Mutagenetix > Incidental Mutation

Incidental Mutation 'R1301:Fbxo47'

158379

Institutional Source

Beutler Lab

Gene Symbol

Fbxo47

Ensembl Gene

ENSMUSG00000070336

Gene Name

F-box protein 47

Synonyms

LOC380724, 2900052P03Rik

MMRRC Submission

039367-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1301 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

97744652-97774980 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 97759427 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Isoleucine at position 166 (M166I)

Ref Sequence

ENSEMBL: ENSMUSP00000091471 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000093939]

AlphaFold

A2A6H3

Predicted Effect

probably benign
Transcript: ENSMUST00000093939
AA Change: M166I

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

SMART Domains

Protein: ENSMUSP00000091471
Gene: ENSMUSG00000070336
AA Change: M166I

Domain	Start	End	E-Value	Type
Pfam:F-box	43	80	2e-6	PFAM

Meta Mutation Damage Score

0.0655

Coding Region Coverage

1x: 98.7%
3x: 97.5%
10x: 93.3%
20x: 82.6%

Validation Efficiency

96% (67/70)

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4fm2	T	A	4: 144,291,635 (GRCm39)	I24L	probably benign	Het
Ano1	A	G	7: 144,187,426 (GRCm39)	W447R	possibly damaging	Het
Blm	T	A	7: 80,105,165 (GRCm39)	K103*	probably null	Het
Camta2	A	G	11: 70,567,230 (GRCm39)	I675T	probably benign	Het
Catsperz	G	A	19: 6,902,450 (GRCm39)	R15C	probably damaging	Het
Chd1l	T	C	3: 97,510,964 (GRCm39)		probably benign	Het
Corin	C	A	5: 72,462,276 (GRCm39)	E844D	possibly damaging	Het
Cyb5rl	T	G	4: 106,938,104 (GRCm39)	M127R	probably damaging	Het
Dcdc2a	A	T	13: 25,286,569 (GRCm39)	N164I	possibly damaging	Het
Dnah6	A	G	6: 73,185,528 (GRCm39)		probably null	Het
Emilin2	T	C	17: 71,562,960 (GRCm39)		probably benign	Het
Epb41l2	T	A	10: 25,319,800 (GRCm39)	V211D	probably damaging	Het
Golm1	T	C	13: 59,786,187 (GRCm39)	D335G	probably damaging	Het
Gpn1	T	A	5: 31,660,773 (GRCm39)	M188K	probably damaging	Het
Gpr84	T	A	15: 103,217,646 (GRCm39)	S144C	probably damaging	Het
Grm8	G	T	6: 27,981,200 (GRCm39)	Q237K	possibly damaging	Het
Gsdmd	C	A	15: 75,738,908 (GRCm39)		probably null	Het
Hmgcr	G	A	13: 96,795,528 (GRCm39)	T347I	probably damaging	Het
Hsd17b7	T	A	1: 169,788,774 (GRCm39)		probably benign	Het
Hsd3b9	G	A	3: 98,354,182 (GRCm39)	Q106*	probably null	Het
Klhl7	T	G	5: 24,364,489 (GRCm39)	W508G	probably damaging	Het
Lrp2	C	A	2: 69,258,948 (GRCm39)	D4581Y	probably damaging	Het
Lrrc7	T	C	3: 157,840,968 (GRCm39)	N1357D	probably benign	Het
Macf1	T	C	4: 123,380,451 (GRCm39)		probably benign	Het
Mroh7	T	C	4: 106,577,692 (GRCm39)	T329A	probably damaging	Het
Mroh9	C	T	1: 162,871,552 (GRCm39)		probably null	Het
Mta2	A	G	19: 8,926,550 (GRCm39)		probably benign	Het
Myo3a	A	T	2: 22,271,906 (GRCm39)		probably benign	Het
Nrip2	A	G	6: 128,384,352 (GRCm39)	D153G	probably benign	Het
Nup133	T	C	8: 124,644,156 (GRCm39)		probably benign	Het
Nup210	C	T	6: 91,019,329 (GRCm39)	V259M	possibly damaging	Het
Or10ak14	C	T	4: 118,610,816 (GRCm39)	M308I	probably benign	Het
Or5b112	A	T	19: 13,319,211 (GRCm39)	I30F	probably benign	Het
Or9i14	A	T	19: 13,792,726 (GRCm39)	V76D	probably damaging	Het
Otog	C	T	7: 45,939,113 (GRCm39)	R2048C	probably damaging	Het
Pacc1	T	C	1: 191,080,632 (GRCm39)	V284A	probably damaging	Het
Paqr7	T	C	4: 134,235,124 (GRCm39)	L327P	probably damaging	Het
Parl	A	G	16: 20,105,676 (GRCm39)	S249P	probably damaging	Het
Phc1	A	G	6: 122,302,833 (GRCm39)	I230T	probably benign	Het
Pitpnm1	T	G	19: 4,160,831 (GRCm39)		probably null	Het
Plpp1	A	G	13: 112,971,477 (GRCm39)	Y48C	probably damaging	Het
Pxdc1	A	G	13: 34,812,870 (GRCm39)	F194L	probably benign	Het
Rp1	A	T	1: 4,416,159 (GRCm39)	V1651D	possibly damaging	Het
Serpinb1c	T	A	13: 33,080,943 (GRCm39)	R47*	probably null	Het
Sis	T	C	3: 72,853,915 (GRCm39)	T521A	possibly damaging	Het
Slc16a9	A	G	10: 70,118,308 (GRCm39)	D209G	probably benign	Het
Slc26a4	A	T	12: 31,575,567 (GRCm39)	C706*	probably null	Het
Slc37a2	A	G	9: 37,148,177 (GRCm39)	V325A	probably benign	Het
Speg	T	A	1: 75,378,145 (GRCm39)	D784E	probably damaging	Het
Sycp1	T	C	3: 102,827,938 (GRCm39)	I270V	probably benign	Het
Tatdn2	T	A	6: 113,681,076 (GRCm39)	F309I	probably damaging	Het
Tmem67	T	C	4: 12,089,400 (GRCm39)		probably benign	Het
Trpm1	T	A	7: 63,852,801 (GRCm39)		probably null	Het
Wrn	T	C	8: 33,782,714 (GRCm39)	R496G	probably damaging	Het
Zfhx2	A	G	14: 55,300,854 (GRCm39)	V2299A	probably benign	Het
Zfp819	T	A	7: 43,266,524 (GRCm39)	S260T	possibly damaging	Het

Other mutations in Fbxo47

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00885:Fbxo47	APN	11	97,768,946 (GRCm39)	missense	probably benign	0.25
IGL01488:Fbxo47	APN	11	97,759,504 (GRCm39)	splice site	probably benign
IGL01924:Fbxo47	APN	11	97,746,986 (GRCm39)	missense	probably damaging	0.99
R0076:Fbxo47	UTSW	11	97,748,481 (GRCm39)	splice site	probably benign
R0076:Fbxo47	UTSW	11	97,748,481 (GRCm39)	splice site	probably benign
R0100:Fbxo47	UTSW	11	97,759,432 (GRCm39)	missense	probably damaging	1.00
R4688:Fbxo47	UTSW	11	97,747,049 (GRCm39)	missense	probably damaging	0.99
R4746:Fbxo47	UTSW	11	97,770,254 (GRCm39)	missense	probably benign	0.32
R5170:Fbxo47	UTSW	11	97,748,520 (GRCm39)	missense	probably benign	0.21
R6544:Fbxo47	UTSW	11	97,747,089 (GRCm39)	missense	probably damaging	1.00
R7467:Fbxo47	UTSW	11	97,755,993 (GRCm39)	missense	probably benign	0.02
R7513:Fbxo47	UTSW	11	97,747,055 (GRCm39)	missense	probably damaging	0.96
R8118:Fbxo47	UTSW	11	97,770,341 (GRCm39)	missense	probably benign
R9323:Fbxo47	UTSW	11	97,770,254 (GRCm39)	missense	probably benign	0.32
R9418:Fbxo47	UTSW	11	97,747,067 (GRCm39)	missense	possibly damaging	0.94

Predicted Primers

PCR Primer
(F):5'- TGGAGTCCTGAGGTGTGTGCTAAA -3'
(R):5'- aggtgaatctctgAAGCCTGTGTCA -3'

Sequencing Primer
(F):5'- aagacacaagagcagcaaatc -3'
(R):5'- gAAGCCTGTGTCAGGGGG -3'

Posted On

2014-02-18