Mutagenetix > Incidental Mutation

Incidental Mutation 'R9081:Fbxo31'

690018

Institutional Source

Beutler Lab

Gene Symbol

Fbxo31

Ensembl Gene

ENSMUSG00000052934

Gene Name

F-box protein 31

Synonyms

Fbxo14, 2310046N15Rik, Fbx14, 1110003O08Rik

MMRRC Submission

068900-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9081 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

122276179-122305545 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 122281136 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Cysteine at position 337 (R337C)

Ref Sequence

ENSEMBL: ENSMUSP00000057573 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000059018] [ENSMUST00000127664]

AlphaFold

Q3TQF0

Predicted Effect

probably damaging
Transcript: ENSMUST00000059018
AA Change: R337C

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000057573
Gene: ENSMUSG00000052934
AA Change: R337C

Domain	Start	End	E-Value	Type
low complexity region	14	24	N/A	INTRINSIC
low complexity region	25	42	N/A	INTRINSIC
FBOX	56	96	3.45e-8	SMART
low complexity region	358	379	N/A	INTRINSIC
low complexity region	385	412	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000127664

SMART Domains

Protein: ENSMUSP00000118564
Gene: ENSMUSG00000092329

Domain	Start	End	E-Value	Type
Pfam:Glycos_transf_2	104	287	7.4e-31	PFAM
Pfam:Glyco_transf_7C	261	331	4.9e-8	PFAM
RICIN	406	531	9.28e-27	SMART

Meta Mutation Damage Score

0.6329

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

100% (71/71)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the F-box family. Members are classified into three classes according to the substrate interaction domain, FBW for WD40 repeats, FBL for leucing-rich repeats, and FBXO for other domains. This protein, classified into the last category because of the lack of a recognizable substrate binding domain, has been proposed to be a component of the SCF ubiquitination complex. It is thought to bind and recruit substrate for ubiquitination and degradation. This protein may have a role in regulating the cell cycle as well as dendrite growth and neuronal migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aaas	A	T	15: 102,248,502 (GRCm39)	V271E	probably damaging	Het
Abca1	A	G	4: 53,109,162 (GRCm39)		probably null	Het
Abcb11	C	T	2: 69,122,388 (GRCm39)	C365Y	possibly damaging	Het
Abcd2	A	T	15: 91,075,772 (GRCm39)	W14R	probably damaging	Het
Acmsd	A	G	1: 127,687,468 (GRCm39)	D250G	possibly damaging	Het
Ahnak	T	A	19: 8,985,890 (GRCm39)	D2391E	possibly damaging	Het
Apol11b	C	T	15: 77,524,771 (GRCm39)	E5K	possibly damaging	Het
Cbr1	G	T	16: 93,406,994 (GRCm39)	G237*	probably null	Het
Cdr2l	T	A	11: 115,284,939 (GRCm39)	V425E	probably damaging	Het
Chd9	A	T	8: 91,704,144 (GRCm39)	K693*	probably null	Het
Clgn	T	G	8: 84,153,169 (GRCm39)	D590E	probably damaging	Het
Col14a1	T	A	15: 55,291,387 (GRCm39)	S952T	unknown	Het
Crip3	T	C	17: 46,740,959 (GRCm39)	L90P	probably benign	Het
Dchs1	A	G	7: 105,403,636 (GRCm39)	S2969P	probably benign	Het
Dnai2	T	A	11: 114,629,493 (GRCm39)	D173E	probably damaging	Het
Dnpep	A	T	1: 75,291,060 (GRCm39)	F257Y	probably damaging	Het
Egln2	A	G	7: 26,864,286 (GRCm39)	V213A	probably benign	Het
Epha8	G	T	4: 136,665,897 (GRCm39)	L420M	probably damaging	Het
Eps8	A	G	6: 137,504,415 (GRCm39)	I106T	probably benign	Het
Evi5	A	G	5: 107,963,571 (GRCm39)	F379L	probably benign	Het
Fpgs	A	T	2: 32,577,500 (GRCm39)		probably benign	Het
Garnl3	T	G	2: 32,896,920 (GRCm39)	D573A	possibly damaging	Het
Gja8	A	G	3: 96,826,676 (GRCm39)	S329P	probably damaging	Het
Gzf1	T	A	2: 148,525,317 (GRCm39)		probably benign	Het
Hgs	T	A	11: 120,366,076 (GRCm39)		probably benign	Het
Ifi203	A	G	1: 173,757,048 (GRCm39)	I245T	unknown	Het
Ighv1-74	C	A	12: 115,766,454 (GRCm39)	W55C	probably damaging	Het
Iqcb1	A	G	16: 36,656,006 (GRCm39)	K131R	probably null	Het
Kit	A	T	5: 75,801,218 (GRCm39)	M539L	probably benign	Het
Klk1	A	G	7: 43,874,952 (GRCm39)		probably benign	Het
Krt84	C	T	15: 101,440,814 (GRCm39)	G126D	unknown	Het
Lama5	A	T	2: 179,833,930 (GRCm39)	C1473*	probably null	Het
Loxl3	T	C	6: 83,025,638 (GRCm39)	V332A	possibly damaging	Het
Mcf2l	T	A	8: 13,068,697 (GRCm39)	Y1120N	probably damaging	Het
Meioc	G	A	11: 102,565,001 (GRCm39)	V150M	probably benign	Het
Mybpc1	T	G	10: 88,389,168 (GRCm39)	Y400S	probably damaging	Het
Ncmap	T	C	4: 135,104,292 (GRCm39)		probably benign	Het
Noc2l	A	G	4: 156,326,224 (GRCm39)	Y437C	probably damaging	Het
Nol8	A	T	13: 49,814,881 (GRCm39)	M330L	probably benign	Het
Or10d4c	A	T	9: 39,558,196 (GRCm39)	Y58F	probably damaging	Het
Or5b113	C	T	19: 13,342,019 (GRCm39)	T9I	probably benign	Het
P4ha1	T	C	10: 59,184,185 (GRCm39)	Y216H	probably damaging	Het
Pamr1	A	T	2: 102,441,933 (GRCm39)	D174V	probably damaging	Het
Pdcd1	C	T	1: 93,968,880 (GRCm39)		probably null	Het
Plec	A	G	15: 76,059,908 (GRCm39)	V3343A	probably damaging	Het
Pnliprp1	A	T	19: 58,723,406 (GRCm39)	I266F	probably benign	Het
Poglut2	T	A	1: 44,153,966 (GRCm39)	Q161L	probably benign	Het
Ppp1r12b	C	T	1: 134,705,085 (GRCm39)	V868I	probably benign	Het
Ppp2r2b	A	T	18: 42,781,825 (GRCm39)	H325Q	probably benign	Het
Rif1	C	T	2: 52,000,989 (GRCm39)	T1481I	probably damaging	Het
Rnf213	A	T	11: 119,357,062 (GRCm39)	D4204V		Het
Rps6kl1	T	C	12: 85,185,881 (GRCm39)	N409S	probably damaging	Het
Rundc1	T	G	11: 101,316,053 (GRCm39)	W42G	probably damaging	Het
Sec1	C	T	7: 45,333,987 (GRCm39)		probably benign	Het
Sez6	G	A	11: 77,865,121 (GRCm39)	E623K	possibly damaging	Het
Shc2	T	C	10: 79,462,762 (GRCm39)		probably null	Het
Slc19a1	T	C	10: 76,877,750 (GRCm39)	V95A	possibly damaging	Het
Slc22a5	A	T	11: 53,762,447 (GRCm39)	D333E	probably damaging	Het
Specc1	A	C	11: 62,010,051 (GRCm39)	R522S	possibly damaging	Het
Syne2	C	T	12: 76,016,290 (GRCm39)	Q3291*	probably null	Het
Taar7e	G	A	10: 23,913,893 (GRCm39)	V128I	probably benign	Het
Tdrd3	A	G	14: 87,743,717 (GRCm39)	N555S	probably benign	Het
Themis	C	T	10: 28,544,582 (GRCm39)		probably benign	Het
Tjp1	A	G	7: 64,964,010 (GRCm39)	V945A	possibly damaging	Het
Tom1	G	A	8: 75,778,151 (GRCm39)	V78I	probably damaging	Het
Usp13	A	G	3: 32,935,542 (GRCm39)	T323A	probably benign	Het
Usp49	T	C	17: 47,984,236 (GRCm39)	S414P	possibly damaging	Het
Vmn1r104	G	A	7: 20,268,378 (GRCm39)	S206N	probably damaging	Het
Vps45	A	T	3: 95,940,125 (GRCm39)	V446E	probably benign	Het
Wwc1	T	C	11: 35,782,331 (GRCm39)	K222R	probably benign	Het
Zc3h13	CAGAGACCGGGACAGAAGGAGAGAC	CAGAGAC	14: 75,569,381 (GRCm39)		probably benign	Het

Other mutations in Fbxo31

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00983:Fbxo31	APN	8	122,281,069 (GRCm39)	missense	possibly damaging	0.92
IGL02155:Fbxo31	APN	8	122,285,814 (GRCm39)	missense	probably damaging	1.00
IGL02551:Fbxo31	APN	8	122,293,083 (GRCm39)	missense	probably damaging	0.99
IGL03092:Fbxo31	APN	8	122,286,757 (GRCm39)	missense	probably benign
Archive	UTSW	8	122,281,967 (GRCm39)	missense	probably benign
Repository	UTSW	8	122,281,136 (GRCm39)	missense	probably damaging	0.98
R0377:Fbxo31	UTSW	8	122,285,841 (GRCm39)	unclassified	probably benign
R0730:Fbxo31	UTSW	8	122,282,103 (GRCm39)	unclassified	probably benign
R1132:Fbxo31	UTSW	8	122,279,019 (GRCm39)	frame shift	probably null
R1132:Fbxo31	UTSW	8	122,279,015 (GRCm39)	frame shift	probably null
R1626:Fbxo31	UTSW	8	122,286,745 (GRCm39)	missense	probably damaging	1.00
R1796:Fbxo31	UTSW	8	122,287,177 (GRCm39)	nonsense	probably null
R2215:Fbxo31	UTSW	8	122,293,050 (GRCm39)	missense	probably benign	0.01
R3726:Fbxo31	UTSW	8	122,305,248 (GRCm39)	missense	probably damaging	1.00
R3761:Fbxo31	UTSW	8	122,287,169 (GRCm39)	missense	possibly damaging	0.94
R4646:Fbxo31	UTSW	8	122,286,755 (GRCm39)	missense	probably benign
R4782:Fbxo31	UTSW	8	122,279,180 (GRCm39)	missense	probably damaging	1.00
R4782:Fbxo31	UTSW	8	122,279,178 (GRCm39)	nonsense	probably null
R5103:Fbxo31	UTSW	8	122,279,101 (GRCm39)	missense	probably damaging	1.00
R5715:Fbxo31	UTSW	8	122,305,302 (GRCm39)	missense	probably damaging	1.00
R6347:Fbxo31	UTSW	8	122,305,198 (GRCm39)	missense	possibly damaging	0.69
R6551:Fbxo31	UTSW	8	122,291,443 (GRCm39)	intron	probably benign
R7027:Fbxo31	UTSW	8	122,305,224 (GRCm39)	missense	probably damaging	1.00
R7156:Fbxo31	UTSW	8	122,281,060 (GRCm39)	missense	possibly damaging	0.83
R7271:Fbxo31	UTSW	8	122,305,503 (GRCm39)	unclassified	probably benign
R7594:Fbxo31	UTSW	8	122,279,107 (GRCm39)	missense	probably damaging	1.00
R7860:Fbxo31	UTSW	8	122,291,384 (GRCm39)	splice site	probably null
R8039:Fbxo31	UTSW	8	122,285,794 (GRCm39)	missense	probably damaging	1.00
R8116:Fbxo31	UTSW	8	122,287,127 (GRCm39)	missense	probably damaging	1.00
R8284:Fbxo31	UTSW	8	122,287,181 (GRCm39)	missense	probably benign	0.01
R8726:Fbxo31	UTSW	8	122,282,014 (GRCm39)	nonsense	probably null
R8867:Fbxo31	UTSW	8	122,281,967 (GRCm39)	missense	probably benign
R9082:Fbxo31	UTSW	8	122,281,136 (GRCm39)	missense	probably damaging	0.98
R9093:Fbxo31	UTSW	8	122,281,136 (GRCm39)	missense	probably damaging	0.98
R9094:Fbxo31	UTSW	8	122,281,136 (GRCm39)	missense	probably damaging	0.98
R9095:Fbxo31	UTSW	8	122,281,136 (GRCm39)	missense	probably damaging	0.98
R9098:Fbxo31	UTSW	8	122,281,136 (GRCm39)	missense	probably damaging	0.98
R9667:Fbxo31	UTSW	8	122,305,208 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TCTTTGCCGTCCTTAGCAGG -3'
(R):5'- CCCACATACTAAACAAGTGGGG -3'

Sequencing Primer
(F):5'- TTAGCAGGTGGCCCATCAG -3'
(R):5'- CACATACTAAACAAGTGGGGGTCTC -3'

Posted On

2021-11-19