Incidental Mutation 'IGL01808:Gm5885'
ID 155727
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5885
Ensembl Gene ENSMUSG00000095412
Gene Name predicted gene 5885
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # IGL01808
Quality Score
Chromosome 6
Chromosomal Location 133506185-133508453 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 133508181 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: ENSMUST00000178578
SMART Domains Protein: ENSMUSP00000136262
Gene: ENSMUSG00000095412

Pfam:Pro-rich 1 166 2.5e-13 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203357
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ager A T 17: 34,818,431 (GRCm39) Q266L probably damaging Het
Amz1 A G 5: 140,727,034 (GRCm39) probably benign Het
Ebf2 C T 14: 67,651,932 (GRCm39) A488V probably benign Het
Gnas T C 2: 174,140,490 (GRCm39) S220P probably damaging Het
Gpr171 G A 3: 59,005,572 (GRCm39) P68S probably damaging Het
H2ax T C 9: 44,246,246 (GRCm39) I63T possibly damaging Het
H2-M9 A T 17: 36,952,711 (GRCm39) probably null Het
Igsf9 T C 1: 172,312,370 (GRCm39) V27A probably benign Het
Kcnh6 G T 11: 105,914,753 (GRCm39) probably benign Het
Mapkbp1 A G 2: 119,853,650 (GRCm39) probably null Het
Mllt6 C A 11: 97,563,310 (GRCm39) H298N possibly damaging Het
Mtmr3 A G 11: 4,447,404 (GRCm39) I352T probably damaging Het
Mtrr T C 13: 68,714,212 (GRCm39) D509G probably benign Het
Ncan C T 8: 70,560,090 (GRCm39) probably null Het
Or51aa2 T A 7: 103,187,781 (GRCm39) Y220F probably damaging Het
Pcdhb4 T C 18: 37,442,067 (GRCm39) V459A probably damaging Het
Phrf1 C A 7: 140,840,879 (GRCm39) P1274Q probably damaging Het
Slc4a2 T C 5: 24,645,205 (GRCm39) L1125P probably damaging Het
Synpo T C 18: 60,735,280 (GRCm39) I650V probably benign Het
Tsc1 G A 2: 28,552,519 (GRCm39) R86H probably damaging Het
Ugt2a3 A G 5: 87,473,414 (GRCm39) V501A probably benign Het
Vmn1r203 T C 13: 22,708,717 (GRCm39) I166T probably benign Het
Vps13a A G 19: 16,687,650 (GRCm39) C933R probably damaging Het
Zfp142 A T 1: 74,615,184 (GRCm39) F342Y probably damaging Het
Other mutations in Gm5885
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02026:Gm5885 APN 6 133,508,291 (GRCm39) exon noncoding transcript
IGL02364:Gm5885 APN 6 133,507,092 (GRCm39) splice site noncoding transcript
R1613:Gm5885 UTSW 6 133,508,205 (GRCm39) exon noncoding transcript
R2141:Gm5885 UTSW 6 133,506,238 (GRCm39) exon noncoding transcript
R4352:Gm5885 UTSW 6 133,508,152 (GRCm39) exon noncoding transcript
Posted On 2014-02-04