Incidental Mutation 'R3740:Gm6489'
ID 270322
Institutional Source Beutler Lab
Gene Symbol Gm6489
Ensembl Gene ENSMUSG00000094215
Gene Name predicted gene 6489
Synonyms
MMRRC Submission 040726-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.412) question?
Stock # R3740 (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: 95.3%
Validation Efficiency 94% (29/31)
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrb3 T C 1: 25,865,535 (GRCm39) R103G probably benign Het
Atp8b2 C G 3: 89,853,338 (GRCm39) A726P probably benign Het
Bbox1 A G 2: 110,135,922 (GRCm39) I19T possibly damaging 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
Fam135a A T 1: 24,053,892 (GRCm39) M1215K probably damaging Het
Fam174b T C 7: 73,390,578 (GRCm39) probably null Het
Fgfr1op2 A G 6: 146,496,731 (GRCm39) I190V possibly damaging Het
Flt1 G A 5: 147,536,403 (GRCm39) R813W probably damaging Het
Hacd3 T C 9: 64,928,755 (GRCm39) E24G possibly damaging Het
Kat6b T G 14: 21,720,112 (GRCm39) M1488R probably damaging Het
Kcnk3 T C 5: 30,779,274 (GRCm39) V108A possibly damaging Het
Kif5a A G 10: 127,079,337 (GRCm39) I287T probably damaging Het
Mical1 A C 10: 41,355,067 (GRCm39) D192A probably benign Het
Mov10l1 A G 15: 88,896,345 (GRCm39) N678D possibly damaging Het
Nup210l A T 3: 90,114,701 (GRCm39) M1759L probably benign Het
Optn C A 2: 5,039,009 (GRCm39) M371I possibly damaging Het
Pik3cg T C 12: 32,255,223 (GRCm39) K255E probably damaging Het
Rims1 A T 1: 22,443,667 (GRCm39) V380D probably damaging Het
Serpinb6e T A 13: 34,022,943 (GRCm39) I147F probably benign Het
Slc13a1 T C 6: 24,134,476 (GRCm39) M136V 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
Ttn T A 2: 76,620,703 (GRCm39) K13995* probably null Het
Vmn1r225 A G 17: 20,723,261 (GRCm39) Q234R possibly damaging Het
Vmn2r107 A G 17: 20,595,151 (GRCm39) N568S probably benign Het
Zfp605 G T 5: 110,276,564 (GRCm39) G561W probably damaging Het
Zfp69 T A 4: 120,788,071 (GRCm39) probably null 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
R3741:Gm6489 UTSW 1 31,326,764 (GRCm39) unclassified noncoding transcript
R3742: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'- AAGAAACCCTGGCTCTGGAG -3'
(R):5'- AAGTTGAAAATGCCACCTTCAC -3'

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