Incidental Mutation 'R5836:Gm5108'
ID 449583
Institutional Source Beutler Lab
Gene Symbol Gm5108
Ensembl Gene ENSMUSG00000094719
Gene Name predicted gene 5108
Synonyms
MMRRC Submission 043222-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # R5836 (G1)
Quality Score 225
Status Not validated
Chromosome 5
Chromosomal Location 68099012-68134413 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to G at 68101953 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000136067 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000177616] [ENSMUST00000177891]
AlphaFold J3QP01
Predicted Effect probably benign
Transcript: ENSMUST00000177616
Predicted Effect unknown
Transcript: ENSMUST00000177891
AA Change: T30A
Predicted Effect noncoding transcript
Transcript: ENSMUST00000201190
Predicted Effect noncoding transcript
Transcript: ENSMUST00000201736
Predicted Effect noncoding transcript
Transcript: ENSMUST00000201798
Predicted Effect noncoding transcript
Transcript: ENSMUST00000202730
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 G T 17: 36,272,918 (GRCm39) A243D possibly damaging Het
Azin2 C T 4: 128,842,670 (GRCm39) G128D probably damaging Het
Babam1 A G 8: 71,855,687 (GRCm39) E260G probably benign Het
Brwd1 A T 16: 95,865,958 (GRCm39) S275T probably damaging Het
Cd8a T C 6: 71,350,775 (GRCm39) V80A possibly damaging Het
Clec4a3 T C 6: 122,929,861 (GRCm39) F12S possibly damaging Het
Dennd2b A T 7: 109,140,552 (GRCm39) S225T possibly damaging Het
Dnah5 A C 15: 28,383,738 (GRCm39) N2987H probably damaging Het
Dock9 A G 14: 121,918,763 (GRCm39) F78S probably damaging Het
Eml3 A G 19: 8,918,659 (GRCm39) T885A possibly damaging Het
Esr1 T C 10: 4,662,817 (GRCm39) V145A probably benign Het
Gpr179 T C 11: 97,229,882 (GRCm39) S758G probably benign Het
Heatr1 T A 13: 12,423,617 (GRCm39) L538Q probably damaging Het
Ikzf2 A G 1: 69,578,546 (GRCm39) I176T probably damaging Het
Lrp3 A G 7: 34,902,747 (GRCm39) V533A probably damaging Het
Nkx2-5 A T 17: 27,058,063 (GRCm39) V297E possibly damaging Het
Or13a19 G A 7: 139,902,827 (GRCm39) V72I probably benign Het
Or2y16 T C 11: 49,335,353 (GRCm39) L225P probably damaging Het
Or8g23 T C 9: 38,971,918 (GRCm39) T15A probably benign Het
Pclo T A 5: 14,728,549 (GRCm39) probably benign Het
Pdgfra T C 5: 75,324,435 (GRCm39) W97R possibly damaging Het
Plekha5 T C 6: 140,372,250 (GRCm39) Y67H probably damaging Het
Plin5 A T 17: 56,422,549 (GRCm39) probably null Het
Pramel11 A G 4: 143,623,490 (GRCm39) V228A probably benign Het
Prickle1 T A 15: 93,400,898 (GRCm39) K529* probably null Het
Ptbp2 G A 3: 119,519,746 (GRCm39) T107I probably damaging Het
Ptpn12 C T 5: 21,214,544 (GRCm39) W197* probably null Het
Rhobtb1 T C 10: 69,105,819 (GRCm39) V128A probably damaging Het
Ryr2 T C 13: 11,618,618 (GRCm39) T3866A probably damaging Het
Serpina3m T C 12: 104,355,509 (GRCm39) Y59H probably damaging Het
Slc12a6 T C 2: 112,172,343 (GRCm39) V414A possibly damaging Het
Slc34a1 T C 13: 55,561,278 (GRCm39) M581T probably benign Het
Slco1c1 A G 6: 141,515,040 (GRCm39) Y596C probably damaging Het
Stoml1 T C 9: 58,168,123 (GRCm39) L278P probably benign Het
Tecpr2 C T 12: 110,897,945 (GRCm39) A399V possibly damaging Het
Tmem229a T C 6: 24,955,016 (GRCm39) E246G probably damaging Het
Vmn1r224 A T 17: 20,639,953 (GRCm39) I177L probably benign Het
Zswim5 C T 4: 116,842,000 (GRCm39) T860I probably benign Het
Other mutations in Gm5108
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2394:Gm5108 UTSW 5 68,132,475 (GRCm39) splice site probably benign
R4233:Gm5108 UTSW 5 68,132,496 (GRCm39) missense unknown
R5185:Gm5108 UTSW 5 68,101,953 (GRCm39) intron probably benign
R5927:Gm5108 UTSW 5 68,134,214 (GRCm39) missense unknown
R6994:Gm5108 UTSW 5 68,102,012 (GRCm39) intron probably benign
R8919:Gm5108 UTSW 5 68,134,299 (GRCm39) makesense probably null
Predicted Primers PCR Primer
(F):5'- GCACAGACCTTGCTGATTGC -3'
(R):5'- TGGTGATGGATTCAGGAAGCTAATG -3'

Sequencing Primer
(F):5'- TTGGGAATAAGGCTAGAGGT -3'
(R):5'- GCTATTTATCACTGAAGTGC -3'
Posted On 2016-12-20