Incidental Mutation 'IGL02689:Anapc15-ps'
ID 303650
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Anapc15-ps
Ensembl Gene ENSMUSG00000074780
Gene Name anaphase promoting complex C subunit 15, pseudogene
Synonyms Gm6843
Accession Numbers
Essential gene? Probably essential (E-score: 0.771) question?
Stock # IGL02689
Quality Score
Status
Chromosome 10
Chromosomal Location 95508853-95509313 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 95508993 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 87 (S87G)
Ref Sequence ENSEMBL: ENSMUSP00000151380 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099328] [ENSMUST00000218771]
AlphaFold A0A140T8L6
Predicted Effect probably benign
Transcript: ENSMUST00000099328
AA Change: S96G

PolyPhen 2 Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000096931
Gene: ENSMUSG00000074780
AA Change: S96G

DomainStartEndE-ValueType
Pfam:ANAPC15 22 113 8.2e-36 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000218771
AA Change: S87G

PolyPhen 2 Score 0.423 (Sensitivity: 0.89; Specificity: 0.90)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acer2 G T 4: 86,835,692 (GRCm39) A235S probably benign Het
Add2 A G 6: 86,084,388 (GRCm39) I479V possibly damaging Het
Anapc11 T A 11: 120,490,168 (GRCm39) M28K probably benign Het
Atraid T C 5: 31,209,826 (GRCm39) L46P probably damaging Het
Ccdc80 T A 16: 44,916,772 (GRCm39) Y509* probably null Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cecr2 T A 6: 120,739,128 (GRCm39) L1257Q probably damaging Het
Csn1s2b A G 5: 87,957,780 (GRCm39) I5V probably benign Het
Dhps T C 8: 85,800,379 (GRCm39) Y221H possibly damaging Het
Dmxl1 T C 18: 49,997,962 (GRCm39) S717P probably damaging Het
Dppa5a G T 9: 78,275,113 (GRCm39) S63Y probably damaging Het
Eif3l A T 15: 78,970,719 (GRCm39) D331V possibly damaging Het
Folh1 G T 7: 86,412,253 (GRCm39) probably null Het
Gbp9 G T 5: 105,253,662 (GRCm39) Q18K probably benign Het
Grm5 A G 7: 87,251,918 (GRCm39) K56R probably damaging Het
H2-M3 T A 17: 37,581,432 (GRCm39) Y31* probably null Het
Herc2 T C 7: 55,815,031 (GRCm39) probably benign Het
Itga7 G T 10: 128,782,687 (GRCm39) A675S possibly damaging Het
Lipo5 G A 19: 33,445,186 (GRCm39) H128Y unknown Het
Or2bd2 T C 7: 6,443,574 (GRCm39) L225P possibly damaging Het
Or5b121 A G 19: 13,507,171 (GRCm39) I89V probably benign Het
Pdk4 C T 6: 5,487,408 (GRCm39) V281I probably benign Het
Pkn3 G A 2: 29,970,858 (GRCm39) G202D probably damaging Het
Rcbtb1 A G 14: 59,462,149 (GRCm39) N260S probably damaging Het
Sipa1l1 T C 12: 82,487,594 (GRCm39) F1623L probably benign Het
Slfn8 A G 11: 82,907,934 (GRCm39) F203S probably damaging Het
St6gal2 T C 17: 55,789,596 (GRCm39) L210S probably damaging Het
Taf5 T C 19: 47,065,704 (GRCm39) probably benign Het
Taok2 A G 7: 126,475,270 (GRCm39) F226S probably damaging Het
Timm10b A G 7: 105,289,839 (GRCm39) probably benign Het
Tmx3 A G 18: 90,555,240 (GRCm39) N319S possibly damaging Het
Trmt1 G T 8: 85,426,385 (GRCm39) probably benign Het
Other mutations in Anapc15-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02692:Anapc15-ps APN 10 95,509,089 (GRCm39) missense probably benign 0.06
R0029:Anapc15-ps UTSW 10 95,508,857 (GRCm39) missense probably damaging 1.00
R0308:Anapc15-ps UTSW 10 95,508,954 (GRCm39) missense probably benign 0.09
R0391:Anapc15-ps UTSW 10 95,509,139 (GRCm39) missense probably damaging 1.00
R0558:Anapc15-ps UTSW 10 95,508,983 (GRCm39) missense probably damaging 1.00
R1843:Anapc15-ps UTSW 10 95,509,176 (GRCm39) missense probably benign 0.28
R6421:Anapc15-ps UTSW 10 95,509,076 (GRCm39) missense probably benign 0.29
R9299:Anapc15-ps UTSW 10 95,509,077 (GRCm39) missense probably damaging 1.00
R9624:Anapc15-ps UTSW 10 95,508,965 (GRCm39) missense probably benign 0.01
Posted On 2015-04-16