Incidental Mutation 'R6442:Gm826'
ID519044
Institutional Source Beutler Lab
Gene Symbol Gm826
Ensembl Gene ENSMUSG00000074623
Gene Namepredicted gene 826
SynonymsLOC329554
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.100) question?
Stock #R6442 (G1)
Quality Score140.008
Status Not validated
Chromosome2
Chromosomal Location160311393-160334162 bp(-) (GRCm38)
Type of Mutationstart gained
DNA Base Change (assembly) T to A at 160327408 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000096729 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099127]
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
9530053A07Rik C T 7: 28,144,186 T833I possibly damaging Het
Atp9a T C 2: 168,649,561 T695A probably benign Het
Btla A G 16: 45,224,458 N36D probably benign Het
Btla T C 16: 45,250,350 V224A possibly damaging Het
Cep126 T C 9: 8,100,563 N657D probably benign Het
Cops3 T A 11: 59,827,954 K171N probably benign Het
Crocc2 A G 1: 93,185,053 R193G probably benign Het
Dis3l T C 9: 64,307,555 I911V probably benign Het
Dpp6 G A 5: 27,718,509 probably null Het
Efcab5 A T 11: 77,105,434 Y1100* probably null Het
Galnt10 A G 11: 57,765,622 T211A probably benign Het
Gdf9 A G 11: 53,433,688 T95A probably benign Het
Hsd17b6 C T 10: 127,993,767 probably null Het
Hyal4 A G 6: 24,765,850 N401S probably benign Het
Itga8 C T 2: 12,230,143 V435I probably benign Het
Nr1h5 G A 3: 102,941,111 P418L probably damaging Het
Olfr1309 G A 2: 111,983,529 P182S probably damaging Het
Olfr1499 T C 19: 13,815,628 probably benign Het
Olfr399 G A 11: 74,054,679 R27W probably benign Het
Olfr732 T G 14: 50,281,369 K295Q probably damaging Het
Olfr807 C A 10: 129,755,408 G14V probably damaging Het
Prdm11 G A 2: 92,975,645 A320V probably benign Het
Ptpn5 T C 7: 47,083,083 probably null Het
Reln T A 5: 21,932,776 I2473L probably benign Het
Rmnd5a A T 6: 71,394,675 C180* probably null Het
Rsrc1 C T 3: 66,994,649 P44L unknown Het
Sapcd2 T A 2: 25,376,122 probably benign Het
Sec24b A G 3: 129,996,701 L462S probably damaging Het
Slc26a9 A T 1: 131,758,817 Y425F possibly damaging Het
Sult1b1 T C 5: 87,535,053 D11G probably benign Het
Tgs1 T A 4: 3,604,760 Y727* probably null Het
Tmem80 T C 7: 141,335,926 V83A probably benign Het
Ttn T C 2: 76,721,634 T31220A probably benign Het
Usp46 A T 5: 74,016,716 D167E probably benign Het
Vmn2r67 T A 7: 85,155,838 D22V possibly damaging Het
Zswim5 C A 4: 116,951,005 P262Q probably damaging Het
Other mutations in Gm826
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03182:Gm826 APN 2 160327115 missense unknown
R2365:Gm826 UTSW 2 160327210 missense unknown
R3762:Gm826 UTSW 2 160313503 intron probably benign
R3769:Gm826 UTSW 2 160327245 missense unknown
R4564:Gm826 UTSW 2 160311993 utr 3 prime probably benign
R6125:Gm826 UTSW 2 160327114 missense unknown
R7048:Gm826 UTSW 2 160327106 nonsense probably null
R7074:Gm826 UTSW 2 160311890 missense unknown
R7491:Gm826 UTSW 2 160312022 missense unknown
R7883:Gm826 UTSW 2 160327293 missense unknown
Predicted Primers
Posted On2018-05-24