Incidental Mutation 'R4401:Gm6712'
ID 500608
Institutional Source Beutler Lab
Gene Symbol Gm6712
Ensembl Gene ENSMUSG00000072761
Gene Name predicted gene 6712
Synonyms
MMRRC Submission 041132-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.142) question?
Stock # R4401 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 17514705-17539847 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 17538366 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: ENSMUST00000105311
SMART Domains Protein: ENSMUSP00000100948
Gene: ENSMUSG00000072761

DomainStartEndE-ValueType
KRAB 3 63 1.9e-15 SMART
ZnF_C2H2 121 143 1.08e1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186431
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb1a A G 5: 8,752,390 (GRCm39) I454V possibly damaging Het
Acvr2a A G 2: 48,789,714 (GRCm39) T486A probably benign Het
Ap3b1 C A 13: 94,554,607 (GRCm39) L248I probably damaging Het
Atad2b T A 12: 4,990,145 (GRCm39) C157S probably damaging Het
Cage1 T A 13: 38,207,078 (GRCm39) I256F probably damaging Het
Cct2 A G 10: 116,893,714 (GRCm39) I287T possibly damaging Het
Cntn4 A G 6: 106,466,625 (GRCm39) T176A possibly damaging Het
Cracd G A 5: 76,996,763 (GRCm39) V74I probably damaging Het
Cyp2c54 T C 19: 40,060,615 (GRCm39) N122S probably benign Het
Cytip T C 2: 58,023,947 (GRCm39) D291G probably benign Het
Eef1d C T 15: 75,774,769 (GRCm39) V213I probably benign Het
Fnbp4 A G 2: 90,577,102 (GRCm39) T145A possibly damaging Het
Fras1 C A 5: 96,790,479 (GRCm39) T951K probably damaging Het
Gm11937 C T 11: 99,500,901 (GRCm39) V39M probably damaging Het
Hira A G 16: 18,744,470 (GRCm39) I352V probably damaging Het
Homer3 G A 8: 70,742,793 (GRCm39) probably null Het
Lpcat2 T C 8: 93,599,683 (GRCm39) V217A possibly damaging Het
Mroh2a G T 1: 88,182,657 (GRCm39) R1195L possibly damaging Het
Or2a25 G T 6: 42,889,260 (GRCm39) E268* probably null Het
Or4k35 A G 2: 111,100,178 (GRCm39) F178S probably damaging Het
Or51f5 C T 7: 102,424,006 (GRCm39) R92* probably null Het
Pla2g1b T A 5: 115,608,947 (GRCm39) Y47* probably null Het
Rfng A T 11: 120,673,306 (GRCm39) V245E possibly damaging Het
Rpf2 A G 10: 40,112,124 (GRCm39) V104A possibly damaging Het
Rps6kc1 G T 1: 190,532,155 (GRCm39) H616N probably benign Het
Slc66a1 T C 4: 139,033,854 (GRCm39) I22V probably benign Het
Slc9b2 T C 3: 135,042,305 (GRCm39) V528A probably benign Het
Srgap1 T C 10: 121,640,826 (GRCm39) probably null Het
Trrap A G 5: 144,780,128 (GRCm39) T3240A possibly damaging Het
Vmn2r68 TCC TC 7: 84,870,758 (GRCm39) probably null Het
Zfhx4 C A 3: 5,468,405 (GRCm39) Y2854* probably null Het
Zfp986 C T 4: 145,625,513 (GRCm39) R58C probably benign Het
Other mutations in Gm6712
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0315:Gm6712 UTSW 17 17,536,380 (GRCm39) exon noncoding transcript
R6033:Gm6712 UTSW 17 17,514,678 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- ATCTTCAAAGGGATGGACCAAG -3'
(R):5'- ATTCATAGGGTTTCTCTCCAGTATG -3'

Sequencing Primer
(F):5'- CTTCAAAGGGATGGACCAAGTAATAC -3'
(R):5'- GTATTGTGCCATGCAAACGC -3'
Posted On 2017-12-01