Mutagenetix > Incidental Mutation

Incidental Mutation 'R4992:Cdc23'

386309

Institutional Source

Beutler Lab

Gene Symbol

Cdc23

Ensembl Gene

ENSMUSG00000024370

Gene Name

CDC23 cell division cycle 23

Synonyms

D18Ertd243e

MMRRC Submission

042586-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.960) question?

Stock #

R4992 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

34764004-34784788 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 34779972 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 119 (M119L)

Ref Sequence

ENSEMBL: ENSMUSP00000122420 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025228] [ENSMUST00000133181]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000025228
AA Change: M119L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000025228
Gene: ENSMUSG00000024370
AA Change: M119L

Domain	Start	End	E-Value	Type
Pfam:APC8	22	152	1.9e-42	PFAM
Blast:TPR	175	202	4e-10	BLAST
TPR	263	296	4.21e1	SMART
TPR	331	364	1.74e-4	SMART
TPR	365	398	1.83e-3	SMART
TPR	399	432	1.37e-2	SMART
TPR	433	466	8.97e0	SMART
TPR	510	543	1.82e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000082923

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133162

Predicted Effect

probably benign
Transcript: ENSMUST00000133181
AA Change: M119L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000122420
Gene: ENSMUSG00000024370
AA Change: M119L

Domain	Start	End	E-Value	Type
low complexity region	2	24	N/A	INTRINSIC
Pfam:ANAPC8	28	151	6.9e-31	PFAM
Blast:TPR	175	202	4e-10	BLAST
TPR	263	296	4.21e1	SMART
TPR	331	364	1.74e-4	SMART
TPR	365	398	1.83e-3	SMART
TPR	399	432	1.37e-2	SMART
TPR	433	466	8.97e0	SMART
TPR	510	543	1.82e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135208

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136943

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151409

Meta Mutation Damage Score

0.1364

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.7%

Validation Efficiency

98% (84/86)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae Cdc23, a protein essential for cell cycle progression through the G2/M transition. This protein is a component of anaphase-promoting complex (APC), which is composed of eight protein subunits and highly conserved in eukaryotic cells. APC catalyzes the formation of cyclin B-ubiquitin conjugate that is responsible for the ubiquitin-mediated proteolysis of B-type cyclins. This protein and 3 other members of the APC complex contain the TPR (tetratricopeptide repeat), a protein domain important for protein-protein interaction. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930407I10Rik	G	A	15: 81,948,203 (GRCm39)	R700Q	possibly damaging	Het
4930444P10Rik	T	A	1: 16,151,101 (GRCm39)	E27V	probably damaging	Het
Acsm4	T	A	7: 119,310,640 (GRCm39)	I509N	probably benign	Het
Asb18	T	C	1: 89,880,585 (GRCm39)	M143V	probably benign	Het
Birc6	A	G	17: 74,996,251 (GRCm39)	D4475G	probably benign	Het
Bsn	A	T	9: 107,992,747 (GRCm39)	S1002T	probably damaging	Het
Bub3	T	C	7: 131,162,535 (GRCm39)	S33P	probably damaging	Het
Ccna1	T	A	3: 54,957,311 (GRCm39)	R35S	probably damaging	Het
Ces1a	A	G	8: 93,771,650 (GRCm39)	V49A	probably benign	Het
Chi3l1	A	T	1: 134,116,364 (GRCm39)	E282D	probably benign	Het
Crocc	G	A	4: 140,773,977 (GRCm39)	A220V	probably damaging	Het
Cstf1	A	G	2: 172,219,720 (GRCm39)	Y277C	probably damaging	Het
D930020B18Rik	C	G	10: 121,490,666 (GRCm39)	P89A	probably damaging	Het
D930020B18Rik	C	T	10: 121,490,667 (GRCm39)	P89L	probably damaging	Het
Dennd5a	A	G	7: 109,493,919 (GRCm39)	S1262P	probably damaging	Het
Dnajb5	G	A	4: 42,953,386 (GRCm39)		probably null	Het
E330034G19Rik	A	G	14: 24,357,064 (GRCm39)	K200R	unknown	Het
Ect2l	A	G	10: 18,048,477 (GRCm39)	F156S	probably benign	Het
Egf	T	C	3: 129,505,179 (GRCm39)		probably null	Het
Elmo1	T	C	13: 20,526,689 (GRCm39)	F413S	probably damaging	Het
Elmo3	T	A	8: 106,036,133 (GRCm39)	Y607*	probably null	Het
Eno3	A	G	11: 70,549,473 (GRCm39)	D98G	probably damaging	Het
Ephb2	A	G	4: 136,388,150 (GRCm39)	V651A	probably damaging	Het
Fbp1	C	T	13: 63,012,888 (GRCm39)	V102I	probably benign	Het
Gcn1	T	C	5: 115,737,225 (GRCm39)	V1321A	probably benign	Het
Gimd1	A	T	3: 132,340,718 (GRCm39)	Y78F	probably benign	Het
Glmn	T	G	5: 107,705,167 (GRCm39)	D483A	probably damaging	Het
Gsr	C	T	8: 34,183,941 (GRCm39)	T401I	probably damaging	Het
Htr3b	G	A	9: 48,870,518 (GRCm39)	H62Y	possibly damaging	Het
Ifna6	T	C	4: 88,745,777 (GRCm39)	V42A	probably benign	Het
Igkv4-80	A	C	6: 68,993,649 (GRCm39)	S81A	probably benign	Het
Inpp4b	A	T	8: 82,759,837 (GRCm39)	R627S	probably damaging	Het
Kif13a	C	T	13: 46,930,639 (GRCm39)	V142M	probably damaging	Het
Lims1	A	C	10: 58,246,063 (GRCm39)		probably benign	Het
Ltn1	T	C	16: 87,202,475 (GRCm39)	T1059A	possibly damaging	Het
Lyst	T	C	13: 13,835,748 (GRCm39)	L1810P	probably damaging	Het
Mboat1	T	G	13: 30,386,343 (GRCm39)	I119R	possibly damaging	Het
Mgat3	T	A	15: 80,096,743 (GRCm39)	D523E	probably benign	Het
Mphosph9	T	C	5: 124,442,253 (GRCm39)	E395G	probably damaging	Het
Mtcl1	G	T	17: 66,649,834 (GRCm39)	P1877Q	probably damaging	Het
Myo6	T	C	9: 80,190,792 (GRCm39)	V781A	possibly damaging	Het
Ncoa3	T	A	2: 165,911,859 (GRCm39)	M1395K	probably benign	Het
Nhlrc2	T	A	19: 56,558,966 (GRCm39)	D150E	probably benign	Het
Nlrp9a	T	C	7: 26,256,811 (GRCm39)	V54A	probably benign	Het
Or1e32	G	A	11: 73,705,146 (GRCm39)	T254I	probably damaging	Het
Or3a1d	A	G	11: 74,238,023 (GRCm39)	I129T	probably damaging	Het
Parp14	A	T	16: 35,661,512 (GRCm39)	C1479S	probably benign	Het
Pdcd1lg2	T	C	19: 29,423,484 (GRCm39)	V176A	probably damaging	Het
Pibf1	T	A	14: 99,388,103 (GRCm39)	N416K	probably damaging	Het
Pip4p1	A	G	14: 51,166,690 (GRCm39)	V179A	probably damaging	Het
Polb	A	T	8: 23,135,087 (GRCm39)	V115E	probably damaging	Het
Polq	T	A	16: 36,881,524 (GRCm39)	N1229K	possibly damaging	Het
Ppp1r21	A	T	17: 88,876,508 (GRCm39)	D440V	probably benign	Het
Ppp2ca	T	A	11: 52,004,033 (GRCm39)	H63Q	possibly damaging	Het
Prl7a1	C	T	13: 27,819,669 (GRCm39)		probably null	Het
Rgs1	C	A	1: 144,122,060 (GRCm39)	K77N	probably damaging	Het
Rnf112	T	A	11: 61,343,537 (GRCm39)	I100F	possibly damaging	Het
Rnf139	G	T	15: 58,770,325 (GRCm39)	E117*	probably null	Het
Robo1	G	A	16: 72,776,756 (GRCm39)	V743I	probably damaging	Het
Scarf1	T	C	11: 75,416,841 (GRCm39)	V761A	probably benign	Het
Scarf1	T	C	11: 75,413,056 (GRCm39)	L434P	probably damaging	Het
Sgsm1	A	T	5: 113,430,486 (GRCm39)	S300T	possibly damaging	Het
Slc26a7	T	G	4: 14,565,508 (GRCm39)	T192P	probably damaging	Het
Smarcc2	A	G	10: 128,310,579 (GRCm39)	K403E	probably damaging	Het
Snai3	G	A	8: 123,183,071 (GRCm39)	T158M	possibly damaging	Het
Spata31d1a	T	C	13: 59,850,965 (GRCm39)	N388D	probably benign	Het
Sptlc3	G	A	2: 139,437,923 (GRCm39)	V406I	probably benign	Het
Tgds	A	C	14: 118,355,175 (GRCm39)	Y197D	probably damaging	Het
Tll1	G	T	8: 64,546,978 (GRCm39)	R323S	probably damaging	Het
Trim14	A	G	4: 46,507,110 (GRCm39)	Y369H	probably damaging	Het
Ube2nl	C	T	7: 61,199,112 (GRCm39)		noncoding transcript	Het
Ube3a	T	A	7: 58,934,568 (GRCm39)	D560E	possibly damaging	Het
Vmn2r10	A	G	5: 109,145,592 (GRCm39)	V505A	possibly damaging	Het
Vmn2r114	T	G	17: 23,510,765 (GRCm39)	I572L	probably benign	Het
Vmn2r26	A	T	6: 124,003,070 (GRCm39)	Q160L	probably benign	Het
Vmn2r75	A	C	7: 85,815,375 (GRCm39)		probably null	Het
Vps8	A	G	16: 21,280,158 (GRCm39)	K336E	possibly damaging	Het
Zfp324	T	C	7: 12,703,300 (GRCm39)	S32P	probably benign	Het
Zfp366	T	C	13: 99,366,003 (GRCm39)	I388T	possibly damaging	Het
Zfp68	A	T	5: 138,605,599 (GRCm39)	N203K	possibly damaging	Het
Zhx2	A	T	15: 57,686,983 (GRCm39)	N784I	probably damaging	Het

Other mutations in Cdc23

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01140:Cdc23	APN	18	34,769,385 (GRCm39)	missense	probably benign	0.01
IGL01302:Cdc23	APN	18	34,767,697 (GRCm39)	missense	probably benign	0.19
IGL01859:Cdc23	APN	18	34,784,459 (GRCm39)	missense	probably benign	0.01
IGL02307:Cdc23	APN	18	34,774,442 (GRCm39)	missense	possibly damaging	0.71
IGL03081:Cdc23	APN	18	34,769,757 (GRCm39)	missense	probably damaging	1.00
IGL03086:Cdc23	APN	18	34,770,239 (GRCm39)	unclassified	probably benign
IGL03089:Cdc23	APN	18	34,767,513 (GRCm39)	missense	probably damaging	1.00
IGL03249:Cdc23	APN	18	34,777,069 (GRCm39)	splice site	probably benign
R0217:Cdc23	UTSW	18	34,784,718 (GRCm39)	missense	unknown
R0790:Cdc23	UTSW	18	34,784,666 (GRCm39)	missense	possibly damaging	0.94
R1593:Cdc23	UTSW	18	34,769,379 (GRCm39)	missense	possibly damaging	0.88
R2929:Cdc23	UTSW	18	34,770,371 (GRCm39)	frame shift	probably null
R2930:Cdc23	UTSW	18	34,770,371 (GRCm39)	frame shift	probably null
R3963:Cdc23	UTSW	18	34,779,972 (GRCm39)	missense	probably benign	0.01
R3983:Cdc23	UTSW	18	34,770,539 (GRCm39)	unclassified	probably benign
R4245:Cdc23	UTSW	18	34,770,100 (GRCm39)	unclassified	probably benign
R4415:Cdc23	UTSW	18	34,770,371 (GRCm39)	frame shift	probably null
R4417:Cdc23	UTSW	18	34,770,371 (GRCm39)	frame shift	probably null
R5037:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5071:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5072:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5073:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5074:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5081:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5082:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5083:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5110:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5111:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5122:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5131:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5132:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R5166:Cdc23	UTSW	18	34,784,742 (GRCm39)	missense	unknown
R7186:Cdc23	UTSW	18	34,770,175 (GRCm39)	missense	probably damaging	1.00
R7359:Cdc23	UTSW	18	34,774,394 (GRCm39)	missense	probably benign	0.40
R7732:Cdc23	UTSW	18	34,769,755 (GRCm39)	critical splice donor site	probably null
R7832:Cdc23	UTSW	18	34,780,072 (GRCm39)	missense	probably benign	0.11
R8031:Cdc23	UTSW	18	34,784,741 (GRCm39)	missense	unknown
R8185:Cdc23	UTSW	18	34,774,197 (GRCm39)	missense	probably benign	0.00
R8345:Cdc23	UTSW	18	34,767,150 (GRCm39)	missense	probably benign	0.17
R8716:Cdc23	UTSW	18	34,784,735 (GRCm39)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- TCAAGTTGAGGGTCAGCCTG -3'
(R):5'- GTGAACTCTGGCTGTCTGAG -3'

Sequencing Primer
(F):5'- TCAGACCTCTGCTGGTACTAGG -3'
(R):5'- GAACTCTGGCTGTCTGAGACCTAAC -3'

Posted On

2016-05-10