Incidental Mutation 'IGL03282:Gm10073'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10073
Ensembl Gene ENSMUSG00000060019
Gene Namepredicted pseudogene 10073
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL03282
Quality Score
Chromosomal Location106572966-106573461 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 106573340 bp
Amino Acid Change Valine to Aspartic acid at position 4 (V4D)
Ref Sequence ENSEMBL: ENSMUSP00000129695 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073722]
Predicted Effect probably benign
Transcript: ENSMUST00000073722
AA Change: V4D

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000129695
Gene: ENSMUSG00000060019
AA Change: V4D

Pfam:Ribosomal_60s 22 113 4.2e-29 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atl1 A G 12: 69,954,464 I333M possibly damaging Het
Atxn2 A G 5: 121,785,235 T52A probably benign Het
Atxn7 T A 14: 14,100,564 L750H probably damaging Het
Cadps T C 14: 12,465,856 probably benign Het
Cts6 T A 13: 61,196,447 I264F possibly damaging Het
Dnah6 G T 6: 73,053,647 probably benign Het
Epg5 A G 18: 77,986,426 S1335G probably benign Het
Gpld1 T A 13: 24,971,408 M342K probably benign Het
Herc1 T A 9: 66,451,459 F2607L probably benign Het
Ighv2-9-1 T C 12: 113,769,865 Y112C probably damaging Het
Itga4 A T 2: 79,325,594 H968L probably damaging Het
Me1 C T 9: 86,613,596 R286Q probably damaging Het
Med1 G A 11: 98,156,817 T1051M probably damaging Het
Msh2 T G 17: 87,689,002 D379E probably benign Het
Mup4 T A 4: 59,958,547 M118L possibly damaging Het
Ostm1 A T 10: 42,698,231 S152C probably damaging Het
Pla2g1b A G 5: 115,470,880 N45D probably damaging Het
Rab21 A G 10: 115,298,898 probably benign Het
Rapgef4 G A 2: 72,205,752 probably benign Het
Slc38a8 G T 8: 119,499,716 N111K probably damaging Het
Snrnp35 A G 5: 124,490,309 T62A probably damaging Het
Strn3 T C 12: 51,627,209 I540V probably benign Het
Tgm1 A G 14: 55,711,070 V208A probably damaging Het
Vmn1r62 A T 7: 5,675,548 D76V possibly damaging Het
Vmn1r90 T A 7: 14,561,501 H224L probably benign Het
Vmn1r90 A T 7: 14,562,168 S2T possibly damaging Het
Other mutations in Gm10073
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01520:Gm10073 APN 8 106573269 missense probably benign 0.13
IGL02433:Gm10073 APN 8 106573319 missense probably benign 0.05
R1664:Gm10073 UTSW 8 106573232 missense probably damaging 1.00
Posted On2016-08-02