Incidental Mutation 'IGL03282:Gm10073'
ID 415631
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10073
Ensembl Gene ENSMUSG00000060019
Gene Name predicted pseudogene 10073
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL03282
Quality Score
Status
Chromosome 8
Chromosomal Location 107299641-107299982 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 107299972 bp (GRCm39)
Zygosity Heterozygous
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]
AlphaFold no structure available at present
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

DomainStartEndE-ValueType
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: 70,001,238 (GRCm39) I333M possibly damaging Het
Atxn2 A G 5: 121,923,298 (GRCm39) T52A probably benign Het
Atxn7 T A 14: 14,100,564 (GRCm38) L750H probably damaging Het
Cadps T C 14: 12,465,856 (GRCm38) probably benign Het
Cts6 T A 13: 61,344,261 (GRCm39) I264F possibly damaging Het
Dnah6 G T 6: 73,030,630 (GRCm39) probably benign Het
Epg5 A G 18: 78,029,641 (GRCm39) S1335G probably benign Het
Gpld1 T A 13: 25,155,391 (GRCm39) M342K probably benign Het
Herc1 T A 9: 66,358,741 (GRCm39) F2607L probably benign Het
Ighv2-9-1 T C 12: 113,733,485 (GRCm39) Y112C probably damaging Het
Itga4 A T 2: 79,155,938 (GRCm39) H968L probably damaging Het
Me1 C T 9: 86,495,649 (GRCm39) R286Q probably damaging Het
Med1 G A 11: 98,047,643 (GRCm39) T1051M probably damaging Het
Msh2 T G 17: 87,996,430 (GRCm39) D379E probably benign Het
Mup4 T A 4: 59,958,547 (GRCm39) M118L possibly damaging Het
Ostm1 A T 10: 42,574,227 (GRCm39) S152C probably damaging Het
Pla2g1b A G 5: 115,608,939 (GRCm39) N45D probably damaging Het
Rab21 A G 10: 115,134,803 (GRCm39) probably benign Het
Rapgef4 G A 2: 72,036,096 (GRCm39) probably benign Het
Slc38a8 G T 8: 120,226,455 (GRCm39) N111K probably damaging Het
Snrnp35 A G 5: 124,628,372 (GRCm39) T62A probably damaging Het
Strn3 T C 12: 51,673,992 (GRCm39) I540V probably benign Het
Tgm1 A G 14: 55,948,527 (GRCm39) V208A probably damaging Het
Vmn1r62 A T 7: 5,678,547 (GRCm39) D76V possibly damaging Het
Vmn1r90 T A 7: 14,295,426 (GRCm39) H224L probably benign Het
Vmn1r90 A T 7: 14,296,093 (GRCm39) S2T possibly damaging Het
Other mutations in Gm10073
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01520:Gm10073 APN 8 107,299,901 (GRCm39) missense probably benign 0.13
IGL02433:Gm10073 APN 8 107,299,951 (GRCm39) missense probably benign 0.05
R1664:Gm10073 UTSW 8 107,299,864 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02