Incidental Mutation 'R2394:Gm5108'
ID 247905
Institutional Source Beutler Lab
Gene Symbol Gm5108
Ensembl Gene ENSMUSG00000094719
Gene Name predicted gene 5108
Synonyms
MMRRC Submission 040362-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # R2394 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 68099012-68134413 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 68132475 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000137034 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000177891]
AlphaFold J3QP01
Predicted Effect probably benign
Transcript: ENSMUST00000177891
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: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.0%
Validation Efficiency 100% (41/41)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700020L13Rik A T 7: 29,980,053 (GRCm39) probably benign Het
Abca17 T C 17: 24,500,190 (GRCm39) probably null Het
Atxn7 T C 14: 14,100,237 (GRCm38) V641A probably damaging Het
C3 G A 17: 57,529,303 (GRCm39) Q30* probably null Het
Ccdc162 A G 10: 41,445,894 (GRCm39) I426T probably damaging Het
Col9a2 C G 4: 120,911,455 (GRCm39) R599G probably damaging Het
Cwc27 A C 13: 104,932,942 (GRCm39) D253E probably benign Het
Cyp1a1 T A 9: 57,607,432 (GRCm39) V20D probably benign Het
Dmbt1 T A 7: 130,696,464 (GRCm39) Y892* probably null Het
Dnhd1 T A 7: 105,369,438 (GRCm39) Y4354N probably benign Het
Dync2li1 T A 17: 84,952,175 (GRCm39) I202K possibly damaging Het
Dyrk1a T A 16: 94,485,991 (GRCm39) V446E probably benign Het
Efcab3 C A 11: 104,629,121 (GRCm39) T933K probably benign Het
Fam186b T C 15: 99,178,058 (GRCm39) I423V probably benign Het
Htr3a A G 9: 48,817,643 (GRCm39) V110A probably benign Het
Itsn2 C A 12: 4,757,005 (GRCm39) S1365Y possibly damaging Het
Lrrc46 T C 11: 96,929,657 (GRCm39) I60V probably damaging Het
Mtrex A T 13: 113,019,702 (GRCm39) Y803N probably benign Het
Nlrp14 T C 7: 106,797,031 (GRCm39) V307A probably benign Het
Nt5c2 A G 19: 46,878,506 (GRCm39) probably null Het
Obox2 C T 7: 15,130,935 (GRCm39) P56S possibly damaging Het
Olfml2b A G 1: 170,477,319 (GRCm39) I151M possibly damaging Het
Oog3 T A 4: 143,885,884 (GRCm39) D238V probably benign Het
Pde11a T C 2: 75,889,405 (GRCm39) T690A probably benign Het
Ppa1 A G 10: 61,508,163 (GRCm39) probably benign Het
Ppfia2 A G 10: 106,655,351 (GRCm39) E306G probably damaging Het
Ppic G A 18: 53,544,119 (GRCm39) R89C probably damaging Het
Ptprk T G 10: 28,427,713 (GRCm39) I764S probably damaging Het
Ripk2 T C 4: 16,132,774 (GRCm39) probably benign Het
Rnf123 A G 9: 107,940,735 (GRCm39) M702T probably benign Het
Slco1b2 T C 6: 141,615,100 (GRCm39) I335T probably damaging Het
Ssbp1 T A 6: 40,453,743 (GRCm39) D96E probably benign Het
Tpp2 T A 1: 44,022,346 (GRCm39) S915T possibly damaging Het
Unc5c A T 3: 141,383,892 (GRCm39) Q90L probably damaging Het
Vmn2r57 A G 7: 41,049,619 (GRCm39) I710T possibly damaging Het
Wdr90 G A 17: 26,070,429 (GRCm39) P1104L probably damaging Het
Other mutations in Gm5108
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4233:Gm5108 UTSW 5 68,132,496 (GRCm39) missense unknown
R5185:Gm5108 UTSW 5 68,101,953 (GRCm39) intron probably benign
R5836: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'- AAAAGTGACTCCTGCCCTTG -3'
(R):5'- AATGGCTAACACCTCCTGC -3'

Sequencing Primer
(F):5'- TGCCCTTGGGCAAGATG -3'
(R):5'- AGGTACACTAGCCCTGTAAGGTC -3'
Posted On 2014-11-11