Mutagenetix > Incidental Mutation

Incidental Mutation 'R5568:Anapc5'

457953

Institutional Source

Beutler Lab

Gene Symbol

Anapc5

Ensembl Gene

ENSMUSG00000029472

Gene Name

anaphase-promoting complex subunit 5

Synonyms

2510006G12Rik

MMRRC Submission

043125-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.951) question?

Stock #

R5568 (G1)

Quality Score

199

Status

Not validated

Chromosome

Chromosomal Location

122925522-122959402 bp(-) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

G to A at 122929988 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000143169 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000086216] [ENSMUST00000196423] [ENSMUST00000196640] [ENSMUST00000197074] [ENSMUST00000197719] [ENSMUST00000199406] [ENSMUST00000200645]

AlphaFold

Q8BTZ4

Predicted Effect

silent
Transcript: ENSMUST00000086216

SMART Domains

Protein: ENSMUSP00000083393
Gene: ENSMUSG00000029472

Domain	Start	End	E-Value	Type
low complexity region	48	57	N/A	INTRINSIC
Pfam:ANAPC5	239	339	3.5e-34	PFAM
Pfam:ANAPC5	383	478	3.1e-3	PFAM
Blast:TPR	526	559	8e-12	BLAST
Blast:TPR	566	599	5e-9	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000196423

SMART Domains

Protein: ENSMUSP00000143169
Gene: ENSMUSG00000029472

Domain	Start	End	E-Value	Type
low complexity region	48	57	N/A	INTRINSIC
Pfam:Apc5	239	339	1.9e-31	PFAM

Predicted Effect

silent
Transcript: ENSMUST00000196640

SMART Domains

Protein: ENSMUSP00000142429
Gene: ENSMUSG00000029472

Domain	Start	End	E-Value	Type
low complexity region	48	57	N/A	INTRINSIC
Pfam:Apc5	239	339	4.8e-31	PFAM
Pfam:Apc5	383	478	5.1e0	PFAM
Blast:TPR	526	559	7e-12	BLAST
Blast:TPR	566	599	5e-9	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196753

Predicted Effect

silent
Transcript: ENSMUST00000197074

SMART Domains

Protein: ENSMUSP00000143053
Gene: ENSMUSG00000029472

Domain	Start	End	E-Value	Type
low complexity region	48	57	N/A	INTRINSIC
Pfam:Apc5	239	339	3.9e-34	PFAM
Pfam:Apc5	375	470	4.1e-3	PFAM
Blast:TPR	518	551	7e-12	BLAST
Blast:TPR	558	591	5e-9	BLAST

Predicted Effect

silent
Transcript: ENSMUST00000197719

SMART Domains

Protein: ENSMUSP00000142579
Gene: ENSMUSG00000029472

Domain	Start	End	E-Value	Type
low complexity region	48	57	N/A	INTRINSIC
Pfam:Apc5	239	339	4.7e-31	PFAM
Pfam:Apc5	370	465	5e0	PFAM
Blast:TPR	513	546	7e-12	BLAST
Blast:TPR	553	586	5e-9	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000199025

Predicted Effect

unknown
Transcript: ENSMUST00000199191
AA Change: R25C

Predicted Effect

silent
Transcript: ENSMUST00000199406

SMART Domains

Protein: ENSMUSP00000142341
Gene: ENSMUSG00000029472

Domain	Start	End	E-Value	Type
low complexity region	48	57	N/A	INTRINSIC
Pfam:Apc5	239	339	4.1e-31	PFAM
Pfam:TPR_10	287	322	2.7e-1	PFAM
Pfam:Apc5	383	478	4.4e0	PFAM
Pfam:TPR_10	533	577	2e-1	PFAM

Predicted Effect

silent
Transcript: ENSMUST00000199130

Predicted Effect

silent
Transcript: ENSMUST00000200645

SMART Domains

Protein: ENSMUSP00000142922
Gene: ENSMUSG00000029472

Domain	Start	End	E-Value	Type
low complexity region	48	57	N/A	INTRINSIC
Pfam:Apc5	239	339	3.9e-34	PFAM
Pfam:Apc5	370	465	4.1e-3	PFAM
Blast:TPR	513	546	7e-12	BLAST
Blast:TPR	553	586	5e-9	BLAST

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.3%
20x: 95.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a tetratricopeptide repeat-containing component of the anaphase promoting complex/cyclosome (APC/C), a large E3 ubiquitin ligase that controls cell cycle progression by targeting a number of cell cycle regulators such as B-type cyclins for 26S proteasome-mediated degradation through ubiquitination. The encoded protein is required for the proper ubiquitination function of APC/C and for the interaction of APC/C with transcription coactivators. It also interacts with polyA binding protein and represses internal ribosome entry site-mediated translation. Multiple transcript variants encoding different isoforms have been found for this gene. These differences cause translation initiation at a downstream AUG and result in a shorter protein (isoform b), compared to isoform a. [provided by RefSeq, Nov 2008]

Allele List at MGI

Other mutations in this stock

Total: 96 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4	T	C	4: 144,349,364 (GRCm39)	V207A	probably benign	Het
Abcc10	C	A	17: 46,614,834 (GRCm39)		probably null	Het
Abcc9	A	C	6: 142,634,742 (GRCm39)	V174G	possibly damaging	Het
Abl1	C	T	2: 31,669,086 (GRCm39)	A155V	probably damaging	Het
Aco2	T	A	15: 81,787,787 (GRCm39)	D212E	probably damaging	Het
Adam26b	A	T	8: 43,973,529 (GRCm39)	M491K	probably benign	Het
Atf7	A	G	15: 102,471,757 (GRCm39)	I46T	probably damaging	Het
Cacna1b	A	G	2: 24,497,612 (GRCm39)	S2100P	probably damaging	Het
Capn5	T	A	7: 97,775,137 (GRCm39)	D501V	probably damaging	Het
Cc2d2a	A	G	5: 43,866,433 (GRCm39)	M748V	probably damaging	Het
Cd300c2	T	C	11: 114,891,662 (GRCm39)	T71A	probably damaging	Het
Chmp2a	T	C	7: 12,767,758 (GRCm39)	M56V	probably benign	Het
Cilp	A	C	9: 65,187,515 (GRCm39)	R1203S	probably benign	Het
Clp1	T	A	2: 84,556,322 (GRCm39)	K53*	probably null	Het
Crhbp	T	A	13: 95,578,737 (GRCm39)	D128V	probably damaging	Het
Crispld1	T	A	1: 17,820,495 (GRCm39)	I292N	probably benign	Het
Cyp2c68	A	T	19: 39,677,526 (GRCm39)	I488N	probably benign	Het
Cyp3a57	A	T	5: 145,307,456 (GRCm39)	M149L	probably benign	Het
Ddx24	T	A	12: 103,390,547 (GRCm39)	Q59L	possibly damaging	Het
Ddx27	A	G	2: 166,871,439 (GRCm39)	H512R	possibly damaging	Het
Dlgap4	T	A	2: 156,604,821 (GRCm39)	*993K	probably null	Het
Dmxl2	A	T	9: 54,330,643 (GRCm39)		probably null	Het
Dus4l	A	T	12: 31,696,712 (GRCm39)	F88L	probably damaging	Het
Ep400	A	T	5: 110,904,071 (GRCm39)	V176E	probably damaging	Het
Fat3	T	A	9: 16,288,219 (GRCm39)	K435*	probably null	Het
Fsip2	T	C	2: 82,816,908 (GRCm39)	C4214R	probably benign	Het
Garin5a	T	G	7: 44,150,428 (GRCm39)	S207A	probably damaging	Het
Gfral	T	C	9: 76,072,087 (GRCm39)	*394W	probably null	Het
Glis1	T	C	4: 107,476,832 (GRCm39)	S518P	probably damaging	Het
H2-T10	A	G	17: 36,430,079 (GRCm39)		probably null	Het
Hsbp1l1	T	C	18: 80,278,679 (GRCm39)	T35A	possibly damaging	Het
Ighv5-12	A	G	12: 113,665,837 (GRCm39)	F87S	probably damaging	Het
Ints13	A	C	6: 146,477,855 (GRCm39)	D31E	probably damaging	Het
Kbtbd12	C	T	6: 88,595,609 (GRCm39)	D74N	probably damaging	Het
Klrb1c	A	G	6: 128,765,877 (GRCm39)		probably benign	Het
Kmt5b	A	T	19: 3,836,538 (GRCm39)	H25L	probably benign	Het
Krt28	A	T	11: 99,262,210 (GRCm39)	M260K	probably damaging	Het
Krt79	A	G	15: 101,838,220 (GRCm39)	S512P	probably damaging	Het
Lama1	A	T	17: 68,075,293 (GRCm39)		probably null	Het
Maneal	T	C	4: 124,750,937 (GRCm39)	E273G	possibly damaging	Het
Map4k3	T	A	17: 80,971,427 (GRCm39)	Y80F	possibly damaging	Het
Mbd6	A	G	10: 127,119,297 (GRCm39)	V946A	possibly damaging	Het
Mfsd14b	A	T	13: 65,219,936 (GRCm39)		probably null	Het
Mrpl46	C	G	7: 78,430,242 (GRCm39)	W176S	probably damaging	Het
Muc19	A	G	15: 91,768,468 (GRCm39)		noncoding transcript	Het
Mup3	T	G	4: 62,002,809 (GRCm39)	E184A	possibly damaging	Het
Myo9a	A	G	9: 59,781,911 (GRCm39)	H1699R	probably benign	Het
Ndrg2	T	A	14: 52,144,420 (GRCm39)	T269S	probably damaging	Het
Nfatc1	A	T	18: 80,693,037 (GRCm39)	V688D	probably benign	Het
Ninj2	T	C	6: 120,175,670 (GRCm39)	I101T	probably benign	Het
Nlrp10	T	A	7: 108,523,468 (GRCm39)	M671L	probably benign	Het
Npsr1	T	A	9: 24,224,510 (GRCm39)	L296I	probably damaging	Het
Or10d5	A	G	9: 39,861,983 (GRCm39)	L28P	probably benign	Het
Or52r1b	G	T	7: 102,691,517 (GRCm39)	R272L	possibly damaging	Het
Pacsin1	T	A	17: 27,927,022 (GRCm39)	D242E	probably damaging	Het
Pcdh1	T	C	18: 38,330,420 (GRCm39)	Y861C	probably damaging	Het
Pcdha12	T	C	18: 37,153,443 (GRCm39)	L54P	probably damaging	Het
Pcdhb18	T	A	18: 37,624,853 (GRCm39)	S728T	probably benign	Het
Phyhd1	T	A	2: 30,167,022 (GRCm39)	H108Q	probably damaging	Het
Plcb1	A	T	2: 135,212,513 (GRCm39)	I1035F	probably damaging	Het
Plcl1	T	C	1: 55,735,309 (GRCm39)	S217P	possibly damaging	Het
Plppr2	G	A	9: 21,852,425 (GRCm39)	R103H	probably damaging	Het
Plxnb2	G	A	15: 89,041,638 (GRCm39)	T1722I	probably damaging	Het
Pole3	T	C	4: 62,442,668 (GRCm39)	N53S	probably damaging	Het
Ptk6	A	T	2: 180,841,488 (GRCm39)	N140K	possibly damaging	Het
Rab12	C	T	17: 66,804,418 (GRCm39)	R180H	probably damaging	Het
Rab36	G	T	10: 74,888,311 (GRCm39)	V252L	probably benign	Het
Ranbp3	T	C	17: 57,008,543 (GRCm39)		probably null	Het
Rapgef2	A	G	3: 79,011,308 (GRCm39)	L259P	probably damaging	Het
Rigi	T	A	4: 40,222,140 (GRCm39)	M380L	probably benign	Het
Scaf4	GGCTGCTGCTGCTGCTGCTGCTGCTG	GGCTGCTGCTGCTGCTGCTGCTG	16: 90,026,745 (GRCm39)		probably benign	Het
Scd2	T	C	19: 44,288,142 (GRCm39)	F178S	probably damaging	Het
Shmt2	A	G	10: 127,356,250 (GRCm39)	S87P	probably damaging	Het
Slf1	T	A	13: 77,194,823 (GRCm39)	D834V	probably damaging	Het
Sorcs2	A	C	5: 36,203,874 (GRCm39)	Y540*	probably null	Het
Srpk2	T	A	5: 23,730,697 (GRCm39)	Q274L	possibly damaging	Het
Stradb	T	A	1: 59,031,901 (GRCm39)	M271K	possibly damaging	Het
Tfec	T	A	6: 16,867,592 (GRCm39)	Q16L	possibly damaging	Het
Tfg	T	C	16: 56,521,450 (GRCm39)	T63A	probably benign	Het
Ticrr	G	A	7: 79,339,715 (GRCm39)		probably null	Het
Ticrr	T	A	7: 79,345,044 (GRCm39)	C1636*	probably null	Het
Tln2	A	G	9: 67,219,147 (GRCm39)	I266T	probably damaging	Het
Tmcc1	G	C	6: 115,999,071 (GRCm39)	R323G	possibly damaging	Het
Tnnt3	A	G	7: 142,065,777 (GRCm39)	E138G	probably damaging	Het
Tpm2	C	A	4: 43,522,692 (GRCm39)	E75*	probably null	Het
Ttn	T	G	2: 76,580,922 (GRCm39)	T23324P	probably damaging	Het
Ubr4	T	G	4: 139,119,349 (GRCm39)	L176R	probably damaging	Het
Uhrf2	G	T	19: 30,016,488 (GRCm39)	D46Y	probably damaging	Het
Ulbp1	A	C	10: 7,423,281 (GRCm39)	S21A	unknown	Het
Usp17lb	C	T	7: 104,490,415 (GRCm39)	G170R	probably damaging	Het
Utp15	T	C	13: 98,394,433 (GRCm39)	N153S	probably benign	Het
Vcan	T	A	13: 89,836,790 (GRCm39)	E2918V	probably damaging	Het
Vmn1r174	T	A	7: 23,453,919 (GRCm39)	I195K	probably damaging	Het
Vmn1r76	C	T	7: 11,665,062 (GRCm39)	V16I	probably benign	Het
Xdh	T	C	17: 74,250,880 (GRCm39)	D24G	possibly damaging	Het
Xylb	T	A	9: 119,190,198 (GRCm39)	H68Q	probably benign	Het

Other mutations in Anapc5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02209:Anapc5	APN	5	122,938,676 (GRCm39)	missense	possibly damaging	0.95
IGL03158:Anapc5	APN	5	122,955,960 (GRCm39)	missense	probably benign
R0137:Anapc5	UTSW	5	122,938,695 (GRCm39)	missense	probably damaging	1.00
R0319:Anapc5	UTSW	5	122,956,919 (GRCm39)	missense	probably damaging	0.99
R0326:Anapc5	UTSW	5	122,952,667 (GRCm39)	missense	probably benign	0.40
R0399:Anapc5	UTSW	5	122,929,816 (GRCm39)	missense	probably damaging	0.99
R0633:Anapc5	UTSW	5	122,938,695 (GRCm39)	missense	probably damaging	1.00
R1173:Anapc5	UTSW	5	122,926,481 (GRCm39)	missense	possibly damaging	0.49
R1723:Anapc5	UTSW	5	122,937,406 (GRCm39)	missense	probably damaging	0.96
R2018:Anapc5	UTSW	5	122,938,587 (GRCm39)	missense	probably damaging	1.00
R2114:Anapc5	UTSW	5	122,926,001 (GRCm39)	missense	probably benign	0.06
R4211:Anapc5	UTSW	5	122,955,968 (GRCm39)	missense	probably benign
R4287:Anapc5	UTSW	5	122,938,664 (GRCm39)	missense	probably benign	0.02
R4533:Anapc5	UTSW	5	122,929,798 (GRCm39)	missense	possibly damaging	0.86
R4905:Anapc5	UTSW	5	122,955,973 (GRCm39)	missense	probably benign	0.00
R5336:Anapc5	UTSW	5	122,945,400 (GRCm39)	missense	probably damaging	1.00
R5499:Anapc5	UTSW	5	122,926,476 (GRCm39)	missense	probably damaging	1.00
R6481:Anapc5	UTSW	5	122,938,607 (GRCm39)	missense	probably benign	0.27
R7461:Anapc5	UTSW	5	122,956,928 (GRCm39)	missense	probably damaging	1.00
R7613:Anapc5	UTSW	5	122,956,928 (GRCm39)	missense	probably damaging	1.00
R7681:Anapc5	UTSW	5	122,940,202 (GRCm39)	missense	probably benign	0.01
R7912:Anapc5	UTSW	5	122,931,498 (GRCm39)	critical splice donor site	probably null
R8007:Anapc5	UTSW	5	122,929,963 (GRCm39)	missense	probably benign
R8080:Anapc5	UTSW	5	122,945,401 (GRCm39)	missense	probably damaging	1.00
R8488:Anapc5	UTSW	5	122,956,033 (GRCm39)	makesense	probably null
R8517:Anapc5	UTSW	5	122,959,093 (GRCm39)	missense	probably benign
R9036:Anapc5	UTSW	5	122,957,716 (GRCm39)	missense	possibly damaging	0.46
R9464:Anapc5	UTSW	5	122,940,209 (GRCm39)	missense	probably benign	0.00
R9471:Anapc5	UTSW	5	122,944,308 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

Posted On

2017-02-16