Incidental Mutation 'R4343:Gm8674'
ID 324236
Institutional Source Beutler Lab
Gene Symbol Gm8674
Ensembl Gene ENSMUSG00000093976
Gene Name predicted gene 8674
Synonyms
MMRRC Submission 041665-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # R4343 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 50053085-50056359 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 50053742 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: ENSMUST00000179367
SMART Domains Protein: ENSMUSP00000137219
Gene: ENSMUSG00000093976

DomainStartEndE-ValueType
low complexity region 70 86 N/A INTRINSIC
Pfam:FAM75 92 444 3.6e-27 PFAM
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cd38 A C 5: 44,026,431 (GRCm39) I72L probably benign Het
Diras1 T A 10: 80,858,018 (GRCm39) K78* probably null Het
Gm5878 G A 6: 85,102,633 (GRCm39) R31* probably null Het
Gnal T C 18: 67,268,659 (GRCm39) S182P probably benign Het
Grik1 T C 16: 87,693,140 (GRCm39) T932A probably benign Het
Igf2r C T 17: 12,928,398 (GRCm39) E982K possibly damaging Het
Lepr G A 4: 101,622,349 (GRCm39) probably null Het
Mical3 C A 6: 120,911,799 (GRCm39) E1083* probably null Het
Mki67 A G 7: 135,296,847 (GRCm39) V2729A probably benign Het
Mmp20 GA GAA 9: 7,628,346 (GRCm39) probably null Het
Myo7b A G 18: 32,116,680 (GRCm39) F976L probably damaging Het
Nfasc A G 1: 132,559,443 (GRCm39) F229S probably damaging Het
Npc1l1 G A 11: 6,167,773 (GRCm39) T1006I probably benign Het
Or5g9 T A 2: 85,552,592 (GRCm39) V281E probably damaging Het
Plekha5 A G 6: 140,501,780 (GRCm39) E656G probably damaging Het
Prep C A 10: 44,996,866 (GRCm39) S381R probably damaging Het
Rab31 C T 17: 65,961,414 (GRCm39) R192H probably benign Het
Rbm5 T C 9: 107,629,395 (GRCm39) D319G probably damaging Het
Rexo2 T C 9: 48,380,148 (GRCm39) E228G possibly damaging Het
Rrn3 A G 16: 13,601,986 (GRCm39) D80G probably benign Het
Slc38a3 A G 9: 107,533,671 (GRCm39) V224A possibly damaging Het
Slc66a2 A G 18: 80,327,004 (GRCm39) probably benign Het
Sycp2 T C 2: 178,022,740 (GRCm39) T464A probably damaging Het
Tpcn1 A T 5: 120,698,285 (GRCm39) L79H probably damaging Het
Trim30a T C 7: 104,084,799 (GRCm39) Q137R probably benign Het
Tyrp1 A G 4: 80,768,078 (GRCm39) D92G possibly damaging Het
Ugt1a6a T C 1: 88,066,248 (GRCm39) L18P probably damaging Het
Ugt2b5 A T 5: 87,287,582 (GRCm39) V195E probably damaging Het
Zmym2 T A 14: 57,159,019 (GRCm39) M598K probably damaging Het
Other mutations in Gm8674
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0355:Gm8674 UTSW 13 50,055,975 (GRCm39) exon noncoding transcript
R0357:Gm8674 UTSW 13 50,056,149 (GRCm39) exon noncoding transcript
R0627:Gm8674 UTSW 13 50,053,751 (GRCm39) exon noncoding transcript
R0833:Gm8674 UTSW 13 50,058,611 (GRCm39) exon noncoding transcript
R1300:Gm8674 UTSW 13 50,055,758 (GRCm39) exon noncoding transcript
R1452:Gm8674 UTSW 13 50,054,553 (GRCm39) exon noncoding transcript
R1542:Gm8674 UTSW 13 50,054,039 (GRCm39) exon noncoding transcript
R1613:Gm8674 UTSW 13 50,056,474 (GRCm39) intron noncoding transcript
R1643:Gm8674 UTSW 13 50,055,394 (GRCm39) exon noncoding transcript
R1732:Gm8674 UTSW 13 50,055,962 (GRCm39) exon noncoding transcript
R1824:Gm8674 UTSW 13 50,054,844 (GRCm39) exon noncoding transcript
R1840:Gm8674 UTSW 13 50,055,801 (GRCm39) exon noncoding transcript
R1915:Gm8674 UTSW 13 50,054,889 (GRCm39) exon noncoding transcript
R1934:Gm8674 UTSW 13 50,055,471 (GRCm39) exon noncoding transcript
R2040:Gm8674 UTSW 13 50,055,705 (GRCm39) exon noncoding transcript
R2214:Gm8674 UTSW 13 50,055,396 (GRCm39) exon noncoding transcript
R2421:Gm8674 UTSW 13 50,054,699 (GRCm39) exon noncoding transcript
R3423:Gm8674 UTSW 13 50,055,792 (GRCm39) exon noncoding transcript
R3425:Gm8674 UTSW 13 50,055,792 (GRCm39) exon noncoding transcript
R3886:Gm8674 UTSW 13 50,056,199 (GRCm39) splice site noncoding transcript
R4083:Gm8674 UTSW 13 50,055,047 (GRCm39) exon noncoding transcript
R4570:Gm8674 UTSW 13 50,056,570 (GRCm39) intron noncoding transcript
R4936:Gm8674 UTSW 13 50,054,791 (GRCm39) exon noncoding transcript
R4967:Gm8674 UTSW 13 50,056,034 (GRCm39) exon noncoding transcript
R5065:Gm8674 UTSW 13 50,056,613 (GRCm39) intron noncoding transcript
R5067:Gm8674 UTSW 13 50,053,870 (GRCm39) exon noncoding transcript
R5120:Gm8674 UTSW 13 50,055,984 (GRCm39) exon noncoding transcript
R5208:Gm8674 UTSW 13 50,055,957 (GRCm39) exon noncoding transcript
R5268:Gm8674 UTSW 13 50,055,390 (GRCm39) exon noncoding transcript
R5471:Gm8674 UTSW 13 50,054,849 (GRCm39) exon noncoding transcript
R5773:Gm8674 UTSW 13 50,055,912 (GRCm39) exon noncoding transcript
R5809:Gm8674 UTSW 13 50,055,924 (GRCm39) exon noncoding transcript
R8162:Gm8674 UTSW 13 50,054,407 (GRCm39) missense noncoding transcript
R8239:Gm8674 UTSW 13 50,054,262 (GRCm39) missense noncoding transcript
Z1088:Gm8674 UTSW 13 50,055,284 (GRCm39) exon noncoding transcript
Z1088:Gm8674 UTSW 13 50,054,830 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- GAATTTCTTTCCCCGTGGGC -3'
(R):5'- TGCTGAGCATACAAAGAAAGTCC -3'

Sequencing Primer
(F):5'- CATGTGGAGCTGGTCAAAGCAC -3'
(R):5'- GCATACAAAGAAAGTCCCAACAAGG -3'
Posted On 2015-06-24