Incidental Mutation 'R5334:Anapc15'
ID 423410
Institutional Source Beutler Lab
Gene Symbol Anapc15
Ensembl Gene ENSMUSG00000030649
Gene Name anaphase promoting complex C subunit 15
Synonyms 6330414C15Rik, 3200002M19Rik
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5334 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 101530508-101551056 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 101547810 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Leucine at position 68 (P68L)
Ref Sequence ENSEMBL: ENSMUSP00000095839 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035395] [ENSMUST00000098237] [ENSMUST00000106969] [ENSMUST00000106970] [ENSMUST00000106973] [ENSMUST00000178851] [ENSMUST00000106978] [ENSMUST00000143835] [ENSMUST00000144207] [ENSMUST00000210984] [ENSMUST00000209334]
AlphaFold P60007
Predicted Effect noncoding transcript
Transcript: ENSMUST00000032884
Predicted Effect probably damaging
Transcript: ENSMUST00000035395
AA Change: P77L

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000040286
Gene: ENSMUSG00000030649
AA Change: P77L

DomainStartEndE-ValueType
Pfam:ANAPC15 21 115 9.5e-44 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000098237
AA Change: P68L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000095839
Gene: ENSMUSG00000030649
AA Change: P68L

DomainStartEndE-ValueType
Pfam:ANAPC15 13 104 6.5e-43 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000106969
SMART Domains Protein: ENSMUSP00000102582
Gene: ENSMUSG00000078630

DomainStartEndE-ValueType
Pfam:Methyltransf_3 64 226 1.2e-16 PFAM
Pfam:Methyltransf_24 103 212 5.5e-13 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000106970
SMART Domains Protein: ENSMUSP00000102583
Gene: ENSMUSG00000078630

DomainStartEndE-ValueType
Pfam:Methyltransf_3 65 223 9.1e-19 PFAM
Pfam:Methyltransf_24 103 212 4.5e-13 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000106973
AA Change: P57L

PolyPhen 2 Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000102586
Gene: ENSMUSG00000030649
AA Change: P57L

DomainStartEndE-ValueType
Pfam:ANAPC15 1 95 2.8e-47 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000178851
AA Change: P68L

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000136164
Gene: ENSMUSG00000030649
AA Change: P68L

DomainStartEndE-ValueType
Pfam:ANAPC15 12 106 3.7e-47 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000106978
AA Change: P68L

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000102591
Gene: ENSMUSG00000030649
AA Change: P68L

DomainStartEndE-ValueType
Pfam:ANAPC15 12 106 3.7e-47 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000143835
AA Change: P68L

PolyPhen 2 Score 0.851 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000120373
Gene: ENSMUSG00000030649
AA Change: P68L

DomainStartEndE-ValueType
Pfam:ANAPC15 12 106 6.8e-47 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000144207
AA Change: P68L

PolyPhen 2 Score 0.673 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000114771
Gene: ENSMUSG00000030649
AA Change: P68L

DomainStartEndE-ValueType
Pfam:ANAPC15 12 106 3.7e-47 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000210984
AA Change: P68L

PolyPhen 2 Score 0.851 (Sensitivity: 0.83; Specificity: 0.93)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146286
Predicted Effect noncoding transcript
Transcript: ENSMUST00000131269
Predicted Effect probably benign
Transcript: ENSMUST00000209334
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150018
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129641
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137949
Meta Mutation Damage Score 0.0693 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap4s1 C T 12: 51,785,454 (GRCm39) S142L probably benign Het
Apol11a A G 15: 77,400,953 (GRCm39) T147A probably benign Het
Aqp9 T C 9: 71,030,292 (GRCm39) probably null Het
Arhgap25 T A 6: 87,440,243 (GRCm39) N468I possibly damaging Het
Arhgef2 T A 3: 88,553,636 (GRCm39) S924R probably damaging Het
Atad3a A T 4: 155,840,146 (GRCm39) L144Q probably damaging Het
Ccbe1 T C 18: 66,216,316 (GRCm39) I136V probably damaging Het
Col24a1 C A 3: 145,167,280 (GRCm39) P1119Q possibly damaging Het
Dgkd T C 1: 87,865,989 (GRCm39) probably null Het
Dnah7a A G 1: 53,542,805 (GRCm39) I2455T probably benign Het
Dock2 T C 11: 34,178,643 (GRCm39) T1795A probably benign Het
Dpp6 A T 5: 27,914,538 (GRCm39) E541V probably benign Het
Edem1 T C 6: 108,825,793 (GRCm39) probably null Het
Fbxo41 A G 6: 85,455,465 (GRCm39) V573A probably damaging Het
Fech A C 18: 64,597,191 (GRCm39) V256G probably damaging Het
Gad1-ps G A 10: 99,281,009 (GRCm39) noncoding transcript Het
Gal3st4 T G 5: 138,263,983 (GRCm39) K339Q probably benign Het
Gpr158 T A 2: 21,832,316 (GRCm39) S1139T probably benign Het
Gpr180 A T 14: 118,397,468 (GRCm39) S321C probably damaging Het
Grik1 CGG CGGG 16: 87,720,082 (GRCm39) probably null Het
Grin2c T G 11: 115,146,881 (GRCm39) N438T possibly damaging Het
Hcn2 T C 10: 79,562,125 (GRCm39) S374P probably damaging Het
Hmcn1 T A 1: 150,631,123 (GRCm39) I892F probably damaging Het
Ifi207 C T 1: 173,555,097 (GRCm39) V869I probably benign Het
Itgad T C 7: 127,788,458 (GRCm39) Y390H probably damaging Het
Itgb4 C T 11: 115,874,983 (GRCm39) R447W probably benign Het
Kcnj15 A G 16: 95,097,508 (GRCm39) K377E probably damaging Het
Kcnq3 A G 15: 65,897,073 (GRCm39) S276P probably damaging Het
Klhl26 T C 8: 70,904,968 (GRCm39) D280G probably damaging Het
Lmnb2 C T 10: 80,739,791 (GRCm39) V376I probably benign Het
Lrrc37 T C 11: 103,504,699 (GRCm39) Q2423R probably benign Het
Mepce T A 5: 137,784,889 (GRCm39) R29S probably benign Het
Mlh3 A G 12: 85,292,535 (GRCm39) probably null Het
Mlip T A 9: 77,150,958 (GRCm39) T33S probably damaging Het
Msantd5f6 T A 4: 73,321,754 (GRCm39) M94L probably benign Het
Mtpn C T 6: 35,489,225 (GRCm39) D100N probably benign Het
Ncapg2 T C 12: 116,390,257 (GRCm39) I402T probably damaging Het
Or2aj6 C G 16: 19,443,241 (GRCm39) G203A probably benign Het
Or5m13b T C 2: 85,754,058 (GRCm39) Y149H probably damaging Het
Pcsk5 T C 19: 17,439,215 (GRCm39) D1301G probably benign Het
Pilrb1 T C 5: 137,853,165 (GRCm39) M213V probably benign Het
Plxdc1 T C 11: 97,846,931 (GRCm39) T163A possibly damaging Het
Pnpla2 T C 7: 141,039,406 (GRCm39) L373P probably damaging Het
Prickle2 A G 6: 92,402,665 (GRCm39) Y52H probably damaging Het
Rnf220 A G 4: 117,129,548 (GRCm39) C294R probably damaging Het
Slc12a1 A G 2: 125,059,809 (GRCm39) D903G probably damaging Het
Slc34a1 T C 13: 24,003,034 (GRCm39) F228S probably damaging Het
Sptbn1 T C 11: 30,087,364 (GRCm39) E1025G possibly damaging Het
Sult1c2 T G 17: 54,271,758 (GRCm39) D143A probably damaging Het
Taar1 T G 10: 23,796,443 (GRCm39) I47R probably damaging Het
Tctn3 G T 19: 40,591,266 (GRCm39) Q514K probably benign Het
Tg T C 15: 66,549,904 (GRCm39) F222S probably damaging Het
Tmem236 C A 2: 14,223,871 (GRCm39) T220K possibly damaging Het
Trim50 C T 5: 135,396,330 (GRCm39) T426M probably damaging Het
Vmn1r237 T C 17: 21,534,942 (GRCm39) F222L probably benign Het
Wrap73 G A 4: 154,229,731 (GRCm39) R34Q probably damaging Het
Zfp85 T C 13: 67,899,803 (GRCm39) Y52C probably damaging Het
Other mutations in Anapc15
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0426:Anapc15 UTSW 7 101,547,240 (GRCm39) missense probably benign 0.10
R0513:Anapc15 UTSW 7 101,547,747 (GRCm39) splice site probably benign
R4625:Anapc15 UTSW 7 101,550,239 (GRCm39) unclassified probably benign
R4846:Anapc15 UTSW 7 101,546,974 (GRCm39) missense probably benign 0.05
R5318:Anapc15 UTSW 7 101,547,810 (GRCm39) missense probably damaging 1.00
R5337:Anapc15 UTSW 7 101,547,810 (GRCm39) missense probably damaging 1.00
R5396:Anapc15 UTSW 7 101,547,810 (GRCm39) missense probably damaging 1.00
R5398:Anapc15 UTSW 7 101,547,810 (GRCm39) missense probably damaging 1.00
R5399:Anapc15 UTSW 7 101,547,810 (GRCm39) missense probably damaging 1.00
R5427:Anapc15 UTSW 7 101,547,810 (GRCm39) missense probably damaging 1.00
R7719:Anapc15 UTSW 7 101,550,236 (GRCm39) missense unknown
R7903:Anapc15 UTSW 7 101,547,193 (GRCm39) missense probably benign 0.07
Z1177:Anapc15 UTSW 7 101,550,246 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TGCATCTTCCTGAGAACTGG -3'
(R):5'- AACCTTGCCTGCCTTGAGTC -3'

Sequencing Primer
(F):5'- GGGGGAGAAGCTTTGTTTCAAC -3'
(R):5'- TGCTGCATGACCTGAAGG -3'
Posted On 2016-08-04