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: 0.097) question?
Stock # IGL01808
Quality Score
Chromosome 6
Chromosomal Location 133529189-133532762 bp(+) (GRCm38)
Type of Mutation exon
DNA Base Change (assembly) A to T at 133531218 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: 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: 34,599,457 Q266L probably damaging Het
Amz1 A G 5: 140,741,279 probably benign Het
Ebf2 C T 14: 67,414,483 A488V probably benign Het
Gnas T C 2: 174,298,697 S220P probably damaging Het
Gpr171 G A 3: 59,098,151 P68S probably damaging Het
H2afx T C 9: 44,334,949 I63T possibly damaging Het
H2-M9 A T 17: 36,641,819 probably null Het
Igsf9 T C 1: 172,484,803 V27A probably benign Het
Kcnh6 G T 11: 106,023,927 probably benign Het
Mapkbp1 A G 2: 120,023,169 probably null Het
Mllt6 C A 11: 97,672,484 H298N possibly damaging Het
Mtmr3 A G 11: 4,497,404 I352T probably damaging Het
Mtrr T C 13: 68,566,093 D509G probably benign Het
Ncan C T 8: 70,107,440 probably null Het
Olfr612 T A 7: 103,538,574 Y220F probably damaging Het
Pcdhb4 T C 18: 37,309,014 V459A probably damaging Het
Phrf1 C A 7: 141,260,966 P1274Q probably damaging Het
Slc4a2 T C 5: 24,440,207 L1125P probably damaging Het
Synpo T C 18: 60,602,208 I650V probably benign Het
Tsc1 G A 2: 28,662,507 R86H probably damaging Het
Ugt2a3 A G 5: 87,325,555 V501A probably benign Het
Vmn1r203 T C 13: 22,524,547 I166T probably benign Het
Vps13a A G 19: 16,710,286 C933R probably damaging Het
Zfp142 A T 1: 74,576,025 F342Y probably damaging Het
Other mutations in Gm5885
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02026:Gm5885 APN 6 133531328 exon noncoding transcript
IGL02364:Gm5885 APN 6 133530129 splice site noncoding transcript
R1613:Gm5885 UTSW 6 133531242 exon noncoding transcript
R2141:Gm5885 UTSW 6 133529275 exon noncoding transcript
R4352:Gm5885 UTSW 6 133531189 exon noncoding transcript
Posted On 2014-02-04