Mutagenetix > Incidental Mutation

Incidental Mutation 'R1498:Fbxw8'

169023

Institutional Source

Beutler Lab

Gene Symbol

Fbxw8

Ensembl Gene

ENSMUSG00000032867

Gene Name

F-box and WD-40 domain protein 8

Synonyms

4930438M06Rik, Fbx29, FBXO29, FBW6, FBW8

MMRRC Submission

039549-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.520) question?

Stock #

R1498 (G1)

Quality Score

139

Status

Validated

Chromosome

Chromosomal Location

118203046-118293523 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

G to A at 118203850 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000138436 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031304] [ENSMUST00000049474] [ENSMUST00000124648]

AlphaFold

Q8BIA4

Predicted Effect

probably benign
Transcript: ENSMUST00000031304

SMART Domains

Protein: ENSMUSP00000031304
Gene: ENSMUSG00000029359

Domain	Start	End	E-Value	Type
PDB:2CT9\|B	1	212	2e-29	PDB
SCOP:d1auib_	13	203	2e-14	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000031305

Predicted Effect

probably benign
Transcript: ENSMUST00000049474

SMART Domains

Protein: ENSMUSP00000047012
Gene: ENSMUSG00000032867

Domain	Start	End	E-Value	Type
low complexity region	16	39	N/A	INTRINSIC
low complexity region	51	75	N/A	INTRINSIC
low complexity region	76	91	N/A	INTRINSIC
FBOX	119	159	5e-5	SMART
WD40	198	236	6.16e0	SMART
WD40	248	285	7.1e1	SMART
WD40	289	327	7.36e1	SMART
Blast:WD40	373	418	2e-8	BLAST
WD40	421	461	1.6e0	SMART
WD40	464	501	2.15e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000124648

SMART Domains

Protein: ENSMUSP00000138436
Gene: ENSMUSG00000029359

Domain	Start	End	E-Value	Type
PDB:2CT9\|B	9	138	3e-19	PDB
SCOP:d1dgua_	9	138	1e-13	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135540

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151792

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.2%
20x: 92.6%

Validation Efficiency

97% (83/86)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the F-box protein family, members of which are characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into three classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene contains a WD-40 domain, in addition to an F-box motif, so it belongs to the Fbw class. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null allele display partial late embryonic lethality with embryonic growth retardation and abnormal placental morphology. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acly	A	G	11: 100,374,627 (GRCm39)	S799P	probably benign	Het
Acvr1b	T	C	15: 101,091,891 (GRCm39)	F57S	probably benign	Het
Adamts5	T	A	16: 85,696,990 (GRCm39)	T56S	possibly damaging	Het
Adrb2	T	C	18: 62,312,004 (GRCm39)	T274A	probably damaging	Het
Agr3	A	T	12: 35,984,379 (GRCm39)		probably null	Het
Ankrd6	A	G	4: 32,810,289 (GRCm39)	M405T	probably benign	Het
Aoc1l2	A	G	6: 48,908,305 (GRCm39)	H435R	probably benign	Het
Aqp5	T	C	15: 99,491,128 (GRCm39)	I60T	probably damaging	Het
Arf5	G	T	6: 28,426,153 (GRCm39)	R180L	probably benign	Het
Asap3	A	G	4: 135,966,505 (GRCm39)	N528D	probably benign	Het
Atmin	G	A	8: 117,681,540 (GRCm39)	E180K	probably benign	Het
Bcl11a	A	T	11: 24,114,005 (GRCm39)	E449D	probably damaging	Het
Cep128	A	T	12: 91,333,191 (GRCm39)	F25I	probably benign	Het
Cfp	GCAC	GC	X: 20,795,905 (GRCm39)		probably null	Het
Chpt1	T	A	10: 88,312,966 (GRCm39)	Y282F	possibly damaging	Het
Cul7	A	G	17: 46,966,636 (GRCm39)	D355G	probably benign	Het
Daxx	T	C	17: 34,131,227 (GRCm39)	Y385H	probably damaging	Het
Dnah2	A	C	11: 69,411,493 (GRCm39)		probably null	Het
Dscc1	CTGAATGAAT	CTGAAT	15: 54,943,572 (GRCm39)		probably benign	Het
Erc2	T	A	14: 28,024,855 (GRCm39)	M578K	probably benign	Het
Evc	T	A	5: 37,481,044 (GRCm39)	H267L	possibly damaging	Het
Exosc10	A	C	4: 148,666,243 (GRCm39)	Q837P	possibly damaging	Het
Fasn	G	A	11: 120,706,245 (GRCm39)	T1033I	probably damaging	Het
Fat1	C	A	8: 45,478,521 (GRCm39)	Y2522*	probably null	Het
Fyn	A	G	10: 39,408,120 (GRCm39)	D321G	possibly damaging	Het
Grm6	G	A	11: 50,748,083 (GRCm39)	V398M	probably damaging	Het
Gtpbp1	T	A	15: 79,603,222 (GRCm39)		probably null	Het
Hnf1a	A	G	5: 115,108,596 (GRCm39)	V103A	probably damaging	Het
Hsp90aa1	A	T	12: 110,662,122 (GRCm39)		probably null	Het
Iqgap2	C	T	13: 95,783,313 (GRCm39)	V1288I	probably benign	Het
Irx5	A	G	8: 93,086,514 (GRCm39)	D199G	probably damaging	Het
Klrh1	A	G	6: 129,748,703 (GRCm39)	S105P	probably damaging	Het
Krt9	G	T	11: 100,079,195 (GRCm39)	C732*	probably null	Het
Lifr	T	C	15: 7,220,099 (GRCm39)	S910P	probably damaging	Het
Lrig1	G	A	6: 94,604,968 (GRCm39)	A209V	possibly damaging	Het
Lrrk1	T	A	7: 65,952,419 (GRCm39)	R506*	probably null	Het
Lyst	T	A	13: 13,824,960 (GRCm39)	I1525K	possibly damaging	Het
Mad2l1	C	T	6: 66,516,826 (GRCm39)	Q173*	probably null	Het
Mcoln1	T	A	8: 3,562,861 (GRCm39)	I524N	probably damaging	Het
Mmp3	A	T	9: 7,446,967 (GRCm39)	D49V	possibly damaging	Het
Morc3	A	T	16: 93,650,743 (GRCm39)	N321I	probably damaging	Het
Mrpl48	T	C	7: 100,195,695 (GRCm39)		probably benign	Het
Myo6	T	A	9: 80,214,961 (GRCm39)	D1231E	probably damaging	Het
Nlrc4	A	G	17: 74,753,408 (GRCm39)	I325T	probably benign	Het
Or1j19	A	T	2: 36,677,358 (GRCm39)	I274F	probably damaging	Het
Or2ag17	T	C	7: 106,389,623 (GRCm39)	Y195C	possibly damaging	Het
Or4f61	A	T	2: 111,922,938 (GRCm39)	M36K	probably benign	Het
Or8c16	C	G	9: 38,130,676 (GRCm39)	P183A	probably damaging	Het
Or8k32	A	G	2: 86,368,902 (GRCm39)	V117A	probably benign	Het
Parvg	T	A	15: 84,218,832 (GRCm39)	S230T	possibly damaging	Het
Pcca	T	C	14: 122,854,230 (GRCm39)	I118T	probably damaging	Het
Pde6a	A	G	18: 61,365,932 (GRCm39)	N219S	possibly damaging	Het
Phldb1	G	T	9: 44,612,915 (GRCm39)	P935Q	possibly damaging	Het
Plppr5	T	C	3: 117,456,261 (GRCm39)	S261P	probably damaging	Het
Ppl	T	C	16: 4,922,629 (GRCm39)	N260S	probably benign	Het
Ppp1r3e	A	T	14: 55,113,882 (GRCm39)	H263Q	probably benign	Het
Ppp3cb	T	C	14: 20,559,567 (GRCm39)		probably null	Het
Ppt2	A	T	17: 34,842,075 (GRCm39)	D185E	probably benign	Het
Prr27	A	T	5: 87,998,600 (GRCm39)		probably benign	Het
Ptcd3	A	T	6: 71,870,479 (GRCm39)	V327E	probably damaging	Het
Pwwp4a	G	T	X: 72,171,261 (GRCm39)	G218C	probably damaging	Het
Rsf1	GCG	GCGACG	7: 97,229,114 (GRCm39)		probably benign	Het
Rtp1	A	T	16: 23,249,970 (GRCm39)	M112L	probably benign	Het
Slc22a5	A	T	11: 53,760,140 (GRCm39)	L392Q	probably damaging	Het
Slc6a7	A	G	18: 61,129,764 (GRCm39)	I614T	probably benign	Het
Slu7	C	A	11: 43,329,044 (GRCm39)	P89T	possibly damaging	Het
Smarcc2	T	C	10: 128,318,061 (GRCm39)	V618A	probably benign	Het
Sorl1	C	T	9: 41,952,369 (GRCm39)	R729Q	probably damaging	Het
Sptbn2	T	C	19: 4,794,274 (GRCm39)	F1493L	possibly damaging	Het
Sulf1	C	T	1: 12,918,574 (GRCm39)	T66I	probably damaging	Het
Tgtp2	A	G	11: 48,950,165 (GRCm39)	Y136H	probably damaging	Het
Tmem117	T	C	15: 94,536,242 (GRCm39)	F92S	probably damaging	Het
Tmprss9	T	A	10: 80,730,934 (GRCm39)	V820E	probably benign	Het
Tpcn2	A	G	7: 144,822,648 (GRCm39)	Y266H	probably damaging	Het
Trat1	A	G	16: 48,555,304 (GRCm39)	S143P	probably benign	Het
Vmn1r49	T	A	6: 90,049,298 (GRCm39)	R235W	probably damaging	Het
Vmn1r71	A	T	7: 10,482,575 (GRCm39)	C38S	probably benign	Het
Vmn2r6	T	A	3: 64,463,890 (GRCm39)	T315S	probably damaging	Het
Wdr36	A	G	18: 32,986,021 (GRCm39)	D575G	possibly damaging	Het
Zfp292	G	T	4: 34,805,397 (GRCm39)	A2549E	possibly damaging	Het
Zfp354a	A	T	11: 50,961,073 (GRCm39)	H426L	probably damaging	Het
Zfp407	C	T	18: 84,577,898 (GRCm39)	A1072T	probably benign	Het
Zfp648	T	A	1: 154,081,119 (GRCm39)	I426N	probably damaging	Het
Zfp87	T	C	13: 74,520,736 (GRCm39)	N114S	probably benign	Het

Other mutations in Fbxw8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00272:Fbxw8	APN	5	118,206,162 (GRCm39)	missense	probably benign	0.00
IGL00435:Fbxw8	APN	5	118,206,202 (GRCm39)	missense	probably benign	0.01
IGL00674:Fbxw8	APN	5	118,233,658 (GRCm39)	missense	possibly damaging	0.94
IGL01306:Fbxw8	APN	5	118,251,785 (GRCm39)	missense	possibly damaging	0.88
IGL02389:Fbxw8	APN	5	118,267,020 (GRCm39)	missense	possibly damaging	0.57
IGL02438:Fbxw8	APN	5	118,233,758 (GRCm39)	missense	probably benign	0.09
IGL02553:Fbxw8	APN	5	118,204,125 (GRCm39)	unclassified	probably benign
IGL02752:Fbxw8	APN	5	118,280,815 (GRCm39)	missense	probably damaging	1.00
IGL02975:Fbxw8	APN	5	118,215,760 (GRCm39)	missense	probably benign	0.02
IGL03177:Fbxw8	APN	5	118,267,045 (GRCm39)	splice site	probably benign
IGL03333:Fbxw8	APN	5	118,233,660 (GRCm39)	missense	possibly damaging	0.94
IGL03407:Fbxw8	APN	5	118,280,741 (GRCm39)	missense	probably damaging	1.00
ANU23:Fbxw8	UTSW	5	118,251,785 (GRCm39)	missense	possibly damaging	0.88
R0135:Fbxw8	UTSW	5	118,208,552 (GRCm39)	missense	probably damaging	1.00
R0760:Fbxw8	UTSW	5	118,203,966 (GRCm39)	splice site	probably null
R1115:Fbxw8	UTSW	5	118,215,636 (GRCm39)	splice site	probably benign
R1689:Fbxw8	UTSW	5	118,215,682 (GRCm39)	missense	probably damaging	0.97
R1897:Fbxw8	UTSW	5	118,266,941 (GRCm39)	missense	probably benign	0.16
R2160:Fbxw8	UTSW	5	118,263,053 (GRCm39)	missense	probably damaging	1.00
R2345:Fbxw8	UTSW	5	118,203,872 (GRCm39)	unclassified	probably benign
R3743:Fbxw8	UTSW	5	118,251,704 (GRCm39)	missense	probably damaging	1.00
R3935:Fbxw8	UTSW	5	118,233,783 (GRCm39)	missense	probably benign	0.38
R4910:Fbxw8	UTSW	5	118,263,092 (GRCm39)	splice site	probably null
R5220:Fbxw8	UTSW	5	118,233,776 (GRCm39)	missense	possibly damaging	0.69
R5628:Fbxw8	UTSW	5	118,230,622 (GRCm39)	missense	probably damaging	1.00
R6161:Fbxw8	UTSW	5	118,230,740 (GRCm39)	missense	possibly damaging	0.94
R6184:Fbxw8	UTSW	5	118,251,814 (GRCm39)	missense	probably damaging	1.00
R6582:Fbxw8	UTSW	5	118,263,028 (GRCm39)	missense	probably benign	0.28
R6617:Fbxw8	UTSW	5	118,280,731 (GRCm39)	critical splice donor site	probably null
R6785:Fbxw8	UTSW	5	118,230,754 (GRCm39)	missense	probably damaging	1.00
R7363:Fbxw8	UTSW	5	118,263,057 (GRCm39)	missense	probably damaging	0.97
R7395:Fbxw8	UTSW	5	118,206,280 (GRCm39)	missense	probably damaging	1.00
R7674:Fbxw8	UTSW	5	118,263,036 (GRCm39)	nonsense	probably null
R8428:Fbxw8	UTSW	5	118,215,763 (GRCm39)	missense	probably benign	0.02
R9161:Fbxw8	UTSW	5	118,251,727 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TTCGAGACGTGAACAAAGCCCC -3'
(R):5'- TTCTCCCTGGAACAGAAGAGGAGC -3'

Sequencing Primer
(F):5'- ACAAAGCCCCTCTGTTAGGTG -3'
(R):5'- AGAGGAGCACCAGCCTG -3'

Posted On

2014-04-13