Incidental Mutation 'R3742:Gm6489'
ID 270392
Institutional Source Beutler Lab
Gene Symbol Gm6489
Ensembl Gene ENSMUSG00000094215
Gene Name predicted gene 6489
Synonyms
MMRRC Submission 040728-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.286) question?
Stock # R3742 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 31326026-31326787 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 31326764 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: ENSMUST00000178167
SMART Domains Protein: ENSMUSP00000136938
Gene: ENSMUSG00000094215

DomainStartEndE-ValueType
RRM 84 156 5.62e-18 SMART
FoP_duplication 165 253 2.91e-4 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 97% (32/33)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp8b2 C G 3: 89,853,338 (GRCm39) A726P probably benign Het
B4galt3 C A 1: 171,101,613 (GRCm39) H196N probably damaging Het
Bclaf3 T A X: 158,334,828 (GRCm39) H41Q probably benign Het
Bsn C A 9: 107,982,938 (GRCm39) R3605M unknown Het
Ctso G A 3: 81,859,556 (GRCm39) V288I probably benign Het
Dab1 C T 4: 104,588,948 (GRCm39) A524V probably benign Het
Dnah11 A G 12: 118,095,076 (GRCm39) M718T probably benign Het
Dsg4 A T 18: 20,604,058 (GRCm39) T842S probably damaging Het
Epb41l5 T C 1: 119,532,973 (GRCm39) Q388R probably benign Het
Fbxo6 A G 4: 148,234,090 (GRCm39) probably benign Het
Frem1 A C 4: 82,930,104 (GRCm39) Y281D probably damaging Het
Gtpbp2 A G 17: 46,476,808 (GRCm39) T329A probably benign Het
Hemgn T C 4: 46,396,421 (GRCm39) T272A possibly damaging Het
Hinfp A G 9: 44,213,812 (GRCm39) C22R probably damaging Het
Hoxc13 G A 15: 102,829,873 (GRCm39) G84D possibly damaging Het
Ing5 T A 1: 93,740,398 (GRCm39) S106R probably damaging Het
Mbd6 G A 10: 127,120,812 (GRCm39) probably benign Het
Nsf C T 11: 103,821,578 (GRCm39) E26K possibly damaging Het
Nup210l A T 3: 90,114,701 (GRCm39) M1759L probably benign Het
Or10ag52 A G 2: 87,043,340 (GRCm39) I35V probably benign Het
Or5b106 A G 19: 13,123,258 (GRCm39) F255S probably damaging Het
Or7e168 A T 9: 19,720,195 (GRCm39) I194F probably benign Het
Or7g25 A G 9: 19,159,979 (GRCm39) S239P possibly damaging Het
Pde4d T G 13: 109,877,013 (GRCm39) V53G probably benign Het
Shisa9 G A 16: 12,085,528 (GRCm39) R379Q probably damaging Het
Syngr4 T C 7: 45,545,194 (GRCm39) E5G possibly damaging Het
Tiam2 A G 17: 3,464,388 (GRCm39) D39G possibly damaging Het
Tmem88b A G 4: 155,869,884 (GRCm39) L59P probably damaging Het
Zfp386 T A 12: 116,023,170 (GRCm39) L296* probably null Het
Zfp605 G T 5: 110,276,564 (GRCm39) G561W probably damaging Het
Other mutations in Gm6489
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01578:Gm6489 APN 1 31,326,416 (GRCm39) exon noncoding transcript
R1957:Gm6489 UTSW 1 31,326,452 (GRCm39) exon noncoding transcript
R3740:Gm6489 UTSW 1 31,326,764 (GRCm39) unclassified noncoding transcript
R3741:Gm6489 UTSW 1 31,326,764 (GRCm39) unclassified noncoding transcript
R4489:Gm6489 UTSW 1 31,326,320 (GRCm39) exon noncoding transcript
R5239:Gm6489 UTSW 1 31,326,351 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- ATGGCAAGAAACCCTGGCTC -3'
(R):5'- GTTGAAAATGCCACCTTCACAAAAG -3'

Sequencing Primer
(F):5'- CAAGAAACCCTGGCTCTGGAG -3'
(R):5'- AGTACAAAACTGGTGCATTTCAG -3'
Posted On 2015-03-18