Incidental Mutation 'R3277:Gm7104'
ID 258282
Institutional Source Beutler Lab
Gene Symbol Gm7104
Ensembl Gene ENSMUSG00000094635
Gene Name predicted gene 7104
Accession Numbers
Essential gene? Possibly essential (E-score: 0.682) question?
Stock # R3277 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 88284535-88286055 bp(-) (GRCm38)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 88285728 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179741
SMART Domains Protein: ENSMUSP00000136935
Gene: ENSMUSG00000094635

Pfam:EloA-BP1 80 248 1.6e-64 PFAM
EXOIII 345 504 5.07e-38 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223359
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921509C19Rik T C 2: 151,472,100 (GRCm38) R553G possibly damaging Het
Adarb2 A G 13: 8,752,627 (GRCm38) N646S probably damaging Het
Adcy8 C T 15: 64,699,159 (GRCm38) G1242S probably benign Het
Ano9 T A 7: 141,104,124 (GRCm38) T543S probably damaging Het
Btnl10 A G 11: 58,922,390 (GRCm38) K282E probably benign Het
Btnl9 T C 11: 49,169,676 (GRCm38) D330G probably damaging Het
Ccdc178 G T 18: 22,067,652 (GRCm38) A416E possibly damaging Het
Cdx2 A T 5: 147,303,192 (GRCm38) S225T probably benign Het
Clca4b T C 3: 144,911,359 (GRCm38) I843M probably benign Het
Cntn4 G A 6: 106,437,964 (GRCm38) probably null Het
Cyp4f18 T C 8: 71,993,200 (GRCm38) D317G possibly damaging Het
Dennd4a G T 9: 64,888,993 (GRCm38) R767L probably damaging Het
Dgkb G A 12: 38,084,217 (GRCm38) V41M probably damaging Het
Duox1 T C 2: 122,340,116 (GRCm38) Y1206H probably damaging Het
Dync1i1 T C 6: 5,972,211 (GRCm38) probably null Het
Fbxw2 T C 2: 34,822,750 (GRCm38) T100A probably benign Het
Fcgbp C A 7: 28,091,661 (GRCm38) H782Q probably damaging Het
Flg2 A T 3: 93,214,888 (GRCm38) Q1455L unknown Het
Frrs1 T C 3: 116,899,224 (GRCm38) F49S probably damaging Het
Gli3 A T 13: 15,725,982 (GRCm38) Q1318L probably benign Het
Gm5592 A G 7: 41,288,380 (GRCm38) E362G probably benign Het
Gpatch2l A G 12: 86,244,315 (GRCm38) T91A possibly damaging Het
Hacd4 T C 4: 88,437,510 (GRCm38) H46R probably damaging Het
Herc2 T C 7: 56,153,428 (GRCm38) V2175A probably benign Het
Hey1 T C 3: 8,664,891 (GRCm38) S169G probably benign Het
Hivep2 C A 10: 14,128,969 (GRCm38) T437K probably benign Het
Hlf T C 11: 90,345,835 (GRCm38) K199E probably damaging Het
Hpgd C A 8: 56,298,413 (GRCm38) A92E probably damaging Het
Hsp90aa1 T A 12: 110,695,680 (GRCm38) M1L possibly damaging Het
Hsp90aa1 C A 12: 110,695,681 (GRCm38) probably null Het
Itgad C A 7: 128,190,981 (GRCm38) H651N possibly damaging Het
Itgav A G 2: 83,776,542 (GRCm38) D409G probably damaging Het
Kif2a A G 13: 106,976,756 (GRCm38) I455T probably damaging Het
Klk14 G A 7: 43,692,077 (GRCm38) C51Y probably damaging Het
Lamc3 G T 2: 31,908,625 (GRCm38) G448C probably damaging Het
Ltbp1 T A 17: 75,359,278 (GRCm38) probably null Het
Ltbp1 G A 17: 75,276,480 (GRCm38) G425D possibly damaging Het
Mag C T 7: 30,901,648 (GRCm38) probably null Het
Mdh1b G A 1: 63,711,531 (GRCm38) T426M possibly damaging Het
Nr1h4 G A 10: 89,478,788 (GRCm38) T282I possibly damaging Het
Nsf C T 11: 103,930,752 (GRCm38) E26K possibly damaging Het
Or4c1 C T 2: 89,303,218 (GRCm38) V125M possibly damaging Het
Or52k2 T C 7: 102,604,576 (GRCm38) V74A possibly damaging Het
Or9s27 A G 1: 92,588,813 (GRCm38) N161S probably benign Het
Padi6 A G 4: 140,735,389 (GRCm38) L307P probably damaging Het
Parp9 T C 16: 35,948,208 (GRCm38) S20P probably damaging Het
Pdcd11 T C 19: 47,113,264 (GRCm38) F963L probably damaging Het
Pwp1 C T 10: 85,882,079 (GRCm38) L294F probably benign Het
Radil A G 5: 142,506,856 (GRCm38) L339P probably damaging Het
Raver1 G A 9: 21,079,277 (GRCm38) P316S possibly damaging Het
Rell1 A G 5: 63,926,987 (GRCm38) probably null Het
Rxrg A G 1: 167,635,700 (GRCm38) D257G possibly damaging Het
Sema4c C T 1: 36,549,879 (GRCm38) R722H possibly damaging Het
Sgk1 C T 10: 21,996,601 (GRCm38) R171W probably damaging Het
Spata7 A G 12: 98,637,598 (GRCm38) N75D possibly damaging Het
Ttc23l A G 15: 10,547,232 (GRCm38) F99L possibly damaging Het
Unc13a A C 8: 71,629,695 (GRCm38) C1642G probably benign Het
Usp36 C T 11: 118,276,759 (GRCm38) probably null Het
Wrn A G 8: 33,317,554 (GRCm38) M292T probably damaging Het
Zfp423 A G 8: 87,782,331 (GRCm38) Y462H probably damaging Het
Zscan5b T A 7: 6,231,346 (GRCm38) Y124N possibly damaging Het
Zswim9 T C 7: 13,277,270 (GRCm38) T51A possibly damaging Het
Other mutations in Gm7104
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0630:Gm7104 UTSW 12 88,285,709 (GRCm38) unclassified noncoding transcript
R1485:Gm7104 UTSW 12 88,285,563 (GRCm38) unclassified noncoding transcript
R2044:Gm7104 UTSW 12 88,285,781 (GRCm38) unclassified noncoding transcript
R2567:Gm7104 UTSW 12 88,285,472 (GRCm38) unclassified noncoding transcript
R3177:Gm7104 UTSW 12 88,285,728 (GRCm38) unclassified noncoding transcript
R3778:Gm7104 UTSW 12 88,285,671 (GRCm38) unclassified noncoding transcript
R3910:Gm7104 UTSW 12 88,284,594 (GRCm38) unclassified noncoding transcript
R3946:Gm7104 UTSW 12 88,286,042 (GRCm38) unclassified noncoding transcript
R4754:Gm7104 UTSW 12 88,285,995 (GRCm38) unclassified noncoding transcript
R5022:Gm7104 UTSW 12 88,285,759 (GRCm38) unclassified noncoding transcript
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2015-01-23