551,978 (GRCm39) T31220A probably benign Het
Usp46 A T 5: 74,177,377 (GRCm39) D167E probably benign Het
Vmn2r67 T A 7: 84,805,046 (GRCm39) D22V possibly damaging Het
Zswim5 C A 4: 116,808,202 (GRCm39) P262Q 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
R3762:Gm826 UTSW 2 160,155,423 (GRCm39) intron probably benign
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
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 2018-05-24